Evidence map›Paper›PMID 27547348›Full record

ArticleEcology and evolution2016

Born blonde: a recessive loss-of-function mutation in the melanocortin 1 receptor is associated with cream coat coloration in Antarctic fur seals.

Lucy Peters, Emily Humble, Nicole Kröcker, Birgit Fuchs, Jaume Forcada, Joseph I Hoffman

Open access · goldAbstract read
In one paragraph

Article in Ecology and evolution, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

8 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Lucy PetersDepartment of Animal Behaviour University of Bielefeld Postfach 100131 33501 Bielefeld Germany; College of Medical, Veterinary & Life Sciences University of Glasgow Graham Kerr Building Glasgow G12 8QQ UK.
Emily HumbleDepartment of Animal Behaviour University of Bielefeld Postfach 100131 33501 Bielefeld Germany; British Antarctic Survey High Cross, Madingley Road Cambridge CB3 OET UK.
Nicole KröckerDepartment of Animal Behaviour University of Bielefeld Postfach 100131 33501 Bielefeld Germany.
Birgit FuchsDepartment of Animal Behaviour University of Bielefeld Postfach 100131 33501 Bielefeld Germany.
Jaume ForcadaBritish Antarctic Survey High Cross, Madingley Road Cambridge CB3 OET UK.
Joseph I HoffmanDepartment of Animal Behaviour University of Bielefeld Postfach 100131 33501 Bielefeld Germany.
Bielefeld University · DEBritish Antarctic Survey · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although the genetic basis of color variation has been extensively studied in humans and domestic animals, the genetic polymorphisms responsible for different color morphs remain to be elucidated in many wild vertebrate species. For example, hypopigmentation has been observed in numerous marine mammal species but the underlying mutations have not been identified. A particularly compelling candidate gene for explaining color polymorphism is the melanocortin 1 receptor (MC1R), which plays a key role in the regulation of pigment production. We therefore used Antarctic fur seals (Arctocephalus gazella) as a highly tractable marine mammal system with which to test for an association between nucleotide variation at the MC1R and melanin-based coat color phenotypes. By sequencing 70 wild-type individuals with dark-colored coats and 26 hypopigmented individuals with cream-colored coats, we identified a nonsynonymous mutation that results in the substitution of serine with phenylalanine at an evolutionarily highly conserved structural domain. All of the hypopigmented individuals were homozygous for the allele coding for phenylalanine, consistent with a recessive loss-of-function allele. In order to test for cryptic population structure, which can generate artefactual associations, and to evaluate whether homozygosity at the MC1R could be indicative of low genome-wide heterozygosity, we also genotyped all of the individuals at 50 polymorphic microsatellite loci. We were unable to detect any population structure and also found that wild-type and hypopigmented individuals did not differ significantly in their standardized multilocus heterozygosity. Such a lack of association implies that hypopigmented individuals are unlikely to suffer disproportionately from inbreeding depression, and hence, we have no reason to believe that they are at a selective disadvantage in the wider population.

Indexed as

Antarctic fur seal (Arctocephalus gazella)candidate genecoat colorationinbreedingmelanocortin 1 receptor

Identifiers

PMID27547348
PMCPMC4983585
OpenAlexW2487603519

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.