RRC ID 30214
Author Yokoo R, Zawadzki KA, Nabeshima K, Drake M, Arur S, Villeneuve AM.
Title COSA-1 reveals robust homeostasis and separable licensing and reinforcement steps governing meiotic crossovers.
Journal Cell
Abstract Crossovers (COs) between homologous chromosomes ensure their faithful segregation during meiosis. We identify C. elegans COSA-1, a cyclin-related protein conserved in metazoa, as a key component required to convert meiotic double-strand breaks (DSBs) into COs. During late meiotic prophase, COSA-1 localizes to foci that correspond to the single CO site on each homolog pair and indicate sites of eventual concentration of other conserved CO proteins. Chromosomes gain and lose competence to load CO proteins during meiotic progression, with competence to load COSA-1 requiring prior licensing. Our data further suggest a self-reinforcing mechanism maintaining CO designation. Modeling of a nonlinear dose-response relationship between IR-induced DSBs and COSA-1 foci reveals efficient conversion of DSBs into COs when DSBs are limiting and a robust capacity to limit cytologically differentiated CO sites when DSBs are in excess. COSA-1 foci serve as a unique live cell readout for investigating CO formation and CO interference.
Volume 149(1)
Pages 75-87
Published 2012-3-30
DOI 10.1016/j.cell.2012.01.052
PII S0092-8674(12)00286-3
PMID 22464324
PMC PMC3339199
MeSH Animals Caenorhabditis elegans / cytology* Caenorhabditis elegans / genetics Caenorhabditis elegans / metabolism Caenorhabditis elegans Proteins / genetics Caenorhabditis elegans Proteins / metabolism* Chromosomes / metabolism Crossing Over, Genetic* Cyclins / genetics Cyclins / metabolism* DNA Breaks, Double-Stranded DNA-Binding Proteins / genetics DNA-Binding Proteins / metabolism* Meiosis* Models, Molecular Mutation
IF 38.637
Times Cited 105
WOS Category BIOCHEMISTRY & MOLECULAR BIOLOGY CELL BIOLOGY
Resource
C.elegans tm3298