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首页> 外文期刊>Annales Zoologici Fennici >Sequence variation in the melanocortin-1 receptor gene (Mc1r) does not explain variation in the degree of melanism in a widespread amphibian
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Sequence variation in the melanocortin-1 receptor gene (Mc1r) does not explain variation in the degree of melanism in a widespread amphibian

机译:melanocortin-1受体基因(Mc1r)中的序列变异不能解释在广泛的两栖动物中黑色素化程度的变异

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Variation in nucleotide sequence of the melanocortin-1 receptor gene (Meir) is associated with melanism in several mammalian, avian and reptilian species, but no attempts have been made to understand the genetic underpinnings of melanism in amphibians. We isolated the complete coding sequence (945 bps) of McIr from the common frog ( Rana temporaria) and compared the predicted amino acid sequence with that of fish, reptiles, birds and mammals. We investigated associations between nucleotide substitutions and the level of dorsal melanism among 28 individuals from two populations with pronounced differences in melanism. According to our results, the transmembrane regions of Mclr are conserved across vertebrates. In the population comparison, we only found five nucleotide sites with synonymous substitutions; none is being associated with the level of melanism. Our results suggest that either other genes or regulatory regions outside the coding sequence of Mclr are responsible for expression of melanism in R. temporaria.
机译:melanocortin-1受体基因(Meir)核苷酸序列的变异与几种哺乳动物,鸟类和爬虫类动物的黑色素症有关,但尚未尝试了解两栖动物黑色素症的遗传基础。我们从普通青蛙(Rana temporaria)中分离了McIr的完整编码序列(945 bps),并将预测的氨基酸序列与鱼类,爬行动物,鸟类和哺乳动物的氨基酸序列进行了比较。我们调查了来自两个人群的28名个体之间的核苷酸取代和背黑素病水平之间的关联,黑素病存在明显差异。根据我们的结果,Mclr的跨膜区域在整个脊椎动物中都是保守的。在总体比较中,我们仅发现了五个具有同义替换的核苷酸位点。没有什么与忧郁症的程度有关。我们的研究结果表明,Mclr编码序列之外的其他基因或调控区域是造成颞下叶黑素病黑色素表达的原因。

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