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

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  • Adam D. Hargreaves
    University of Oxford
  • Long Zhou
    China National Genebank, Shanghai
  • Josef Christensen
    Novo Nordisk
  • Ferdinand Marletaz
    University of Oxford
  • Shiping Liu
    China National Genebank, Shenzen.
  • Fang Li
    China National Genebank, Shenzen.
  • Peter Gildsig Jansen
    Novo Nordisk
  • Enrico Spiga
    Francis Crick Institute, London.
  • Matilde Thye Hansen
    Novo Nordisk
  • Signe Vendelbo Horn Pedersen
    Novo Nordisk
  • Shameek Biswas
    Novo Nordisk Research Centre, Seattle.
  • Kyle Seriwaka
    Novo Nordisk Research Centre, Seattle.
  • Brian A. Fox
    Novo Nordisk Research Centre, Seattle.
  • William R. Taylor
    Francis Crick Institute, London.
  • John Mulley
  • Guojie Zhang
    China National Genebank, Shenzen.
  • R. Scott Heller
    Novo Nordisk
  • Peter W. H. Holland
    University of Oxford
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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