Recurrent Evolution of Melanism in South American Felids
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2015Metadata
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Schneider, Alexsandra
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Recurrent Evolution of Melanism in South American Felids
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Abstract
Morphological variation in natural populations is a genomic test bed for studying the interface
between molecular evolution and population genetics, but some of the most interesting
questions involve non-model organisms that lack well annotated reference genomes. Many
felid species exhibit polymorphism for melanism but the relative roles played by genetic
drift, natural selection, and interspecies hybridization remain uncertain. We identify mutations
of Agouti signaling protein (ASIP) or the Melanocortin 1 receptor (MC1R) as independent
causes of melanism in three closely related South American species: the pampas cat
(Leopardus colocolo), the kodkod (Leopardus guigna), and Geoffroy’s cat (Leopardus geoffroyi).
To assess population level variation in the regions surrounding the causative mutations
we apply genomic resources from the domestic cat to carry out clone-based capture
and targeted resequencing of 299 kb and 251 kb segments that contain ASIP and MC1R,
respectively, from 54 individuals (13–21 per species), achieving enrichment of ~500–2500-
fold and ~150x coverage. Our analysis points to unique evolutionary histories for each of
the three species, with a strong selective sweep in the pampas cat, a distinctive but short
melanism-specific haplotype in the Geoffroy’s cat, and reduced nucleotide diversity for both
ancestral and melanism-bearing chromosomes in the kodkod. These results reveal an important
role for natural selection in a trait of longstanding interest to ecologists, geneticists,
and the lay community, and provide a platform for comparative studies of morphological variation
in other natural populations.
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Artículo de publicación ISI
Patrocinador
Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq), Brazil
Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES), Brazil
Intramural Research Program of the NIH
Frederick National Laboratory
Center for Cancer Research
National Cancer Institute
HudsonAlpha Institute for Biotechnology
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URI: https://repositorio.uchile.cl/handle/2250/132413
DOI: DOI: 10.1371/journal.pgen.1004892
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PLOS Genetics, February 19, 2015
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