Verma Preeti, Sharma Ankita, Sodhi Monika, Tiwari Manish, Vivek Prince, Kataria Ranjit S, Nirajan S K, Bharti Vijay K, Singh Pawan, Lathwal S S, Sharma Vishal, Masharing Nampher, Mukesh Manishi
Animal Biotechnology Division, ICAR-National Bureau of Animal Genetic Resources, Karnal, India.
Animal Biotechnology Center, ICAR-National Dairy Research Institute, Karnal, India.
Front Genet. 2022 Feb 1;12:730599. doi: 10.3389/fgene.2021.730599. eCollection 2021.
To estimate gene expression in a reliable manner, quantitative real-time polymerase chain reaction data require normalisation using a panel of stably expressed reference genes (RGs). To date, information on an appropriate panel of RGs in cattle populations reared at cold arid high-altitude hypoxia and hot arid tropical normoxia environments is not available. Therefore, the present study was carried out to identify a panel of stably expressed RGs from 10 candidate genes ( and ) in peripheral blood mononuclear cells (PBMCs) of cattle populations reared at cold arid high-altitude hypoxia and hot arid normoxia environments. Four different statistical algorithms: geNorm, NormFinder, BestKeeper, and RefFinder were used to assess the stability of these genes. A total of 30 blood samples were collected: six adult heifers each of Ladakhi (LAC) and Holstein Frisian crosses (HFX) and 4 Jersey (JYC) cows from cold arid high-altitude hypoxia environments (group I) and five adult heifers each of Sahiwal (SAC), Karan Fries (KFC), and Holstein Friesian (HFC) cows from hot arid normoxia environments (group II). Combined analysis of group I and group II resulted in identification of a panel of RGs like and that could act as a useful resource to unravel the accurate transcriptional profile of PBMCs from diverse cattle populations adapted to distinct altitudes.
为了以可靠的方式估计基因表达,定量实时聚合酶链反应数据需要使用一组稳定表达的参考基因(RGs)进行标准化。迄今为止,关于在寒冷干旱高海拔低氧和炎热干旱热带常氧环境中饲养的牛群中合适的RGs组的信息尚不可用。因此,本研究旨在从在寒冷干旱高海拔低氧和炎热干旱常氧环境中饲养的牛群的外周血单核细胞(PBMCs)中的10个候选基因(和)中鉴定一组稳定表达的RGs。使用四种不同的统计算法:geNorm、NormFinder、BestKeeper和RefFinder来评估这些基因的稳定性。总共收集了30份血样:来自寒冷干旱高海拔低氧环境(第一组)的6头成年拉达克母牛(LAC)和荷斯坦弗里生杂交母牛(HFX)以及4头泽西母牛(JYC),以及来自炎热干旱常氧环境(第二组)的5头成年萨希瓦尔母牛(SAC)、卡兰弗里生母牛(KFC)和荷斯坦弗里生母牛(HFC)。对第一组和第二组的联合分析导致鉴定出一组RGs,如和,它们可以作为一种有用的资源,用于揭示来自适应不同海拔的不同牛群的PBMCs的准确转录谱。