Research
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The 7 research groups show a high level of interaction and integration. They all share a common management of their fundings, the human ressources, the research and the IT infrastructure.
We are interested in understanding at atomic level the interaction between proteins and RNA at the heart of pre-mRNA splicing and/or RNA editing.
Our focus is on determining the structures of protein-RNA complexes using Nuclear Magnetic Resonance (NMR) in solution. In addition we also employ other biophysical and biochemical methods to gain further insights.
We use the budding yeast Saccharomyces cerevisiae as our main model to study how asymmetric cell division contributes to the generation of cell diversity in eukaryotes. We follow three axes of research. First, we investigate how the mitotic spindle senses and orients along the polarity axis of the cell to reproducibly segregate its oldest centrosome to the bud. Second, we investigate the role of diffusion barriers in the coordination of cell polarity with the plane of division, and in the asymmetric segregation of fate determinants between mother and bud. Third, we are particularly interested in understanding the nature and segregation of age determinants. This leads us to investigate the intriguing possibility that part of the aging process may consist in the accumulation of memory traces by the yeast mother cell. More...
Our group studies interactions that occur between animal viruses and their host cells during the early infectious cycle; how virus particles bind to cells, how they are internalized by endocytosis, how they are transported to various organelles such as endosomes and the endoplasmic reticulum, how they penetrate into the cytosol, and how the genome is uncoated. Since viruses take advantage of host cell factors and processes during their entry, we combine virological techniques with cell biological approaches, molecular biology, advanced imaging, and systems biology. The virus systems presently analyzed include enveloped and non-enveloped viruses; influenza virus, vaccinia virus, uukuniemi virus, semliki forest virus, human cytomegalovirus, respiratory syncytial virus, and simian virus 40. In addition, we study the dynamics of caveolae and their role in endocytosis. More...
We are broadly interested in exploring the function(s) of satellite DNA repeats at a cellular and organismal level and in determining whether the widely observed divergence of satellite DNAs is one of the fundamental barriers that reproductively isolates different species. More...
Our laboratory is interested in the organization, function and dynamics of the human cell nucleus. The nucleus is a truly fascinating organelle that is perfectly adapted to its functions as cellular command center and protective home of our genome. We are investigating different aspects of nuclear biology, including the fundamental biosynthetic function of the nucleus in the assembly of ribosomal subunits, the role of the nuclear envelope in nucleo-cytoplasmic communication and genome organization as well as the dynamics of the nuclear compartment during the cell cycle. By our research, we seek to improve our understanding of how nuclear dysfunction contributes to human diseases such as ribosomopathies, nuclear envelopathies and cancer. More...
From bacteria to higher eukaryotes all cells of a specific cell type have a very characteristic size. Why tight regulation of cell size is so critical for cell function is largely unexplored. This question is interesting for two reasons: Deviation from normal cell size occurs during non-physiological conditions such as during cell senescence and in tumors and coincides with altered cell function, strongly suggesting that having a specific cell size is critical for cell function. On the other hand, cells in multicellular organisms exist at sizes that span several orders of magnitude, but every cell type has a well-defined size. This raises the possibility that cell size may contribute to defining cell type specific cell function. In our lab we use a combination of genetic, live cell microscopy and molecular biology approaches to understand how cell size affects different aspects of cell physiology.
Regulation of cell growth and division by selective degradation mechanisms. Every living organism requires a tight coordination of cell growth and cell division, and defects in these regulatory systems are intimately linked to metabolic disorders and cellular transformation. Cell growth is manifested by an increase in cell mass, and thus involves the homeostasis and regulation of metabolic pathways, ribosome biogenesis and protein translation, and catabolic pathways including autophagy and ubiquitin-dependent degradation. Cell division requires the precise duplication of chromosomes and their partitioning between two daughter cells. The morphological transitions that lead to chromosome segregation during mitosis need to be coordinated in space and time with subsequent cytoplasm separation during cytokinesis. However, the molecular mechanisms that govern cell growth and division, and the different intra- and extracellular signals that regulate these pathways, are still poorly understood. More...
The interest of our laboratory is centered on very fundamental questions in eukaryotic cell biology: how are macromolecules properly localized within a cell, and how do eukaryotes take advantage of transport and compartmentalization to regulate their gene expression programs? Our work particularly focuses on studying transport processes between the nucleus and the cytoplasm. The exchange of macromolecules between the nucleus and the cytoplasm is absolutely essential to establish and maintain order in eukaryotic cells, and constitutes an important step in the regulation of gene expression. Our laboratory combines genetic, biochemical, cell biological and biophysical approaches in Saccharomyces cerevisiae and in metazoan cells to characterize and analyze the molecular machinery that is responsible for the transport of macromolecules into and out of the nucleus.
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