DNA cross-link repair safeguards genomic stability during premeiotic germ cell development

Nat Genet. 2019 Aug;51(8):1283-1294. doi: 10.1038/s41588-019-0471-2. Epub 2019 Jul 31.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehydes / metabolism
  • Aldehydes / toxicity
  • Animals
  • Apoptosis / drug effects
  • Cell Differentiation*
  • Cross-Linking Reagents
  • DNA / chemistry*
  • DNA / genetics
  • DNA Damage
  • DNA Repair*
  • DNA-Binding Proteins / physiology
  • Endonucleases / physiology
  • Female
  • Fertility
  • Genome
  • Genomic Instability*
  • Germ Cells / cytology*
  • Germ Cells / physiology
  • Male
  • Meiosis / physiology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout

Substances

  • Aldehydes
  • Cross-Linking Reagents
  • DNA-Binding Proteins
  • DNA
  • Endonucleases
  • Ercc1 protein, mouse