Key mediators of somatic ATR signaling localize to unpaired chromosomes in spermatocytes

Development. 2015 Sep 1;142(17):2972-80. doi: 10.1242/dev.126078. Epub 2015 Jul 24.

Abstract

Meiotic silencing of unpaired chromatin (MSUC) occurs during the first meiotic prophase, as chromosomes that fail to pair are sequestered into a transcriptionally repressive nuclear domain. This phenomenon is exemplified by the heterologous sex chromosomes of male mammals, where the ATR DNA damage response kinase is crucial for this silencing event. However, the mechanisms underlying the initiation of MSUC remain unknown. Here, we show that essential components of ATR signaling in murine somatic cells are spatially confined to unpaired chromosomes in spermatocytes, including the ATR-dependent phosphorylation of the single-stranded DNA (ssDNA)-binding complex replication protein A (RPA) and the checkpoint kinase CHK1. These observations support a model in which ssDNA plays a central role in the recruitment of ATR during MSUC, and provide a link to meiotic progression through activation of CHK1.

Keywords: CHEK1; Meiosis; Mouse; Spermatogenesis; Transcriptional regulation.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Antibody Specificity
  • Ataxia Telangiectasia Mutated Proteins / metabolism
  • Cells, Cultured
  • Checkpoint Kinase 1
  • Chromatin / metabolism
  • Chromosome Pairing*
  • Chromosomes, Mammalian / metabolism*
  • DNA Breaks, Double-Stranded
  • Endodeoxyribonucleases / deficiency
  • Endodeoxyribonucleases / metabolism
  • Male
  • Meiosis
  • Mice
  • Phosphorylation
  • Phosphoserine / metabolism
  • Protein Kinases / metabolism
  • Protein Transport
  • Replication Protein A / metabolism
  • Sex Chromosomes / metabolism
  • Signal Transduction*
  • Spermatocytes / metabolism*

Substances

  • Chromatin
  • Replication Protein A
  • Phosphoserine
  • Protein Kinases
  • Atr protein, mouse
  • Ataxia Telangiectasia Mutated Proteins
  • Checkpoint Kinase 1
  • Chek1 protein, mouse
  • Endodeoxyribonucleases
  • meiotic recombination protein SPO11