Peters Lucy, Humble Emily, Kröcker Nicole, Fuchs Birgit, Forcada Jaume, Hoffman Joseph I
Department 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.
Department of Animal Behaviour University of Bielefeld Postfach 100131 33501 Bielefeld Germany; British Antarctic Survey High Cross, Madingley Road Cambridge CB3 OET UK.
Ecol Evol. 2016 Jul 22;6(16):5705-17. doi: 10.1002/ece3.2290. eCollection 2016 Aug.
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.
尽管在人类和家畜中已经广泛研究了颜色变异的遗传基础,但在许多野生脊椎动物物种中,导致不同颜色形态的遗传多态性仍有待阐明。例如,在众多海洋哺乳动物物种中都观察到了色素沉着不足的现象,但尚未确定其潜在的突变。一个特别有说服力的解释颜色多态性的候选基因是黑皮质素1受体(MC1R),它在色素生成的调节中起关键作用。因此,我们使用南极毛皮海狮(南极海狗)作为一个易于处理的海洋哺乳动物系统,来测试MC1R基因座的核苷酸变异与基于黑色素的毛色表型之间的关联。通过对70只深色皮毛的野生型个体和26只奶油色皮毛的色素沉着不足个体进行测序,我们在一个进化上高度保守的结构域中发现了一个非同义突变,该突变导致丝氨酸被苯丙氨酸取代。所有色素沉着不足的个体都是编码苯丙氨酸的等位基因的纯合子,这与隐性功能丧失等位基因一致。为了测试可能产生人为关联的潜在种群结构,并评估MC1R基因座的纯合性是否可能指示全基因组杂合性较低,我们还对所有个体的50个多态性微卫星基因座进行了基因分型。我们未能检测到任何种群结构,并且还发现野生型个体和色素沉着不足的个体在标准化多位点杂合性方面没有显著差异。这种缺乏关联意味着色素沉着不足的个体不太可能过度遭受近亲繁殖衰退的影响,因此,我们没有理由相信它们在更广泛的种群中处于选择劣势。