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黑素皮质素 1 受体(MC1R)基因的多态性解释了火鸡(Meleagris gallopavo)青铜色位点的分离。

Variability of the melanocortin 1 receptor (MC1R) gene explains the segregation of the bronze locus in turkey (Meleagris gallopavo).

机构信息

Departament de Biologia, Universitat de Girona, E-17071 Girona, Catalonia, Spain.

出版信息

Poult Sci. 2010 Aug;89(8):1599-602. doi: 10.3382/ps.2010-00726.

Abstract

By sequencing the full coding region of the turkey melanocortin 1 receptor (MC1R) gene, we have found 4 mutations (c.96G > A, c.364A > T, c.450C > T, and c.887C > T) that are organized in 5 different haplotypes (MC1R1 to MC1R5). These haplotypes correlate perfectly with the 3 alleles of the bronze locus (i.e., B, b(+), and b(1)). We suggest that the dominant black phenotype, associated with the B allele, results from the constitutive activation of the receptor, an effect that might be mediated by the missense mutation c.364A > T (p.Ile122Phe). Moreover, we propose that the recessive black-winged bronze phenotype (linked to b(1)) might be produced by 2 deleterious mutations of MC1R (c.96G > A and c.887C > T). This is an unexpected finding because in mammals, MC1R deleterious polymorphisms are usually related with either red or lighter fur colors.

摘要

通过对火鸡黑色素皮质素 1 受体 (MC1R) 基因的完整编码区进行测序,我们发现了 4 种突变(c.96G > A、c.364A > T、c.450C > T 和 c.887C > T),它们组织在 5 种不同的单倍型(MC1R1 至 MC1R5)中。这些单倍型与青铜基因座的 3 个等位基因(即 B、b(+) 和 b(1))完全相关。我们认为,与 B 等位基因相关的显性黑色表型是由于受体的组成性激活所致,这种效应可能是由错义突变 c.364A > T(p.Ile122Phe)介导的。此外,我们提出隐性黑翅青铜表型(与 b(1)相关)可能是由 MC1R 的 2 种有害突变(c.96G > A 和 c.887C > T)引起的。这是一个意外的发现,因为在哺乳动物中,MC1R 的有害多态性通常与红色或更浅的毛色有关。

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