共 11 条
Coupling crossover and synaptonemal complex in meiosis
被引:14
作者:

Grey, Corinne
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Univ Montpellier, Ctr Natl Rech Sci, Inst Genet Humaine IGH, F-34396 Montpellier, France Univ Montpellier, Ctr Natl Rech Sci, Inst Genet Humaine IGH, F-34396 Montpellier, France

de Massy, Bernard
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Univ Montpellier, Ctr Natl Rech Sci, Inst Genet Humaine IGH, F-34396 Montpellier, France Univ Montpellier, Ctr Natl Rech Sci, Inst Genet Humaine IGH, F-34396 Montpellier, France
机构:
[1] Univ Montpellier, Ctr Natl Rech Sci, Inst Genet Humaine IGH, F-34396 Montpellier, France
关键词:
aneuploidy;
crossing over;
homologous recombination;
meiosis;
chromosome segregation;
DSB repair;
protein-protein interactions;
homologous synapsis;
D O I:
10.1101/gad.349286.121
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
During meiosis, a molecular program induces DNA double-strand breaks (DSBs) and their repair by homologous recombination. DSBs can be repaired with or without crossovers. ZMM proteins promote the repair toward crossover. The sites of DSB repair are also sites where the axes of homologous chromosomes are juxtaposed and stabilized, and where a structure called the synaptonemal complex initiates, providing further regulation of both DSB formation and repair. How crossover formation and synapsis initiation are linked has remained unknown. The study by Pyatnitskaya and colleagues (pp. 53-69) in this issue of Genes & Development highlights the central role of the Saccharomyces cerevisiae ZMM protein Zip4 in this process.
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页码:4 / 6
页数:3
相关论文
共 11 条
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