Kishore Amit, Mukesh M, Sobti R C, Kataria R S, Mishra B P, Sodhi Monika
National Bureau of Animal Genetics Resources, PO Box-129, Karnal 132 001, Haryana, India ; Department of Biotechnology, Panjab University, Chandigarh 160 014, India.
National Bureau of Animal Genetics Resources, PO Box-129, Karnal 132 001, Haryana, India.
Meta Gene. 2014 Oct 24;2:769-81. doi: 10.1016/j.mgene.2014.10.001. eCollection 2014 Dec.
The promoter region of kappa-casein (κ-CN) gene in Indian native cattle and buffalo breeds was sequenced and analyzed for nucleotide variations. Sequence comparison across breeds of Indian cattle revealed a total of 7 variations in the promoter region, of which - 515 G/T, - 427 C/T, - 385 C/T, - 283 A/G and - 251 C/T were located within consensus binding sites for octamer-binding protein (OCT1)/pregnancy specific mammary nuclear factor (PMF), activator protein-2 (AP2), hepatocyte nuclear factor (HNF-1) and GAL4 transcription factors (TFs), respectively. These variations might be involved in gain or loss of potential transcription factor binding sites (TFBSs). Unlike the other 4 variants, the - 283 (A/G) variant located within HNF-1 TFBS was specific to Indian cattle as this change has not been observed in the Bos taurus sequence. Other TFBSs viz., MGF, TBP, NF-1, milk box and C/EBP were conserved across species. For the Indian native buffalo breeds, only 3 changes were identified in the promoter region; - 305 (A/C), - 160 (T/C) and - 141 (A/G) and most of the TFBSs were found to be conserved. However, deletion of two adjacent nucleotides located in and around binding site for C/EBP TF was identified in buffalo when compared with promoter sequence of bovine κ-CN. For κ-CN of Indian native cattle, a strong linkage disequilibrium (LD) was observed for variations 515 G/T, - 427 C/T and - 385 C/T in the promoter region; and for variations at codons 136 and 148 of exon-IV. Further, among intragenic haplotypes, variation - 427 C/T was found to be in LD with variations at codons 136 and 148. The information generated in the present work provides comprehensive characterization of κ-CN gene promoter and coding regions in Indian cattle and buffaloes and reported variations could become important candidates for carrying out further research in dairy traits.
对印度本土牛和水牛品种的κ-酪蛋白(κ-CN)基因启动子区域进行了测序,并分析了核苷酸变异。对印度牛不同品种的序列比较显示,启动子区域共有7个变异,其中-515 G/T、-427 C/T、-385 C/T、-283 A/G和-251 C/T分别位于八聚体结合蛋白(OCT1)/妊娠特异性乳腺核因子(PMF)、激活蛋白-2(AP2)、肝细胞核因子(HNF-1)和GAL4转录因子(TFs)的共有结合位点内。这些变异可能参与潜在转录因子结合位点(TFBSs)的增减。与其他4个变异不同,位于HNF-1 TFBS内的-283(A/G)变异是印度牛特有的,因为在Bos taurus序列中未观察到这种变化。其他TFBSs,即MGF、TBP、NF-1、乳盒和C/EBP在物种间是保守的。对于印度本土水牛品种,在启动子区域仅鉴定出3个变化;-305(A/C)、-160(T/C)和-141(A/G),并且发现大多数TFBSs是保守的。然而,与牛κ-CN的启动子序列相比,在水牛中鉴定出C/EBP TF结合位点及其周围两个相邻核苷酸的缺失。对于印度本土牛的κ-CN,在启动子区域的变异515 G/T、-427 C/T和-385 C/T;以及外显子IV的第136和148密码子的变异中观察到强烈的连锁不平衡(LD)。此外,在基因内单倍型中,发现变异-427 C/T与第136和148密码子的变异处于LD状态。本研究产生的信息提供了印度牛和水牛中κ-CN基因启动子和编码区域的全面特征,所报道的变异可能成为进一步研究奶牛性状的重要候选对象。