Pioneering meiotic recombination

  1. Satoshi H. Namekawa1,2,3
  1. 1Division of Reproductive Sciences, University of Cincinnati College of Medicine, Cincinnati, Ohio, 45229, USA;
  2. 2Division of Developmental Biology, University of Cincinnati College of Medicine, Cincinnati, Ohio, 45229, USA;
  3. 3Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, 45229, USA
  1. Corresponding author: satoshi.namekawa{at}cchmc.org

Abstract

To induce cell type-specific forms of gene regulation, pioneer factors open tightly packed, inaccessible chromatin sites, enabling the molecular machinery to act on functionally significant information encoded in DNA. While previous studies of pioneer factors have revealed their functions in transcriptional regulation, pioneer factors that open chromatin for other physiological events remain undetermined. In this issue of Genes & Development, Spruce and colleagues (pp. 398–412) report the functional significance of a “pioneer complex” in mouse meiotic recombination. This complex, comprised of the zinc finger DNA-binding protein PRDM9 and the SNF2 family chromatin remodeler HELLS, exposes nucleosomal DNA to designate the sites of DNA double-strand breaks that initiate meiotic recombination. Both HELLS and PRDM9 are required for the determination of these recombination hot spots. Through the identification of a pioneer complex for meiotic recombination, this study broadens the conceptual scope of pioneer factors, indicating their functional significance in biological processes beyond transcriptional regulation.

Keywords

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