DS0405 - Génétique et génomique: relation génotype-phénotype, interactions génome-environnement, épigénétique

Role of Condensin in Gene Silencing – GeneSilencingByCondensin

Role of condensin in the regulation of gene expression

Condensins are universal chromosome organizers that play key role in the assembly and segregation of chromosomes. Condensins have been implicated in the regulation of gene expression but the underlying mechanisms remain unknown. The objectives of the first phase of this research project aimed at determining the role played by condensin in the regulation of gene expression by using the fission yeast as a model system.

Define the role played by condensin in the regulation of gene expression in fission yeast

Aim 1 : Identify the pathway in which condensin regulates genes.<br />State : achieved.<br />Our results indicate that condensine preserves gene expression by promoting accurate chromosomes segregation during mitosis. Aneuploidy caused by condensin deficiency alters gene expression.<br /><br />Aim2. Define condensin’s proteome.<br />State : final phase. <br />The aim was to identify condensin’s binding partners by an unbiased approach<br /><br />Aim 3. Cell cycle analyses.<br />State : achieved<br />The aim was to determine during which phase of the cell cycle condensin was required for proper gene expression. We found that condensin is required solely during anaphase for proper gene expression, and not during interphase.<br /><br />Aim 4. Condensin’s localisation on DNA/RNA.<br />State : achieved<br />We found that condensin is bound to the genes it regulates but this binding is not instrumental for gene regulation. <br /><br />Aim 5. Publication 1.<br />State: in progress<br />Our work has been presented at three major meetings in the field (Gordon Conference Chromosome Dynamics- Italy 2017, Cold Spring Harbour Symposium on chromosome segregation -2017, SMC meeting 20017 - Japan). A manuscript is in preparation and should be submitted during the second semester of 2017.<br />

Aim 1 : Identify the pathway in which condensin regulates genes.
Genetics, transcriptomics (RNA-seq) and RT-qPCR

Aim2. Define condensin’s proteome.
TAP tagging, purification and mass spec analyses

Aim 3. Cell cycle analyses.
Fission yeast cells were synchronized in the cell cycle by conditional arrest, condensin was inactivated, cells were released in the cell and gene expression assessed by RT-qPCR as cells progressed in the different phases (S, G2, M, G1)


Aim 4. Condensin’s localisation on DNA/RNA.
Condensin localisation on DNA or RNA was assessed by ChIP (DNA) and RNA-IP (RNA)


We discovered that condensin preserves proper gene expression in fission yeast by preserving genome stability throughout mitosis. This result is crucial for the scientific community that studies chromosome biology, and will have to be taken into account for the conception of future experiments based on condensin inactivation on proliferative cells.

Assess the role of condensin I and condensin II in gene expression in human cells and determine whether results obtained in fission yeast are transposable to human cells.

Two talks selected on abstracts at international meetings : Gordon conference Italy 2017 and SMC meeting 2017 Japan. One poster presentation at the 82nd cold spring Harbour symposium on chromosome structure and segregation.

Understanding how chromosome organization and hence chromosome organizing factors regulate gene expression has become an important challenge of modern biology. Studies performed during the past two decades identified the condensin complex as a universal chromosome organizing enzyme, conserved from bacteria to human, which condenses the genome and regulates its expression, mostly by silencing genes. Yet, how condensin drives chromosome condensation and represses gene expression remain poorly understood. Notably, the extent to which those two activities are related to each other is still unclear. Indeed, the mechanisms underlying condensin-mediated gene regulation have been poorly investigated thus far and the few available data lead to divergent conclusions. Some studies suggest that condensin complexes repress gene expression by compacting chromatin, thereby limiting access to RNA polymerases. Others imply that condensin-mediated chromosome condensation is insufficient to ensure a robust transcriptional silencing. In that context, we decided to investigate the role of condensin is gene silencing in the fission yeast Schizosaccharomyces pombe which is the model of choice for studying chromatin and gene silencing. Consistent with the idea of an evolutionarily-conserved mechanism, we found that condensin takes part in gene silencing in fission yeast as well. However, and most importantly, our results point towards an unexpected mechanism and suggest that the model of a transcriptional silencing based on chromatin condensation must be reconsidered. We collected robust preliminary data suggesting that condensin silences genes, at least in part, at the post-transcriptional level, through controlled RNA degradation. We found condensin bound to a ribonuclease and RNA-binding proteins. Moreover, those interactions seem conserved in human, suggesting that condensin regulates gene expression within a conserved network of functional and physical interactions with RNA processing factors. This opens the possibility of hitherto ignored functional links between condensin, genome architecture and controlled RNA turn-over. The objective of this research project is to further decipher the mode of action of condensin in gene silencing in both fission yeast and human cells. For that, we propose to identify and characterize critical interactions between condensin, silencing factors, chromatin regions and/or RNAs that engage condensin into gene silencing in both fission yeast and human cells. This ambitious and ground-breaking project is based on robust preliminary data and will combine innovative and interdisciplinary approaches conducted by three complementary laboratories which are already productive as a consortium. Since the organization of the genome, the condensation of chromosomes and the gene silencing operated by condensin are all ubiquitous processes, the knowledge generated by this project will be of general interest.

Project coordination

Pascal BERNARD (LABORATOIRE DE BIOLOGIE MOLECULAIRE DE LA CELLULE)

The author of this summary is the project coordinator, who is responsible for the content of this summary. The ANR declines any responsibility as for its contents.

Partner

INSERM/UJF U823 Institut Albert Bonniot
LBMC/ENS de Lyon Laboratoire de Biologie Moléculaire de la Cellule
LBMC CNRS/ENS-Lyon LABORATOIRE DE BIOLOGIE MOLECULAIRE DE LA CELLULE

Help of the ANR 522,152 euros
Beginning and duration of the scientific project: September 2015 - 48 Months

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