The formation and repair of DNA double-strand breaks in mammalian meiosis

被引:16
|
作者
Qu, Wei [1 ]
Liu, Cong [1 ]
Xu, Ya-Ting [1 ]
Xu, Yu-Min [1 ]
Luo, Meng-Cheng [1 ]
机构
[1] Wuhan Univ, Hubei Prov Key Lab Dev Originated Dis, Sch Basic Med Sci, Wuhan 430072, Peoples R China
基金
中国国家自然科学基金;
关键词
CHROMOSOME SYNAPSIS; MRE11-RAD50-NBS1; COMPLEX; CROSSING-OVER; MICE LACKING; RECOMBINATION; PROTEIN; MUTATION; GENE; AZOOSPERMIA; SYCE1;
D O I
10.4103/aja202191
中图分类号
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
摘要
Programmed DNA double-strand breaks (DSBs) are necessary for meiosis in mammals. A sufficient number of DSBs ensure the normal pairing/synapsis of homologous chromosomes. Abnormal DSB repair undermines meiosis, leading to sterility in mammals. The DSBs that initiate recombination are repaired as crossovers and noncrossovers, and crossovers are required for correct chromosome separation. Thus, the placement, timing, and frequency of crossover formation must be tightly controlled. Importantly, mutations in many genes related to the formation and repair of DSB result in infertility in humans. These mutations cause nonobstructive azoospermia in men, premature ovarian insufficiency and ovarian dysgenesis in women. Here, we have illustrated the formation and repair of DSB in mammals, summarized major factors influencing the formation of DSB and the theories of crossover regulation.
引用
收藏
页码:572 / 579
页数:8
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