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牛 MITF 基因的单倍型变异性与荷斯坦和西门塔尔牛的花斑病的关联。

Haplotype variability in the bovine MITF gene and association with piebaldism in Holstein and Simmental cattle breeds.

机构信息

DIPROVAL, Sezione di Allevamenti Zootecnici, Faculty of Agriculture, University of Bologna, Italy.

出版信息

Anim Genet. 2012 Jun;43(3):250-6. doi: 10.1111/j.1365-2052.2011.02242.x. Epub 2011 Sep 15.

DOI:10.1111/j.1365-2052.2011.02242.x
PMID:22486495
Abstract

Candidate gene analysis, quantitative trait locus mapping in outbreed and experimental cross-populations and a genomewide association study in Holstein have reported that a few chromosome regions contribute to great variability in the degree of white/black spotting in cattle. In particular, an important region affecting this trait was localized on bovine chromosome 22 in the region containing the microphthalmia-associated transcription factor (MITF) gene. We sequenced a total of 7258 bp of the MITF gene in 40 cattle of different breeds, including 20 animals from spotted breeds (10 Italian Holstein and 10 Italian Simmental) and 20 animals from solid coloured breeds (10 Italian Brown and 10 Reggiana), and identified 17 single nucleotide polymorphisms (SNPs). The allele frequencies of one polymorphism (g.32386957A>T) were clearly different between spotted (A = 0.875; T = 0.125) and non-spotted breeds (A = 0.125; T = 0.875) (P = 8.2E-12). This result was confirmed by genotyping additional animals of these four breeds (P < 1.0E-20). A total of 21 different haplotypes were inferred from the sequenced animals. Considering similarities among haplotypes, spotted and non-spotted groups of cattle showed significant differences in their haplotype distribution (P = 0.001), which was further supported by the analysis of molecular variance (amova) of two genotyped SNPs in an enlarged sample of cattle. Variability in the MITF gene clearly explained the differences between spotted and non-spotted phenotypes but, at the same time, it is evident that this gene is not the only genetic factor determining piebaldism in Italian Holstein and Italian Simmental cattle breeds.

摘要

候选基因分析、异交和实验杂交群体的数量性状位点作图以及荷斯坦牛的全基因组关联研究表明,几个染色体区域对牛的黑白斑点程度的巨大变异性有贡献。特别是,一个影响该性状的重要区域位于包含小眼相关转录因子(MITF)基因的牛 22 号染色体上。我们对来自不同品种的 40 头牛的 MITF 基因进行了总共 7258bp 的测序,包括 20 头斑点品种的动物(10 头意大利荷斯坦牛和 10 头意大利西门塔尔牛)和 20 头纯色品种的动物(10 头意大利棕色牛和 10 头雷焦亚纳牛),并鉴定出 17 个单核苷酸多态性(SNP)。一个多态性(g.32386957A>T)的等位基因频率在斑点(A = 0.875;T = 0.125)和非斑点品种(A = 0.125;T = 0.875)之间明显不同(P = 8.2E-12)。这一结果通过对这四个品种的额外动物进行基因分型得到了证实(P < 1.0E-20)。从测序的动物中推断出 21 个不同的单倍型。考虑到单倍型之间的相似性,斑点和非斑点牛群在单倍型分布上存在显著差异(P = 0.001),这一结果通过对一个更大的牛样本中两个基因分型 SNP 的分子方差分析(amova)得到了进一步支持。MITF 基因的变异性清楚地解释了斑点和非斑点表型之间的差异,但同时也表明,该基因不是决定意大利荷斯坦牛和意大利西门塔尔牛品种中花斑现象的唯一遗传因素。

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