| Literature DB >> 33748134 |
Vikash Kumar Yadav1, Corentin Claeys Bouuaert1.
Abstract
Developmentally programmed formation of DNA double-strand breaks (DSBs) by Spo11 initiates a recombination mechanism that promotes synapsis and the subsequent segregation of homologous chromosomes during meiosis. Although DSBs are induced to high levels in meiosis, their formation and repair are tightly regulated to minimize potentially dangerous consequences for genomic integrity. In S. cerevisiae, nine proteins participate with Spo11 in DSB formation, but their molecular functions have been challenging to define. Here, we describe our current view of the mechanism of meiotic DSB formation based on recent advances in the characterization of the structure and function of DSB proteins and discuss regulatory pathways in the light of recent models.Entities:
Keywords: DNA recombination; Spo11; double-strand break; meiosis; phase separation
Year: 2021 PMID: 33748134 PMCID: PMC7968521 DOI: 10.3389/fcell.2021.642737
Source DB: PubMed Journal: Front Cell Dev Biol ISSN: 2296-634X