In vivo binding of PRDM9 reveals interactions with noncanonical genomic sites

Genome Res. 2017 Apr;27(4):580-590. doi: 10.1101/gr.217240.116. Epub 2017 Mar 23.

Abstract

In mouse and human meiosis, DNA double-strand breaks (DSBs) initiate homologous recombination and occur at specific sites called hotspots. The localization of these sites is determined by the sequence-specific DNA binding domain of the PRDM9 histone methyl transferase. Here, we performed an extensive analysis of PRDM9 binding in mouse spermatocytes. Unexpectedly, we identified a noncanonical recruitment of PRDM9 to sites that lack recombination activity and the PRDM9 binding consensus motif. These sites include gene promoters, where PRDM9 is recruited in a DSB-dependent manner. Another subset reveals DSB-independent interactions between PRDM9 and genomic sites, such as the binding sites for the insulator protein CTCF. We propose that these DSB-independent sites result from interactions between hotspot-bound PRDM9 and genomic sequences located on the chromosome axis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CCCTC-Binding Factor / metabolism
  • DNA Breaks, Double-Stranded
  • Genome*
  • Histone-Lysine N-Methyltransferase / metabolism*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Nucleotide Motifs*
  • Promoter Regions, Genetic
  • Protein Binding
  • Spermatocytes / metabolism

Substances

  • CCCTC-Binding Factor
  • Ctcf protein, mouse
  • Histone-Lysine N-Methyltransferase
  • prdm9 protein, mouse