Chromosome dynamics and recombination

Valérie Borde

Valérie Borde Team Leader

We study the process of recombination, that ensures genome stability and faithful chromosome segregation, during the production of haploid gametes at meiosis. Homologous recombination takes place when a broken or damaged chromosome uses a homologous sequence as a template for repair. Defects in homologous recombination have severe consequences and are linked to several disorders, such as certain inherited cancers and genetic instability syndromes.

Recombination can be due to accidental lesions, following exposure to genotoxic agents or replication failures, but lesions can also be deliberately self-inflicted by the cell, such as during meiosis. During meiosis, the genome is halved, with only one of each pair of parental homologous chromosomes being transmitted to progeny for sexual reproduction. Recombination ensures that physical links between homologous chromosomes, called crossing over, are created, necessary for their correct segregation during the first meiotic division. Errors in the meiotic recombination process lead to sterility or aneuploidy and are a major cause of chromosome abnormalities, such as in Downs Syndrome.

Recombination is initiated by programmed double-strand break (DSB) formation (Fig. 1A) along chromosomes, at hotspots whose determinants are poorly understood. Furthermore, only a subset of DSBs is processed to undergo crossing over, involving an important decision at the time of DSB repair. We study the factors that control DSB and crossing over formation and, in particular, the influence of chromatin, chromosome and nuclear organization on their positioning. One remarkable feature of meiosis is its conservation between species. Our model organism is the budding yeast Saccharomyces cerevisiae, among the closest to mammals in terms of meiotic recombination mechanisms and which allows a large panel of molecular, genetic and biochemical approaches.

Borde
Figure 1 : Chromatin modifications and proteins involved at meiotic recombination hotspots. A: Overview of the process of DSB formation and repair by homologous recombination. At sites of DSB formation, histones are modified, and specific proteins are bound at each step of DSB repair. B: Model to illustrate how chromatin regions that bear H3K4me3 modification are selected by a specific PHD finger module to experience DSB formation by interaction with the proteins located on the chromosomal axis (from Sommermeyer et al, 2013).

Meiotic chromosomes are organized into linear arrays of loops anchored at their base to the chromosome axis structure. We have recently found that a chromatin modification, histone H3K4 methylation, promoted by the Set1 complex, is important for DSB formation. We have further shown that a sub-unit of the Set1 complex directly binds H3K4me3 through a PHD finger module and interacts with the proteins necessary for DSB formation on the axes, making the molecular bridge between these two chromosomal regions for DSB formation (Figure 1B).

We also investigate which mechanisms drive the repair of meiotic DSBs through crossover versus noncrossover. By genome-wide mapping of a crossover-associated protein, Zip3, we have uncovered specific chromosome features associated with high or low crossover frequency. We are currently applying proteomic approaches to decipher protein complexes involved in crossover repair of meiotic DSBs.

Finally, we study how chromatin is modified upon DSB formation. We found that two histone chaperones CAF-1 and Hir, are specifically recruited to meiotic DSBs, implying that new histones are incorporated into chromatin to replace those evicted by recombination, potentially altering the local composition of chromatin.

Our research should allow better understanding of the mechanisms allowing faithful transmission of genetic information during reproduction and also shed light on the involvement of chromatin and its modifications in somatic DSB repair by recombination, potentially contributing to epigenetic changes underlying disease and abnormal development.

 

Key publications

Year of publication 2018

Adam C, Guérois R, Citarella A, Verardi L, Adolphe F Béneut C, Sommermeyer V, Ramus C, Govin J, Couté Y, Borde V (2018 Feb 1)

The PHD finger protein Spp1 has distinct functions in the Set1 and the meiotic DSB formation complexes

PLoS Genetics : 14(2) : DOI : 10.1371/journal.pgen.1007223
De Muyt A, Pyatnitskaya A, Andréani J, Ranjha L, Ramus C, Laureau R, Fernandez-Vega A, Holoch D, Girard E, Govin J, Margueron R, Couté Y, Cejka P, Guérois R, Borde V. (2018 Feb 1)

A meiotic XPF-ERCC1-like complex recognizes joint molecule recombination intermediates to promote crossover formation

Genes & Development : DOI : 10.1101/gad.308510.117

Year of publication 2017

Yann Duroc, Rajeev Kumar, Lepakshi Ranjha, Céline Adam, Raphaël Guérois, Khan Md Muntaz, Marie-Claude Marsolier-Kergoat, Florent Dingli, Raphaëlle Laureau, Damarys Loew, Bertrand Llorente, Jean-Baptiste Charbonnier, Petr Cejka, Valérie Borde (2017 Jan 5)

Concerted action of the MutLβ heterodimer and Mer3 helicase regulates the global extent of meiotic gene conversion.

eLife : DOI : 10.7554/eLife.21900

Year of publication 2013

Maria-Elisabetta Serrentino, Emmanuel Chaplais, Vérane Sommermeyer, Valérie Borde (2013 Apr 9)

Differential association of the conserved SUMO ligase Zip3 with meiotic double-strand break sites reveals regional variations in the outcome of meiotic recombination.

PLoS genetics : e1003416 : DOI : 10.1371/journal.pgen.1003416
Valérie Borde, Bernard de Massy (2013 Apr 2)

Programmed induction of DNA double strand breaks during meiosis: setting up communication between DNA and the chromosome structure.

Current opinion in genetics & development : 147-55 : DOI : 10.1016/j.gde.2012.12.002
Vérane Sommermeyer, Claire Béneut, Emmanuel Chaplais, Maria Elisabetta Serrentino, Valérie Borde (2013 Jan 10)

Spp1, a member of the Set1 Complex, promotes meiotic DSB formation in promoters by tethering histone H3K4 methylation sites to chromosome axes.

Molecular cell : 43-54 : DOI : 10.1016/j.molcel.2012.11.008
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