PRDM9 drives the location and rapid evolution of recombination hotspots in salmonids

• Published in: bioRxiv
• Main Authors: Raynaud, Marie, Sanna, Paola, Julien, Joseph, Clément, Julie, Imai, Yukiko, Jean-Jacques Lareyre, Laurent, Audrey, Galtier, Nicolas, Baudat, Frédéric, Duret, Laurent, Pierre-Alexandre Gagnaire, De Massy, Bernard
• Format: Paper
• Language: English
• Published: Cold Spring Harbor Cold Spring Harbor Laboratory Press 07.03.2024
• Subjects: DNA damage; Evolution; Gene mapping; Gene polymorphism; Genomes; Meiosis; Oncorhynchus kisutch; Oncorhynchus mykiss; Promoters; Recombination hot spots; Salmo salar; Salmonidae; Zinc finger proteins
• DOI: 10.1101/2024.03.06.583651

In many eukaryotes, meiotic recombination occurs preferentially at discrete sites, called recombination hotspots. In various lineages, recombination hotspots are located in regions with promoter-like features and are evolutionarily stable. Conversely, in some mammals, hotspots are driven by PRDM9 that targets recombination away from promoters. Paradoxically, PRDM9 induces the self-destruction of its targets and this triggers an ultra-fast evolution of mammalian hotspots. PRDM9 is ancestral to all animals, suggesting a critical importance for the meiotic program, but has been lost in many lineages with surprisingly little effect on meiosis success. However, it is unclear whether the function of PRDM9 described in mammals is shared by other species. To investigate this, we analyzed the recombination landscape of several salmonids, the genome of which harbors one full-length PRDM9 and several truncated paralogs. We identified recombination initiation sites in Oncorhynchus mykiss by mapping meiotic DNA double-strand breaks (DSBs). We found that DNA DSBs clustered at hotspots positioned away from promoters, enriched for the H3K4me3 and H3K4me36 marks and the location of which depended on the genotype of full-length Prdm9. We observed a high level of polymorphism in the zinc finger domain of full-length Prdm9, but not of the truncated paralogs. Moreover, population-scaled recombination maps in O. mykiss, Oncorhynchus kisutch and Salmo salar revealed a rapid turnover of recombination hotspots caused by PRDM9 target motif erosion. Our results imply that PRDM9 function is conserved across vertebrates and that the peculiar evolutionary runaway caused by PRDM9 has been active for several hundred million years.Competing Interest StatementThe authors have declared no competing interest.