Genome sequence of a diabetes-prone rodent reveals a mutation hotspot around the ParaHox gene cluster

Adam D. Hargreaves, Long Zhou, Josef Christensen, Ferdinand Marletaz, Shiping Liu, Fang Li, Peter Gildsig Jansen, Enrico Spiga, Matilde Thye Hansen, Signe Vendelbo Horn Pedersen, Shameek Biswas, Kyle Seriwaka, Brian A. Fox, William R. Taylor, John Mulley, Guojie Zhang, R. Scott Heller, Peter W. H. Holland

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    Abstract

    The sand rat Psammomys obesus is a gerbil species native to deserts of North Africa and the Middle East, and is constrained in its ecology because high carbohydrate diets induce obesity and type II diabetes that, in extreme cases, can lead to pancreatic failure and death. We report the sequencing of the sand rat genome and discovery of an unusual, extensive, and mutationally biased GC-rich genomic domain. This highly divergent genomic region encompasses several functionally essential genes, and spans the ParaHox cluster which includes the insulin-regulating homeobox gene Pdx1. The sequence of sand rat Pdx1 has been grossly affected by GC-biased mutation, leading to the highest divergence observed for this gene across the Bilateria. In addition to genomic insights into restricted caloric intake in a desert species, the discovery of a localized chromosomal region subject to elevated mutation suggests that mutational heterogeneity within genomes could influence the course of evolution.
    Original languageEnglish
    Pages (from-to)7677–7682
    JournalProceedings of the National Academy of Sciences of the United States of America: PNAS
    Volume114
    Issue number29
    Early online date3 Jul 2017
    DOIs
    Publication statusPublished - 18 Jul 2017

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