MRC Laboratory of Molecular Biology, Cambridge, UK.
Nat Genet. 2019 Aug;51(8):1283-1294. doi: 10.1038/s41588-019-0471-2. Epub 2019 Jul 31.
Germline de novo mutations are the basis of evolutionary diversity but also of genetic disease. However, the molecular origin, mechanisms and timing of germline mutagenesis are not fully understood. Here, we define a fundamental role for DNA interstrand cross-link repair in the germline. This repair process is essential for primordial germ cell (PGC) maturation during embryonic development. Inactivation of cross-link repair leads to genetic instability that is restricted to PGCs within the genital ridge during a narrow temporal window. Having successfully activated the PGC transcriptional program, a potent quality control mechanism detects and drives damaged PGCs into apoptosis. Therefore, these findings define a source of DNA damage and the nature of the subsequent DNA repair response in germ cells, which ensures faithful transmission of the genome between generations.
胚系新生突变是进化多样性的基础,但也是遗传疾病的基础。然而,胚系突变的分子起源、机制和时间尚不完全清楚。在这里,我们定义了 DNA 链间交联修复在胚系中的基本作用。这一修复过程对于胚胎发育过程中原始生殖细胞(PGC)的成熟是必不可少的。交联修复的失活会导致遗传不稳定性,这种不稳定性在狭窄的时间窗口内仅限于生殖嵴内的 PGC。一旦成功激活了 PGC 的转录程序,一个强大的质量控制机制就会检测到并促使受损的 PGC 进入凋亡。因此,这些发现定义了生殖细胞中 DNA 损伤的来源和随后的 DNA 修复反应的性质,这确保了基因组在代际之间的忠实传递。