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首页> 外文期刊>The Journal of Heredity >Identification of a mutation that is associated with the saddle tan and black-and-tan phenotypes in Basset Hounds and Pembroke Welsh Corgis
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Identification of a mutation that is associated with the saddle tan and black-and-tan phenotypes in Basset Hounds and Pembroke Welsh Corgis

机译:鉴定与巴塞特猎犬和彭布罗克威尔士柯基犬图片中的鞍形棕褐色和黑色棕褐色表型相关的突变

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摘要

The causative mutation for the black-and-tan (at) phenotype in dogs was previously shown to be a SINE insertion in the 5′ region of Agouti Signaling Protein (ASIP). Dogs with the black-and-tan phenotype, as well as dogs with the saddle tan phenotype, genotype as at/- at this locus. We have identified a 16-bp duplication (g.1875-1890dupCCCCAGGTCAGAGTTT) in an intron of hnRNP associated with lethal yellow (RALY), which segregates with the black-and-tan phenotype in a group of 99 saddle tan and black-and-tan Basset Hounds and Pembroke Welsh Corgis. In these breeds, all dogs with the saddle tan phenotype had RALY genotypes of +/+ or +/dup, whereas dogs with the black-and-tan phenotype were homozygous for the duplication. The presence of an ay/- fawn or e/e red genotype is epistatic to the +/- saddle tan genotype. Genotypes from 10 wolves and 1 coyote indicated that the saddle tan (+) allele is the ancestral allele, suggesting that black-and-tan is a modification of saddle tan. An additional 95 dogs from breeds that never have the saddle tan phenotype have all three of the possible RALY genotypes. We suggest that a multi-gene interaction involving ASIP, RALY, MC1R, DEFB103, and a yet-unidentified modifier gene is required for expression of saddle tan.
机译:先前已证明狗中黑色和棕褐色(at)表型的致病突变是在Agouti信号蛋白(ASIP)5'区的SINE插入。具有黑色和棕褐色表型的狗,以及具有鞍形棕褐色表型的狗,在此基因座处的基因型为at /-。我们在与致死黄(RALY)相关的hnRNP内含子中鉴定出16 bp重复序列(g.1875-1890dupCCCCAGGTCAGAGTTT),该基因与黑色和棕褐色表型隔离在一组99个鞍形棕褐色和黑色和棕褐色的巴塞特猎犬和彭布罗克威尔士柯基犬图片。在这些犬种中,所有具有棕褐色棕褐色表型的狗的RALY基因型均为+ / +或+ / dup,而具有棕褐色棕褐色表型的狗是纯合的。 ay / -fawn或e / e红色基因型的存在比+/-鞍形棕褐色的基因型上位。来自10头狼和1头土狼的基因型表明,鞍形棕褐色(+)等位基因是祖先等位基因,表明黑棕褐色是鞍形棕褐色的修饰。从未有鞍形棕褐色表型的其他品种的95只犬具有所有三种可能的RALY基因型。我们建议表达鞍鞍棕褐色需要一个涉及ASIP,RALY,MC1R,DEFB103和一个尚未鉴定的修饰基因的多基因相互作用。

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