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

机译:出生的金发女郎:黑皮素1受体的隐性功能丧失突变与南极毛皮海豹的乳膏外皮着色有关

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摘要

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.
机译:尽管已经在人和家畜中广泛研究了颜色变化的遗传基础,但是在许多野生脊椎动物物种中仍需阐明造成不同颜色形态的遗传多态性。例如,已经在许多海洋哺乳动物物种中观察到色素沉着不足,但尚未发现潜在的突变。用于解释颜色多态性的特别引人注目的候选基因是黑皮质素1受体(MC1R),它在调节色素生成中起关键作用。因此,我们使用南极海狗(Arctocephalus gazella)作为高度易处理的海洋哺乳动物系统,用以测试MC1R的核苷酸变异与基于黑色素的皮毛颜色表型之间的关联。通过对深色外套的70个野生型个体和奶油色外套的26个色素沉着的个体进行测序,我们确定了一个非同义突变,该突变导致在进化上高度保守的结构域中丝氨酸被苯丙氨酸取代。所有色素减低的个体均是编码苯丙氨酸的等位基因纯合子,与隐性功能丧失等位基因一致。为了测试可以生成人工产物关联的隐性种群结构,并评估MC1R上的纯合子是否可以指示整个基因组范围内的低杂合子,我们还对50个多态性微卫星基因座上的所有个体进行了基因分型。我们无法检测到任何种群结构,还发现野生型和色素沉着个体的标准化多基因座杂合性没有显着差异。缺乏这种联系意味着色素沉着的个体不太可能遭受近交性抑郁症的折磨,因此,我们没有理由相信他们在更广泛的人群中处于选择性的劣势。

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