[{"publication_status":"published","department":[{"_id":"MiLe"}],"publisher":"American Physical Society","year":"2017","date_updated":"2023-02-23T12:36:07Z","date_created":"2018-12-11T11:45:46Z","volume":999,"author":[{"full_name":"Camus, Nicolas","first_name":"Nicolas","last_name":"Camus"},{"last_name":"Yakaboylu","first_name":"Enderalp","orcid":"0000-0001-5973-0874","id":"38CB71F6-F248-11E8-B48F-1D18A9856A87","full_name":"Yakaboylu, Enderalp"},{"full_name":"Fechner, Lutz","first_name":"Lutz","last_name":"Fechner"},{"first_name":"Michael","last_name":"Klaiber","full_name":"Klaiber, Michael"},{"full_name":"Laux, Martin","last_name":"Laux","first_name":"Martin"},{"full_name":"Mi, Yonghao","last_name":"Mi","first_name":"Yonghao"},{"full_name":"Hatsagortsyan, Karen","first_name":"Karen","last_name":"Hatsagortsyan"},{"full_name":"Pfeifer, Thomas","first_name":"Thomas","last_name":"Pfeifer"},{"last_name":"Keitel","first_name":"Cristoph","full_name":"Keitel, Cristoph"},{"full_name":"Moshammer, Robert","last_name":"Moshammer","first_name":"Robert"}],"related_material":{"record":[{"status":"public","relation":"later_version","id":"6013"}]},"article_number":"012004","license":"https://creativecommons.org/licenses/by/4.0/","file_date_updated":"2020-07-14T12:46:00Z","publist_id":"7552","quality_controlled":"1","external_id":{"arxiv":["1611.03701"]},"tmp":{"name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","short":"CC BY (4.0)","image":"/images/cc_by.png"},"oa":1,"language":[{"iso":"eng"}],"conference":{"name":"Annual International Laser Physics Workshop LPHYS","start_date":"2017-08-17","location":"Kazan, Russian Federation","end_date":"2017-08-21"},"doi":"10.1088/1742-6596/999/1/012004","month":"07","publication_identifier":{"issn":["17426588"]},"status":"public","ddc":["530"],"title":"Experimental evidence for Wigner's tunneling time","intvolume":" 999","_id":"313","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","oa_version":"Published Version","file":[{"checksum":"6e70b525a84f6d5fb175c48e9f5cb59a","date_updated":"2020-07-14T12:46:00Z","date_created":"2019-01-22T08:34:10Z","relation":"main_file","file_id":"5871","file_size":949321,"content_type":"application/pdf","creator":"dernst","access_level":"open_access","file_name":"2017_Physics_Camus.pdf"}],"alternative_title":["Journal of Physics: Conference Series"],"type":"conference","abstract":[{"text":"Tunneling of a particle through a potential barrier remains one of the most remarkable quantum phenomena. Owing to advances in laser technology, electric fields comparable to those electrons experience in atoms are readily generated and open opportunities to dynamically investigate the process of electron tunneling through the potential barrier formed by the superposition of both laser and atomic fields. Attosecond-time and angstrom-space resolution of the strong laser-field technique allow to address fundamental questions related to tunneling, which are still open and debated: Which time is spent under the barrier and what momentum is picked up by the particle in the meantime? In this combined experimental and theoretical study we demonstrate that for strong-field ionization the leading quantum mechanical Wigner treatment for the time resolved description of tunneling is valid. We achieve a high sensitivity on the tunneling barrier and unambiguously isolate its effects by performing a differential study of two systems with almost identical tunneling geometry. Moreover, working with a low frequency laser, we essentially limit the non-adiabaticity of the process as a major source of uncertainty. The agreement between experiment and theory implies two substantial corrections with respect to the widely employed quasiclassical treatment: In addition to a non-vanishing longitudinal momentum along the laser field-direction we provide clear evidence for a non-zero tunneling time delay. This addresses also the fundamental question how the transition occurs from the tunnel barrier to free space classical evolution of the ejected electron.","lang":"eng"}],"issue":"1","citation":{"ieee":"N. Camus et al., “Experimental evidence for Wigner’s tunneling time,” presented at the Annual International Laser Physics Workshop LPHYS, Kazan, Russian Federation, 2017, vol. 999, no. 1.","apa":"Camus, N., Yakaboylu, E., Fechner, L., Klaiber, M., Laux, M., Mi, Y., … Moshammer, R. (2017). Experimental evidence for Wigner’s tunneling time (Vol. 999). Presented at the Annual International Laser Physics Workshop LPHYS, Kazan, Russian Federation: American Physical Society. https://doi.org/10.1088/1742-6596/999/1/012004","ista":"Camus N, Yakaboylu E, Fechner L, Klaiber M, Laux M, Mi Y, Hatsagortsyan K, Pfeifer T, Keitel C, Moshammer R. 2017. Experimental evidence for Wigner’s tunneling time. Annual International Laser Physics Workshop LPHYS, Journal of Physics: Conference Series, vol. 999, 012004.","ama":"Camus N, Yakaboylu E, Fechner L, et al. Experimental evidence for Wigner’s tunneling time. In: Vol 999. American Physical Society; 2017. doi:10.1088/1742-6596/999/1/012004","chicago":"Camus, Nicolas, Enderalp Yakaboylu, Lutz Fechner, Michael Klaiber, Martin Laux, Yonghao Mi, Karen Hatsagortsyan, Thomas Pfeifer, Cristoph Keitel, and Robert Moshammer. “Experimental Evidence for Wigner’s Tunneling Time,” Vol. 999. American Physical Society, 2017. https://doi.org/10.1088/1742-6596/999/1/012004.","short":"N. Camus, E. Yakaboylu, L. Fechner, M. Klaiber, M. Laux, Y. Mi, K. Hatsagortsyan, T. Pfeifer, C. Keitel, R. Moshammer, in:, American Physical Society, 2017.","mla":"Camus, Nicolas, et al. Experimental Evidence for Wigner’s Tunneling Time. Vol. 999, no. 1, 012004, American Physical Society, 2017, doi:10.1088/1742-6596/999/1/012004."},"date_published":"2017-07-14T00:00:00Z","scopus_import":1,"day":"14","has_accepted_license":"1"},{"citation":{"ista":"Xu Y, Bernecky C, Lee C, Maier K, Schwalb B, Tegunov D, Plitzko J, Urlaub H, Cramer P. 2017. Architecture of the RNA polymerase II-Paf1C-TFIIS transcription elongation complex. Nature Communications. 8, 15741.","apa":"Xu, Y., Bernecky, C., Lee, C., Maier, K., Schwalb, B., Tegunov, D., … Cramer, P. (2017). Architecture of the RNA polymerase II-Paf1C-TFIIS transcription elongation complex. Nature Communications. Nature Publishing Group. https://doi.org/10.1038/ncomms15741","ieee":"Y. Xu et al., “Architecture of the RNA polymerase II-Paf1C-TFIIS transcription elongation complex,” Nature Communications, vol. 8. Nature Publishing Group, 2017.","ama":"Xu Y, Bernecky C, Lee C, et al. Architecture of the RNA polymerase II-Paf1C-TFIIS transcription elongation complex. Nature Communications. 2017;8. doi:10.1038/ncomms15741","chicago":"Xu, Youwei, Carrie Bernecky, Chung Lee, Kerstin Maier, Björn Schwalb, Dimitri Tegunov, Jürgen Plitzko, Henning Urlaub, and Patrick Cramer. “Architecture of the RNA Polymerase II-Paf1C-TFIIS Transcription Elongation Complex.” Nature Communications. Nature Publishing Group, 2017. https://doi.org/10.1038/ncomms15741.","mla":"Xu, Youwei, et al. “Architecture of the RNA Polymerase II-Paf1C-TFIIS Transcription Elongation Complex.” Nature Communications, vol. 8, 15741, Nature Publishing Group, 2017, doi:10.1038/ncomms15741.","short":"Y. Xu, C. Bernecky, C. Lee, K. Maier, B. Schwalb, D. Tegunov, J. Plitzko, H. Urlaub, P. Cramer, Nature Communications 8 (2017)."},"publication":"Nature Communications","date_published":"2017-06-06T00:00:00Z","article_processing_charge":"No","has_accepted_license":"1","day":"06","_id":"601","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","intvolume":" 8","ddc":["570"],"title":"Architecture of the RNA polymerase II-Paf1C-TFIIS transcription elongation complex","status":"public","oa_version":"Published Version","file":[{"file_size":3018075,"content_type":"application/pdf","creator":"dernst","access_level":"open_access","file_name":"2017_NatureComm_Xu.pdf","checksum":"940742282a9a285dc4aeae0c2b5ebe96","date_created":"2019-01-21T14:48:10Z","date_updated":"2020-07-14T12:47:16Z","relation":"main_file","file_id":"5865"}],"type":"journal_article","abstract":[{"lang":"eng","text":"The conserved polymerase-Associated factor 1 complex (Paf1C) plays multiple roles in chromatin transcription and genomic regulation. Paf1C comprises the five subunits Paf1, Leo1, Ctr9, Cdc73 and Rtf1, and binds to the RNA polymerase II (Pol II) transcription elongation complex (EC). Here we report the reconstitution of Paf1C from Saccharomyces cerevisiae, and a structural analysis of Paf1C bound to a Pol II EC containing the elongation factor TFIIS. Cryo-electron microscopy and crosslinking data reveal that Paf1C is highly mobile and extends over the outer Pol II surface from the Rpb2 to the Rpb3 subunit. The Paf1-Leo1 heterodimer and Cdc73 form opposite ends of Paf1C, whereas Ctr9 bridges between them. Consistent with the structural observations, the initiation factor TFIIF impairs Paf1C binding to Pol II, whereas the elongation factor TFIIS enhances it. We further show that Paf1C is globally required for normal mRNA transcription in yeast. These results provide a three-dimensional framework for further analysis of Paf1C function in transcription through chromatin. "}],"tmp":{"name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","short":"CC BY (4.0)","image":"/images/cc_by.png"},"oa":1,"quality_controlled":"1","doi":"10.1038/ncomms15741","language":[{"iso":"eng"}],"publication_identifier":{"issn":["20411723"]},"month":"06","year":"2017","publisher":"Nature Publishing Group","publication_status":"published","author":[{"full_name":"Xu, Youwei","first_name":"Youwei","last_name":"Xu"},{"full_name":"Bernecky, Carrie A","last_name":"Bernecky","first_name":"Carrie A","orcid":"0000-0003-0893-7036","id":"2CB9DFE2-F248-11E8-B48F-1D18A9856A87"},{"full_name":"Lee, Chung","first_name":"Chung","last_name":"Lee"},{"last_name":"Maier","first_name":"Kerstin","full_name":"Maier, Kerstin"},{"full_name":"Schwalb, Björn","first_name":"Björn","last_name":"Schwalb"},{"last_name":"Tegunov","first_name":"Dimitri","full_name":"Tegunov, Dimitri"},{"last_name":"Plitzko","first_name":"Jürgen","full_name":"Plitzko, Jürgen"},{"full_name":"Urlaub, Henning","last_name":"Urlaub","first_name":"Henning"},{"first_name":"Patrick","last_name":"Cramer","full_name":"Cramer, Patrick"}],"volume":8,"date_created":"2018-12-11T11:47:25Z","date_updated":"2021-01-12T08:05:40Z","article_number":"15741","publist_id":"7203","file_date_updated":"2020-07-14T12:47:16Z","extern":"1"},{"oa":1,"main_file_link":[{"open_access":"1","url":"https://arxiv.org/abs/1611.03701"}],"external_id":{"arxiv":["1611.03701"]},"quality_controlled":"1","doi":"10.1103/PhysRevLett.119.023201","language":[{"iso":"eng"}],"month":"07","publication_identifier":{"eissn":["1079-7114"],"issn":["0031-9007"]},"year":"2017","publication_status":"published","department":[{"_id":"MiLe"}],"publisher":"American Physical Society","author":[{"first_name":"Nicolas","last_name":"Camus","full_name":"Camus, Nicolas"},{"full_name":"Yakaboylu, Enderalp","id":"38CB71F6-F248-11E8-B48F-1D18A9856A87","orcid":"0000-0001-5973-0874","first_name":"Enderalp","last_name":"Yakaboylu"},{"first_name":"Lutz","last_name":"Fechner","full_name":"Fechner, Lutz"},{"last_name":"Klaiber","first_name":"Michael","full_name":"Klaiber, Michael"},{"last_name":"Laux","first_name":"Martin","full_name":"Laux, Martin"},{"full_name":"Mi, Yonghao","first_name":"Yonghao","last_name":"Mi"},{"last_name":"Hatsagortsyan","first_name":"Karen Z.","full_name":"Hatsagortsyan, Karen Z."},{"full_name":"Pfeifer, Thomas","last_name":"Pfeifer","first_name":"Thomas"},{"full_name":"Keitel, Christoph H.","last_name":"Keitel","first_name":"Christoph H."},{"full_name":"Moshammer, Robert","first_name":"Robert","last_name":"Moshammer"}],"related_material":{"record":[{"id":"313","relation":"earlier_version","status":"public"}]},"date_created":"2019-02-14T15:24:13Z","date_updated":"2023-02-23T11:13:36Z","volume":119,"article_number":"023201","publication":"Physical Review Letters","citation":{"ieee":"N. Camus et al., “Experimental evidence for quantum tunneling time,” Physical Review Letters, vol. 119, no. 2. American Physical Society, 2017.","apa":"Camus, N., Yakaboylu, E., Fechner, L., Klaiber, M., Laux, M., Mi, Y., … Moshammer, R. (2017). Experimental evidence for quantum tunneling time. Physical Review Letters. American Physical Society. https://doi.org/10.1103/PhysRevLett.119.023201","ista":"Camus N, Yakaboylu E, Fechner L, Klaiber M, Laux M, Mi Y, Hatsagortsyan KZ, Pfeifer T, Keitel CH, Moshammer R. 2017. Experimental evidence for quantum tunneling time. Physical Review Letters. 119(2), 023201.","ama":"Camus N, Yakaboylu E, Fechner L, et al. Experimental evidence for quantum tunneling time. Physical Review Letters. 2017;119(2). doi:10.1103/PhysRevLett.119.023201","chicago":"Camus, Nicolas, Enderalp Yakaboylu, Lutz Fechner, Michael Klaiber, Martin Laux, Yonghao Mi, Karen Z. Hatsagortsyan, Thomas Pfeifer, Christoph H. Keitel, and Robert Moshammer. “Experimental Evidence for Quantum Tunneling Time.” Physical Review Letters. American Physical Society, 2017. https://doi.org/10.1103/PhysRevLett.119.023201.","short":"N. Camus, E. Yakaboylu, L. Fechner, M. Klaiber, M. Laux, Y. Mi, K.Z. Hatsagortsyan, T. Pfeifer, C.H. Keitel, R. Moshammer, Physical Review Letters 119 (2017).","mla":"Camus, Nicolas, et al. “Experimental Evidence for Quantum Tunneling Time.” Physical Review Letters, vol. 119, no. 2, 023201, American Physical Society, 2017, doi:10.1103/PhysRevLett.119.023201."},"date_published":"2017-07-14T00:00:00Z","scopus_import":1,"day":"14","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","_id":"6013","title":"Experimental evidence for quantum tunneling time","status":"public","intvolume":" 119","oa_version":"Preprint","type":"journal_article","abstract":[{"lang":"eng","text":"The first hundred attoseconds of the electron dynamics during strong field tunneling ionization are investigated. We quantify theoretically how the electron’s classical trajectories in the continuum emerge from the tunneling process and test the results with those achieved in parallel from attoclock measurements. An especially high sensitivity on the tunneling barrier is accomplished here by comparing the momentum distributions of two atomic species of slightly deviating atomic potentials (argon and krypton) being ionized under absolutely identical conditions with near-infrared laser pulses (1300 nm). The agreement between experiment and theory provides clear evidence for a nonzero tunneling time delay and a nonvanishing longitudinal momentum of the electron at the “tunnel exit.”"}],"issue":"2"},{"language":[{"iso":"eng"}],"date_published":"2017-10-05T00:00:00Z","doi":"10.1038/nsmb.3465","quality_controlled":"1","page":"809 - 815","publication":"Nature Structural and Molecular Biology","citation":{"short":"C. Bernecky, J. Plitzko, P. Cramer, Nature Structural and Molecular Biology 24 (2017) 809–815.","mla":"Bernecky, Carrie, et al. “Structure of a Transcribing RNA Polymerase II-DSIF Complex Reveals a Multidentate DNA-RNA Clamp.” Nature Structural and Molecular Biology, vol. 24, no. 10, Nature Publishing Group, 2017, pp. 809–15, doi:10.1038/nsmb.3465.","chicago":"Bernecky, Carrie, Jürgen Plitzko, and Patrick Cramer. “Structure of a Transcribing RNA Polymerase II-DSIF Complex Reveals a Multidentate DNA-RNA Clamp.” Nature Structural and Molecular Biology. Nature Publishing Group, 2017. https://doi.org/10.1038/nsmb.3465.","ama":"Bernecky C, Plitzko J, Cramer P. Structure of a transcribing RNA polymerase II-DSIF complex reveals a multidentate DNA-RNA clamp. Nature Structural and Molecular Biology. 2017;24(10):809-815. doi:10.1038/nsmb.3465","ieee":"C. Bernecky, J. Plitzko, and P. Cramer, “Structure of a transcribing RNA polymerase II-DSIF complex reveals a multidentate DNA-RNA clamp,” Nature Structural and Molecular Biology, vol. 24, no. 10. Nature Publishing Group, pp. 809–815, 2017.","apa":"Bernecky, C., Plitzko, J., & Cramer, P. (2017). Structure of a transcribing RNA polymerase II-DSIF complex reveals a multidentate DNA-RNA clamp. Nature Structural and Molecular Biology. Nature Publishing Group. https://doi.org/10.1038/nsmb.3465","ista":"Bernecky C, Plitzko J, Cramer P. 2017. Structure of a transcribing RNA polymerase II-DSIF complex reveals a multidentate DNA-RNA clamp. Nature Structural and Molecular Biology. 24(10), 809–815."},"month":"10","day":"05","publication_identifier":{"issn":["15459993"]},"article_processing_charge":"No","date_created":"2018-12-11T11:47:26Z","date_updated":"2021-01-12T08:05:47Z","volume":24,"oa_version":"None","author":[{"full_name":"Bernecky, Carrie A","orcid":"0000-0003-0893-7036","id":"2CB9DFE2-F248-11E8-B48F-1D18A9856A87","last_name":"Bernecky","first_name":"Carrie A"},{"full_name":"Plitzko, Jürgen","last_name":"Plitzko","first_name":"Jürgen"},{"last_name":"Cramer","first_name":"Patrick","full_name":"Cramer, Patrick"}],"publication_status":"published","title":"Structure of a transcribing RNA polymerase II-DSIF complex reveals a multidentate DNA-RNA clamp","status":"public","publisher":"Nature Publishing Group","intvolume":" 24","year":"2017","_id":"603","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","extern":"1","abstract":[{"lang":"eng","text":"During transcription, RNA polymerase II (Pol II) associates with the conserved elongation factor DSIF. DSIF renders the elongation complex stable and functions during Pol II pausing and RNA processing. We combined cryo-EM and X-ray crystallography to determine the structure of the mammalian Pol II-DSIF elongation complex at a nominal resolution of 3.4. Human DSIF has a modular structure with two domains forming a DNA clamp, two domains forming an RNA clamp, and one domain buttressing the RNA clamp. The clamps maintain the transcription bubble, position upstream DNA, and retain the RNA transcript in the exit tunnel. The mobile C-terminal region of DSIF is located near exiting RNA, where it can recruit factors for RNA processing. The structure provides insight into the roles of DSIF during mRNA synthesis."}],"publist_id":"7202","issue":"10","type":"journal_article"},{"_id":"605","user_id":"3E5EF7F0-F248-11E8-B48F-1D18A9856A87","intvolume":" 10677","title":"Position based cryptography and multiparty communication complexity","status":"public","oa_version":"Submitted Version","type":"conference","alternative_title":["LNCS"],"abstract":[{"lang":"eng","text":"Position based cryptography (PBC), proposed in the seminal work of Chandran, Goyal, Moriarty, and Ostrovsky (SIAM J. Computing, 2014), aims at constructing cryptographic schemes in which the identity of the user is his geographic position. Chandran et al. construct PBC schemes for secure positioning and position-based key agreement in the bounded-storage model (Maurer, J. Cryptology, 1992). Apart from bounded memory, their security proofs need a strong additional restriction on the power of the adversary: he cannot compute joint functions of his inputs. Removing this assumption is left as an open problem. We show that an answer to this question would resolve a long standing open problem in multiparty communication complexity: finding a function that is hard to compute with low communication complexity in the simultaneous message model, but easy to compute in the fully adaptive model. On a more positive side: we also show some implications in the other direction, i.e.: we prove that lower bounds on the communication complexity of certain multiparty problems imply existence of PBC primitives. Using this result we then show two attractive ways to “bypass” our hardness result: the first uses the random oracle model, the second weakens the locality requirement in the bounded-storage model to online computability. The random oracle construction is arguably one of the simplest proposed so far in this area. Our results indicate that constructing improved provably secure protocols for PBC requires a better understanding of multiparty communication complexity. This is yet another example where negative results in one area (in our case: lower bounds in multiparty communication complexity) can be used to construct secure cryptographic schemes."}],"citation":{"short":"J. Brody, S. Dziembowski, S. Faust, K.Z. Pietrzak, in:, Y. Kalai, L. Reyzin (Eds.), Springer, 2017, pp. 56–81.","mla":"Brody, Joshua, et al. Position Based Cryptography and Multiparty Communication Complexity. Edited by Yael Kalai and Leonid Reyzin, vol. 10677, Springer, 2017, pp. 56–81, doi:10.1007/978-3-319-70500-2_3.","chicago":"Brody, Joshua, Stefan Dziembowski, Sebastian Faust, and Krzysztof Z Pietrzak. “Position Based Cryptography and Multiparty Communication Complexity.” edited by Yael Kalai and Leonid Reyzin, 10677:56–81. Springer, 2017. https://doi.org/10.1007/978-3-319-70500-2_3.","ama":"Brody J, Dziembowski S, Faust S, Pietrzak KZ. Position based cryptography and multiparty communication complexity. In: Kalai Y, Reyzin L, eds. Vol 10677. Springer; 2017:56-81. doi:10.1007/978-3-319-70500-2_3","ieee":"J. Brody, S. Dziembowski, S. Faust, and K. Z. Pietrzak, “Position based cryptography and multiparty communication complexity,” presented at the TCC: Theory of Cryptography Conference, Baltimore, MD, United States, 2017, vol. 10677, pp. 56–81.","apa":"Brody, J., Dziembowski, S., Faust, S., & Pietrzak, K. Z. (2017). Position based cryptography and multiparty communication complexity. In Y. Kalai & L. Reyzin (Eds.) (Vol. 10677, pp. 56–81). Presented at the TCC: Theory of Cryptography Conference, Baltimore, MD, United States: Springer. https://doi.org/10.1007/978-3-319-70500-2_3","ista":"Brody J, Dziembowski S, Faust S, Pietrzak KZ. 2017. Position based cryptography and multiparty communication complexity. TCC: Theory of Cryptography Conference, LNCS, vol. 10677, 56–81."},"page":"56 - 81","date_published":"2017-11-05T00:00:00Z","scopus_import":1,"day":"05","year":"2017","editor":[{"first_name":"Yael","last_name":"Kalai","full_name":"Kalai, Yael"},{"first_name":"Leonid","last_name":"Reyzin","full_name":"Reyzin, Leonid"}],"publisher":"Springer","department":[{"_id":"KrPi"}],"publication_status":"published","author":[{"last_name":"Brody","first_name":"Joshua","full_name":"Brody, Joshua"},{"full_name":"Dziembowski, Stefan","last_name":"Dziembowski","first_name":"Stefan"},{"full_name":"Faust, Sebastian","first_name":"Sebastian","last_name":"Faust"},{"first_name":"Krzysztof Z","last_name":"Pietrzak","id":"3E04A7AA-F248-11E8-B48F-1D18A9856A87","orcid":"0000-0002-9139-1654","full_name":"Pietrzak, Krzysztof Z"}],"volume":10677,"date_created":"2018-12-11T11:47:27Z","date_updated":"2021-01-12T08:05:53Z","publist_id":"7200","ec_funded":1,"main_file_link":[{"url":"https://eprint.iacr.org/2016/536","open_access":"1"}],"oa":1,"project":[{"_id":"258AA5B2-B435-11E9-9278-68D0E5697425","grant_number":"682815","name":"Teaching Old Crypto New Tricks","call_identifier":"H2020"}],"quality_controlled":"1","doi":"10.1007/978-3-319-70500-2_3","conference":{"name":"TCC: Theory of Cryptography Conference","end_date":"2017-11-15","location":"Baltimore, MD, United States","start_date":"2017-11-12"},"language":[{"iso":"eng"}],"publication_identifier":{"isbn":["978-331970499-9"]},"month":"11"},{"oa_version":"Submitted Version","status":"public","title":"Molecular impurities interacting with a many-particle environment: From ultracold gases to helium nanodroplets","intvolume":" 11","user_id":"4435EBFC-F248-11E8-B48F-1D18A9856A87","_id":"604","abstract":[{"lang":"eng","text":"In several settings of physics and chemistry one has to deal with molecules interacting with some kind of an external environment, be it a gas, a solution, or a crystal surface. Understanding molecular processes in the presence of such a many-particle bath is inherently challenging, and usually requires large-scale numerical computations. Here, we present an alternative approach to the problem, based on the notion of the angulon quasiparticle. We show that molecules rotating inside superfluid helium nanodroplets and Bose–Einstein condensates form angulons, and therefore can be described by straightforward solutions of a simple microscopic Hamiltonian. Casting the problem in the language of angulons allows us not only to greatly simplify it, but also to gain insights into the origins of the observed phenomena and to make predictions for future experimental studies."}],"alternative_title":["Theoretical and Computational Chemistry Series"],"type":"book_chapter","date_published":"2017-12-14T00:00:00Z","page":"444 - 495","publication":"Cold Chemistry: Molecular Scattering and Reactivity Near Absolute Zero ","citation":{"short":"M. Lemeshko, R. Schmidt, in:, O. Dulieu, A. Osterwalder (Eds.), Cold Chemistry: Molecular Scattering and Reactivity Near Absolute Zero , The Royal Society of Chemistry, 2017, pp. 444–495.","mla":"Lemeshko, Mikhail, and Richard Schmidt. “Molecular Impurities Interacting with a Many-Particle Environment: From Ultracold Gases to Helium Nanodroplets.” Cold Chemistry: Molecular Scattering and Reactivity Near Absolute Zero , edited by Oliver Dulieu and Andreas Osterwalder, vol. 11, The Royal Society of Chemistry, 2017, pp. 444–95, doi:10.1039/9781782626800-00444.","chicago":"Lemeshko, Mikhail, and Richard Schmidt. “Molecular Impurities Interacting with a Many-Particle Environment: From Ultracold Gases to Helium Nanodroplets.” In Cold Chemistry: Molecular Scattering and Reactivity Near Absolute Zero , edited by Oliver Dulieu and Andreas Osterwalder, 11:444–95. Theoretical and Computational Chemistry Series. The Royal Society of Chemistry, 2017. https://doi.org/10.1039/9781782626800-00444.","ama":"Lemeshko M, Schmidt R. Molecular impurities interacting with a many-particle environment: From ultracold gases to helium nanodroplets. In: Dulieu O, Osterwalder A, eds. Cold Chemistry: Molecular Scattering and Reactivity Near Absolute Zero . Vol 11. Theoretical and Computational Chemistry Series. The Royal Society of Chemistry; 2017:444-495. doi:10.1039/9781782626800-00444","apa":"Lemeshko, M., & Schmidt, R. (2017). Molecular impurities interacting with a many-particle environment: From ultracold gases to helium nanodroplets. In O. Dulieu & A. Osterwalder (Eds.), Cold Chemistry: Molecular Scattering and Reactivity Near Absolute Zero (Vol. 11, pp. 444–495). The Royal Society of Chemistry. https://doi.org/10.1039/9781782626800-00444","ieee":"M. Lemeshko and R. Schmidt, “Molecular impurities interacting with a many-particle environment: From ultracold gases to helium nanodroplets,” in Cold Chemistry: Molecular Scattering and Reactivity Near Absolute Zero , vol. 11, O. Dulieu and A. Osterwalder, Eds. The Royal Society of Chemistry, 2017, pp. 444–495.","ista":"Lemeshko M, Schmidt R. 2017.Molecular impurities interacting with a many-particle environment: From ultracold gases to helium nanodroplets. In: Cold Chemistry: Molecular Scattering and Reactivity Near Absolute Zero . Theoretical and Computational Chemistry Series, vol. 11, 444–495."},"day":"14","series_title":"Theoretical and Computational Chemistry Series","scopus_import":1,"date_created":"2018-12-11T11:47:27Z","date_updated":"2021-01-12T08:05:50Z","volume":11,"author":[{"full_name":"Lemeshko, Mikhail","last_name":"Lemeshko","first_name":"Mikhail","orcid":"0000-0002-6990-7802","id":"37CB05FA-F248-11E8-B48F-1D18A9856A87"},{"full_name":"Schmidt, Richard","last_name":"Schmidt","first_name":"Richard"}],"publication_status":"published","editor":[{"full_name":"Dulieu, Oliver","last_name":"Dulieu","first_name":"Oliver"},{"full_name":"Osterwalder, Andreas","last_name":"Osterwalder","first_name":"Andreas"}],"department":[{"_id":"MiLe"}],"publisher":"The Royal Society of Chemistry","year":"2017","publist_id":"7201","language":[{"iso":"eng"}],"doi":"10.1039/9781782626800-00444","quality_controlled":"1","main_file_link":[{"url":"https://arxiv.org/abs/1703.06753","open_access":"1"}],"oa":1,"month":"12","publication_identifier":{"issn":["20413181"]}},{"date_created":"2019-02-26T13:45:17Z","date_updated":"2021-01-12T08:05:57Z","volume":112,"oa_version":"None","author":[{"last_name":"Balta","first_name":"Emre","full_name":"Balta, Emre"},{"full_name":"Stopp, Julian A","id":"489E3F00-F248-11E8-B48F-1D18A9856A87","last_name":"Stopp","first_name":"Julian A"},{"full_name":"Castelletti, Laura","first_name":"Laura","last_name":"Castelletti"},{"last_name":"Kirchgessner","first_name":"Henning","full_name":"Kirchgessner, Henning"},{"full_name":"Samstag, Yvonne","last_name":"Samstag","first_name":"Yvonne"},{"full_name":"Wabnitz, Guido H.","first_name":"Guido H.","last_name":"Wabnitz"}],"related_material":{"link":[{"url":"http://dx.doi.org/10.1016/j.ymeth.2016.09.013","relation":"supplementary_material"}]},"status":"public","publication_status":"published","title":"Qualitative and quantitative analysis of PMN/T-cell interactions by InFlow and super-resolution microscopy","intvolume":" 112","publisher":"Elsevier","_id":"6059","year":"2017","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","pmid":1,"extern":"1","abstract":[{"text":"Neutrophils or polymorphonuclear cells (PMN) eliminate bacteria via phagocytosis and/or NETosis. Apartfrom these conventional roles, PMN also have immune-regulatory functions. They can transdifferentiateand upregulate MHCII as well as ligands for costimulatory receptors which enables them to behave asantigen presenting cells (APC). The initial step for activating T-cells is the formation of an immunesynapse between T-cells and antigen-presenting cells. However, the immune synapse that develops atthe PMN/T-cell contact zone is as yet hardly investigated due to the non-availability of methods foranalysis of large number of PMN interactions. In order to overcome these obstacles, we introduce herea workflow to analyse the immune synapse of primary human PMN and T-cells using multispectral imag-ing flow cytometry (InFlow microscopy) and super-resolution microscopy. For that purpose, we used CD3and CD66b as the lineage markers for T-cells and PMN, respectively. Thereafter, we applied and criticallydiscussed various ‘‘masks” for identification of T-cell PMN interactions. Using this approach, we foundthat a small fraction of transdifferentiated PMN (CD66b+CD86high) formed stable PMN/T-cell conjugates.Interestingly, while both CD3 and CD66b accumulation in the immune synapse was dependent on thematuration state of the PMN, only CD3 accumulation was greatly enhanced by the presence of superanti-gen. The actin cytoskeleton was weakly rearranged at the PMN side on the immune synapse upon contactwith a T-cell in the presence of superantigen. A more detailed analysis using super-resolution microscopy(structured-illumination microscopy, SIM) confirmed this finding. Together, we present an InFlow micro-scopy based approach for the large scale analysis of PMN/T-cell interactions and – combined with SIM – apossibility for an in-depth analysis of protein translocation at the site of interactions.","lang":"eng"}],"issue":"1","type":"journal_article","language":[{"iso":"eng"}],"doi":"10.1016/j.ymeth.2016.09.013","date_published":"2017-01-01T00:00:00Z","quality_controlled":"1","page":"25-38","publication":"Methods","citation":{"ama":"Balta E, Stopp JA, Castelletti L, Kirchgessner H, Samstag Y, Wabnitz GH. Qualitative and quantitative analysis of PMN/T-cell interactions by InFlow and super-resolution microscopy. Methods. 2017;112(1):25-38. doi:10.1016/j.ymeth.2016.09.013","apa":"Balta, E., Stopp, J. A., Castelletti, L., Kirchgessner, H., Samstag, Y., & Wabnitz, G. H. (2017). Qualitative and quantitative analysis of PMN/T-cell interactions by InFlow and super-resolution microscopy. Methods. Elsevier. https://doi.org/10.1016/j.ymeth.2016.09.013","ieee":"E. Balta, J. A. Stopp, L. Castelletti, H. Kirchgessner, Y. Samstag, and G. H. Wabnitz, “Qualitative and quantitative analysis of PMN/T-cell interactions by InFlow and super-resolution microscopy,” Methods, vol. 112, no. 1. Elsevier, pp. 25–38, 2017.","ista":"Balta E, Stopp JA, Castelletti L, Kirchgessner H, Samstag Y, Wabnitz GH. 2017. Qualitative and quantitative analysis of PMN/T-cell interactions by InFlow and super-resolution microscopy. Methods. 112(1), 25–38.","short":"E. Balta, J.A. Stopp, L. Castelletti, H. Kirchgessner, Y. Samstag, G.H. Wabnitz, Methods 112 (2017) 25–38.","mla":"Balta, Emre, et al. “Qualitative and Quantitative Analysis of PMN/T-Cell Interactions by InFlow and Super-Resolution Microscopy.” Methods, vol. 112, no. 1, Elsevier, 2017, pp. 25–38, doi:10.1016/j.ymeth.2016.09.013.","chicago":"Balta, Emre, Julian A Stopp, Laura Castelletti, Henning Kirchgessner, Yvonne Samstag, and Guido H. Wabnitz. “Qualitative and Quantitative Analysis of PMN/T-Cell Interactions by InFlow and Super-Resolution Microscopy.” Methods. Elsevier, 2017. https://doi.org/10.1016/j.ymeth.2016.09.013."},"external_id":{"pmid":["27693880"]},"month":"01","day":"01","publication_identifier":{"issn":["1046-2023"]}},{"_id":"609","user_id":"3E5EF7F0-F248-11E8-B48F-1D18A9856A87","intvolume":" 10677","status":"public","title":"Moderately hard functions: Definition, instantiations, and applications","oa_version":"Submitted Version","type":"conference","alternative_title":["LNCS"],"abstract":[{"lang":"eng","text":"Several cryptographic schemes and applications are based on functions that are both reasonably efficient to compute and moderately hard to invert, including client puzzles for Denial-of-Service protection, password protection via salted hashes, or recent proof-of-work blockchain systems. Despite their wide use, a definition of this concept has not yet been distilled and formalized explicitly. Instead, either the applications are proven directly based on the assumptions underlying the function, or some property of the function is proven, but the security of the application is argued only informally. The goal of this work is to provide a (universal) definition that decouples the efforts of designing new moderately hard functions and of building protocols based on them, serving as an interface between the two. On a technical level, beyond the mentioned definitions, we instantiate the model for four different notions of hardness. We extend the work of Alwen and Serbinenko (STOC 2015) by providing a general tool for proving security for the first notion of memory-hard functions that allows for provably secure applications. The tool allows us to recover all of the graph-theoretic techniques developed for proving security under the older, non-composable, notion of security used by Alwen and Serbinenko. As an application of our definition of moderately hard functions, we prove the security of two different schemes for proofs of effort (PoE). We also formalize and instantiate the concept of a non-interactive proof of effort (niPoE), in which the proof is not bound to a particular communication context but rather any bit-string chosen by the prover."}],"citation":{"ista":"Alwen JF, Tackmann B. 2017. Moderately hard functions: Definition, instantiations, and applications. TCC: Theory of Cryptography, LNCS, vol. 10677, 493–526.","apa":"Alwen, J. F., & Tackmann, B. (2017). Moderately hard functions: Definition, instantiations, and applications. In Y. Kalai & L. Reyzin (Eds.) (Vol. 10677, pp. 493–526). Presented at the TCC: Theory of Cryptography, Baltimore, MD, United States: Springer. https://doi.org/10.1007/978-3-319-70500-2_17","ieee":"J. F. Alwen and B. Tackmann, “Moderately hard functions: Definition, instantiations, and applications,” presented at the TCC: Theory of Cryptography, Baltimore, MD, United States, 2017, vol. 10677, pp. 493–526.","ama":"Alwen JF, Tackmann B. Moderately hard functions: Definition, instantiations, and applications. In: Kalai Y, Reyzin L, eds. Vol 10677. Springer; 2017:493-526. doi:10.1007/978-3-319-70500-2_17","chicago":"Alwen, Joel F, and Björn Tackmann. “Moderately Hard Functions: Definition, Instantiations, and Applications.” edited by Yael Kalai and Leonid Reyzin, 10677:493–526. Springer, 2017. https://doi.org/10.1007/978-3-319-70500-2_17.","mla":"Alwen, Joel F., and Björn Tackmann. Moderately Hard Functions: Definition, Instantiations, and Applications. Edited by Yael Kalai and Leonid Reyzin, vol. 10677, Springer, 2017, pp. 493–526, doi:10.1007/978-3-319-70500-2_17.","short":"J.F. Alwen, B. Tackmann, in:, Y. Kalai, L. Reyzin (Eds.), Springer, 2017, pp. 493–526."},"page":"493 - 526","date_published":"2017-11-05T00:00:00Z","scopus_import":1,"day":"05","year":"2017","publisher":"Springer","department":[{"_id":"KrPi"}],"editor":[{"full_name":"Kalai, Yael","first_name":"Yael","last_name":"Kalai"},{"first_name":"Leonid","last_name":"Reyzin","full_name":"Reyzin, Leonid"}],"publication_status":"published","author":[{"last_name":"Alwen","first_name":"Joel F","id":"2A8DFA8C-F248-11E8-B48F-1D18A9856A87","full_name":"Alwen, Joel F"},{"full_name":"Tackmann, Björn","last_name":"Tackmann","first_name":"Björn"}],"volume":10677,"date_created":"2018-12-11T11:47:28Z","date_updated":"2021-01-12T08:06:04Z","publist_id":"7196","oa":1,"main_file_link":[{"url":"https://eprint.iacr.org/2017/945","open_access":"1"}],"quality_controlled":"1","doi":"10.1007/978-3-319-70500-2_17","conference":{"location":"Baltimore, MD, United States","start_date":"2017-11-12","end_date":"2017-11-15","name":"TCC: Theory of Cryptography"},"language":[{"iso":"eng"}],"publication_identifier":{"isbn":["978-331970499-9"]},"month":"11"},{"publication":"Israel Journal of Mathematics","citation":{"ista":"Goaoc X, Mabillard I, Paták P, Patakova Z, Tancer M, Wagner U. 2017. On generalized Heawood inequalities for manifolds: A van Kampen–Flores type nonembeddability result. Israel Journal of Mathematics. 222(2), 841–866.","apa":"Goaoc, X., Mabillard, I., Paták, P., Patakova, Z., Tancer, M., & Wagner, U. (2017). On generalized Heawood inequalities for manifolds: A van Kampen–Flores type nonembeddability result. Israel Journal of Mathematics. Springer. https://doi.org/10.1007/s11856-017-1607-7","ieee":"X. Goaoc, I. Mabillard, P. Paták, Z. Patakova, M. Tancer, and U. Wagner, “On generalized Heawood inequalities for manifolds: A van Kampen–Flores type nonembeddability result,” Israel Journal of Mathematics, vol. 222, no. 2. Springer, pp. 841–866, 2017.","ama":"Goaoc X, Mabillard I, Paták P, Patakova Z, Tancer M, Wagner U. On generalized Heawood inequalities for manifolds: A van Kampen–Flores type nonembeddability result. Israel Journal of Mathematics. 2017;222(2):841-866. doi:10.1007/s11856-017-1607-7","chicago":"Goaoc, Xavier, Isaac Mabillard, Pavel Paták, Zuzana Patakova, Martin Tancer, and Uli Wagner. “On Generalized Heawood Inequalities for Manifolds: A van Kampen–Flores Type Nonembeddability Result.” Israel Journal of Mathematics. Springer, 2017. https://doi.org/10.1007/s11856-017-1607-7.","mla":"Goaoc, Xavier, et al. “On Generalized Heawood Inequalities for Manifolds: A van Kampen–Flores Type Nonembeddability Result.” Israel Journal of Mathematics, vol. 222, no. 2, Springer, 2017, pp. 841–66, doi:10.1007/s11856-017-1607-7.","short":"X. Goaoc, I. Mabillard, P. Paták, Z. Patakova, M. Tancer, U. Wagner, Israel Journal of Mathematics 222 (2017) 841–866."},"page":"841 - 866","date_published":"2017-10-01T00:00:00Z","scopus_import":1,"day":"01","_id":"610","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","status":"public","title":"On generalized Heawood inequalities for manifolds: A van Kampen–Flores type nonembeddability result","intvolume":" 222","oa_version":"Preprint","type":"journal_article","abstract":[{"text":"The fact that the complete graph K5 does not embed in the plane has been generalized in two independent directions. On the one hand, the solution of the classical Heawood problem for graphs on surfaces established that the complete graph Kn embeds in a closed surface M (other than the Klein bottle) if and only if (n−3)(n−4) ≤ 6b1(M), where b1(M) is the first Z2-Betti number of M. On the other hand, van Kampen and Flores proved that the k-skeleton of the n-dimensional simplex (the higher-dimensional analogue of Kn+1) embeds in R2k if and only if n ≤ 2k + 1. Two decades ago, Kühnel conjectured that the k-skeleton of the n-simplex embeds in a compact, (k − 1)-connected 2k-manifold with kth Z2-Betti number bk only if the following generalized Heawood inequality holds: (k+1 n−k−1) ≤ (k+1 2k+1)bk. This is a common generalization of the case of graphs on surfaces as well as the van Kampen–Flores theorem. In the spirit of Kühnel’s conjecture, we prove that if the k-skeleton of the n-simplex embeds in a compact 2k-manifold with kth Z2-Betti number bk, then n ≤ 2bk(k 2k+2)+2k+4. This bound is weaker than the generalized Heawood inequality, but does not require the assumption that M is (k−1)-connected. Our results generalize to maps without q-covered points, in the spirit of Tverberg’s theorem, for q a prime power. Our proof uses a result of Volovikov about maps that satisfy a certain homological triviality condition.","lang":"eng"}],"issue":"2","main_file_link":[{"url":"https://arxiv.org/abs/1610.09063","open_access":"1"}],"oa":1,"quality_controlled":"1","project":[{"grant_number":"291734","_id":"25681D80-B435-11E9-9278-68D0E5697425","name":"International IST Postdoc Fellowship Programme","call_identifier":"FP7"}],"doi":"10.1007/s11856-017-1607-7","language":[{"iso":"eng"}],"month":"10","acknowledgement":"The work by Z. P. was partially supported by the Israel Science Foundation grant ISF-768/12. The work by Z. P. and M. T. was partially supported by the project CE-ITI (GACR P202/12/G061) of the Czech Science Foundation and by the ERC Advanced Grant No. 267165. Part of the research work of M.T. was conducted at IST Austria, supported by an IST Fellowship. The research of P. P. was supported by the ERC Advanced grant no. 320924. The work by I. M. and U. W. was supported by the Swiss National Science Foundation (grants SNSF-200020-138230 and SNSF-PP00P2-138948). The collaboration between U. W. and X. G. was partially supported by the LabEx Bézout (ANR-10-LABX-58).","year":"2017","publication_status":"published","publisher":"Springer","department":[{"_id":"UlWa"}],"author":[{"first_name":"Xavier","last_name":"Goaoc","full_name":"Goaoc, Xavier"},{"full_name":"Mabillard, Isaac","last_name":"Mabillard","first_name":"Isaac","id":"32BF9DAA-F248-11E8-B48F-1D18A9856A87"},{"last_name":"Paták","first_name":"Pavel","full_name":"Paták, Pavel"},{"full_name":"Patakova, Zuzana","first_name":"Zuzana","last_name":"Patakova","id":"48B57058-F248-11E8-B48F-1D18A9856A87","orcid":"0000-0002-3975-1683"},{"full_name":"Tancer, Martin","first_name":"Martin","last_name":"Tancer","id":"38AC689C-F248-11E8-B48F-1D18A9856A87","orcid":"0000-0002-1191-6714"},{"full_name":"Wagner, Uli","id":"36690CA2-F248-11E8-B48F-1D18A9856A87","orcid":"0000-0002-1494-0568","first_name":"Uli","last_name":"Wagner"}],"related_material":{"record":[{"id":"1511","relation":"earlier_version","status":"public"}]},"date_created":"2018-12-11T11:47:29Z","date_updated":"2023-02-23T10:02:13Z","volume":222,"publist_id":"7194","ec_funded":1},{"publication":"Proceedings of the National Academy of Sciences","citation":{"ista":"Fenk LA, de Bono M. 2017. Memory of recent oxygen experience switches pheromone valence inCaenorhabditis elegans. Proceedings of the National Academy of Sciences. 114(16), 4195–4200.","apa":"Fenk, L. A., & de Bono, M. (2017). Memory of recent oxygen experience switches pheromone valence inCaenorhabditis elegans. Proceedings of the National Academy of Sciences. National Academy of Sciences. https://doi.org/10.1073/pnas.1618934114","ieee":"L. A. Fenk and M. de Bono, “Memory of recent oxygen experience switches pheromone valence inCaenorhabditis elegans,” Proceedings of the National Academy of Sciences, vol. 114, no. 16. National Academy of Sciences, pp. 4195–4200, 2017.","ama":"Fenk LA, de Bono M. Memory of recent oxygen experience switches pheromone valence inCaenorhabditis elegans. Proceedings of the National Academy of Sciences. 2017;114(16):4195-4200. doi:10.1073/pnas.1618934114","chicago":"Fenk, Lorenz A., and Mario de Bono. “Memory of Recent Oxygen Experience Switches Pheromone Valence InCaenorhabditis Elegans.” Proceedings of the National Academy of Sciences. National Academy of Sciences, 2017. https://doi.org/10.1073/pnas.1618934114.","mla":"Fenk, Lorenz A., and Mario de Bono. “Memory of Recent Oxygen Experience Switches Pheromone Valence InCaenorhabditis Elegans.” Proceedings of the National Academy of Sciences, vol. 114, no. 16, National Academy of Sciences, 2017, pp. 4195–200, doi:10.1073/pnas.1618934114.","short":"L.A. Fenk, M. de Bono, Proceedings of the National Academy of Sciences 114 (2017) 4195–4200."},"page":"4195-4200","date_published":"2017-04-18T00:00:00Z","day":"18","has_accepted_license":"1","user_id":"3E5EF7F0-F248-11E8-B48F-1D18A9856A87","_id":"6115","title":"Memory of recent oxygen experience switches pheromone valence inCaenorhabditis elegans","status":"public","ddc":["570"],"intvolume":" 114","oa_version":"Published Version","file":[{"content_type":"application/pdf","file_size":1217696,"creator":"kschuh","file_name":"2017_PNAS_Fenk.pdf","access_level":"open_access","date_created":"2019-03-19T14:00:42Z","date_updated":"2020-07-14T12:47:20Z","checksum":"1801bc8319b752fa17598004ec375279","relation":"main_file","file_id":"6116"}],"type":"journal_article","abstract":[{"lang":"eng","text":"Animals adjust their behavioral priorities according to momentary needs and prior experience. We show that Caenorhabditis elegans changes how it processes sensory information according to the oxygen environment it experienced recently. C. elegans acclimated to 7% O2 are aroused by CO2 and repelled by pheromones that attract animals acclimated to 21% O2. This behavioral plasticity arises from prolonged activity differences in a circuit that continuously signals O2 levels. A sustained change in the activity of O2-sensing neurons reprograms the properties of their postsynaptic partners, the RMG hub interneurons. RMG is gap-junctionally coupled to the ASK and ADL pheromone sensors that respectively drive pheromone attraction and repulsion. Prior O2 experience has opposite effects on the pheromone responsiveness of these neurons. These circuit changes provide a physiological correlate of altered pheromone valence. Our results suggest C. elegans stores a memory of recent O2 experience in the RMG circuit and illustrate how a circuit is flexibly sculpted to guide behavioral decisions in a context-dependent manner."}],"issue":"16","external_id":{"pmid":["28373553"]},"oa":1,"quality_controlled":"1","doi":"10.1073/pnas.1618934114","language":[{"iso":"eng"}],"month":"04","publication_identifier":{"issn":["0027-8424","1091-6490"]},"year":"2017","pmid":1,"publication_status":"published","publisher":"National Academy of Sciences","author":[{"full_name":"Fenk, Lorenz A.","first_name":"Lorenz A.","last_name":"Fenk"},{"first_name":"Mario","last_name":"de Bono","id":"4E3FF80E-F248-11E8-B48F-1D18A9856A87","orcid":"0000-0001-8347-0443","full_name":"de Bono, Mario"}],"date_created":"2019-03-19T13:46:36Z","date_updated":"2021-01-12T08:06:11Z","volume":114,"file_date_updated":"2020-07-14T12:47:20Z","extern":"1"},{"author":[{"full_name":"Chen, Changchun","last_name":"Chen","first_name":"Changchun"},{"full_name":"Itakura, Eisuke","last_name":"Itakura","first_name":"Eisuke"},{"first_name":"Geoffrey M.","last_name":"Nelson","full_name":"Nelson, Geoffrey M."},{"last_name":"Sheng","first_name":"Ming","full_name":"Sheng, Ming"},{"last_name":"Laurent","first_name":"Patrick","full_name":"Laurent, Patrick"},{"last_name":"Fenk","first_name":"Lorenz A.","full_name":"Fenk, Lorenz A."},{"first_name":"Rebecca A.","last_name":"Butcher","full_name":"Butcher, Rebecca A."},{"last_name":"Hegde","first_name":"Ramanujan S.","full_name":"Hegde, Ramanujan S."},{"orcid":"0000-0001-8347-0443","id":"4E3FF80E-F248-11E8-B48F-1D18A9856A87","last_name":"de Bono","first_name":"Mario","full_name":"de Bono, Mario"}],"date_updated":"2021-01-12T08:06:12Z","date_created":"2019-03-19T14:06:41Z","volume":542,"year":"2017","pmid":1,"publication_status":"published","publisher":"Springer Nature","extern":"1","doi":"10.1038/nature20818","language":[{"iso":"eng"}],"oa":1,"external_id":{"pmid":[" 28099418"]},"main_file_link":[{"open_access":"1","url":"https://www.ncbi.nlm.nih.gov/pubmed/28099418"}],"quality_controlled":"1","month":"02","publication_identifier":{"issn":["0028-0836","1476-4687"]},"oa_version":"Submitted Version","_id":"6117","user_id":"3E5EF7F0-F248-11E8-B48F-1D18A9856A87","title":"IL-17 is a neuromodulator of Caenorhabditis elegans sensory responses","status":"public","intvolume":" 542","abstract":[{"text":"Interleukin-17 (IL-17) is a major pro-inflammatory cytokine: it mediates responses to pathogens or tissue damage, and drives autoimmune diseases. Little is known about its role in the nervous system. Here we show that IL-17 has neuromodulator-like properties in Caenorhabditis elegans. IL-17 can act directly on neurons to alter their response properties and contribution to behaviour. Using unbiased genetic screens, we delineate an IL-17 signalling pathway and show that it acts in the RMG hub interneurons. Disrupting IL-17 signalling reduces RMG responsiveness to input from oxygen sensors, and renders sustained escape from 21% oxygen transient and contingent on additional stimuli. Over-activating IL-17 receptors abnormally heightens responses to 21% oxygen in RMG neurons and whole animals. IL-17 deficiency can be bypassed by optogenetic stimulation of RMG. Inducing IL-17 expression in adults can rescue mutant defects within 6 h. These findings reveal a non-immunological role of IL-17 modulating circuit function and behaviour.","lang":"eng"}],"issue":"7639","type":"journal_article","date_published":"2017-02-02T00:00:00Z","publication":"Nature","citation":{"ista":"Chen C, Itakura E, Nelson GM, Sheng M, Laurent P, Fenk LA, Butcher RA, Hegde RS, de Bono M. 2017. IL-17 is a neuromodulator of Caenorhabditis elegans sensory responses. Nature. 542(7639), 43–48.","apa":"Chen, C., Itakura, E., Nelson, G. M., Sheng, M., Laurent, P., Fenk, L. A., … de Bono, M. (2017). IL-17 is a neuromodulator of Caenorhabditis elegans sensory responses. Nature. Springer Nature. https://doi.org/10.1038/nature20818","ieee":"C. Chen et al., “IL-17 is a neuromodulator of Caenorhabditis elegans sensory responses,” Nature, vol. 542, no. 7639. Springer Nature, pp. 43–48, 2017.","ama":"Chen C, Itakura E, Nelson GM, et al. IL-17 is a neuromodulator of Caenorhabditis elegans sensory responses. Nature. 2017;542(7639):43-48. doi:10.1038/nature20818","chicago":"Chen, Changchun, Eisuke Itakura, Geoffrey M. Nelson, Ming Sheng, Patrick Laurent, Lorenz A. Fenk, Rebecca A. Butcher, Ramanujan S. Hegde, and Mario de Bono. “IL-17 Is a Neuromodulator of Caenorhabditis Elegans Sensory Responses.” Nature. Springer Nature, 2017. https://doi.org/10.1038/nature20818.","mla":"Chen, Changchun, et al. “IL-17 Is a Neuromodulator of Caenorhabditis Elegans Sensory Responses.” Nature, vol. 542, no. 7639, Springer Nature, 2017, pp. 43–48, doi:10.1038/nature20818.","short":"C. Chen, E. Itakura, G.M. Nelson, M. Sheng, P. Laurent, L.A. Fenk, R.A. Butcher, R.S. Hegde, M. de Bono, Nature 542 (2017) 43–48."},"page":"43-48","day":"02"},{"language":[{"iso":"eng"}],"doi":"10.1126/science.aao3526","date_published":"2017-11-17T00:00:00Z","page":"925 - 928","quality_controlled":"1","citation":{"ama":"Bradley D, Xu P, Mohorianu I, et al. Evolution of flower color pattern through selection on regulatory small RNAs. Science. 2017;358(6365):925-928. doi:10.1126/science.aao3526","ista":"Bradley D, Xu P, Mohorianu I, Whibley A, Field D, Tavares H, Couchman M, Copsey L, Carpenter R, Li M, Li Q, Xue Y, Dalmay T, Coen E. 2017. Evolution of flower color pattern through selection on regulatory small RNAs. Science. 358(6365), 925–928.","apa":"Bradley, D., Xu, P., Mohorianu, I., Whibley, A., Field, D., Tavares, H., … Coen, E. (2017). Evolution of flower color pattern through selection on regulatory small RNAs. Science. American Association for the Advancement of Science. https://doi.org/10.1126/science.aao3526","ieee":"D. Bradley et al., “Evolution of flower color pattern through selection on regulatory small RNAs,” Science, vol. 358, no. 6365. American Association for the Advancement of Science, pp. 925–928, 2017.","mla":"Bradley, Desmond, et al. “Evolution of Flower Color Pattern through Selection on Regulatory Small RNAs.” Science, vol. 358, no. 6365, American Association for the Advancement of Science, 2017, pp. 925–28, doi:10.1126/science.aao3526.","short":"D. Bradley, P. Xu, I. Mohorianu, A. Whibley, D. Field, H. Tavares, M. Couchman, L. Copsey, R. Carpenter, M. Li, Q. Li, Y. Xue, T. Dalmay, E. Coen, Science 358 (2017) 925–928.","chicago":"Bradley, Desmond, Ping Xu, Irina Mohorianu, Annabel Whibley, David Field, Hugo Tavares, Matthew Couchman, et al. “Evolution of Flower Color Pattern through Selection on Regulatory Small RNAs.” Science. American Association for the Advancement of Science, 2017. https://doi.org/10.1126/science.aao3526."},"publication":"Science","publication_identifier":{"issn":["00368075"]},"month":"11","day":"17","scopus_import":1,"oa_version":"None","volume":358,"date_updated":"2021-01-12T08:06:10Z","date_created":"2018-12-11T11:47:29Z","author":[{"full_name":"Bradley, Desmond","first_name":"Desmond","last_name":"Bradley"},{"first_name":"Ping","last_name":"Xu","full_name":"Xu, Ping"},{"full_name":"Mohorianu, Irina","last_name":"Mohorianu","first_name":"Irina"},{"full_name":"Whibley, Annabel","first_name":"Annabel","last_name":"Whibley"},{"orcid":"0000-0002-4014-8478","id":"419049E2-F248-11E8-B48F-1D18A9856A87","last_name":"Field","first_name":"David","full_name":"Field, David"},{"last_name":"Tavares","first_name":"Hugo","full_name":"Tavares, Hugo"},{"last_name":"Couchman","first_name":"Matthew","full_name":"Couchman, Matthew"},{"full_name":"Copsey, Lucy","last_name":"Copsey","first_name":"Lucy"},{"full_name":"Carpenter, Rosemary","first_name":"Rosemary","last_name":"Carpenter"},{"last_name":"Li","first_name":"Miaomiao","full_name":"Li, Miaomiao"},{"first_name":"Qun","last_name":"Li","full_name":"Li, Qun"},{"first_name":"Yongbiao","last_name":"Xue","full_name":"Xue, Yongbiao"},{"first_name":"Tamas","last_name":"Dalmay","full_name":"Dalmay, Tamas"},{"full_name":"Coen, Enrico","first_name":"Enrico","last_name":"Coen"}],"publisher":"American Association for the Advancement of Science","department":[{"_id":"NiBa"}],"intvolume":" 358","title":"Evolution of flower color pattern through selection on regulatory small RNAs","publication_status":"published","status":"public","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","_id":"611","year":"2017","publist_id":"7193","issue":"6365","abstract":[{"lang":"eng","text":"Small RNAs (sRNAs) regulate genes in plants and animals. Here, we show that population-wide differences in color patterns in snapdragon flowers are caused by an inverted duplication that generates sRNAs. The complexity and size of the transcripts indicate that the duplication represents an intermediate on the pathway to microRNA evolution. The sRNAs repress a pigment biosynthesis gene, creating a yellow highlight at the site of pollinator entry. The inverted duplication exhibits steep clines in allele frequency in a natural hybrid zone, showing that the allele is under selection. Thus, regulatory interactions of evolutionarily recent sRNAs can be acted upon by selection and contribute to the evolution of phenotypic diversity."}],"type":"journal_article"},{"day":"06","has_accepted_license":"1","date_published":"2017-06-06T00:00:00Z","publication":"Proceedings of the National Academy of Sciences","citation":{"chicago":"Oda, Shigekazu, Yu Toyoshima, and Mario de Bono. “Modulation of Sensory Information Processing by a Neuroglobin in Caenorhabditis Elegans.” Proceedings of the National Academy of Sciences. National Academy of Sciences, 2017. https://doi.org/10.1073/pnas.1614596114.","short":"S. Oda, Y. Toyoshima, M. de Bono, Proceedings of the National Academy of Sciences 114 (2017) E4658–E4665.","mla":"Oda, Shigekazu, et al. “Modulation of Sensory Information Processing by a Neuroglobin in Caenorhabditis Elegans.” Proceedings of the National Academy of Sciences, vol. 114, no. 23, National Academy of Sciences, 2017, pp. E4658–65, doi:10.1073/pnas.1614596114.","ieee":"S. Oda, Y. Toyoshima, and M. de Bono, “Modulation of sensory information processing by a neuroglobin in Caenorhabditis elegans,” Proceedings of the National Academy of Sciences, vol. 114, no. 23. National Academy of Sciences, pp. E4658–E4665, 2017.","apa":"Oda, S., Toyoshima, Y., & de Bono, M. (2017). Modulation of sensory information processing by a neuroglobin in Caenorhabditis elegans. Proceedings of the National Academy of Sciences. National Academy of Sciences. https://doi.org/10.1073/pnas.1614596114","ista":"Oda S, Toyoshima Y, de Bono M. 2017. Modulation of sensory information processing by a neuroglobin in Caenorhabditis elegans. Proceedings of the National Academy of Sciences. 114(23), E4658–E4665.","ama":"Oda S, Toyoshima Y, de Bono M. Modulation of sensory information processing by a neuroglobin in Caenorhabditis elegans. Proceedings of the National Academy of Sciences. 2017;114(23):E4658-E4665. doi:10.1073/pnas.1614596114"},"page":"E4658-E4665","issue":"23","type":"journal_article","file":[{"date_created":"2019-03-19T13:42:58Z","date_updated":"2020-07-14T12:47:19Z","checksum":"9e42ce47090ecdad7d76f2dbdebb924e","file_id":"6114","relation":"main_file","creator":"kschuh","content_type":"application/pdf","file_size":1469622,"file_name":"2017_PNAS_Oda.pdf","access_level":"open_access"}],"oa_version":"Published Version","user_id":"3E5EF7F0-F248-11E8-B48F-1D18A9856A87","_id":"6113","ddc":["570"],"title":"Modulation of sensory information processing by a neuroglobin in Caenorhabditis elegans","status":"public","intvolume":" 114","month":"06","publication_identifier":{"issn":["0027-8424","1091-6490"]},"doi":"10.1073/pnas.1614596114","language":[{"iso":"eng"}],"external_id":{"pmid":["28536200"]},"oa":1,"quality_controlled":"1","file_date_updated":"2020-07-14T12:47:19Z","extern":"1","author":[{"last_name":"Oda","first_name":"Shigekazu","full_name":"Oda, Shigekazu"},{"last_name":"Toyoshima","first_name":"Yu","full_name":"Toyoshima, Yu"},{"full_name":"de Bono, Mario","id":"4E3FF80E-F248-11E8-B48F-1D18A9856A87","orcid":"0000-0001-8347-0443","first_name":"Mario","last_name":"de Bono"}],"date_created":"2019-03-19T13:29:51Z","date_updated":"2021-01-12T08:06:11Z","volume":114,"year":"2017","pmid":1,"publication_status":"published","publisher":"National Academy of Sciences"},{"has_accepted_license":"1","article_processing_charge":"Yes (in subscription journal)","day":"01","scopus_import":1,"date_published":"2017-12-01T00:00:00Z","citation":{"ieee":"R. P. Chait, J. Ruess, T. Bergmiller, G. Tkačik, and C. C. Guet, “Shaping bacterial population behavior through computer interfaced control of individual cells,” Nature Communications, vol. 8, no. 1. Nature Publishing Group, 2017.","apa":"Chait, R. P., Ruess, J., Bergmiller, T., Tkačik, G., & Guet, C. C. (2017). Shaping bacterial population behavior through computer interfaced control of individual cells. Nature Communications. Nature Publishing Group. https://doi.org/10.1038/s41467-017-01683-1","ista":"Chait RP, Ruess J, Bergmiller T, Tkačik G, Guet CC. 2017. Shaping bacterial population behavior through computer interfaced control of individual cells. Nature Communications. 8(1), 1535.","ama":"Chait RP, Ruess J, Bergmiller T, Tkačik G, Guet CC. Shaping bacterial population behavior through computer interfaced control of individual cells. Nature Communications. 2017;8(1). doi:10.1038/s41467-017-01683-1","chicago":"Chait, Remy P, Jakob Ruess, Tobias Bergmiller, Gašper Tkačik, and Calin C Guet. “Shaping Bacterial Population Behavior through Computer Interfaced Control of Individual Cells.” Nature Communications. Nature Publishing Group, 2017. https://doi.org/10.1038/s41467-017-01683-1.","short":"R.P. Chait, J. Ruess, T. Bergmiller, G. Tkačik, C.C. Guet, Nature Communications 8 (2017).","mla":"Chait, Remy P., et al. “Shaping Bacterial Population Behavior through Computer Interfaced Control of Individual Cells.” Nature Communications, vol. 8, no. 1, 1535, Nature Publishing Group, 2017, doi:10.1038/s41467-017-01683-1."},"publication":"Nature Communications","issue":"1","abstract":[{"text":"Bacteria in groups vary individually, and interact with other bacteria and the environment to produce population-level patterns of gene expression. Investigating such behavior in detail requires measuring and controlling populations at the single-cell level alongside precisely specified interactions and environmental characteristics. Here we present an automated, programmable platform that combines image-based gene expression and growth measurements with on-line optogenetic expression control for hundreds of individual Escherichia coli cells over days, in a dynamically adjustable environment. This integrated platform broadly enables experiments that bridge individual and population behaviors. We demonstrate: (i) population structuring by independent closed-loop control of gene expression in many individual cells, (ii) cell-cell variation control during antibiotic perturbation, (iii) hybrid bio-digital circuits in single cells, and freely specifiable digital communication between individual bacteria. These examples showcase the potential for real-time integration of theoretical models with measurement and control of many individual cells to investigate and engineer microbial population behavior.","lang":"eng"}],"type":"journal_article","pubrep_id":"911","file":[{"access_level":"open_access","file_name":"IST-2017-911-v1+1_s41467-017-01683-1.pdf","creator":"system","file_size":1951699,"content_type":"application/pdf","file_id":"5190","relation":"main_file","checksum":"44bb5d0229926c23a9955d9fe0f9723f","date_created":"2018-12-12T10:16:05Z","date_updated":"2020-07-14T12:47:20Z"}],"oa_version":"Published Version","_id":"613","user_id":"3E5EF7F0-F248-11E8-B48F-1D18A9856A87","intvolume":" 8","title":"Shaping bacterial population behavior through computer interfaced control of individual cells","status":"public","ddc":["576","579"],"publication_identifier":{"issn":["20411723"]},"month":"12","doi":"10.1038/s41467-017-01683-1","language":[{"iso":"eng"}],"tmp":{"name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","short":"CC BY (4.0)","image":"/images/cc_by.png"},"oa":1,"project":[{"_id":"25681D80-B435-11E9-9278-68D0E5697425","grant_number":"291734","call_identifier":"FP7","name":"International IST Postdoc Fellowship Programme"},{"call_identifier":"FWF","name":"Biophysics of information processing in gene regulation","_id":"254E9036-B435-11E9-9278-68D0E5697425","grant_number":"P28844-B27"}],"quality_controlled":"1","ec_funded":1,"publist_id":"7191","file_date_updated":"2020-07-14T12:47:20Z","article_number":"1535","author":[{"full_name":"Chait, Remy P","orcid":"0000-0003-0876-3187","id":"3464AE84-F248-11E8-B48F-1D18A9856A87","last_name":"Chait","first_name":"Remy P"},{"id":"4A245D00-F248-11E8-B48F-1D18A9856A87","orcid":"0000-0003-1615-3282","first_name":"Jakob","last_name":"Ruess","full_name":"Ruess, Jakob"},{"id":"2C471CFA-F248-11E8-B48F-1D18A9856A87","orcid":"0000-0001-5396-4346","first_name":"Tobias","last_name":"Bergmiller","full_name":"Bergmiller, Tobias"},{"orcid":"0000-0002-6699-1455","id":"3D494DCA-F248-11E8-B48F-1D18A9856A87","last_name":"Tkacik","first_name":"Gasper","full_name":"Tkacik, Gasper"},{"first_name":"Calin C","last_name":"Guet","id":"47F8433E-F248-11E8-B48F-1D18A9856A87","orcid":"0000-0001-6220-2052","full_name":"Guet, Calin C"}],"volume":8,"date_updated":"2021-01-12T08:06:15Z","date_created":"2018-12-11T11:47:30Z","year":"2017","acknowledgement":"We are grateful to M. Lang, H. Janovjak, M. Khammash, A. Milias-Argeitis, M. Rullan, G. Batt, A. Bosma-Moody, Aryan, S. Leibler, and members of the Guet and Tkačik groups for helpful discussion, comments, and suggestions. We thank A. Moglich, T. Mathes, J. Tabor, and S. Schmidl for kind gifts of strains, and R. Hauschild, B. Knep, M. Lang, T. Asenov, E. Papusheva, T. Menner, T. Adletzberger, and J. Merrin for technical assistance. The research leading to these results has received funding from the People Programme (Marie Curie Actions) of the European Union’s Seventh Framework Programme (FP7/2007–2013) under REA grant agreement no. [291734]. (to R.C. and J.R.), Austrian Science Fund grant FWF P28844 (to G.T.), and internal IST Austria Interdisciplinary Project Support. J.R. acknowledges support from the Agence Nationale de la Recherche (ANR) under Grant Nos. ANR-16-CE33-0018 (MEMIP), ANR-16-CE12-0025 (COGEX) and ANR-10-BINF-06-01 (ICEBERG).","department":[{"_id":"CaGu"},{"_id":"GaTk"}],"publisher":"Nature Publishing Group","publication_status":"published"},{"author":[{"full_name":"Erdös, László","last_name":"Erdös","first_name":"László","orcid":"0000-0001-5366-9603","id":"4DBD5372-F248-11E8-B48F-1D18A9856A87"},{"orcid":"0000-0003-0954-3231","id":"434AD0AE-F248-11E8-B48F-1D18A9856A87","last_name":"Schnelli","first_name":"Kevin","full_name":"Schnelli, Kevin"}],"volume":53,"date_updated":"2021-01-12T08:06:22Z","date_created":"2018-12-11T11:47:30Z","year":"2017","department":[{"_id":"LaEr"}],"publisher":"Institute of Mathematical Statistics","publication_status":"published","publist_id":"7189","ec_funded":1,"doi":"10.1214/16-AIHP765","language":[{"iso":"eng"}],"main_file_link":[{"url":"https://arxiv.org/abs/1504.00650","open_access":"1"}],"oa":1,"project":[{"name":"Random matrices, universality and disordered quantum systems","call_identifier":"FP7","_id":"258DCDE6-B435-11E9-9278-68D0E5697425","grant_number":"338804"}],"quality_controlled":"1","publication_identifier":{"issn":["02460203"]},"month":"11","oa_version":"Submitted Version","_id":"615","user_id":"4435EBFC-F248-11E8-B48F-1D18A9856A87","intvolume":" 53","status":"public","title":"Universality for random matrix flows with time dependent density","issue":"4","abstract":[{"lang":"eng","text":"We show that the Dyson Brownian Motion exhibits local universality after a very short time assuming that local rigidity and level repulsion of the eigenvalues hold. These conditions are verified, hence bulk spectral universality is proven, for a large class of Wigner-like matrices, including deformed Wigner ensembles and ensembles with non-stochastic variance matrices whose limiting densities differ from Wigner's semicircle law."}],"type":"journal_article","date_published":"2017-11-01T00:00:00Z","citation":{"chicago":"Erdös, László, and Kevin Schnelli. “Universality for Random Matrix Flows with Time Dependent Density.” Annales de l’institut Henri Poincare (B) Probability and Statistics. Institute of Mathematical Statistics, 2017. https://doi.org/10.1214/16-AIHP765.","mla":"Erdös, László, and Kevin Schnelli. “Universality for Random Matrix Flows with Time Dependent Density.” Annales de l’institut Henri Poincare (B) Probability and Statistics, vol. 53, no. 4, Institute of Mathematical Statistics, 2017, pp. 1606–56, doi:10.1214/16-AIHP765.","short":"L. Erdös, K. Schnelli, Annales de l’institut Henri Poincare (B) Probability and Statistics 53 (2017) 1606–1656.","ista":"Erdös L, Schnelli K. 2017. Universality for random matrix flows with time dependent density. Annales de l’institut Henri Poincare (B) Probability and Statistics. 53(4), 1606–1656.","apa":"Erdös, L., & Schnelli, K. (2017). Universality for random matrix flows with time dependent density. Annales de l’institut Henri Poincare (B) Probability and Statistics. Institute of Mathematical Statistics. https://doi.org/10.1214/16-AIHP765","ieee":"L. Erdös and K. Schnelli, “Universality for random matrix flows with time dependent density,” Annales de l’institut Henri Poincare (B) Probability and Statistics, vol. 53, no. 4. Institute of Mathematical Statistics, pp. 1606–1656, 2017.","ama":"Erdös L, Schnelli K. Universality for random matrix flows with time dependent density. Annales de l’institut Henri Poincare (B) Probability and Statistics. 2017;53(4):1606-1656. doi:10.1214/16-AIHP765"},"publication":"Annales de l'institut Henri Poincare (B) Probability and Statistics","page":"1606 - 1656","day":"01","scopus_import":1},{"publication_identifier":{"issn":["17563305"]},"month":"06","oa":1,"tmp":{"name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","short":"CC BY (4.0)","image":"/images/cc_by.png"},"quality_controlled":"1","doi":"10.1186/s13071-017-2192-7","language":[{"iso":"eng"}],"article_number":"52","publist_id":"7186","file_date_updated":"2020-07-14T12:47:22Z","extern":"1","year":"2017","publisher":"BioMed Central","publication_status":"published","author":[{"full_name":"Franke, Frederik","first_name":"Frederik","last_name":"Franke"},{"last_name":"Armitage","first_name":"Sophie","full_name":"Armitage, Sophie"},{"full_name":"Kutzer, Megan","id":"29D0B332-F248-11E8-B48F-1D18A9856A87","orcid":"0000-0002-8696-6978","first_name":"Megan","last_name":"Kutzer"},{"last_name":"Kurtz","first_name":"Joachim","full_name":"Kurtz, Joachim"},{"last_name":"Scharsack","first_name":"Jörn","full_name":"Scharsack, Jörn"}],"volume":10,"date_created":"2018-12-11T11:47:31Z","date_updated":"2021-01-12T08:06:35Z","has_accepted_license":"1","day":"02","citation":{"short":"F. Franke, S. Armitage, M. Kutzer, J. Kurtz, J. Scharsack, Parasites & Vectors 10 (2017).","mla":"Franke, Frederik, et al. “Environmental Temperature Variation Influences Fitness Trade-Offs in a Fish-Tapeworm Association .” Parasites & Vectors, vol. 10, no. 252, 52, BioMed Central, 2017, doi:10.1186/s13071-017-2192-7.","chicago":"Franke, Frederik, Sophie Armitage, Megan Kutzer, Joachim Kurtz, and Jörn Scharsack. “Environmental Temperature Variation Influences Fitness Trade-Offs in a Fish-Tapeworm Association .” Parasites & Vectors. BioMed Central, 2017. https://doi.org/10.1186/s13071-017-2192-7.","ama":"Franke F, Armitage S, Kutzer M, Kurtz J, Scharsack J. Environmental temperature variation influences fitness trade-offs in a fish-tapeworm association . Parasites & Vectors. 2017;10(252). doi:10.1186/s13071-017-2192-7","apa":"Franke, F., Armitage, S., Kutzer, M., Kurtz, J., & Scharsack, J. (2017). Environmental temperature variation influences fitness trade-offs in a fish-tapeworm association . Parasites & Vectors. BioMed Central. https://doi.org/10.1186/s13071-017-2192-7","ieee":"F. Franke, S. Armitage, M. Kutzer, J. Kurtz, and J. Scharsack, “Environmental temperature variation influences fitness trade-offs in a fish-tapeworm association ,” Parasites & Vectors, vol. 10, no. 252. BioMed Central, 2017.","ista":"Franke F, Armitage S, Kutzer M, Kurtz J, Scharsack J. 2017. Environmental temperature variation influences fitness trade-offs in a fish-tapeworm association . Parasites & Vectors. 10(252), 52."},"publication":"Parasites & Vectors","date_published":"2017-06-02T00:00:00Z","type":"journal_article","issue":"252","abstract":[{"text":"Background: Increasing temperatures are predicted to strongly impact host-parasite interactions, but empirical tests are rare. Host species that are naturally exposed to a broad temperature spectrum offer the possibility to investigate the effects of elevated temperatures on hosts and parasites. Using three-spined sticklebacks, Gasterosteus aculeatus L., and tapeworms, Schistocephalus solidus (Müller, 1776), originating from a cold and a warm water site of a volcanic lake, we subjected sympatric and allopatric host-parasite combinations to cold and warm conditions in a fully crossed design. We predicted that warm temperatures would promote the development of the parasites, while the hosts might benefit from cooler temperatures. We further expected adaptations to the local temperature and mutual adaptations of local host-parasite pairs. Results: Overall, S. solidus parasites grew faster at warm temperatures and stickleback hosts at cold temperatures. On a finer scale, we observed that parasites were able to exploit their hosts more efficiently at the parasite’s temperature of origin. In contrast, host tolerance towards parasite infection was higher when sticklebacks were infected with parasites at the parasite’s ‘foreign’ temperature. Cold-origin sticklebacks tended to grow faster and parasite infection induced a stronger immune response. Conclusions: Our results suggest that increasing environmental temperatures promote the parasite rather than the host and that host tolerance is dependent on the interaction between parasite infection and temperature. Sticklebacks might use tolerance mechanisms towards parasite infection in combination with their high plasticity towards temperature changes to cope with increasing parasite infection pressures and rising temperatures.","lang":"eng"}],"_id":"618","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","intvolume":" 10","status":"public","title":"Environmental temperature variation influences fitness trade-offs in a fish-tapeworm association ","ddc":["570"],"oa_version":"Published Version","file":[{"relation":"main_file","file_id":"5864","checksum":"742943377a38ee208108705b8e2f4dbf","date_updated":"2020-07-14T12:47:22Z","date_created":"2019-01-21T13:45:36Z","access_level":"open_access","file_name":"2017_Parasites_Franke.pdf","file_size":671807,"content_type":"application/pdf","creator":"dernst"}]},{"publist_id":"7177","author":[{"last_name":"Hill Yardin","first_name":"Elisa","full_name":"Hill Yardin, Elisa"},{"last_name":"Mckeown","first_name":"Sonja","full_name":"Mckeown, Sonja"},{"last_name":"Novarino","first_name":"Gaia","orcid":"0000-0002-7673-7178","id":"3E57A680-F248-11E8-B48F-1D18A9856A87","full_name":"Novarino, Gaia"},{"last_name":"Grabrucker","first_name":"Andreas","full_name":"Grabrucker, Andreas"}],"volume":224,"date_created":"2018-12-11T11:47:33Z","date_updated":"2021-01-12T08:06:46Z","year":"2017","publisher":"Springer","editor":[{"full_name":"Schmeisser, Michael","last_name":"Schmeisser","first_name":"Michael"},{"last_name":"Boekers","first_name":"Tobias","full_name":"Boekers, Tobias"}],"department":[{"_id":"GaNo"}],"publication_status":"published","publication_identifier":{"issn":["03015556"],"isbn":["978-3-319-52496-2"]},"month":"05","doi":"10.1007/978-3-319-52498-6_9","language":[{"iso":"eng"}],"quality_controlled":"1","abstract":[{"text":"Genetic factors might be largely responsible for the development of autism spectrum disorder (ASD) that alone or in combination with specific environmental risk factors trigger the pathology. Multiple mutations identified in ASD patients that impair synaptic function in the central nervous system are well studied in animal models. How these mutations might interact with other risk factors is not fully understood though. Additionally, how systems outside of the brain are altered in the context of ASD is an emerging area of research. Extracerebral influences on the physiology could begin in utero and contribute to changes in the brain and in the development of other body systems and further lead to epigenetic changes. Therefore, multiple recent studies have aimed at elucidating the role of gene-environment interactions in ASD. Here we provide an overview on the extracerebral systems that might play an important associative role in ASD and review evidence regarding the potential roles of inflammation, trace metals, metabolism, genetic susceptibility, enteric nervous system function and the microbiota of the gastrointestinal (GI) tract on the development of endophenotypes in animal models of ASD. By influencing environmental conditions, it might be possible to reduce or limit the severity of ASD pathology.","lang":"eng"}],"type":"book_chapter","alternative_title":["ADVSANAT"],"oa_version":"None","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","_id":"623","intvolume":" 224","title":"Extracerebral dysfunction in animal models of autism spectrum disorder","status":"public","day":"28","scopus_import":1,"series_title":"Advances in Anatomy Embryology and Cell Biology","date_published":"2017-05-28T00:00:00Z","citation":{"ieee":"E. Hill Yardin, S. Mckeown, G. Novarino, and A. Grabrucker, “Extracerebral dysfunction in animal models of autism spectrum disorder,” in Translational Anatomy and Cell Biology of Autism Spectrum Disorder, vol. 224, M. Schmeisser and T. Boekers, Eds. Springer, 2017, pp. 159–187.","apa":"Hill Yardin, E., Mckeown, S., Novarino, G., & Grabrucker, A. (2017). Extracerebral dysfunction in animal models of autism spectrum disorder. In M. Schmeisser & T. Boekers (Eds.), Translational Anatomy and Cell Biology of Autism Spectrum Disorder (Vol. 224, pp. 159–187). Springer. https://doi.org/10.1007/978-3-319-52498-6_9","ista":"Hill Yardin E, Mckeown S, Novarino G, Grabrucker A. 2017.Extracerebral dysfunction in animal models of autism spectrum disorder. In: Translational Anatomy and Cell Biology of Autism Spectrum Disorder. ADVSANAT, vol. 224, 159–187.","ama":"Hill Yardin E, Mckeown S, Novarino G, Grabrucker A. Extracerebral dysfunction in animal models of autism spectrum disorder. In: Schmeisser M, Boekers T, eds. Translational Anatomy and Cell Biology of Autism Spectrum Disorder. Vol 224. Advances in Anatomy Embryology and Cell Biology. Springer; 2017:159-187. doi:10.1007/978-3-319-52498-6_9","chicago":"Hill Yardin, Elisa, Sonja Mckeown, Gaia Novarino, and Andreas Grabrucker. “Extracerebral Dysfunction in Animal Models of Autism Spectrum Disorder.” In Translational Anatomy and Cell Biology of Autism Spectrum Disorder, edited by Michael Schmeisser and Tobias Boekers, 224:159–87. Advances in Anatomy Embryology and Cell Biology. Springer, 2017. https://doi.org/10.1007/978-3-319-52498-6_9.","short":"E. Hill Yardin, S. Mckeown, G. Novarino, A. Grabrucker, in:, M. Schmeisser, T. Boekers (Eds.), Translational Anatomy and Cell Biology of Autism Spectrum Disorder, Springer, 2017, pp. 159–187.","mla":"Hill Yardin, Elisa, et al. “Extracerebral Dysfunction in Animal Models of Autism Spectrum Disorder.” Translational Anatomy and Cell Biology of Autism Spectrum Disorder, edited by Michael Schmeisser and Tobias Boekers, vol. 224, Springer, 2017, pp. 159–87, doi:10.1007/978-3-319-52498-6_9."},"publication":"Translational Anatomy and Cell Biology of Autism Spectrum Disorder","page":"159 - 187"},{"has_accepted_license":"1","day":"01","scopus_import":1,"date_published":"2017-12-01T00:00:00Z","citation":{"apa":"Barton, N. H., Etheridge, A., & Véber, A. (2017). The infinitesimal model: Definition derivation and implications. Theoretical Population Biology. Academic Press. https://doi.org/10.1016/j.tpb.2017.06.001","ieee":"N. H. Barton, A. Etheridge, and A. Véber, “The infinitesimal model: Definition derivation and implications,” Theoretical Population Biology, vol. 118. Academic Press, pp. 50–73, 2017.","ista":"Barton NH, Etheridge A, Véber A. 2017. The infinitesimal model: Definition derivation and implications. Theoretical Population Biology. 118, 50–73.","ama":"Barton NH, Etheridge A, Véber A. The infinitesimal model: Definition derivation and implications. Theoretical Population Biology. 2017;118:50-73. doi:10.1016/j.tpb.2017.06.001","chicago":"Barton, Nicholas H, Alison Etheridge, and Amandine Véber. “The Infinitesimal Model: Definition Derivation and Implications.” Theoretical Population Biology. Academic Press, 2017. https://doi.org/10.1016/j.tpb.2017.06.001.","short":"N.H. Barton, A. Etheridge, A. Véber, Theoretical Population Biology 118 (2017) 50–73.","mla":"Barton, Nicholas H., et al. “The Infinitesimal Model: Definition Derivation and Implications.” Theoretical Population Biology, vol. 118, Academic Press, 2017, pp. 50–73, doi:10.1016/j.tpb.2017.06.001."},"publication":"Theoretical Population Biology","page":"50 - 73","abstract":[{"lang":"eng","text":"Our focus here is on the infinitesimal model. In this model, one or several quantitative traits are described as the sum of a genetic and a non-genetic component, the first being distributed within families as a normal random variable centred at the average of the parental genetic components, and with a variance independent of the parental traits. Thus, the variance that segregates within families is not perturbed by selection, and can be predicted from the variance components. This does not necessarily imply that the trait distribution across the whole population should be Gaussian, and indeed selection or population structure may have a substantial effect on the overall trait distribution. One of our main aims is to identify some general conditions on the allelic effects for the infinitesimal model to be accurate. We first review the long history of the infinitesimal model in quantitative genetics. Then we formulate the model at the phenotypic level in terms of individual trait values and relationships between individuals, but including different evolutionary processes: genetic drift, recombination, selection, mutation, population structure, …. We give a range of examples of its application to evolutionary questions related to stabilising selection, assortative mating, effective population size and response to selection, habitat preference and speciation. We provide a mathematical justification of the model as the limit as the number M of underlying loci tends to infinity of a model with Mendelian inheritance, mutation and environmental noise, when the genetic component of the trait is purely additive. We also show how the model generalises to include epistatic effects. We prove in particular that, within each family, the genetic components of the individual trait values in the current generation are indeed normally distributed with a variance independent of ancestral traits, up to an error of order 1∕M. Simulations suggest that in some cases the convergence may be as fast as 1∕M."}],"type":"journal_article","pubrep_id":"908","file":[{"file_id":"4964","relation":"main_file","date_created":"2018-12-12T10:12:45Z","date_updated":"2020-07-14T12:47:25Z","checksum":"7dd02bfcfe8f244f4a6c19091aedf2c8","file_name":"IST-2017-908-v1+1_1-s2.0-S0040580917300886-main_1_.pdf","access_level":"open_access","creator":"system","file_size":1133924,"content_type":"application/pdf"}],"oa_version":"Published Version","_id":"626","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","intvolume":" 118","status":"public","title":"The infinitesimal model: Definition derivation and implications","ddc":["576"],"publication_identifier":{"issn":["00405809"]},"month":"12","doi":"10.1016/j.tpb.2017.06.001","language":[{"iso":"eng"}],"oa":1,"tmp":{"name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","short":"CC BY (4.0)","image":"/images/cc_by.png"},"project":[{"_id":"25B07788-B435-11E9-9278-68D0E5697425","grant_number":"250152","call_identifier":"FP7","name":"Limits to selection in biology and in evolutionary computation"}],"quality_controlled":"1","publist_id":"7169","ec_funded":1,"file_date_updated":"2020-07-14T12:47:25Z","author":[{"full_name":"Barton, Nicholas H","id":"4880FE40-F248-11E8-B48F-1D18A9856A87","orcid":"0000-0002-8548-5240","first_name":"Nicholas H","last_name":"Barton"},{"last_name":"Etheridge","first_name":"Alison","full_name":"Etheridge, Alison"},{"full_name":"Véber, Amandine","first_name":"Amandine","last_name":"Véber"}],"volume":118,"date_created":"2018-12-11T11:47:34Z","date_updated":"2021-01-12T08:06:50Z","year":"2017","department":[{"_id":"NiBa"}],"publisher":"Academic Press","publication_status":"published"},{"publication_identifier":{"isbn":["978-3-319-63120-2"],"issn":["0302-9743"]},"month":"07","oa":1,"project":[{"name":"Moderne Concurrency Paradigms","call_identifier":"FWF","grant_number":"S11402-N23","_id":"25F5A88A-B435-11E9-9278-68D0E5697425"},{"call_identifier":"FWF","name":"Game Theory","grant_number":"S11407","_id":"25863FF4-B435-11E9-9278-68D0E5697425"},{"name":"The Wittgenstein Prize","call_identifier":"FWF","_id":"25F42A32-B435-11E9-9278-68D0E5697425","grant_number":"Z211"},{"grant_number":"279307","_id":"2581B60A-B435-11E9-9278-68D0E5697425","name":"Quantitative Graph Games: Theory and Applications","call_identifier":"FP7"},{"grant_number":"ICT15-003","_id":"25892FC0-B435-11E9-9278-68D0E5697425","name":"Efficient Algorithms for Computer Aided Verification"}],"quality_controlled":"1","doi":"10.1007/978-3-319-63121-9_18","language":[{"iso":"eng"}],"ec_funded":1,"publist_id":"7170","file_date_updated":"2020-07-14T12:47:25Z","year":"2017","acknowledgement":"This research was supported in part by the Austrian Science Fund (FWF) under grants S11402-N23 and S11407-N23 (RiSE/SHiNE), and Z211-N23 (Wittgenstein Award), ERC Start grant (279307: Graph Games), Vienna Science and Technology Fund (WWTF) through project ICT15-003.","editor":[{"first_name":"Luca","last_name":"Aceto","full_name":"Aceto, Luca"},{"first_name":"Giorgio","last_name":"Bacci","full_name":"Bacci, Giorgio"},{"full_name":"Ingólfsdóttir, Anna","last_name":"Ingólfsdóttir","first_name":"Anna"},{"last_name":"Legay","first_name":"Axel","full_name":"Legay, Axel"},{"first_name":"Radu","last_name":"Mardare","full_name":"Mardare, Radu"}],"publisher":"Springer","department":[{"_id":"KrCh"},{"_id":"ToHe"}],"publication_status":"published","author":[{"full_name":"Chatterjee, Krishnendu","orcid":"0000-0002-4561-241X","id":"2E5DCA20-F248-11E8-B48F-1D18A9856A87","last_name":"Chatterjee","first_name":"Krishnendu"},{"full_name":"Doyen, Laurent","last_name":"Doyen","first_name":"Laurent"},{"id":"40876CD8-F248-11E8-B48F-1D18A9856A87","orcid":"0000−0002−2985−7724","first_name":"Thomas A","last_name":"Henzinger","full_name":"Henzinger, Thomas A"}],"volume":10460,"date_updated":"2022-05-23T08:54:02Z","date_created":"2018-12-11T11:47:34Z","scopus_import":"1","series_title":"Theoretical Computer Science and General Issues","has_accepted_license":"1","article_processing_charge":"No","day":"25","citation":{"ama":"Chatterjee K, Doyen L, Henzinger TA. The cost of exactness in quantitative reachability. In: Aceto L, Bacci G, Ingólfsdóttir A, Legay A, Mardare R, eds. Models, Algorithms, Logics and Tools. Vol 10460. Theoretical Computer Science and General Issues. Springer; 2017:367-381. doi:10.1007/978-3-319-63121-9_18","ista":"Chatterjee K, Doyen L, Henzinger TA. 2017.The cost of exactness in quantitative reachability. In: Models, Algorithms, Logics and Tools. LNCS, vol. 10460, 367–381.","apa":"Chatterjee, K., Doyen, L., & Henzinger, T. A. (2017). The cost of exactness in quantitative reachability. In L. Aceto, G. Bacci, A. Ingólfsdóttir, A. Legay, & R. Mardare (Eds.), Models, Algorithms, Logics and Tools (Vol. 10460, pp. 367–381). Springer. https://doi.org/10.1007/978-3-319-63121-9_18","ieee":"K. Chatterjee, L. Doyen, and T. A. Henzinger, “The cost of exactness in quantitative reachability,” in Models, Algorithms, Logics and Tools, vol. 10460, L. Aceto, G. Bacci, A. Ingólfsdóttir, A. Legay, and R. Mardare, Eds. Springer, 2017, pp. 367–381.","mla":"Chatterjee, Krishnendu, et al. “The Cost of Exactness in Quantitative Reachability.” Models, Algorithms, Logics and Tools, edited by Luca Aceto et al., vol. 10460, Springer, 2017, pp. 367–81, doi:10.1007/978-3-319-63121-9_18.","short":"K. Chatterjee, L. Doyen, T.A. Henzinger, in:, L. Aceto, G. Bacci, A. Ingólfsdóttir, A. Legay, R. Mardare (Eds.), Models, Algorithms, Logics and Tools, Springer, 2017, pp. 367–381.","chicago":"Chatterjee, Krishnendu, Laurent Doyen, and Thomas A Henzinger. “The Cost of Exactness in Quantitative Reachability.” In Models, Algorithms, Logics and Tools, edited by Luca Aceto, Giorgio Bacci, Anna Ingólfsdóttir, Axel Legay, and Radu Mardare, 10460:367–81. Theoretical Computer Science and General Issues. Springer, 2017. https://doi.org/10.1007/978-3-319-63121-9_18."},"publication":"Models, Algorithms, Logics and Tools","page":"367 - 381","date_published":"2017-07-25T00:00:00Z","type":"book_chapter","alternative_title":["LNCS"],"abstract":[{"text":"In the analysis of reactive systems a quantitative objective assigns a real value to every trace of the system. The value decision problem for a quantitative objective requires a trace whose value is at least a given threshold, and the exact value decision problem requires a trace whose value is exactly the threshold. We compare the computational complexity of the value and exact value decision problems for classical quantitative objectives, such as sum, discounted sum, energy, and mean-payoff for two standard models of reactive systems, namely, graphs and graph games.","lang":"eng"}],"user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","_id":"625","intvolume":" 10460","title":"The cost of exactness in quantitative reachability","ddc":["000"],"status":"public","oa_version":"Submitted Version","file":[{"file_id":"7048","relation":"main_file","date_created":"2019-11-19T08:06:50Z","date_updated":"2020-07-14T12:47:25Z","checksum":"b2402766ec02c79801aac634bd8f9f6c","file_name":"2017_ModelsAlgorithms_Chatterjee.pdf","access_level":"open_access","creator":"dernst","content_type":"application/pdf","file_size":192826}]},{"date_published":"2017-09-21T00:00:00Z","publication":"PeerJ","citation":{"ista":"Nikolic N, Didara Z, Moll I. 2017. MazF activation promotes translational heterogeneity of the grcA mRNA in Escherichia coli populations. PeerJ. 2017(9), 3830.","ieee":"N. Nikolic, Z. Didara, and I. Moll, “MazF activation promotes translational heterogeneity of the grcA mRNA in Escherichia coli populations,” PeerJ, vol. 2017, no. 9. PeerJ, 2017.","apa":"Nikolic, N., Didara, Z., & Moll, I. (2017). MazF activation promotes translational heterogeneity of the grcA mRNA in Escherichia coli populations. PeerJ. PeerJ. https://doi.org/10.7717/peerj.3830","ama":"Nikolic N, Didara Z, Moll I. MazF activation promotes translational heterogeneity of the grcA mRNA in Escherichia coli populations. PeerJ. 2017;2017(9). doi:10.7717/peerj.3830","chicago":"Nikolic, Nela, Zrinka Didara, and Isabella Moll. “MazF Activation Promotes Translational Heterogeneity of the GrcA MRNA in Escherichia Coli Populations.” PeerJ. PeerJ, 2017. https://doi.org/10.7717/peerj.3830.","mla":"Nikolic, Nela, et al. “MazF Activation Promotes Translational Heterogeneity of the GrcA MRNA in Escherichia Coli Populations.” PeerJ, vol. 2017, no. 9, 3830, PeerJ, 2017, doi:10.7717/peerj.3830.","short":"N. Nikolic, Z. Didara, I. Moll, PeerJ 2017 (2017)."},"day":"21","has_accepted_license":"1","scopus_import":1,"oa_version":"Published Version","file":[{"date_updated":"2020-07-14T12:47:24Z","date_created":"2018-12-12T10:11:51Z","checksum":"3d79ae6b6eabc90b0eaaed82ff3493b0","relation":"main_file","file_id":"4908","file_size":682064,"content_type":"application/pdf","creator":"system","file_name":"IST-2017-909-v1+1_peerj-3830.pdf","access_level":"open_access"}],"pubrep_id":"909","ddc":["579"],"title":"MazF activation promotes translational heterogeneity of the grcA mRNA in Escherichia coli populations","status":"public","intvolume":" 2017","_id":"624","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","abstract":[{"text":"Bacteria adapt to adverse environmental conditions by altering gene expression patterns. Recently, a novel stress adaptation mechanism has been described that allows Escherichia coli to alter gene expression at the post-transcriptional level. The key player in this regulatory pathway is the endoribonuclease MazF, the toxin component of the toxin-antitoxin module mazEF that is triggered by various stressful conditions. In general, MazF degrades the majority of transcripts by cleaving at ACA sites, which results in the retardation of bacterial growth. Furthermore, MazF can process a small subset of mRNAs and render them leaderless by removing their ribosome binding site. MazF concomitantly modifies ribosomes, making them selective for the translation of leaderless mRNAs. In this study, we employed fluorescent reporter-systems to investigate mazEF expression during stressful conditions, and to infer consequences of the mRNA processing mediated by MazF on gene expression at the single-cell level. Our results suggest that mazEF transcription is maintained at low levels in single cells encountering adverse conditions, such as antibiotic stress or amino acid starvation. Moreover, using the grcA mRNA as a model for MazF-mediated mRNA processing, we found that MazF activation promotes heterogeneity in the grcA reporter expression, resulting in a subpopulation of cells with increased levels of GrcA reporter protein.","lang":"eng"}],"issue":"9","type":"journal_article","language":[{"iso":"eng"}],"doi":"10.7717/peerj.3830","quality_controlled":"1","tmp":{"name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","short":"CC BY (4.0)","image":"/images/cc_by.png"},"oa":1,"month":"09","publication_identifier":{"issn":["21678359"]},"date_updated":"2021-01-12T08:06:48Z","date_created":"2018-12-11T11:47:33Z","volume":2017,"author":[{"first_name":"Nela","last_name":"Nikolic","id":"42D9CABC-F248-11E8-B48F-1D18A9856A87","orcid":"0000-0001-9068-6090","full_name":"Nikolic, Nela"},{"first_name":"Zrinka","last_name":"Didara","full_name":"Didara, Zrinka"},{"full_name":"Moll, Isabella","last_name":"Moll","first_name":"Isabella"}],"publication_status":"published","publisher":"PeerJ","department":[{"_id":"CaGu"}],"year":"2017","acknowledgement":"Austrian Science Fund (FWF): M1697, P22249; Swiss National Science Foundation (SNF): 145706; European Commission;FWF Special Research Program: RNA-REG F43","file_date_updated":"2020-07-14T12:47:24Z","publist_id":"7172","article_number":"3830"}]