Baptiste Roelens

ORCID: 0000-0003-0118-0229
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About
Contact & Profiles
Research Areas
  • DNA Repair Mechanisms
  • Genetics, Aging, and Longevity in Model Organisms
  • Genomics and Chromatin Dynamics
  • Photosynthetic Processes and Mechanisms
  • Microtubule and mitosis dynamics
  • Chromosomal and Genetic Variations
  • CRISPR and Genetic Engineering
  • Effects of Radiation Exposure
  • Carcinogens and Genotoxicity Assessment
  • RNA Research and Splicing
  • Mitochondrial Function and Pathology
  • Parasitic Diseases Research and Treatment
  • Parasitic Infections and Diagnostics
  • Parasite Biology and Host Interactions
  • Wheat and Barley Genetics and Pathology
  • Insect Resistance and Genetics
  • Developmental Biology and Gene Regulation
  • Plant Genetic and Mutation Studies
  • Fungal and yeast genetics research
  • Plant Molecular Biology Research

Stanford University
2013-2022

Sorbonne Université
2013-2016

Université Paris Sciences et Lettres
2016

Institut Curie
2010-2016

Centre National de la Recherche Scientifique
2010-2013

During meiotic prophase, a structure called the synaptonemal complex (SC) assembles at interface between aligned pairs of homologous chromosomes, and crossover recombination events occur their DNA molecules. Here we investigate inter-relationships these two hallmark features program in nematode C. elegans, revealing dynamic properties SC that are modulated by recombination. We demonstrate incorporates new subunits switches from more highly dynamic/labile state to stable as germ cells...

10.1371/journal.pgen.1006670 article EN cc-by PLoS Genetics 2017-03-24

It is widely accepted that morphogenetic gradients determine cell identity by concentration-dependent activation of target genes. How precise each step in the gene expression process acts downstream morphogens, however, remains unclear. The Bicoid morphogen a transcription factor directly activating its genes and provides thus simple system to address this issue quantitative manner. Recent studies indicate gradient precisely established Drosophila embryos after eight nuclear divisions (cycle...

10.1242/dev.051300 article EN Development 2010-07-27

During meiosis, chromosomes adopt a specialized organization involving assembly of cohesin-based axis along their lengths, with DNA loops emanating from this axis. We applied novel, quantitative, and widely applicable cytogenetic strategies to elucidate the molecular bases using Caenorhabditis elegans. Analyses wild-type (WT) de novo circular minichromosomes revealed that meiosis-specific HORMA-domain proteins assemble into cohorts in defined numbers co-organize together 2 functionally...

10.1371/journal.pbio.3000817 article EN cc-by PLoS Biology 2020-08-19

Meiotic recombination plays dual roles in the evolution and stable inheritance of genomes: Recombination promotes genetic diversity by reassorting variants, it establishes temporary connections between pairs homologous chromosomes that ensure their future segregation. is initiated generation double-strand DNA breaks (DSBs) conserved topoisomerase-like protein Spo11. Despite strong conservation Spo11 across eukaryotic kingdoms, auxiliary complexes interact with to promote DSB formation are...

10.1073/pnas.2109306118 article EN Proceedings of the National Academy of Sciences 2021-08-13

Significance Double-strand breaks (DSBs) are deleterious DNA lesions, and impairment of the DSB repair machinery can lead to devastating diseases, such as Nijmegen Breakage Syndrome (NBS). During meiosis, DSBs represent a “necessary evil”: they required promote formation crossovers between homologous chromosomes. Crossovers, in turn, ensure correct chromosome inheritance during gamete formation, which is essential for viability normal development embryos. numerous actively created, so...

10.1073/pnas.1719029115 article EN Proceedings of the National Academy of Sciences 2018-04-23

Abstract Meiotic recombination is initiated by the programmed induction of double-strand DNA breaks (DSBs), lesions that pose a potential threat to genome. A subset DSBs induced during meiotic prophase become designated be repaired pathway specifically yields interhomolog crossovers (COs), which mature into chiasmata temporarily connect homologs ensure their proper segregation at meiosis I. The remaining must other mechanisms restore genomic integrity prior divisions. Here we show HIM-6,...

10.1534/genetics.114.161513 article EN Genetics 2014-07-21

Meiotic chromosome segregation requires pairwise association between homologs, stabilized by the synaptonemal complex (SC). Here, we investigate factors contributing to synapsis investigating meiosis in polyploid worms. We devised a strategy, based on transient inhibition of cohesin function, generate derivatives virtually any Caenorhabditis elegans strain. exploited this strategy contribution recombination tetraploid and triploid In otherwise wild-type polyploids, chromosomes first sort...

10.1534/genetics.115.182279 article EN Genetics 2015-10-23

Reduction in ploidy to generate haploid gametes during sexual reproduction is accomplished by the specialized cell division program of meiosis. Pairing between homologous chromosomes and assembly synaptonemal complex at their interface (synapsis) represent intermediate steps meiotic that are essential form crossover recombination-based linkages homologs, which turn enable segregation homologs opposite poles meiosis I division. Here, we challenge mechanisms pairing synapsis C. elegans...

10.1371/journal.pgen.1003963 article EN cc-by PLoS Genetics 2013-12-05

Proper partitioning of homologous chromosomes during meiosis relies on the coordinated execution multiple interconnected events: Homologs must locate, recognize, and align with their correct pairing partners. Further, homolog be coupled to assembly synaptonemal complex (SC), a meiosis-specific tripartite structure that maintains stable associations between axes aligned homologs regulates formation crossovers DNA molecules create linkages enable segregation. Here, we identify HAL-3 (Homolog...

10.1534/genetics.119.302479 article EN Genetics 2019-07-25

In eukaryotic cells, the organization of genomic DNA into chromatin regulates many biological processes, from control gene expression to regulation chromosome segregation. The proper maintenance this structure upon cell division is therefore prime importance during development for identity and genome stability. assembly factor 1 (CAF-1) involved in H3-H4 histone dimers on newly synthesized a higher order structure, heterochromatin, through an interaction its large subunit with...

10.1534/genetics.116.190785 article EN Genetics 2016-11-13

Abstract During meiotic prophase, a structure called the synaptonemal complex (SC) assembles at interface between aligned pairs of homologous chromosomes, and crossover recombination events occur their DNA molecules. Here we investigate inter-relationships these two hallmark features program in nematode C. elegans , revealing dynamic properties SC that are modulated by recombination. We demonstrate incorporates new subunits switches from more highly dynamic/labile state to stable as germ...

10.1101/110064 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2017-02-20

ABSTRACT During meiosis, chromosomes adopt a specialized organization involving assembly of cohesin-based axis along their lengths, with DNA loops emanating from this axis. We applied novel, quantitative and widely applicable cytogenetic strategies to elucidate the molecular bases using C. elegans . Analyses WT de novo circular mini-chromosomes revealed that meiosis-specific HORMA-domain proteins assemble into cohorts in defined numbers co-organize together two functionally-distinct cohesin...

10.1101/724997 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2019-08-05

Abstract Faithful inheritance of genetic information through sexual reproduction relies on the formation crossovers between homologous chromosomes during meiosis, which in turn and repair numerous double-strand DNA breaks (DSBs). As DSBs pose a potential threat to genome, mechanisms that ensure timely error-free DSB are crucial for successful meiosis. Here we identify NBS-1, Caenorhabditis elegans ortholog NBS1 subunit conserved MRE11-RAD50-NBS1/Xrs2 (MRN) complex, as key mediator via...

10.1101/214015 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2017-11-04

Abstract Meiotic recombination plays dual roles in the evolution and stable inheritance of genomes: promotes genetic diversity by reassorting variants, it establishes temporary connections between pairs homologous chromosomes that ensure for their future segregation. is initiated generation double-strand DNA breaks (DSBs) conserved topoisomerase-like protein Spo11. Despite strong conservation Spo11 across eukaryotic kingdoms, auxiliary complexes interact with to promote DSB formation are...

10.1101/2021.05.14.444243 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2021-05-16

Abstract Proper partitioning of homologous chromosomes during meiosis relies on the coordinated execution multiple interconnected events: Homologs must locate, recognize and align with their correct pairing partners. Further, homolog be coupled to assembly synaptonemal complex (SC), a meiosis-specific tripartite structure that maintains stable associations between axes aligned homologs regulates formation crossovers DNA molecules create linkages enable segregation. Here we identify HAL-3 ( H...

10.1101/534339 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2019-01-29

A complex series of interconnected events during meiotic prophase creates the physical connections between homologous chromosomes essential to ensure their proper partitioning first division. HIM-19 is an important factor that regulates progression in C. elegans , but its molecular function(s) and localization have remained unclear. We show here tagged expressed from endogenous locus exhibits dynamic germ cell nuclei support proposed role as a regulator CHK-2 protein kinase.

10.17912/micropub.biology.000624 article EN PubMed 2022-01-01
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