| Literature DB >> 28674003 |
Adam D Hargreaves1, Long Zhou2, Josef Christensen3, Ferdinand Marlétaz1,4, Shiping Liu2, Fang Li2, Peter Gildsig Jansen3, Enrico Spiga5, Matilde Thye Hansen3, Signe Vendelbo Horn Pedersen3, Shameek Biswas6, Kyle Serikawa6, Brian A Fox6, William R Taylor5, John Frederick Mulley7, Guojie Zhang8,9,10, R Scott Heller11, Peter W H Holland12.
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.Entities:
Keywords: Pdx1; desert rodent; gene conversion; homeobox; type 2 diabetes
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Year: 2017 PMID: 28674003 PMCID: PMC5530673 DOI: 10.1073/pnas.1702930114
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205