NBS1 is required for SPO11-linked DNA double-strand break repair in male meiosis

• Published in: Cell death and differentiation Vol. 27; no. 7; pp. 2176 - 2190
• Main Authors: Zhang, Bin, Tang, Zhenghui, Li, Lejun, Lu, Lin-Yu
• Format: Journal Article
• Language: English
• Published: England Nature Publishing Group 01.07.2020; Nature Publishing Group UK
• Subjects: Chromosomes; Deoxyribonucleic acid; DNA; DNA damage; DNA repair; Double-strand break repair; Germ cells; Homologous recombination; Infertility; Meiosis; MRE11 protein; Prophase; Somatic cells; Yeast; Zebrafish
• ISSN: 1350-9047; 1476-5403
• DOI: 10.1038/s41418-020-0493-4

DNA double-strand breaks (DSBs) pose a serious threat to genomic stability. Paradoxically, hundreds of programed DSBs are generated by SPO11 in meiotic prophase, which are exclusively repaired by homologous recombination (HR) to promote obligate crossover between homologous chromosomes. In somatic cells, MRE11-RAD50-NBS1 (MRN) complex-dependent DNA end resection is a prerequisite for HR repair, especially for DSBs that are covalently linked with proteins or chemicals. Interestingly, all meiotic DSBs are linked with SPO11 after being generated. Although MRN complex's function in meiotic DSB repair has been established in lower organisms, the role of MRN complex in mammalian meiotic DSB repair is not clear. Here, we show that MRN complex is essential for repairing meiotic SPO11-linked DSBs in male mice. In male germ cells, conditional inactivation of NBS1, a key component of MRN complex, causes dramatic reduction of DNA end resection and defective HR repair in meiotic prophase. NBS1 loss severely disrupts chromosome synapsis, generates abnormal chromosome structures, and eventually leads to meiotic arrest and male infertility in mice. Unlike in somatic cells, the recruitment of NBS1 to SPO11-linked DSB sites is MDC1-independent but requires other phosphorylated proteins. Collectively, our study not only reveals the significance of MRN complex in repairing meiotic DSBs but also discovers a unique mechanism that recruits MRN complex to SPO11-linked DSB sites.