Literature DB >> 32744506

ZCWPW1 is recruited to recombination hotspots by PRDM9 and is essential for meiotic double strand break repair.

Daniel Wells1,2, Emmanuelle Bitoun1,2, Daniela Moralli1, Gang Zhang1, Anjali Hinch1, Julia Jankowska1, Peter Donnelly1,2, Catherine Green1, Simon R Myers1,2.   

Abstract

During meiosis, homologous chromosomes pair and recombine, enabling balanced segregation and generating genetic diversity. In many vertebrates, double-strand breaks (pan class="Chemical">DSBs) initiate recombination within hotspots where pan class="Gene">PRDM9 binds, and deposits H3K4me3 and H3K36me3. However, no protein(s) recognising this unique combination of histone marks have been identified. We identified Zcwpw1, containing H3K4me3 and H3K36me3 recognition domains, as having highly correlated expression with Prdm9. Here, we show that ZCWPW1 has co-evolved with PRDM9 and, in human cells, is strongly and specifically recruited to PRDM9 binding sites, with higher affinity than sites possessing H3K4me3 alone. Surprisingly, ZCWPW1 also recognises CpG dinucleotides. Male Zcwpw1 knockout mice show completely normal DSB positioning, but persistent DMC1 foci, severe DSB repair and synapsis defects, and downstream sterility. Our findings suggest ZCWPW1 recognition of PRDM9-bound sites at DSB hotspots is critical for synapsis, and hence fertility.
© 2020, Wells et al.

Entities:  

Keywords:  DMC1; PRDM9; ZCWPW1; double strand break repair; genetics; genomics; human; meiosis; mouse; recombination

Mesh:

Substances:

Year:  2020        PMID: 32744506      PMCID: PMC7494361          DOI: 10.7554/eLife.53392

Source DB:  PubMed          Journal:  Elife        ISSN: 2050-084X            Impact factor:   8.140


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