PRDM9 losses in vertebrates are coupled to those of paralogs ZCWPW1 and ZCWPW2

Author:

Cavassim Maria Izabel A.12ORCID,Baker Zachary2ORCID,Hoge Carla2ORCID,Schierup Mikkel H.1ORCID,Schumer Molly3,Przeworski Molly24ORCID

Affiliation:

1. Bioinformatics Research Centre, Aarhus University, Aarhus 8000, Denmark

2. Department of Biological Sciences, Columbia University, New York, NY 10027

3. Department of Biology, Stanford University, Stanford, CA 94305

4. Department of Systems Biology, Columbia University, New York, NY 10027

Abstract

Significance We take a phylogenetic approach to search for molecular partners of PRDM9, a key meiotic recombination gene, by leveraging the fact that the complete PRDM9 gene has been lost at least 13 times independently in vertebrates. We identify two genes, ZCWPW1 and its paralog ZCWPW2 , whose presence or absence across vertebrates is coupled to that of PRDM9 . ZCWPW1 was recently shown to be recruited to sites of PRDM9 binding and to aid in the repair of double strand breaks. ZCWPW2 is likely recruited to sites of PRDM9 binding as well; its tight coevolution with PRDM9 across vertebrates suggests that it too plays an important role in mammals and beyond, either in double strand break formation or repair.

Funder

NIH

RO1

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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