College of Life Science, Henan Normal University, Xinxiang, Henan, 453007, People's Republic of China.
Sci Rep. 2019 Jun 18;9(1):8691. doi: 10.1038/s41598-019-44982-x.
Yellow River carp is widely cultivated in the world due to its economic value in aquaculture, and the faster growth of females compared to males. It is believed that microRNAs (miRNA) are involved in gonadal differentiation and development. qPCR is the most preferred method for miRNA functional analysis. Reliable reference genes for normalization in qRT-PCR are the key to ensuring the accuracy of this method. The aim of present research was to evaluate as well as identify the efficacy of reference genes for miRNA expression using qRT-PCR in Yellow River carp. Nine ncRNAs (miR-101, miR-23a, let7a, miR-26a, miR-146a, miR-451, U6, 5S, and 18S) were chosen and tested in four sample sets: (1) different tissues in adult carp, (2) different tissues in juvenile carp, (3) different early developmental stages of carp, and (4) different developmental stages of carp gonads. The stability and suitability values were calculated using NormFinder, geNorm, and BestKeeper software. The results showed that 5S was a suitable reference gene in different tissues of adult and juvenile carp. The genes 5S, 18S, and U6 were the most stable reference genes in the early developmental stages of carp. Let-7a and miR-23a were considered as the suitable reference genes in the development of gonads. All these reference genes were subsequently validated using miR-430. The results showed that genes 5S and 18S were the most suitable reference genes to normalize miRNA expression under normal growth conditions in early different developmental stages. The genes Let-7a, and miR-23a were the most suitable in different developmental stages. The present study is the first comprehensive study of the stability of miRNA reference genes in Yellow River carp, providing valuable as well as basic data for investigating more accurate miRNA expression during gonadal differentiation and development of carp.
黄河鲤鱼因其在水产养殖中的经济价值以及雌性生长速度快于雄性而在世界范围内广泛养殖。据信,微小 RNA(miRNA)参与了性腺分化和发育。qPCR 是 miRNA 功能分析最常用的方法。在 qRT-PCR 中,用于归一化的可靠参考基因是确保该方法准确性的关键。本研究的目的是评估并确定用于黄河鲤鱼 miRNA 表达 qRT-PCR 的参考基因的功效。选择了 9 种 ncRNA(miR-101、miR-23a、let7a、miR-26a、miR-146a、miR-451、U6、5S 和 18S),并在四个样本组中进行了测试:(1)成年鲤鱼的不同组织,(2)幼鱼的不同组织,(3)鲤鱼的不同早期发育阶段,以及(4)鲤鱼性腺的不同发育阶段。使用 NormFinder、geNorm 和 BestKeeper 软件计算稳定性和适用性值。结果表明,5S 是成年和幼鱼不同组织中合适的参考基因。5S、18S 和 U6 是鲤鱼早期发育阶段最稳定的参考基因。Let-7a 和 miR-23a 被认为是性腺发育的合适参考基因。使用 miR-430 进一步验证了这些参考基因。结果表明,在早期不同发育阶段的正常生长条件下,基因 5S 和 18S 是归一化 miRNA 表达最适合的参考基因。基因 Let-7a 和 miR-23a 是在不同发育阶段最适合的。本研究是首次对黄河鲤鱼 miRNA 参考基因稳定性的全面研究,为研究鲤鱼性腺分化和发育过程中更准确的 miRNA 表达提供了有价值的基础数据。