Kumar Rakesh, Gupta I D, Verma Archana, Kumari Ragini, Verma Nishant
Regional Research Station (Punjab Agricultural University), Ballowal Saunkhri, SBS, Nagar, 144 521, India.
Animal Genetics and Breeding Division, ICAR-NDRI, Karnal, 132001, India.
Trop Anim Health Prod. 2017 Jun;49(5):1059-1063. doi: 10.1007/s11250-017-1235-6. Epub 2017 Mar 31.
Heat shock proteins (HSPs) act as molecular chaperones which are preferentially transcribed in response to severe perturbations of the cellular homeostasis such as heat stress. The present study was undertaken for molecular characterization and detection of genetic polymorphisms of HSPB6 gene in 100 Karan Fries Cattle. HSPB6 gene was mapped on Bos taurus autosome 18 (BTA 18), comprising three exons and two introns. Four sets of primers for HSPB6 gene were designed using Primer3 software (version 0.4.0). For detecting single nucleotide polymorphisms (SNPs), sequence data was analyzed using BioEdit software (version 7.2). Comparative sequence analysis of HSPB6 gene showed five nucleotide polymorphisms, which included three transitions viz. g.161A > G, g.436G > A and g.2152A > G and two transversions viz. g.1743C > G and g.2417A > T compared to B. taurus (NCBI GenBank: AC_000175.1). HSPB6 gene of Karan Fries cattle exhibited a high percentage of nucleotide identity (47.0-100.0%) with the corresponding mammalian homologue. The present study indicated a high degree of genetic variability in the HSPB6 gene in the Karan Fries cattle populations.
热休克蛋白(HSPs)作为分子伴侣,在细胞内稳态受到严重干扰(如热应激)时会优先转录。本研究旨在对100头卡兰弗里牛的HSPB6基因进行分子特征分析和遗传多态性检测。HSPB6基因定位于牛18号常染色体(BTA 18)上,由三个外显子和两个内含子组成。使用Primer3软件(0.4.0版)设计了四组针对HSPB6基因的引物。为检测单核苷酸多态性(SNP),利用BioEdit软件(7.2版)对序列数据进行分析。HSPB6基因的比较序列分析显示有五个核苷酸多态性,其中包括三个转换,即g.161A>G、g.436G>A和g.2152A>G,以及两个颠换,即g.1743C>G和g.2417A>T,与牛(NCBI基因库:AC_000175.1)相比。卡兰弗里牛的HSPB6基因与相应的哺乳动物同源物具有较高的核苷酸同一性百分比(47.0 - 100.0%)。本研究表明卡兰弗里牛群体中HSPB6基因存在高度的遗传变异性。