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How the Leopard Hides Its Spots: ASIP Mutations and Melanism in Wild Cats
The occurrence of melanism (darkening of the background coloration) is documented in 13 felid species, in some cases reaching high frequencies at the population level. Recent analyses have indicated that it arose multiple times in the Felidae, with three different species exhibiting unique mutations...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3520955/ https://www.ncbi.nlm.nih.gov/pubmed/23251368 http://dx.doi.org/10.1371/journal.pone.0050386 |
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author | Schneider, Alexsandra David, Victor A. Johnson, Warren E. O'Brien, Stephen J. Barsh, Gregory S. Menotti-Raymond, Marilyn Eizirik, Eduardo |
author_facet | Schneider, Alexsandra David, Victor A. Johnson, Warren E. O'Brien, Stephen J. Barsh, Gregory S. Menotti-Raymond, Marilyn Eizirik, Eduardo |
author_sort | Schneider, Alexsandra |
collection | PubMed |
description | The occurrence of melanism (darkening of the background coloration) is documented in 13 felid species, in some cases reaching high frequencies at the population level. Recent analyses have indicated that it arose multiple times in the Felidae, with three different species exhibiting unique mutations associated with this trait. The causative mutations in the remaining species have so far not been identified, precluding a broader assessment of the evolutionary dynamics of melanism in the Felidae. Among these, the leopard (Panthera pardus) is a particularly important target for research, given the iconic status of the ‘black panther’ and the extremely high frequency of melanism observed in some Asian populations. Another felid species from the same region, the Asian golden cat (Pardofelis temminckii), also exhibits frequent records of melanism in some areas. We have sequenced the coding region of the Agouti Signaling Protein (ASIP) gene in multiple leopard and Asian golden cat individuals, and identified distinct mutations strongly associated with melanism in each of them. The single nucleotide polymorphism (SNP) detected among the P. pardus individuals was caused by a nonsense mutation predicted to completely ablate ASIP function. A different SNP was identified in P. temminckii, causing a predicted amino acid change that should also induce loss of function. Our results reveal two additional cases of species-specific mutations implicated in melanism in the Felidae, and indicate that ASIP mutations may play an important role in naturally-occurring coloration polymorphism. |
format | Online Article Text |
id | pubmed-3520955 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-35209552012-12-18 How the Leopard Hides Its Spots: ASIP Mutations and Melanism in Wild Cats Schneider, Alexsandra David, Victor A. Johnson, Warren E. O'Brien, Stephen J. Barsh, Gregory S. Menotti-Raymond, Marilyn Eizirik, Eduardo PLoS One Research Article The occurrence of melanism (darkening of the background coloration) is documented in 13 felid species, in some cases reaching high frequencies at the population level. Recent analyses have indicated that it arose multiple times in the Felidae, with three different species exhibiting unique mutations associated with this trait. The causative mutations in the remaining species have so far not been identified, precluding a broader assessment of the evolutionary dynamics of melanism in the Felidae. Among these, the leopard (Panthera pardus) is a particularly important target for research, given the iconic status of the ‘black panther’ and the extremely high frequency of melanism observed in some Asian populations. Another felid species from the same region, the Asian golden cat (Pardofelis temminckii), also exhibits frequent records of melanism in some areas. We have sequenced the coding region of the Agouti Signaling Protein (ASIP) gene in multiple leopard and Asian golden cat individuals, and identified distinct mutations strongly associated with melanism in each of them. The single nucleotide polymorphism (SNP) detected among the P. pardus individuals was caused by a nonsense mutation predicted to completely ablate ASIP function. A different SNP was identified in P. temminckii, causing a predicted amino acid change that should also induce loss of function. Our results reveal two additional cases of species-specific mutations implicated in melanism in the Felidae, and indicate that ASIP mutations may play an important role in naturally-occurring coloration polymorphism. Public Library of Science 2012-12-12 /pmc/articles/PMC3520955/ /pubmed/23251368 http://dx.doi.org/10.1371/journal.pone.0050386 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Schneider, Alexsandra David, Victor A. Johnson, Warren E. O'Brien, Stephen J. Barsh, Gregory S. Menotti-Raymond, Marilyn Eizirik, Eduardo How the Leopard Hides Its Spots: ASIP Mutations and Melanism in Wild Cats |
title | How the Leopard Hides Its Spots: ASIP Mutations and Melanism in Wild Cats |
title_full | How the Leopard Hides Its Spots: ASIP Mutations and Melanism in Wild Cats |
title_fullStr | How the Leopard Hides Its Spots: ASIP Mutations and Melanism in Wild Cats |
title_full_unstemmed | How the Leopard Hides Its Spots: ASIP Mutations and Melanism in Wild Cats |
title_short | How the Leopard Hides Its Spots: ASIP Mutations and Melanism in Wild Cats |
title_sort | how the leopard hides its spots: asip mutations and melanism in wild cats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3520955/ https://www.ncbi.nlm.nih.gov/pubmed/23251368 http://dx.doi.org/10.1371/journal.pone.0050386 |
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