@article{11160, abstract = {Mutations in the chromodomain helicase DNA-binding 8 (CHD8) gene are a frequent cause of autism spectrum disorder (ASD). While its phenotypic spectrum often encompasses macrocephaly, implicating cortical abnormalities, how CHD8 haploinsufficiency affects neurodevelopmental is unclear. Here, employing human cerebral organoids, we find that CHD8 haploinsufficiency disrupted neurodevelopmental trajectories with an accelerated and delayed generation of, respectively, inhibitory and excitatory neurons that yields, at days 60 and 120, symmetrically opposite expansions in their proportions. This imbalance is consistent with an enlargement of cerebral organoids as an in vitro correlate of patients’ macrocephaly. Through an isogenic design of patient-specific mutations and mosaic organoids, we define genotype-phenotype relationships and uncover their cell-autonomous nature. Our results define cell-type-specific CHD8-dependent molecular defects related to an abnormal program of proliferation and alternative splicing. By identifying cell-type-specific effects of CHD8 mutations, our study uncovers reproducible developmental alterations that may be employed for neurodevelopmental disease modeling.}, author = {Villa, Carlo Emanuele and Cheroni, Cristina and Dotter, Christoph and López-Tóbon, Alejandro and Oliveira, Bárbara and Sacco, Roberto and Yahya, Aysan Çerağ and Morandell, Jasmin and Gabriele, Michele and Tavakoli, Mojtaba and Lyudchik, Julia and Sommer, Christoph M and Gabitto, Mariano and Danzl, Johann G and Testa, Giuseppe and Novarino, Gaia}, issn = {2211-1247}, journal = {Cell Reports}, keywords = {General Biochemistry, Genetics and Molecular Biology}, number = {1}, publisher = {Elsevier}, title = {{CHD8 haploinsufficiency links autism to transient alterations in excitatory and inhibitory trajectories}}, doi = {10.1016/j.celrep.2022.110615}, volume = {39}, year = {2022}, } @phdthesis{12364, abstract = {Autism spectrum disorders (ASDs) are a group of neurodevelopmental disorders characterized by behavioral symptoms such as problems in social communication and interaction, as well as repetitive, restricted behaviors and interests. These disorders show a high degree of heritability and hundreds of risk genes have been identifed using high throughput sequencing technologies. This genetic heterogeneity has hampered eforts in understanding the pathogenesis of ASD but at the same time given rise to the concept of convergent mechanisms. Previous studies have identifed that risk genes for ASD broadly converge onto specifc functional categories with transcriptional regulation being one of the biggest groups. In this thesis, I focus on this subgroup of genes and investigate the gene regulatory consequences of some of them in the context of neurodevelopment. First, we showed that mutations in the ASD and intellectual disability risk gene Setd5 lead to perturbations of gene regulatory programs in early cell fate specifcation. In addition, adult animals display abnormal learning behavior which is mirrored at the transcriptional level by altered activity dependent regulation of postsynaptic gene expression. Lastly, we link the regulatory function of Setd5 to its interaction with the Paf1 and the NCoR complex. Second, by modeling the heterozygous loss of the top ASD gene CHD8 in human cerebral organoids we demonstrate profound changes in the developmental trajectories of both inhibitory and excitatory neurons using single cell RNA-sequencing. While the former were generated earlier in CHD8+/- organoids, the generation of the latter was shifted to later times in favor of a prolonged progenitor expansion phase and ultimately increased organoid size. Finally, by modeling heterozygous mutations for four ASD associated chromatin modifers, ASH1L, KDM6B, KMT5B, and SETD5 in human cortical spheroids we show evidence of regulatory convergence across three of those genes. We observe a shift from dorsal cortical excitatory neuron fates towards partially ventralized cell types resembling cells from the lateral ganglionic eminence. As this project is still ongoing at the time of writing, future experiments will aim at elucidating the regulatory mechanisms underlying this shift with the aim of linking these three ASD risk genes through biological convergence.}, author = {Dotter, Christoph}, issn = {2663-337X}, pages = {152}, publisher = {Institute of Science and Technology Austria}, title = {{Transcriptional consequences of mutations in genes associated with Autism Spectrum Disorder}}, doi = {10.15479/at:ista:12094}, year = {2022}, } @article{10614, abstract = {The infiltration of immune cells into tissues underlies the establishment of tissue-resident macrophages and responses to infections and tumors. Yet the mechanisms immune cells utilize to negotiate tissue barriers in living organisms are not well understood, and a role for cortical actin has not been examined. Here, we find that the tissue invasion of Drosophila macrophages, also known as plasmatocytes or hemocytes, utilizes enhanced cortical F-actin levels stimulated by the Drosophila member of the fos proto oncogene transcription factor family (Dfos, Kayak). RNA sequencing analysis and live imaging show that Dfos enhances F-actin levels around the entire macrophage surface by increasing mRNA levels of the membrane spanning molecular scaffold tetraspanin TM4SF, and the actin cross-linking filamin Cheerio, which are themselves required for invasion. Both the filamin and the tetraspanin enhance the cortical activity of Rho1 and the formin Diaphanous and thus the assembly of cortical actin, which is a critical function since expressing a dominant active form of Diaphanous can rescue the Dfos macrophage invasion defect. In vivo imaging shows that Dfos enhances the efficiency of the initial phases of macrophage tissue entry. Genetic evidence argues that this Dfos-induced program in macrophages counteracts the constraint produced by the tension of surrounding tissues and buffers the properties of the macrophage nucleus from affecting tissue entry. We thus identify strengthening the cortical actin cytoskeleton through Dfos as a key process allowing efficient forward movement of an immune cell into surrounding tissues. }, author = {Belyaeva, Vera and Wachner, Stephanie and György, Attila and Emtenani, Shamsi and Gridchyn, Igor and Akhmanova, Maria and Linder, M and Roblek, Marko and Sibilia, M and Siekhaus, Daria E}, issn = {1545-7885}, journal = {PLoS Biology}, number = {1}, pages = {e3001494}, publisher = {Public Library of Science}, title = {{Fos regulates macrophage infiltration against surrounding tissue resistance by a cortical actin-based mechanism in Drosophila}}, doi = {10.1371/journal.pbio.3001494}, volume = {20}, year = {2022}, } @article{12244, abstract = {Environmental cues influence the highly dynamic morphology of microglia. Strategies to characterize these changes usually involve user-selected morphometric features, which preclude the identification of a spectrum of context-dependent morphological phenotypes. Here we develop MorphOMICs, a topological data analysis approach, which enables semiautomatic mapping of microglial morphology into an atlas of cue-dependent phenotypes and overcomes feature-selection biases and biological variability. We extract spatially heterogeneous and sexually dimorphic morphological phenotypes for seven adult mouse brain regions. This sex-specific phenotype declines with maturation but increases over the disease trajectories in two neurodegeneration mouse models, with females showing a faster morphological shift in affected brain regions. Remarkably, microglia morphologies reflect an adaptation upon repeated exposure to ketamine anesthesia and do not recover to control morphologies. Finally, we demonstrate that both long primary processes and short terminal processes provide distinct insights to morphological phenotypes. MorphOMICs opens a new perspective to characterize microglial morphology.}, author = {Colombo, Gloria and Cubero, Ryan J and Kanari, Lida and Venturino, Alessandro and Schulz, Rouven and Scolamiero, Martina and Agerberg, Jens and Mathys, Hansruedi and Tsai, Li-Huei and Chachólski, Wojciech and Hess, Kathryn and Siegert, Sandra}, issn = {1546-1726}, journal = {Nature Neuroscience}, keywords = {General Neuroscience}, number = {10}, pages = {1379--1393}, publisher = {Springer Nature}, title = {{A tool for mapping microglial morphology, morphOMICs, reveals brain-region and sex-dependent phenotypes}}, doi = {10.1038/s41593-022-01167-6}, volume = {25}, year = {2022}, } @phdthesis{11393, abstract = {AMPA receptors (AMPARs) mediate fast excitatory neurotransmission and their role is implicated in complex processes such as learning and memory and various neurological diseases. These receptors are composed of different subunits and the subunit composition can affect channel properties, receptor trafficking and interaction with other associated proteins. Using the high sensitivity SDS-digested freeze-fracture replica labeling (SDS-FRL) for electron microscopy I investigated the number, density, and localization of AMPAR subunits, GluA1, GluA2, GluA3, and GluA1-3 (panAMPA) in pyramidal cells in the CA1 area of mouse hippocampus. I have found that the immunogold labeling for all of these subunits in the postsynaptic sites was highest in stratum radiatum and lowest in stratum lacunosummoleculare. The labeling density for the all subunits in the extrasynaptic sites showed a gradual increase from the pyramidal cell soma towards the distal part of stratum radiatum. The densities of extrasynaptic GluA1, GluA2 and panAMPA labeling reached 10-15% of synaptic densities, while the ratio of extrasynaptic labeling for GluA3 was significantly lower compared than those for other subunits. The labeling patterns for GluA1, GluA2 and GluA1-3 are similar and their densities were higher in the periphery than center of synapses. In contrast, the GluA3- containing receptors were more centrally localized compared to the GluA1- and GluA2- containing receptors. The hippocampus plays a central role in learning and memory. Contextual learning has been shown to require the delivery of AMPA receptors to CA1 synapses in the dorsal hippocampus. However, proximodistal heterogeneity of this plasticity and particular contribution of different AMPA receptor subunits are not fully understood. By combining inhibitory avoidance task, a hippocampus-dependent contextual fear-learning paradigm, with SDS-FRL, I have revealed an increase in synaptic density specific to GluA1-containing AMPA receptors in the CA1 area. The intrasynaptic distribution of GluA1 also changed from the periphery to center-preferred pattern. Furthermore, this synaptic plasticity was evident selectively in stratum radiatum but not stratum oriens, and in the CA1 subregion proximal but not distal to CA2. These findings further contribute to our understanding of how specific hippocampal subregions and AMPA receptor subunits are involved in physiological learning. Although the immunolabeling results above shed light on subunit-specific plasticity in AMPAR distribution, no tools to visualize and study the subunit composition at the single channel level in situ have been available. Electron microscopy with conventional immunogold labeling approaches has limitations in the single channel analysis because of the large size of antibodies and steric hindrance hampering multiple subunit labeling of single channels. I managed to develop a new chemical labeling system using a short peptide tag and small synthetic probes, which form specific covalent bond with a cysteine residue in the tag fused to proteins of interest (reactive tag system). I additionally made substantial progress into adapting this system for AMPA receptor subunits.}, author = {Jevtic, Marijo}, issn = {2663-337X}, pages = {108}, publisher = {Institute of Science and Technology Austria}, title = {{Contextual fear learning induced changes in AMPA receptor subtypes along the proximodistal axis in dorsal hippocampus}}, doi = {10.15479/at:ista:11393}, year = {2022}, } @phdthesis{12366, abstract = {Recent substantial advances in the feld of superconducting circuits have shown its potential as a leading platform for future quantum computing. In contrast to classical computers based on bits that are represented by a single binary value, 0 or 1, quantum bits (or qubits) can be in a superposition of both. Thus, quantum computers can store and handle more information at the same time and a quantum advantage has already been demonstrated for two types of computational tasks. Rapid progress in academic and industry labs accelerates the development of superconducting processors which may soon fnd applications in complex computations, chemical simulations, cryptography, and optimization. Now that these machines are scaled up to tackle such problems the questions of qubit interconnects and networks becomes very relevant. How to route signals on-chip between diferent processor components? What is the most efcient way to entangle qubits? And how to then send and process entangled signals between distant cryostats hosting superconducting processors? In this thesis, we are looking for solutions to these problems by studying the collective behavior of superconducting qubit ensembles. We frst demonstrate on-demand tunable directional scattering of microwave photons from a pair of qubits in a waveguide. Such a device can route microwave photons on-chip with a high diode efciency. Then we focus on studying ultra-strong coupling regimes between light (microwave photons) and matter (superconducting qubits), a regime that could be promising for extremely fast multi-qubit entanglement generation. Finally, we show coherent pulse storage and periodic revivals in a fve qubit ensemble strongly coupled to a resonator. Such a reconfgurable storage device could be used as part of a quantum repeater that is needed for longer-distance quantum communication. The achieved high degree of control over multi-qubit ensembles highlights not only the beautiful physics of circuit quantum electrodynamics, it also represents the frst step toward new quantum simulation and communication methods, and certain techniques may also fnd applications in future superconducting quantum computing hardware. }, author = {Redchenko, Elena}, isbn = {978-3-99078-024-4}, issn = {2663-337X}, pages = {168}, publisher = {Institute of Science and Technology Austria}, title = {{Controllable states of superconducting Qubit ensembles}}, doi = {10.15479/at:ista:12132}, year = {2022}, } @phdthesis{11193, abstract = {The infiltration of immune cells into tissues underlies the establishment of tissue-resident macrophages and responses to infections and tumors. However, the mechanisms immune cells utilize to collectively migrate through tissue barriers in vivo are not yet well understood. In this thesis, I describe two mechanisms that Drosophila immune cells (hemocytes) use to overcome the tissue barrier of the germband in the embryo. One strategy is the strengthening of the actin cortex through developmentally controlled transcriptional regulation induced by the Drosophila proto-oncogene family member Dfos, which I show in Chapter 2. Dfos induces expression of the tetraspanin TM4SF and the filamin Cher leading to higher levels of the activated formin Dia at the cortex and increased cortical F-actin. This enhanced cortical strength allows hemocytes to overcome the physical resistance of the surrounding tissue and translocate their nucleus to move forward. This mechanism affects the speed of migration when hemocytes face a confined environment in vivo. Another aspect of the invasion process is the initial step of the leading hemocytes entering the tissue, which potentially guides the follower cells. In Chapter 3, I describe a novel subpopulation of hemocytes activated by BMP signaling prior to tissue invasion that leads penetration into the germband. Hemocytes that are deficient in BMP signaling activation show impaired persistence at the tissue entry, while their migration speed remains unaffected. This suggests that there might be different mechanisms controlling immune cell migration within the confined environment in vivo, one of these being the general ability to overcome the resistance of the surrounding tissue and another affecting the order of hemocytes that collectively invade the tissue in a stream of individual cells. Together, my findings provide deeper insights into transcriptional changes in immune cells that enable efficient tissue invasion and pave the way for future studies investigating the early colonization of tissues by macrophages in higher organisms. Moreover, they extend the current view of Drosophila immune cell heterogeneity and point toward a potentially conserved role for canonical BMP signaling in specifying immune cells that lead the migration of tissue resident macrophages during embryogenesis.}, author = {Wachner, Stephanie}, issn = {2663-337X}, pages = {170}, publisher = {Institute of Science and Technology Austria}, title = {{Transcriptional regulation by Dfos and BMP-signaling support tissue invasion of Drosophila immune cells}}, doi = {10.15479/at:ista:11193}, year = {2022}, } @phdthesis{12378, abstract = {Environmental cues influence the highly dynamic morphology of microglia. Strategies to characterize these changes usually involve user-selected morphometric features, which preclude the identification of a spectrum of context-dependent morphological phenotypes. Here, we develop MorphOMICs, a topological data analysis approach, which enables semiautomatic mapping of microglial morphology into an atlas of cue-dependent phenotypes, overcomes feature-selection bias and minimizes biological variability. First, with MorphOMICs we derive the morphological spectrum of microglia across seven brain regions during postnatal development and in two distinct Alzheimer’s disease degeneration mouse models. We uncover region-specific and sexually dimorphic morphological trajectories, with females showing an earlier morphological shift than males in the degenerating brain. Overall, we demonstrate that both long primary- and short terminal processes provide distinct insights to morphological phenotypes. Moreover, using machine learning to map novel condition on the spectrum, we observe that microglia morphologies reflect a dose-dependent adaptation upon ketamine anesthesia and do not recover to control morphologies. Next, we took advantage of MorphOMICs to build a high-resolution and layer-specific map of microglial morphological spectrum in the retina, covering postnatal development and rd10 degeneration. Here, following photoreceptor death, microglia assume an early developmentlike morphology. Finally, we map microglial morphology following optic nerve crush on the retinal spectrum and observe a layer- and sex-dependent response. Overall, MorphOMICs opens a new perspective to analyze microglial morphology across multiple conditions, and provides a novel tool to characterize microglial morphology beyond the traditionally dichotomized view of microglia.}, author = {Colombo, Gloria}, issn = {2663-337X}, pages = {142}, publisher = {Institute of Science and Technology Austria}, title = {{MorphOMICs, a tool for mapping microglial morphology, reveals brain region- and sex-dependent phenotypes}}, doi = {10.15479/at:ista:12378}, year = {2022}, } @article{10703, abstract = {When crawling through the body, leukocytes often traverse tissues that are densely packed with extracellular matrix and other cells, and this raises the question: How do leukocytes overcome compressive mechanical loads? Here, we show that the actin cortex of leukocytes is mechanoresponsive and that this responsiveness requires neither force sensing via the nucleus nor adhesive interactions with a substrate. Upon global compression of the cell body as well as local indentation of the plasma membrane, Wiskott-Aldrich syndrome protein (WASp) assembles into dot-like structures, providing activation platforms for Arp2/3 nucleated actin patches. These patches locally push against the external load, which can be obstructing collagen fibers or other cells, and thereby create space to facilitate forward locomotion. We show in vitro and in vivo that this WASp function is rate limiting for ameboid leukocyte migration in dense but not in loose environments and is required for trafficking through diverse tissues such as skin and lymph nodes.}, author = {Gaertner, Florian and Dos Reis Rodrigues, Patricia and De Vries, Ingrid and Hons, Miroslav and Aguilera, Juan and Riedl, Michael and Leithner, Alexander F and Tasciyan, Saren and Kopf, Aglaja and Merrin, Jack and Zheden, Vanessa and Kaufmann, Walter and Hauschild, Robert and Sixt, Michael K}, issn = {1878-1551}, journal = {Developmental Cell}, number = {1}, pages = {47--62.e9}, publisher = {Cell Press}, title = {{WASp triggers mechanosensitive actin patches to facilitate immune cell migration in dense tissues}}, doi = {10.1016/j.devcel.2021.11.024}, volume = {57}, year = {2022}, } @phdthesis{11388, abstract = {In evolve and resequence experiments, a population is sequenced, subjected to selection and then sequenced again, so that genetic changes before and after selection can be observed at the genetic level. Here, I use these studies to better understand the genetic basis of complex traits - traits which depend on more than a few genes. In the first chapter, I discuss the first evolve and resequence experiment, in which a population of mice, the so-called "Longshanks" mice, were selected for tibia length while their body mass was kept constant. The full pedigree is known. We observed a selection response on all chromosomes and used the infinitesimal model with linkage, a model which assumes an infinite number of genes with infinitesimally small effect sizes, as a null model. Results implied a very polygenic basis with a few loci of major effect standing out and changing in parallel. There was large variability between the different chromosomes in this study, probably due to LD. In chapter two, I go on to discuss the impact of LD, on the variability in an allele-frequency based summary statistic, giving an equation based on the initial allele frequencies, average pairwise LD, and the first four moments of the haplotype block copy number distribution. I describe this distribution by referring back to the founder generation. I then demonstrate how to infer selection via a maximum likelihood scheme on the example of a single locus and discuss how to extend this to more realistic scenarios. In chapter three, I discuss the second evolve and resequence experiment, in which a small population of Drosophila melanogaster was selected for increased pupal case size over 6 generations. The experiment was highly replicated with 27 lines selected within family and a known pedigree. We observed a phenotypic selection response of over one standard deviation. I describe the patterns in allele frequency data, including allele frequency changes and patterns of heterozygosity, and give ideas for future work.}, author = {Belohlavy, Stefanie}, isbn = {978-3-99078-018-3}, pages = {98}, publisher = {Institute of Science and Technology Austria}, title = {{The genetic basis of complex traits studied via analysis of evolve and resequence experiments}}, doi = {10.15479/at:ista:11388}, year = {2022}, } @phdthesis{12401, abstract = {Detachment of the cancer cells from the bulk of the tumor is the first step of metastasis, which is the primary cause of cancer related deaths. It is unclear, which factors contribute to this step. Recent studies indicate a crucial role of the tumor microenvironment in malignant transformation and metastasis. Studying cancer cell invasion and detachments quantitatively in the context of its physiological microenvironment is technically challenging. Especially, precise control of microenvironmental properties in vivo is currently not possible. Here, I studied the role of microenvironment geometry in the invasion and detachment of cancer cells from the bulk with a simplistic and reductionist approach. In this approach, I engineered microfluidic devices to mimic a pseudo 3D extracellular matrix environment, where I was able to quantitatively tune the geometrical configuration of the microenvironment and follow tumor cells with fluorescence live imaging. To aid quantitative analysis I developed a widely applicable software application to automatically analyze and visualize particle tracking data. Quantitative analysis of tumor cell invasion in isotropic and anisotropic microenvironments showed that heterogeneity in the microenvironment promotes faster invasion and more frequent detachment of cells. These observations correlated with overall higher speed of cells at the edge of the bulk of the cells. In heterogeneous microenvironments cells preferentially passed through larger pores, thus invading areas of least resistance and generating finger-like invasive structures. The detachments occurred mostly at the tips of these structures. To investigate the potential mechanism, we established a two dimensional model to simulate active Brownian particles representing the cell nuclei dynamics. These simulations backed our in vitro observations without the need of precise fitting the simulation parameters. Our model suggests the importance of the pore heterogeneity in the direction perpendicular to the orientation of bias field (lateral heterogeneity), which causes the interface roughening.}, author = {Tasciyan, Saren}, issn = {2663-337X}, pages = {105}, publisher = {Institute of Science and Technology Austria}, title = {{Role of microenvironment heterogeneity in cancer cell invasion}}, doi = {10.15479/at:ista:12401}, year = {2022}, } @article{12080, abstract = {Endocytosis is a multistep process involving the sequential recruitment and action of numerous proteins. This process can be divided into two phases: an early phase, in which sites of endocytosis are formed, and a late phase in which clathrin-coated vesicles are formed and internalized into the cytosol, but how these phases link to each other remains unclear. In this study, we demonstrate that anchoring the yeast Eps15-like protein Pan1p to the peroxisome triggers most of the events occurring during the late phase at the peroxisome. At this ectopic location, Pan1p recruits most proteins that function in the late phases—including actin nucleation promoting factors—and then initiates actin polymerization. Pan1p also recruited Prk1 kinase and actin depolymerizing factors, thereby triggering disassembly immediately after actin assembly and inducing dissociation of endocytic proteins from the peroxisome. These observations suggest that Pan1p is a key regulator for initiating, processing, and completing the late phase of endocytosis.}, author = {Enshoji, Mariko and Miyano, Yoshiko and Yoshida, Nao and Nagano, Makoto and Watanabe, Minami and Kunihiro, Mayumi and Siekhaus, Daria E and Toshima, Junko Y. and Toshima, Jiro}, issn = {1540-8140}, journal = {Journal of Cell Biology}, number = {10}, publisher = {Rockefeller University Press}, title = {{Eps15/Pan1p is a master regulator of the late stages of the endocytic pathway}}, doi = {10.1083/jcb.202112138}, volume = {221}, year = {2022}, } @misc{10934, abstract = {FtsA is crucial for assembly of the E. coli divisome, as it dynamically links cytoplasmic FtsZ filaments with transmembrane cell division proteins. FtsA allegedly initiates cell division by switching from an inactive polymeric to an active monomeric confirmation, which recruits downstream proteins and stabilizes FtsZ filaments. Here, we use biochemical reconstitution experiments combined with quantitative fluorescence microscopy to study divisome activation in vitro. We compare wildtype-FtsA with FtsA-R286W, a constantly active gain-of-function mutant and find that R286W outperforms the wildtype protein in replicating FtsZ treadmilling dynamics, stabilizing FtsZ filaments and recruiting FtsN. We attribute these differences to a faster membrane exchange of FtsA-R286W and its higher packing density below FtsZ filaments. Using FRET microscopy, we find that FtsN binding does not compete with, but promotes FtsA self-interaction. Our findings suggest a model where FtsA always forms dynamic polymers on the membrane, which re-organize during assembly and activation of the divisome. }, author = {Radler, Philipp}, keywords = {Bacterial cell division, in vitro reconstitution, FtsZ, FtsN, FtsA}, publisher = {Institute of Science and Technology Austria}, title = {{In vitro reconstitution of Escherichia coli divisome activation}}, doi = {10.15479/AT:ISTA:10934}, year = {2022}, } @article{11373, abstract = {The actin-homologue FtsA is essential for E. coli cell division, as it links FtsZ filaments in the Z-ring to transmembrane proteins. FtsA is thought to initiate cell constriction by switching from an inactive polymeric to an active monomeric conformation, which recruits downstream proteins and stabilizes the Z-ring. However, direct biochemical evidence for this mechanism is missing. Here, we use reconstitution experiments and quantitative fluorescence microscopy to study divisome activation in vitro. By comparing wild-type FtsA with FtsA R286W, we find that this hyperactive mutant outperforms FtsA WT in replicating FtsZ treadmilling dynamics, FtsZ filament stabilization and recruitment of FtsN. We could attribute these differences to a faster exchange and denser packing of FtsA R286W below FtsZ filaments. Using FRET microscopy, we also find that FtsN binding promotes FtsA self-interaction. We propose that in the active divisome FtsA and FtsN exist as a dynamic copolymer that follows treadmilling filaments of FtsZ.}, author = {Radler, Philipp and Baranova, Natalia S. and Dos Santos Caldas, Paulo R and Sommer, Christoph M and Lopez Pelegrin, Maria D and Michalik, David and Loose, Martin}, issn = {2041-1723}, journal = {Nature Communications}, keywords = {General Physics and Astronomy, General Biochemistry, Genetics and Molecular Biology, General Chemistry}, publisher = {Springer Nature}, title = {{In vitro reconstitution of Escherichia coli divisome activation}}, doi = {10.1038/s41467-022-30301-y}, volume = {13}, year = {2022}, } @misc{11653, abstract = {Eurasian brine shrimp (genus Artemia) have closely related sexual and asexual lineages of parthenogenetic females, which produce rare males at low frequencies. Although they are known to have ZW chromosomes, these are not well characterized, and it is unclear whether they are shared across the clade. Furthermore, the underlying genetic architecture of the transmission of asexuality, which can occur when rare males mate with closely related sexual females, is not well understood. We produced a chromosome-level assembly for the sexual Eurasian species A. sinica and characterized in detail the pair of sex chromosomes of this species. We combined this new assembly with short-read genomic data for the sexual species A. sp. Kazakhstan and several asexual lineages of A. parthenogenetica, allowing us to perform an in-depth characterization of sex-chromosome evolution across the genus. We identified a small differentiated region of the ZW pair that is shared by all sexual and asexual lineages, supporting the shared ancestry of the sex chromosomes. We also inferred that recombination suppression has spread to larger sections of the chromosome independently in the American and Eurasian lineages. Finally, we took advantage of a rare male, which we backcrossed to sexual females, to explore the genetic basis of asexuality. Our results suggest that parthenogenesis is likely partly controlled by a locus on the Z chromosome, highlighting the interplay between sex determination and asexuality.}, author = {Elkrewi, Marwan N}, publisher = {Institute of Science and Technology Austria}, title = {{Data from Elkrewi, Khauratovich, Toups et al. 2022, "ZW sex-chromosome evolution and contagious parthenogenesis in Artemia brine shrimp"}}, doi = {10.15479/AT:ISTA:11653}, year = {2022}, } @article{12138, abstract = {Complex I is the first enzyme in the respiratory chain, which is responsible for energy production in mitochondria and bacteria1. Complex I couples the transfer of two electrons from NADH to quinone and the translocation of four protons across the membrane2, but the coupling mechanism remains contentious. Here we present cryo-electron microscopy structures of Escherichia coli complex I (EcCI) in different redox states, including catalytic turnover. EcCI exists mostly in the open state, in which the quinone cavity is exposed to the cytosol, allowing access for water molecules, which enable quinone movements. Unlike the mammalian paralogues3, EcCI can convert to the closed state only during turnover, showing that closed and open states are genuine turnover intermediates. The open-to-closed transition results in the tightly engulfed quinone cavity being connected to the central axis of the membrane arm, a source of substrate protons. Consistently, the proportion of the closed state increases with increasing pH. We propose a detailed but straightforward and robust mechanism comprising a ‘domino effect’ series of proton transfers and electrostatic interactions: the forward wave (‘dominoes stacking’) primes the pump, and the reverse wave (‘dominoes falling’) results in the ejection of all pumped protons from the distal subunit NuoL. This mechanism explains why protons exit exclusively from the NuoL subunit and is supported by our mutagenesis data. We contend that this is a universal coupling mechanism of complex I and related enzymes.}, author = {Kravchuk, Vladyslav and Petrova, Olga and Kampjut, Domen and Wojciechowska-Bason, Anna and Breese, Zara and Sazanov, Leonid A}, issn = {1476-4687}, journal = {Nature}, keywords = {Multidisciplinary}, number = {7928}, pages = {808--814}, publisher = {Springer Nature}, title = {{A universal coupling mechanism of respiratory complex I}}, doi = {10.1038/s41586-022-05199-7}, volume = {609}, year = {2022}, } @article{12272, abstract = {Reading, interpreting and crawling along gradients of chemotactic cues is one of the most complex questions in cell biology. In this issue, Georgantzoglou et al. (2022. J. Cell. Biol.https://doi.org/10.1083/jcb.202103207) use in vivo models to map the temporal sequence of how neutrophils respond to an acutely arising gradient of chemoattractant.}, author = {Stopp, Julian A and Sixt, Michael K}, issn = {1540-8140}, journal = {Journal of Cell Biology}, keywords = {Cell Biology}, number = {8}, publisher = {Rockefeller University Press}, title = {{Plan your trip before you leave: The neutrophils’ search-and-run journey}}, doi = {10.1083/jcb.202206127}, volume = {221}, year = {2022}, } @article{11420, abstract = {Understanding the properties of neural networks trained via stochastic gradient descent (SGD) is at the heart of the theory of deep learning. In this work, we take a mean-field view, and consider a two-layer ReLU network trained via noisy-SGD for a univariate regularized regression problem. Our main result is that SGD with vanishingly small noise injected in the gradients is biased towards a simple solution: at convergence, the ReLU network implements a piecewise linear map of the inputs, and the number of “knot” points -- i.e., points where the tangent of the ReLU network estimator changes -- between two consecutive training inputs is at most three. In particular, as the number of neurons of the network grows, the SGD dynamics is captured by the solution of a gradient flow and, at convergence, the distribution of the weights approaches the unique minimizer of a related free energy, which has a Gibbs form. Our key technical contribution consists in the analysis of the estimator resulting from this minimizer: we show that its second derivative vanishes everywhere, except at some specific locations which represent the “knot” points. We also provide empirical evidence that knots at locations distinct from the data points might occur, as predicted by our theory.}, author = {Shevchenko, Aleksandr and Kungurtsev, Vyacheslav and Mondelli, Marco}, issn = {1533-7928}, journal = {Journal of Machine Learning Research}, number = {130}, pages = {1--55}, publisher = {Journal of Machine Learning Research}, title = {{Mean-field analysis of piecewise linear solutions for wide ReLU networks}}, volume = {23}, year = {2022}, } @phdthesis{11932, abstract = {The ability to form and retrieve memories is central to survival. In mammals, the hippocampus is a brain region essential to the acquisition and consolidation of new memories. It is also involved in keeping track of one’s position in space and aids navigation. Although this space-memory has been a source of contradiction, evidence supports the view that the role of the hippocampus in navigation is memory, thanks to the formation of cognitive maps. First introduced by Tolman in 1948, cognitive maps are generally used to organize experiences in memory; however, the detailed mechanisms by which these maps are formed and stored are not yet agreed upon. Some influential theories describe this process as involving three fundamental steps: initial encoding by the hippocampus, interactions between the hippocampus and other cortical areas, and long-term extra-hippocampal consolidation. In this thesis, I will show how the investigation of cognitive maps of space helped to shed light on each of these three memory processes. The first study included in this thesis deals with the initial encoding of spatial memories in the hippocampus. Much is known about encoding at the level of single cells, but less about their co-activity or joint contribution to the encoding of novel spatial information. I will describe the structure of an interaction network that allows for efficient encoding of noisy spatial information during the first exploration of a novel environment. The second study describes the interactions between the hippocampus and the prefrontal cortex (PFC), two areas directly and indirectly connected. It is known that the PFC, in concert with the hippocampus, is involved in various processes, including memory storage and spatial navigation. Nonetheless, the detailed mechanisms by which PFC receives information from the hippocampus are not clear. I will show how a transient improvement in theta phase locking of PFC cells enables interactions of cell pairs across the two regions. The third study describes the learning of behaviorally-relevant spatial locations in the hippocampus and the medial entorhinal cortex. I will show how the accumulation of firing around goal locations, a correlate of learning, can shed light on the transition from short- to long-term spatial memories and the speed of consolidation in different brain areas. The studies included in this thesis represent the main scientific contributions of my Ph.D. They involve statistical analyses and models of neural responses of cells in different brain areas of rats executing spatial tasks. I will conclude the thesis by discussing the impact of the findings on principles of memory formation and retention, including the mechanisms, the speed, and the duration of these processes.}, author = {Nardin, Michele}, issn = {2663-337X}, pages = {136}, publisher = {Institute of Science and Technology Austria}, title = {{On the encoding, transfer, and consolidation of spatial memories}}, doi = {10.15479/at:ista:11932}, year = {2022}, } @article{12248, abstract = {Eurasian brine shrimp (genus Artemia) have closely related sexual and asexual lineages of parthenogenetic females, which produce rare males at low frequencies. Although they are known to have ZW chromosomes, these are not well characterized, and it is unclear whether they are shared across the clade. Furthermore, the underlying genetic architecture of the transmission of asexuality, which can occur when rare males mate with closely related sexual females, is not well understood. We produced a chromosome-level assembly for the sexual Eurasian species Artemia sinica and characterized in detail the pair of sex chromosomes of this species. We combined this new assembly with short-read genomic data for the sexual species Artemia sp. Kazakhstan and several asexual lineages of Artemia parthenogenetica, allowing us to perform an in-depth characterization of sex-chromosome evolution across the genus. We identified a small differentiated region of the ZW pair that is shared by all sexual and asexual lineages, supporting the shared ancestry of the sex chromosomes. We also inferred that recombination suppression has spread to larger sections of the chromosome independently in the American and Eurasian lineages. Finally, we took advantage of a rare male, which we backcrossed to sexual females, to explore the genetic basis of asexuality. Our results suggest that parthenogenesis is likely partly controlled by a locus on the Z chromosome, highlighting the interplay between sex determination and asexuality.}, author = {Elkrewi, Marwan N and Khauratovich, Uladzislava and Toups, Melissa A and Bett, Vincent K and Mrnjavac, Andrea and Macon, Ariana and Fraisse, Christelle and Sax, Luca and Huylmans, Ann K and Hontoria, Francisco and Vicoso, Beatriz}, issn = {1943-2631}, journal = {Genetics}, keywords = {Genetics}, number = {2}, publisher = {Oxford University Press}, title = {{ZW sex-chromosome evolution and contagious parthenogenesis in Artemia brine shrimp}}, doi = {10.1093/genetics/iyac123}, volume = {222}, year = {2022}, }