College of Animal Science and Veterinary Medicine, Jilin University, Changchun, 130062, China.
Mol Biol Rep. 2011 Aug;38(6):4197-204. doi: 10.1007/s11033-010-0541-0. Epub 2010 Dec 1.
Prion protein (PRNP) gene has been located at position q17 of chromosome 13 in cattle. The polymorphisms of PRNP gene might be associated with BSE susceptibility. In the present work, we investigated the polymorphisms of PRNP gene, including SNP in exon 3, 23-bp indel in promoter region, 12-bp indel in intron 1 in 2 Chinese indigenous cattle breeds of northeast China. Eighty-six animals from Yanbian (34) and Chinese Red Steppes (52) were genotyped at PRNP locus by analyzing genomic DNA. A total of 4 single nucleotide polymorphism (SNP) sites were revealed in the PRNP gene exon 3 of the 2 cattle breeds investigated. Three of these SNPs were non-synonymous mutations that resulted in the amino acid exchanges (K119N, S154N, and M177V), and one is silent nucleotide substitutions (A234G). The two amino acid mutations of S154N and M177V were detected only in Yanbian with a very low frequency (0.0147), and they appears to be absent in Chinese Red Steppes. The average gene heterozygosity (He), effective allele numbers (Ne), Shannon's information index (I) and polymorphism information content (PIC) were 0.3088, 1.5013, 0.3814 and 0.2000 in Yanbian, respectively, being relatively higher than that of Chinese Red Steppes (0.2885, 1.4985, 0.3462 and 0.1873, respectively). In 23-bp indel and 12-bp indel loci, three different genotypes were identified in both Yanbian and Chinese Red Steppes breeds. Based 23- and 12-bp indels, four haplotypes was constructed in the 2 Chinese cattle breeds, of which the 23-bp (-)/12-bp (-) was main haplotypes accounting for more than 50% of the total in both Yanbian and Chinese Red Steppes breeds. These results might be useful in understanding the genetic characteristics of PRNP gene in Chinese indigenous cattle breeds.
朊病毒蛋白(PRNP)基因位于牛 13 号染色体的 q17 位置。PRNP 基因的多态性可能与 BSE 的易感性有关。在本工作中,我们研究了中国东北两个本土牛种 PRNP 基因的多态性,包括外显子 3 的 SNP、启动子区 23-bp 缺失、内含子 1 的 12-bp 缺失。从延边(34 只)和中国红草原(52 只)的 86 只动物中,通过分析基因组 DNA 在 PRNP 基因座上进行了基因型分型。在所研究的 2 个牛种的 PRNP 基因外显子 3 中发现了 4 个单核苷酸多态性(SNP)位点。其中 3 个 SNP 是导致氨基酸置换的非同义突变(K119N、S154N 和 M177V),1 个是沉默核苷酸取代(A234G)。S154N 和 M177V 的两个氨基酸突变仅在延边被检测到,频率非常低(0.0147),而在中国红草原似乎不存在。延边的平均基因杂合度(He)、有效等位基因数(Ne)、香农信息指数(I)和多态信息含量(PIC)分别为 0.3088、1.5013、0.3814 和 0.2000,均高于中国红草原的 0.2885、1.4985、0.3462 和 0.1873。在 23-bp 缺失和 12-bp 缺失位点,在延边和中国红草原牛种中均鉴定出三种不同的基因型。基于 23-bp 和 12-bp 缺失,在中国两个牛种中构建了四个单倍型,其中 23-bp(-)/12-bp(-)是主要单倍型,占延边和中国红草原牛种总单倍型的 50%以上。这些结果可能有助于了解中国本土牛种 PRNP 基因的遗传特征。