TY - JOUR T1 - A natural mutator allele shapes mutation spectrum variation in mice JF - bioRxiv DO - 10.1101/2021.03.12.435196 SP - 2021.03.12.435196 AU - Thomas A. Sasani AU - David G. Ashbrook AU - Annabel C. Beichman AU - Lu Lu AU - Abraham A. Palmer AU - Robert W. Williams AU - Jonathan K. Pritchard AU - Kelley Harris Y1 - 2022/01/01 UR - http://biorxiv.org/content/early/2022/01/10/2021.03.12.435196.abstract N2 - Although germline mutation rates and spectra can vary within and between species, genetic modifiers of these traits have long eluded detection. In this study, we searched for loci that influence germline mutagenesis using a uniquely powerful resource: a panel of recombinant inbred mouse lines known as the BXD, descended from the laboratory mouse strains C57BL/6J (B) and DBA/2J (D). Each BXD lineage has been maintained by brother-sister mating in the near absence of natural selection, accumulating de novo mutations for up to 50 years on a known genetic background that is a unique linear mosaic of B and D haplotypes. We show that mice inheriting D haplotypes at a quantitative trait locus (QTL) on chromosome 4 accumulate C>A germline mutations at a 50% higher rate than those inheriting B haplotypes, primarily due to the activity of a C>A-dominated mutational signature known as SBS18. The B and D QTL haplotypes encode different alleles of the DNA repair gene Mutyh, which underlies the heritable colorectal cancer syndrome in which SBS18 was first identified. The B and D Mutyh alleles are present in wild populations of Mus musculus domesticus, providing evidence that common genetic variation modulates germline mutagenesis in a model mammalian species.Competing Interest StatementThe authors have declared no competing interest. ER -