TY - JOUR AB - The fungal bioluminescence pathway can be reconstituted in other organisms allowing luminescence imaging without exogenously supplied substrate. The pathway starts from hispidin biosynthesis—a step catalyzed by a large fungal polyketide synthase that requires a posttranslational modification for activity. Here, we report identification of alternative compact hispidin synthases encoded by a phylogenetically diverse group of plants. A hybrid bioluminescence pathway that combines plant and fungal genes is more compact, not dependent on availability of machinery for posttranslational modifications, and confers autonomous bioluminescence in yeast, mammalian, and plant hosts. The compact size of plant hispidin synthases enables additional modes of delivery of autoluminescence, such as delivery with viral vectors. AU - Palkina, Kseniia A. AU - Karataeva, Tatiana A. AU - Perfilov, Maxim M. AU - Fakhranurova, Liliia I. AU - Markina, Nadezhda M. AU - Gonzalez Somermeyer, Louisa AU - Garcia-Perez, Elena AU - Vazquez-Vilar, Marta AU - Rodriguez-Rodriguez, Marta AU - Vazquez-Vilriales, Victor AU - Shakhova, Ekaterina S. AU - Mitiouchkina, Tatiana AU - Belozerova, Olga A. AU - Kovalchuk, Sergey I. AU - Alekberova, Anna AU - Malyshevskaia, Alena K. AU - Bugaeva, Evgenia N. AU - Guglya, Elena B. AU - Balakireva, Anastasia AU - Sytov, Nikita AU - Bezlikhotnova, Anastasia AU - Boldyreva, Daria I. AU - Babenko, Vladislav V. AU - Kondrashov, Fyodor AU - Choob, Vladimir V. AU - Orzaez, Diego AU - Yampolsky, Ilia V. AU - Mishin, Alexander S. AU - Sarkisyan, Karen S. ID - 15179 IS - 10 JF - Science Advances SN - 2375-2548 TI - A hybrid pathway for self-sustained luminescence VL - 10 ER - TY - JOUR AB - AlphaFold changed the field of structural biology by achieving three-dimensional (3D) structure prediction from protein sequence at experimental quality. The astounding success even led to claims that the protein folding problem is “solved”. However, protein folding problem is more than just structure prediction from sequence. Presently, it is unknown if the AlphaFold-triggered revolution could help to solve other problems related to protein folding. Here we assay the ability of AlphaFold to predict the impact of single mutations on protein stability (ΔΔG) and function. To study the question we extracted the pLDDT and metrics from AlphaFold predictions before and after single mutation in a protein and correlated the predicted change with the experimentally known ΔΔG values. Additionally, we correlated the same AlphaFold pLDDT metrics with the impact of a single mutation on structure using a large scale dataset of single mutations in GFP with the experimentally assayed levels of fluorescence. We found a very weak or no correlation between AlphaFold output metrics and change of protein stability or fluorescence. Our results imply that AlphaFold may not be immediately applied to other problems or applications in protein folding. AU - Pak, Marina A. AU - Markhieva, Karina A. AU - Novikova, Mariia S. AU - Petrov, Dmitry S. AU - Vorobyev, Ilya S. AU - Maksimova, Ekaterina AU - Kondrashov, Fyodor AU - Ivankov, Dmitry N. ID - 12758 IS - 3 JF - PLoS ONE TI - Using AlphaFold to predict the impact of single mutations on protein stability and function VL - 18 ER - TY - JOUR AB - Molecular compatibility between gametes is a prerequisite for successful fertilization. As long as a sperm and egg can recognize and bind each other via their surface proteins, gamete fusion may occur even between members of separate species, resulting in hybrids that can impact speciation. The egg membrane protein Bouncer confers species specificity to gamete interactions between medaka and zebrafish, preventing their cross-fertilization. Here, we leverage this specificity to uncover distinct amino acid residues and N-glycosylation patterns that differentially influence the function of medaka and zebrafish Bouncer and contribute to cross-species incompatibility. Curiously, in contrast to the specificity observed for medaka and zebrafish Bouncer, seahorse and fugu Bouncer are compatible with both zebrafish and medaka sperm, in line with the pervasive purifying selection that dominates Bouncer’s evolution. The Bouncer-sperm interaction is therefore the product of seemingly opposing evolutionary forces that, for some species, restrict fertilization to closely related fish, and for others, allow broad gamete compatibility that enables hybridization. AU - Gert, Krista R.B. AU - Panser, Karin AU - Surm, Joachim AU - Steinmetz, Benjamin S. AU - Schleiffer, Alexander AU - Jovine, Luca AU - Moran, Yehu AU - Kondrashov, Fyodor AU - Pauli, Andrea ID - 13164 JF - Nature Communications TI - Divergent molecular signatures in fish Bouncer proteins define cross-fertilization boundaries VL - 14 ER - TY - JOUR AB - Conflicts and natural disasters affect entire populations of the countries involved and, in addition to the thousands of lives destroyed, have a substantial negative impact on the scientific advances these countries provide. The unprovoked invasion of Ukraine by Russia, the devastating earthquake in Turkey and Syria, and the ongoing conflicts in the Middle East are just a few examples. Millions of people have been killed or displaced, their futures uncertain. These events have resulted in extensive infrastructure collapse, with loss of electricity, transportation, and access to services. Schools, universities, and research centers have been destroyed along with decades’ worth of data, samples, and findings. Scholars in disaster areas face short- and long-term problems in terms of what they can accomplish now for obtaining grants and for employment in the long run. In our interconnected world, conflicts and disasters are no longer a local problem but have wide-ranging impacts on the entire world, both now and in the future. Here, we focus on the current and ongoing impact of war on the scientific community within Ukraine and from this draw lessons that can be applied to all affected countries where scientists at risk are facing hardship. We present and classify examples of effective and feasible mechanisms used to support researchers in countries facing hardship and discuss how these can be implemented with help from the international scientific community and what more is desperately needed. Reaching out, providing accessible training opportunities, and developing collaborations should increase inclusion and connectivity, support scientific advancements within affected communities, and expedite postwar and disaster recovery. AU - Wolfsberger, Walter AU - Chhugani, Karishma AU - Shchubelka, Khrystyna AU - Frolova, Alina AU - Salyha, Yuriy AU - Zlenko, Oksana AU - Arych, Mykhailo AU - Dziuba, Dmytro AU - Parkhomenko, Andrii AU - Smolanka, Volodymyr AU - Gümüş, Zeynep H. AU - Sezgin, Efe AU - Diaz-Lameiro, Alondra AU - Toth, Viktor R. AU - Maci, Megi AU - Bortz, Eric AU - Kondrashov, Fyodor AU - Morton, Patricia M. AU - Łabaj, Paweł P. AU - Romero, Veronika AU - Hlávka, Jakub AU - Mangul, Serghei AU - Oleksyk, Taras K. ID - 13976 JF - GigaScience TI - Scientists without borders: Lessons from Ukraine VL - 12 ER - TY - GEN AU - Rella, Simon AU - Kulikova, Y AU - Minnegalieva, Aygul AU - Kondrashov, Fyodor ID - 14862 IS - Supplement_2 KW - Public Health KW - Environmental and Occupational Health SN - 1101-1262 T2 - European Journal of Public Health TI - Complex vaccination strategies prevent the emergence of vaccine resistance VL - 33 ER - TY - JOUR AB - During the COVID-19 pandemic, genomics and bioinformatics have emerged as essential public health tools. The genomic data acquired using these methods have supported the global health response, facilitated the development of testing methods and allowed the timely tracking of novel SARS-CoV-2 variants. Yet the virtually unlimited potential for rapid generation and analysis of genomic data is also coupled with unique technical, scientific and organizational challenges. Here, we discuss the application of genomic and computational methods for efficient data-driven COVID-19 response, the advantages of the democratization of viral sequencing around the world and the challenges associated with viral genome data collection and processing. AU - Knyazev, Sergey AU - Chhugani, Karishma AU - Sarwal, Varuni AU - Ayyala, Ram AU - Singh, Harman AU - Karthikeyan, Smruthi AU - Deshpande, Dhrithi AU - Baykal, Pelin Icer AU - Comarova, Zoia AU - Lu, Angela AU - Porozov, Yuri AU - Vasylyeva, Tetyana I. AU - Wertheim, Joel O. AU - Tierney, Braden T. AU - Chiu, Charles Y. AU - Sun, Ren AU - Wu, Aiping AU - Abedalthagafi, Malak S. AU - Pak, Victoria M. AU - Nagaraj, Shivashankar H. AU - Smith, Adam L. AU - Skums, Pavel AU - Pasaniuc, Bogdan AU - Komissarov, Andrey AU - Mason, Christopher E. AU - Bortz, Eric AU - Lemey, Philippe AU - Kondrashov, Fyodor AU - Beerenwinkel, Niko AU - Lam, Tommy Tsan Yuk AU - Wu, Nicholas C. AU - Zelikovsky, Alex AU - Knight, Rob AU - Crandall, Keith A. AU - Mangul, Serghei ID - 11187 IS - 4 JF - Nature Methods SN - 1548-7091 TI - Unlocking capacities of genomics for the COVID-19 response and future pandemics VL - 19 ER - TY - JOUR AB - Until recently, Shigella and enteroinvasive Escherichia coli were thought to be primate-restricted pathogens. The base of their pathogenicity is the type 3 secretion system (T3SS) encoded by the pINV virulence plasmid, which facilitates host cell invasion and subsequent proliferation. A large family of T3SS effectors, E3 ubiquitin-ligases encoded by the ipaH genes, have a key role in the Shigella pathogenicity through the modulation of cellular ubiquitination that degrades host proteins. However, recent genomic studies identified ipaH genes in the genomes of Escherichia marmotae, a potential marmot pathogen, and an E. coli extracted from fecal samples of bovine calves, suggesting that non-human hosts may also be infected by these strains, potentially pathogenic to humans. We performed a comparative genomic study of the functional repertoires in the ipaH gene family in Shigella and enteroinvasive Escherichia from human and predicted non-human hosts. We found that fewer than half of Shigella genomes had a complete set of ipaH genes, with frequent gene losses and duplications that were not consistent with the species tree and nomenclature. Non-human host IpaH proteins had a diverse set of substrate-binding domains and, in contrast to the Shigella proteins, two variants of the NEL C-terminal domain. Inconsistencies between strains phylogeny and composition of effectors indicate horizontal gene transfer between E. coli adapted to different hosts. These results provide a framework for understanding of ipaH-mediated host-pathogens interactions and suggest a need for a genomic study of fecal samples from diseased animals. AU - Dranenko, NO AU - Tutukina, MN AU - Gelfand, MS AU - Kondrashov, Fyodor AU - Bochkareva, Olga ID - 11344 JF - Scientific Reports SN - 2045-2322 TI - Chromosome-encoded IpaH ubiquitin ligases indicate non-human enteroinvasive Escherichia VL - 12 ER - TY - JOUR AB - Studies of protein fitness landscapes reveal biophysical constraints guiding protein evolution and empower prediction of functional proteins. However, generalisation of these findings is limited due to scarceness of systematic data on fitness landscapes of proteins with a defined evolutionary relationship. We characterized the fitness peaks of four orthologous fluorescent proteins with a broad range of sequence divergence. While two of the four studied fitness peaks were sharp, the other two were considerably flatter, being almost entirely free of epistatic interactions. Mutationally robust proteins, characterized by a flat fitness peak, were not optimal templates for machine-learning-driven protein design – instead, predictions were more accurate for fragile proteins with epistatic landscapes. Our work paves insights for practical application of fitness landscape heterogeneity in protein engineering. AU - Gonzalez Somermeyer, Louisa AU - Fleiss, Aubin AU - Mishin, Alexander S AU - Bozhanova, Nina G AU - Igolkina, Anna A AU - Meiler, Jens AU - Alaball Pujol, Maria-Elisenda AU - Putintseva, Ekaterina V AU - Sarkisyan, Karen S AU - Kondrashov, Fyodor ID - 11448 JF - eLife KW - General Immunology and Microbiology KW - General Biochemistry KW - Genetics and Molecular Biology KW - General Medicine KW - General Neuroscience SN - 2050-084X TI - Heterogeneity of the GFP fitness landscape and data-driven protein design VL - 11 ER - TY - JOUR AB - Empirical essays of fitness landscapes suggest that they may be rugged, that is having multiple fitness peaks. Such fitness landscapes, those that have multiple peaks, necessarily have special local structures, called reciprocal sign epistasis (Poelwijk et al. in J Theor Biol 272:141–144, 2011). Here, we investigate the quantitative relationship between the number of fitness peaks and the number of reciprocal sign epistatic interactions. Previously, it has been shown (Poelwijk et al. in J Theor Biol 272:141–144, 2011) that pairwise reciprocal sign epistasis is a necessary but not sufficient condition for the existence of multiple peaks. Applying discrete Morse theory, which to our knowledge has never been used in this context, we extend this result by giving the minimal number of reciprocal sign epistatic interactions required to create a given number of peaks. AU - Saona Urmeneta, Raimundo J AU - Kondrashov, Fyodor AU - Khudiakova, Kseniia ID - 11447 IS - 8 JF - Bulletin of Mathematical Biology KW - Computational Theory and Mathematics KW - General Agricultural and Biological Sciences KW - Pharmacology KW - General Environmental Science KW - General Biochemistry KW - Genetics and Molecular Biology KW - General Mathematics KW - Immunology KW - General Neuroscience SN - 0092-8240 TI - Relation between the number of peaks and the number of reciprocal sign epistatic interactions VL - 84 ER - TY - JOUR AB - Russia’s unprovoked attack on Ukraine has destroyed civilian infrastructure, including universities, research centers, and other academic infrastructure (1). Many Ukrainian scholars and researchers remain in Ukraine, and their work has suffered from major setbacks (2–4). We call on international scientists and institutions to support them. AU - Chhugani, Karishma AU - Frolova, Alina AU - Salyha, Yuriy AU - Fiscutean, Andrada AU - Zlenko, Oksana AU - Reinsone, Sanita AU - Wolfsberger, Walter W. AU - Ivashchenko, Oleksandra V. AU - Maci, Megi AU - Dziuba, Dmytro AU - Parkhomenko, Andrii AU - Bortz, Eric AU - Kondrashov, Fyodor AU - Łabaj, Paweł P. AU - Romero, Veronika AU - Hlávka, Jakub AU - Oleksyk, Taras K. AU - Mangul, Serghei ID - 12116 IS - 6626 JF - Science SN - 0036-8075 TI - Remote opportunities for scholars in Ukraine VL - 378 ER - TY - JOUR AB - Adult height inspired the first biometrical and quantitative genetic studies and is a test-case trait for understanding heritability. The studies of height led to formulation of the classical polygenic model, that has a profound influence on the way we view and analyse complex traits. An essential part of the classical model is an assumption of additivity of effects and normality of the distribution of the residuals. However, it may be expected that the normal approximation will become insufficient in bigger studies. Here, we demonstrate that when the height of hundreds of thousands of individuals is analysed, the model complexity needs to be increased to include non-additive interactions between sex, environment and genes. Alternatively, the use of log-normal approximation allowed us to still use the additive effects model. These findings are important for future genetic and methodologic studies that make use of adult height as an exemplar trait. AU - Slavskii, Sergei A. AU - Kuznetsov, Ivan A. AU - Shashkova, Tatiana I. AU - Bazykin, Georgii A. AU - Axenovich, Tatiana I. AU - Kondrashov, Fyodor AU - Aulchenko, Yurii S. ID - 9910 IS - 7 JF - European Journal of Human Genetics SN - 10184813 TI - The limits of normal approximation for adult height VL - 29 ER - TY - JOUR AB - Vaccines are thought to be the best available solution for controlling the ongoing SARS-CoV-2 pandemic. However, the emergence of vaccine-resistant strains may come too rapidly for current vaccine developments to alleviate the health, economic and social consequences of the pandemic. To quantify and characterize the risk of such a scenario, we created a SIR-derived model with initial stochastic dynamics of the vaccine-resistant strain to study the probability of its emergence and establishment. Using parameters realistically resembling SARS-CoV-2 transmission, we model a wave-like pattern of the pandemic and consider the impact of the rate of vaccination and the strength of non-pharmaceutical intervention measures on the probability of emergence of a resistant strain. As expected, we found that a fast rate of vaccination decreases the probability of emergence of a resistant strain. Counterintuitively, when a relaxation of non-pharmaceutical interventions happened at a time when most individuals of the population have already been vaccinated the probability of emergence of a resistant strain was greatly increased. Consequently, we show that a period of transmission reduction close to the end of the vaccination campaign can substantially reduce the probability of resistant strain establishment. Our results suggest that policymakers and individuals should consider maintaining non-pharmaceutical interventions and transmission-reducing behaviours throughout the entire vaccination period. AU - Rella, Simon AU - Kulikova, Yuliya A. AU - Dermitzakis, Emmanouil T. AU - Kondrashov, Fyodor ID - 9905 IS - 1 JF - Scientific Reports TI - Rates of SARS-CoV-2 transmission and vaccination impact the fate of vaccine-resistant strains VL - 11 ER - TY - GEN AB - The main idea behind the Core Project is to teach first year students at IST scientific communication skills and let them practice by presenting their research within an interdisciplinary environment. Over the course of the first semester, students participated in seminars, where they shared their results with the colleagues from other fields and took part in discussions on relevant subjects. The main focus during this sessions was on delivering the information in a simplified and comprehensible way, going into the very basics of a subject if necessary. At the end, the students were asked to present their research in the written form to exercise their writing skills. The reports were gathered in this document. All of them were reviewed by the teaching assistants and write-ups illustrating unique stylistic features and, in general, an outstanding level of writing skills, were honorably mentioned in the section "Selected Reports". AU - Maslov, Mikhail AU - Kondrashov, Fyodor AU - Artner, Christina AU - Hennessey-Wesen, Mike AU - Kavcic, Bor AU - Machnik, Nick N AU - Satapathy, Roshan K AU - Tomanek, Isabella ID - 8151 TI - Core Project Proceedings ER - TY - JOUR AB - In the course of sample preparation for Next Generation Sequencing (NGS), DNA is fragmented by various methods. Fragmentation shows a persistent bias with regard to the cleavage rates of various dinucleotides. With the exception of CpG dinucleotides the previously described biases were consistent with results of the DNA cleavage in solution. Here we computed cleavage rates of all dinucleotides including the methylated CpG and unmethylated CpG dinucleotides using data of the Whole Genome Sequencing datasets of the 1000 Genomes project. We found that the cleavage rate of CpG is significantly higher for the methylated CpG dinucleotides. Using this information, we developed a classifier for distinguishing cancer and healthy tissues based on their CpG islands statuses of the fragmentation. A simple Support Vector Machine classifier based on this algorithm shows an accuracy of 84%. The proposed method allows the detection of epigenetic markers purely based on mechanochemical DNA fragmentation, which can be detected by a simple analysis of the NGS sequencing data. AU - Uroshlev, Leonid A. AU - Abdullaev, Eldar T. AU - Umarova, Iren R. AU - Il’Icheva, Irina A. AU - Panchenko, Larisa A. AU - Polozov, Robert V. AU - Kondrashov, Fyodor AU - Nechipurenko, Yury D. AU - Grokhovsky, Sergei L. ID - 7931 JF - Scientific Reports TI - A method for identification of the methylation level of CpG islands from NGS data VL - 10 ER - TY - JOUR AB - Epistasis, the context-dependence of the contribution of an amino acid substitution to fitness, is common in evolution. To detect epistasis, fitness must be measured for at least four genotypes: the reference genotype, two different single mutants and a double mutant with both of the single mutations. For higher-order epistasis of the order n, fitness has to be measured for all 2n genotypes of an n-dimensional hypercube in genotype space forming a ‘combinatorially complete dataset’. So far, only a handful of such datasets have been produced by manual curation. Concurrently, random mutagenesis experiments have produced measurements of fitness and other phenotypes in a high-throughput manner, potentially containing a number of combinatorially complete datasets. We present an effective recursive algorithm for finding all hypercube structures in random mutagenesis experimental data. To test the algorithm, we applied it to the data from a recent HIS3 protein dataset and found all 199 847 053 unique combinatorially complete genotype combinations of dimensionality ranging from 2 to 12. The algorithm may be useful for researchers looking for higher-order epistasis in their high-throughput experimental data. AU - Esteban, Laura A AU - Lonishin, Lyubov R AU - Bobrovskiy, Daniil M AU - Leleytner, Gregory AU - Bogatyreva, Natalya S AU - Kondrashov, Fyodor AU - Ivankov, Dmitry N ID - 8645 IS - 6 JF - Bioinformatics SN - 1367-4803 TI - HypercubeME: Two hundred million combinatorially complete datasets from a single experiment VL - 36 ER - TY - JOUR AB - Autoluminescent plants engineered to express a bacterial bioluminescence gene cluster in plastids have not been widely adopted because of low light output. We engineered tobacco plants with a fungal bioluminescence system that converts caffeic acid (present in all plants) into luciferin and report self-sustained luminescence that is visible to the naked eye. Our findings could underpin development of a suite of imaging tools for plants. AU - Mitiouchkina, Tatiana AU - Mishin, Alexander S. AU - Gonzalez Somermeyer, Louisa AU - Markina, Nadezhda M. AU - Chepurnyh, Tatiana V. AU - Guglya, Elena B. AU - Karataeva, Tatiana A. AU - Palkina, Kseniia A. AU - Shakhova, Ekaterina S. AU - Fakhranurova, Liliia I. AU - Chekova, Sofia V. AU - Tsarkova, Aleksandra S. AU - Golubev, Yaroslav V. AU - Negrebetsky, Vadim V. AU - Dolgushin, Sergey A. AU - Shalaev, Pavel V. AU - Shlykov, Dmitry AU - Melnik, Olesya A. AU - Shipunova, Victoria O. AU - Deyev, Sergey M. AU - Bubyrev, Andrey I. AU - Pushin, Alexander S. AU - Choob, Vladimir V. AU - Dolgov, Sergey V. AU - Kondrashov, Fyodor AU - Yampolsky, Ilia V. AU - Sarkisyan, Karen S. ID - 7889 JF - Nature Biotechnology SN - 1087-0156 TI - Plants with genetically encoded autoluminescence VL - 38 ER - TY - JOUR AB - Characterizing the fitness landscape, a representation of fitness for a large set of genotypes, is key to understanding how genetic information is interpreted to create functional organisms. Here we determined the evolutionarily-relevant segment of the fitness landscape of His3, a gene coding for an enzyme in the histidine synthesis pathway, focusing on combinations of amino acid states found at orthologous sites of extant species. Just 15% of amino acids found in yeast His3 orthologues were always neutral while the impact on fitness of the remaining 85% depended on the genetic background. Furthermore, at 67% of sites, amino acid replacements were under sign epistasis, having both strongly positive and negative effect in different genetic backgrounds. 46% of sites were under reciprocal sign epistasis. The fitness impact of amino acid replacements was influenced by only a few genetic backgrounds but involved interaction of multiple sites, shaping a rugged fitness landscape in which many of the shortest paths between highly fit genotypes are inaccessible. AU - Pokusaeva, Victoria AU - Usmanova, Dinara R. AU - Putintseva, Ekaterina V. AU - Espinar, Lorena AU - Sarkisyan, Karen AU - Mishin, Alexander S. AU - Bogatyreva, Natalya S. AU - Ivankov, Dmitry AU - Akopyan, Arseniy AU - Avvakumov, Sergey AU - Povolotskaya, Inna S. AU - Filion, Guillaume J. AU - Carey, Lucas B. AU - Kondrashov, Fyodor ID - 6419 IS - 4 JF - PLoS Genetics TI - An experimental assay of the interactions of amino acids from orthologous sequences shaping a complex fitness landscape VL - 15 ER - TY - GEN AU - Pokusaeva, Victoria AU - Usmanova, Dinara R. AU - Putintseva, Ekaterina V. AU - Espinar, Lorena AU - Sarkisyan, Karen AU - Mishin, Alexander S. AU - Bogatyreva, Natalya S. AU - Ivankov, Dmitry AU - Akopyan, Arseniy AU - Avvakumov, Sergey AU - Povolotskaya, Inna S. AU - Filion, Guillaume J. AU - Carey, Lucas B. AU - Kondrashov, Fyodor ID - 9790 TI - A statistical summary of segment libraries and sequencing results ER - TY - GEN AU - Pokusaeva, Victoria AU - Usmanova, Dinara R. AU - Putintseva, Ekaterina V. AU - Espinar, Lorena AU - Sarkisyan, Karen AU - Mishin, Alexander S. AU - Bogatyreva, Natalya S. AU - Ivankov, Dmitry AU - Akopyan, Arseniy AU - Povolotskaya, Inna S. AU - Filion, Guillaume J. AU - Carey, Lucas B. AU - Kondrashov, Fyodor ID - 9797 TI - A statistical summary of segment libraries and sequencing results ER - TY - GEN AU - Pokusaeva, Victoria AU - Usmanova, Dinara R. AU - Putintseva, Ekaterina V. AU - Espinar, Lorena AU - Sarkisyan, Karen AU - Mishin, Alexander S. AU - Bogatyreva, Natalya S. AU - Ivankov, Dmitry AU - Akopyan, Arseniy AU - Avvakumov, Sergey AU - Povolotskaya, Inna S. AU - Filion, Guillaume J. AU - Carey, Lucas B. AU - Kondrashov, Fyodor ID - 9789 TI - Multiple alignment of His3 orthologues ER -