Evidence map›Paper›PMID 25695801›Full record

ArticlePLoS genetics2015

Recurrent evolution of melanism in South American felids.

Alexsandra Schneider, Corneliu Henegar, Kenneth Day, Devin Absher, Constanza Napolitano, Leandro Silveira, Victor A David, Stephen J O'Brien, Marilyn Menotti-Raymond, Gregory S Barsh and 1 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.0field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 62 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 6 institutions in 4 countries.

Alexsandra SchneiderLaboratório de Biologia Genômica e Molecular, Faculdade de Biociências, Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS), Porto Alegre, Brazil.
Corneliu HenegarHudsonAlpha Institute for Biotechnology, Huntsville, Alabama, United States of America.
Kenneth DayHudsonAlpha Institute for Biotechnology, Huntsville, Alabama, United States of America.
Devin AbsherHudsonAlpha Institute for Biotechnology, Huntsville, Alabama, United States of America.
Constanza NapolitanoLaboratorio de Ecología Molecular & Instituto de Ecologia y Biodiversidad, Departamento de Ciencias Ecológicas, Facultad de Ciencias, Universidad de Chile, Santiago, Chile.
Leandro SilveiraJaguar Conservation Fund, Instituto Onça-Pintada, Mineiros, Goiás, Brazil.
Victor A DavidBasic Research Laboratory, Frederick National Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, United States of America.
Stephen J O'BrienTheodosius Dobzhansky Center for Genome Informatics, St. Petersburg State University, St. Petersburg, Russia.
Marilyn Menotti-RaymondBasic Research Laboratory, Frederick National Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, Maryland, United States of America.
Gregory S BarshHudsonAlpha Institute for Biotechnology, Huntsville, Alabama, United States of America.
Eduardo EizirikLaboratório de Biologia Genômica e Molecular, Faculdade de Biociências, Pontifícia Universidade Católica do Rio Grande do Sul (PUCRS), Porto Alegre, Brazil; Instituto Pró-Carnívoros, Atibaia, São Paulo, Brazil.
HudsonAlpha Institute for Biotechnology · USPontifícia Universidade Católica do Rio Grande do Sul · BRCenter for Cancer Research · USInstitute of Ecology and Biodiversity · CLNational Cancer Institute · USSt Petersburg University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Evolution, MolecularAgouti Signaling ProteinAnimalsCatsGenetics, PopulationGenetic VariationHaplotypesMelanosisMutationPhylogenyReceptor, Melanocortin, Type 1Selection, GeneticSouth AmericaSpecies SpecificityAgouti Signaling ProteinReceptor, Melanocortin, Type 1

Identifiers

PMID25695801
PMCPMC4335015
OpenAlexW2094461845

What OpenQuestion holds

Textmetadata
LicenceCC0
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.