Repeated losses of PRDM9-directed recombination despite the conservation of PRDM9 across vertebrates

• DOI: 10.7554/elife.24133
• Publication Date: 2017-06-06T12:00:13Z
• Authors: Zachary Baker; Molly Schumer; Yuki Haba; Lisa Bashkirova; Chris Holland; Gil G Rosenthal; Molly Przeworski
• Keywords: Recombination, Genetic; 0301 basic medicine; QH301-705.5; Science; Q; R; Xiphophorus; Histone-Lysine N-Methyltransferase; Recombination; Evolution, Molecular; Meiosis; 03 medical and health sciences; Hotspot; Genomics and Evolutionary Biology; Vertebrates; Medicine; Animals; Biology (General); PRDM9

Studies of highly diverged species have revealed two mechanisms by which meiotic recombination is directed to the genome—through PRDM9 binding or by targeting promoter-like features—that lead to dramatically different evolutionary dynamics of hotspots. Here, we identify PRDM9 orthologs from genome and transcriptome data in 225 species. We find the complete PRDM9 ortholog across distantly related vertebrates but, despite this broad conservation, infer a minimum of six partial and three complete losses. Strikingly, taxa carrying the complete ortholog of PRDM9 are precisely those with rapid evolution of its predicted binding affinity, suggesting that all domains are necessary for directing recombination. Indeed, as we show, swordtail fish carrying only a partial but conserved ortholog share recombination properties with PRDM9 knock-outs.