Guo Rong, Guo Hongyan, Zhang Qingying, Guo Mengbi, Xu Yanping, Zeng Min, Lv Pin, Chen Xuan, Yang Ming
a Industrial Crop Research Institute, Yunnan Academy of Agricultural Sciences , Kunming , People's Republic of China.
b Biotechnology and Germplasm Resources Institute, Yunnan Academy of Agricultural Sciences , Kunming , People's Republic of China.
Biosci Biotechnol Biochem. 2018 Nov;82(11):1902-1910. doi: 10.1080/09168451.2018.1506253. Epub 2018 Aug 21.
RT-qPCR has been widely used for gene expression analysis in recent years. The accuracy of this technique largely depends on the selection of suitable reference genes. In order to facilitate gene expression analysis in wild and cultivated Cannabis, the expression stability of seven candidate reference genes (ACT2, 18S rRNA, GAPDH, UBQ, TUB, PP2A and EF1α) were assessed in leaves samples of different development stages and different organs of both wild and cultivated Cannabis in the present study. Their expression stabilities were evaluated through three software packages (GeNorm, Normfinder and Bestkeeper). Results showed that UBQ and EF1α were the highly ranked genes in different leaves samples, and PP2A was the most stable reference gene in different organs, while GAPDH was the least stable one. And the validation of the reference genes selected was further confirmed by the expression patterns of MDS and OLS.
近年来,逆转录定量聚合酶链反应(RT-qPCR)已广泛用于基因表达分析。该技术的准确性很大程度上取决于合适的内参基因的选择。为便于对野生和栽培大麻进行基因表达分析,本研究在野生和栽培大麻不同发育阶段的叶片样本以及不同器官中评估了7个候选内参基因(ACT2、18S rRNA、GAPDH、UBQ、TUB、PP2A和EF1α)的表达稳定性。通过三个软件包(GeNorm、Normfinder和Bestkeeper)评估了它们的表达稳定性。结果表明,UBQ和EF1α在不同叶片样本中排名靠前,PP2A在不同器官中是最稳定的内参基因,而GAPDH是最不稳定的。并且通过MDS和OLS的表达模式进一步证实了所选内参基因的有效性。