@article{3113, abstract = {A cell membrane can be considered a liquid-phase plane in which lipids and proteins theoretically are free to diffuse. Numerous reports,however, describe retarded diffusion ofmembrane proteins in animal cells. This anomalous diffusion results from a combination of structuring factors including protein-protein interactions, cytoskeleton corralling, and lipid organization into microdomains. In plant cells, plasma-membrane (PM) proteins have been described as relatively immobile, but the control mechanisms that structure the PM have not been studied. Here, we use fluorescence recovery after photobleaching to estimate mobility of a set of minimal PM proteins. These proteins consist only of a PM-anchoring domain fused to a fluorescent protein, but their mobilities remained limited, as is the case for many full-length proteins. Neither the cytoskeleton nor membrane microdomain structure was involved in constraining the diffusion of these proteins. The cell wall, however, was shown to have a crucial role in immobilizing PM proteins. In addition, by single-molecule fluorescence imaging we confirmed that the pattern of cellulose deposition in the cell wall affects the trajectory and speed ofPMprotein diffusion. Regulation ofPMprotein dynamics by the plant cell wall can be interpreted as a mechanism for regulating protein interactions in processes such as trafficking and signal transduction.}, author = {Martinière, Alexandre and Lavagi, Irene and Nageswaran, Gayathri and Rolfe, Daniel J and Maneta-Peyret, Lilly and Luu, Doan-Trung and Botchway, Stanley W and Webb, Stephen E and Mongrand, Sebastien and Maurel, Christophe and Martin-Fernandez, Marisa L and Kleine-Vehn, Jürgen and Jirí Friml and Moreau, Patrick and Runions, John}, journal = {PNAS}, number = {31}, pages = {12805 -- 12810}, publisher = {National Academy of Sciences}, title = {{Cell wall constrains lateral diffusion of plant plasma membrane proteins}}, doi = {10.1073/pnas.1202040109}, volume = {109}, year = {2012}, } @article{3114, abstract = {Auxin is a key coordinative signal required for many aspects of plant development and its levels are controlled by auxin metabolism and intercellular auxin transport. Here we find that a member of PIN auxin transporter family, PIN8 is expressed in male gametophyte of Arabidopsis thaliana and has a crucial role in pollen development and functionality. Ectopic expression in sporophytic tissues establishes a role of PIN8 in regulating auxin homoeostasis and metabolism. PIN8 co-localizes with PIN5 to the endoplasmic reticulum (ER) where it acts as an auxin transporter. Genetic analyses reveal an antagonistic action of PIN5 and PIN8 in the regulation of intracellular auxin homoeostasis and gametophyte as well as sporophyte development. Our results reveal a role of the auxin transport in male gametophyte development in which the distinct actions of ER-localized PIN transporters regulate cellular auxin homoeostasis and maintain the auxin levels optimal for pollen development and pollen tube growth.}, author = {Ding, Zhaojun and Wang, Bangjun and Moreno, Ignacio and Dupláková, Nikoleta and Sibu Simon and Carraro, Nicola and Reemmer, Jesica and Pěnčík, Aleš and Xu Chen and Tejos, Ricardo I and Skůpa, Petr and Pollmann, Stephan and Mravec, Jozef and Petrášek, Jan and Zažímalová, Eva and Honys, David and Rolčík, Jakub and Murphy, Angus S and Orellana, Ariel and Geisler, Markus and Jirí Friml}, journal = {Nature Communications}, number = {AN 941}, publisher = {Nature Publishing Group}, title = {{ER-localized auxin transporter PIN8 regulates auxin homeostasis and male gametophyte development in Arabidopsis}}, doi = {10.1038/ncomms1941}, volume = {3}, year = {2012}, } @article{3111, abstract = {PIN-FORMED (PIN) protein-mediated auxin polar transport is critically important for development, pattern formation, and morphogenesis in plants. Auxin has been implicated in the regulation of polar auxin transport by inhibiting PIN endocytosis [1, 2], but how auxin regulates this process is poorly understood. Our genetic screen identified the Arabidopsis SPIKE1 (SPK1) gene whose loss-of-function mutations increased lateral root density and retarded gravitropic responses, as do pin2 knockout mutations [3]. SPK1 belongs to the conserved DHR2-Dock family of Rho guanine nucleotide exchange factors [4-6]. The spk1 mutations induced PIN2 internalization that was not suppressed by auxin, as did the loss-of-function mutations for Rho-like GTPase from Plants 6 (ROP6)-GTPase or its effector RIC1. Furthermore, SPK1 was required for auxin induction of ROP6 activation. Our results have established a Rho GTPase-based auxin signaling pathway that maintains PIN2 polar distribution to the plasma membrane via inhibition of its internalization in Arabidopsis roots. Our findings provide new insights into signaling mechanisms that underlie the regulation of the dynamic trafficking of PINs required for long-distance auxin transport and that link auxin signaling to PIN-mediated pattern formation and morphogenesis.}, author = {Lin, Deshu and Nagawa, Shingo and Chen, Jisheng and Cao, Lingyan and Xu Chen and Xu, Tongda and Hongjiang Li and Dhonukshe, Pankaj and Yamamuro, Chizuko and Jirí Friml and Scheres, Ben and Fu, Ying and Yang, Zhenbiao}, journal = {Current Biology}, number = {14}, pages = {1319 -- 1325}, publisher = {Cell Press}, title = {{A ROP GTPase dependent auxin signaling pathway regulates the subcellular distribution of PIN2 in Arabidopsis roots}}, doi = {10.1016/j.cub.2012.05.019}, volume = {22}, year = {2012}, } @article{3112, abstract = {The dynamic spatial and temporal distribution of the crucial plant signaling molecule auxin is achieved by feedback coordination of auxin signaling and intercellular auxin transport pathways [1, 2]. Developmental roles of auxin have been attributed predominantly to its effect on transcription; however, an alternative pathway involving AUXIN BINDING PROTEIN1 (ABP1) has been proposed to regulate clathrin-mediated endocytosis in roots and Rho-like GTPase (ROP)-dependent pavement cell interdigitation in leaves [3, 4]. In this study, we show that ROP6 and its downstream effector RIC1 regulate clathrin association with the plasma membrane for clathrin-mediated endocytosis, as well as for its feedback regulation by auxin. Genetic analysis revealed that ROP6/RIC1 acts downstream of ABP1 to regulate endocytosis. This signaling circuit is also involved in the feedback regulation of PIN-FORMED 1 (PIN1) and PIN2 auxin transporters activity (via its constitutive endocytosis) and corresponding auxin transport-mediated processes, including root gravitropism and leave vascular tissue patterning. Our findings suggest that the signaling module auxin-ABP1-ROP6/RIC1-clathrin-PIN1/PIN2 is a shared component of the feedback regulation of auxin transport during both root and aerial development.}, author = {Xu Chen and Naramoto, Satoshi and Robert, Stéphanie and Tejos, Ricardo and Löfke, Christian and Lin, Deshu and Yang, Zhenbiao and Jirí Friml}, journal = {Current Biology}, number = {14}, pages = {1326 -- 1332}, publisher = {Cell Press}, title = {{ABP1 and ROP6 GTPase signaling regulate clathrin mediated endocytosis in Arabidopsis roots}}, doi = {10.1016/j.cub.2012.05.020}, volume = {22}, year = {2012}, } @article{3128, abstract = {We consider two-player zero-sum stochastic games on graphs with ω-regular winning conditions specified as parity objectives. These games have applications in the design and control of reactive systems. We survey the complexity results for the problem of deciding the winner in such games, and in classes of interest obtained as special cases, based on the information and the power of randomization available to the players, on the class of objectives and on the winning mode. On the basis of information, these games can be classified as follows: (a) partial-observation (both players have partial view of the game); (b) one-sided partial-observation (one player has partial-observation and the other player has complete-observation); and (c) complete-observation (both players have complete view of the game). The one-sided partial-observation games have two important subclasses: the one-player games, known as partial-observation Markov decision processes (POMDPs), and the blind one-player games, known as probabilistic automata. On the basis of randomization, (a) the players may not be allowed to use randomization (pure strategies), or (b) they may choose a probability distribution over actions but the actual random choice is external and not visible to the player (actions invisible), or (c) they may use full randomization. Finally, various classes of games are obtained by restricting the parity objective to a reachability, safety, Büchi, or coBüchi condition. We also consider several winning modes, such as sure-winning (i.e., all outcomes of a strategy have to satisfy the winning condition), almost-sure winning (i.e., winning with probability 1), limit-sure winning (i.e., winning with probability arbitrarily close to 1), and value-threshold winning (i.e., winning with probability at least ν, where ν is a given rational). }, author = {Chatterjee, Krishnendu and Doyen, Laurent and Henzinger, Thomas A}, journal = {Formal Methods in System Design}, number = {2}, pages = {268 -- 284}, publisher = {Springer}, title = {{A survey of partial-observation stochastic parity games}}, doi = {10.1007/s10703-012-0164-2}, volume = {43}, year = {2012}, } @inproceedings{3125, abstract = {We propose a new learning method to infer a mid-level feature representation that combines the advantage of semantic attribute representations with the higher expressive power of non-semantic features. The idea lies in augmenting an existing attribute-based representation with additional dimensions for which an autoencoder model is coupled with a large-margin principle. This construction allows a smooth transition between the zero-shot regime with no training example, the unsupervised regime with training examples but without class labels, and the supervised regime with training examples and with class labels. The resulting optimization problem can be solved efficiently, because several of the necessity steps have closed-form solutions. Through extensive experiments we show that the augmented representation achieves better results in terms of object categorization accuracy than the semantic representation alone.}, author = {Sharmanska, Viktoriia and Quadrianto, Novi and Lampert, Christoph}, location = {Florence, Italy}, number = {PART 5}, pages = {242 -- 255}, publisher = {Springer}, title = {{Augmented attribute representations}}, doi = {10.1007/978-3-642-33715-4_18}, volume = {7576}, year = {2012}, } @inproceedings{3129, abstract = {Let K be a simplicial complex and g the rank of its p-th homology group Hp(K) defined with ℤ2 coefficients. We show that we can compute a basis H of Hp(K) and annotate each p-simplex of K with a binary vector of length g with the following property: the annotations, summed over all p-simplices in any p-cycle z, provide the coordinate vector of the homology class [z] in the basis H. The basis and the annotations for all simplices can be computed in O(n ω ) time, where n is the size of K and ω < 2.376 is a quantity so that two n×n matrices can be multiplied in O(n ω ) time. The precomputed annotations permit answering queries about the independence or the triviality of p-cycles efficiently. Using annotations of edges in 2-complexes, we derive better algorithms for computing optimal basis and optimal homologous cycles in 1 - dimensional homology. Specifically, for computing an optimal basis of H1(K) , we improve the previously known time complexity from O(n 4) to O(n ω  + n 2 g ω − 1). Here n denotes the size of the 2-skeleton of K and g the rank of H1(K) . Computing an optimal cycle homologous to a given 1-cycle is NP-hard even for surfaces and an algorithm taking 2 O(g) nlogn time is known for surfaces. We extend this algorithm to work with arbitrary 2-complexes in O(n ω ) + 2 O(g) n 2logn time using annotations. }, author = {Busaryev, Oleksiy and Cabello, Sergio and Chen, Chao and Dey, Tamal and Wang, Yusu}, location = {Helsinki, Finland}, pages = {189 -- 200}, publisher = {Springer}, title = {{Annotating simplices with a homology basis and its applications}}, doi = {10.1007/978-3-642-31155-0_17}, volume = {7357}, year = {2012}, } @inproceedings{3126, abstract = {In this work we propose a new information-theoretic clustering algorithm that infers cluster memberships by direct optimization of a non-parametric mutual information estimate between data distribution and cluster assignment. Although the optimization objective has a solid theoretical foundation it is hard to optimize. We propose an approximate optimization formulation that leads to an efficient algorithm with low runtime complexity. The algorithm has a single free parameter, the number of clusters to find. We demonstrate superior performance on several synthetic and real datasets. }, author = {Müller, Andreas and Nowozin, Sebastian and Lampert, Christoph}, location = {Graz, Austria}, pages = {205 -- 215}, publisher = {Springer}, title = {{Information theoretic clustering using minimal spanning trees}}, doi = {10.1007/978-3-642-32717-9_21}, volume = {7476}, year = {2012}, } @inproceedings{3155, abstract = {We propose synchronous interfaces, a new interface theory for discrete-time systems. We use an application to time-triggered scheduling to drive the design choices for our formalism; in particular, additionally to deriving useful mathematical properties, we focus on providing a syntax which is adapted to natural high-level system modeling. As a result, we develop an interface model that relies on a guarded-command based language and is equipped with shared variables and explicit discrete-time clocks. We define all standard interface operations: compatibility checking, composition, refinement, and shared refinement. Apart from the synchronous interface model, the contribution of this paper is the establishment of a formal relation between interface theories and real-time scheduling, where we demonstrate a fully automatic framework for the incremental computation of time-triggered schedules.}, author = {Delahaye, Benoît and Fahrenberg, Uli and Henzinger, Thomas A and Legay, Axel and Nickovic, Dejan}, location = {Stockholm, Sweden}, pages = {203 -- 218}, publisher = {Springer}, title = {{Synchronous interface theories and time triggered scheduling}}, doi = {10.1007/978-3-642-30793-5_13}, volume = {7273}, year = {2012}, } @article{3159, abstract = {The structure of hierarchical networks in biological and physical systems has long been characterized using the Horton-Strahler ordering scheme. The scheme assigns an integer order to each edge in the network based on the topology of branching such that the order increases from distal parts of the network (e.g., mountain streams or capillaries) to the "root" of the network (e.g., the river outlet or the aorta). However, Horton-Strahler ordering cannot be applied to networks with loops because they they create a contradiction in the edge ordering in terms of which edge precedes another in the hierarchy. Here, we present a generalization of the Horton-Strahler order to weighted planar reticular networks, where weights are assumed to correlate with the importance of network edges, e.g., weights estimated from edge widths may correlate to flow capacity. Our method assigns hierarchical levels not only to edges of the network, but also to its loops, and classifies the edges into reticular edges, which are responsible for loop formation, and tree edges. In addition, we perform a detailed and rigorous theoretical analysis of the sensitivity of the hierarchical levels to weight perturbations. In doing so, we show that the ordering of the reticular edges is more robust to noise in weight estimation than is the ordering of the tree edges. We discuss applications of this generalized Horton-Strahler ordering to the study of leaf venation and other biological networks.}, author = {Mileyko, Yuriy and Edelsbrunner, Herbert and Price, Charles and Weitz, Joshua}, journal = {PLoS One}, number = {6}, publisher = {Public Library of Science}, title = {{Hierarchical ordering of reticular networks}}, doi = {10.1371/journal.pone.0036715}, volume = {7}, year = {2012}, }