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Recent Evolution in Rattus norvegicus Is Shaped by Declining Effective Population Size.
Deinum, Eva E; Halligan, Daniel L; Ness, Rob W; Zhang, Yao-Hua; Cong, Lin; Zhang, Jian-Xu; Keightley, Peter D.
Afiliación
  • Deinum EE; Institute of Evolutionary Biology, University of Edinburgh, Edinburgh, United Kingdom.
  • Halligan DL; Institute of Evolutionary Biology, University of Edinburgh, Edinburgh, United Kingdom.
  • Ness RW; Institute of Evolutionary Biology, University of Edinburgh, Edinburgh, United Kingdom.
  • Zhang YH; State Key Laboratory of Integrated Management of Pest Insects and Rodents in Agriculture, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
  • Cong L; Institute of Plant Protection, Heilongjiang Academy of Agricultural Sciences, Harbin, China.
  • Zhang JX; State Key Laboratory of Integrated Management of Pest Insects and Rodents in Agriculture, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
  • Keightley PD; Institute of Evolutionary Biology, University of Edinburgh, Edinburgh, United Kingdom peter.keightley@ed.ac.uk.
Mol Biol Evol ; 32(10): 2547-58, 2015 Oct.
Article en En | MEDLINE | ID: mdl-26037536
ABSTRACT
The brown rat, Rattus norvegicus, is both a notorious pest and a frequently used model in biomedical research. By analyzing genome sequences of 12 wild-caught brown rats from their presumed ancestral range in NE China, along with the sequence of a black rat, Rattus rattus, we investigate the selective and demographic forces shaping variation in the genome. We estimate that the recent effective population size (Ne) of this species = [Formula see text], based on silent site diversity. We compare patterns of diversity in these genomes with patterns in multiple genome sequences of the house mouse (Mus musculus castaneus), which has a much larger Ne. This reveals an important role for variation in the strength of genetic drift in mammalian genome evolution. By a Pairwise Sequentially Markovian Coalescent analysis of demographic history, we infer that there has been a recent population size bottleneck in wild rats, which we date to approximately 20,000 years ago. Consistent with this, wild rat populations have experienced an increased flux of mildly deleterious mutations, which segregate at higher frequencies in protein-coding genes and conserved noncoding elements. This leads to negative estimates of the rate of adaptive evolution (α) in proteins and conserved noncoding elements, a result which we discuss in relation to the strongly positive estimates observed in wild house mice. As a consequence of the population bottleneck, wild rats also show a markedly slower decay of linkage disequilibrium with physical distance than wild house mice.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Evolución Biológica Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Mol Biol Evol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2015 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Evolución Biológica Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Mol Biol Evol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2015 Tipo del documento: Article País de afiliación: Reino Unido
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