Lühken G, Caroli A, Ibeagha-Awemu E M, Erhardt G
Department of Animal Breeding and Genetics, Justus Liebig University, 35390 Giessen, Germany.
Anim Genet. 2009 Aug;40(4):479-85. doi: 10.1111/j.1365-2052.2009.01861.x. Epub 2009 Mar 20.
The aim of this study was to identify the molecular genetic origin underlying the I variant of alpha(s1)-casein and to develop a DNA-based test for this polymorphism as a tool for genetic analyses independent of milk sample testing. All coding exons and flanking regions of the alpha(s1)-casein gene were sequenced in DNA samples from cattle of known alpha(s1)-casein genotypes (BI, CI, II, CC), determined by isoelectric focusing of milk samples. A nucleotide substitution (A>T) in exon 11 (g.19836A>T) leads to the exchange of Glu with Asp at amino acid position 84 of the mature protein (p.Glu84Asp) and perfectly co-segregated with the presence of the alpha(s1)-casein I variant in the milk of the analysed animals. Genotyping of a total of 680 DNA samples from 31 Bos taurus and Bos indicus cattle breeds and from Bos grunniens, Bison bison and Bison bonasus by restriction fragment length polymorphism analysis revealed the occurrence of Asp at position 84 at low frequencies in Bos taurus and Bos indicus breeds and established its origin from the alpha(s1)-casein C variant (p.Glu192Gly). Ten different intragenic haplotypes in the gene region from intron 8 to intron 12 were observed by sequencing, of which two occurred in Bison bison and one in Bison bonasus only. Using available casein gene complex information, an association of Asp at position 84 to beta-casein A(2) and kappa-casein B was shown in the Bos indicus breed Banyo Gudali. Taken together, we can postulate that the alpha(s1)-casein variant I is caused by a non-synonymous nucleotide substitution in exon 11 of the gene and that it originated within Bos indicus and spread to Bos taurus subsequently.
本研究的目的是确定α(s1)-酪蛋白I变体的分子遗传起源,并开发一种基于DNA的该多态性检测方法,作为独立于牛奶样本检测的遗传分析工具。通过对牛奶样本进行等电聚焦确定已知α(s1)-酪蛋白基因型(BI、CI、II、CC)的牛的DNA样本中,对α(s1)-酪蛋白基因的所有编码外显子和侧翼区域进行了测序。外显子11中的一个核苷酸替换(A>T,g.19836A>T)导致成熟蛋白第84位氨基酸处的谷氨酸被天冬氨酸替换(p.Glu84Asp),并且与被分析动物牛奶中α(s1)-酪蛋白I变体的存在完全共分离。通过限制性片段长度多态性分析对来自31个普通牛和瘤牛品种以及牦牛、美洲野牛和欧洲野牛的总共680个DNA样本进行基因分型,结果显示在普通牛和瘤牛品种中第84位天冬氨酸的出现频率较低,并确定其起源于α(s1)-酪蛋白C变体(p.Glu192Gly)。通过测序观察到基因区域从内含子8到内含子12有10种不同的基因内单倍型,其中两种仅出现在美洲野牛中,一种仅出现在欧洲野牛中。利用现有的酪蛋白基因复合体信息,在瘤牛品种班约古达利中显示了第84位天冬氨酸与β-酪蛋白A(2)和κ-酪蛋白B的关联。综上所述,我们可以推测α(s1)-酪蛋白变体I是由该基因外显子11中的一个非同义核苷酸替换引起的,并且它起源于瘤牛,随后传播到普通牛。