Gaete-Eastman Carlos, Mattus-Araya Elena, Herrera Raúl, Moya-León María Alejandra
Laboratorio de Fisiología Vegetal y Genética Molecular, Instituto de Ciencias Biológicas, Universidad de Talca, Talca, Chile.
Physiol Mol Biol Plants. 2022 Aug;28(8):1535-1544. doi: 10.1007/s12298-022-01227-y. Epub 2022 Sep 9.
Quantitative real-time PCR (RT-qPCR) is used extensively in gene expression studies. For adequate comparisons, the identification and use of reliable reference genes are crucial. Nevertheless, the availability of such genes in strawberry species is limited and has yet to be described for the Chilean strawberry, . In this study, the expression dynamics of a set of 10 candidate reference genes were analyzed in various vegetative tissues (root, runners, stem, leaf, and flower), and fruits at different ripening stages or subjected to different hormonal treatments (ABA, auxin). The expression stability of candidate genes was examined by a series of algorithms, such as geNorm, NormFinder, BestKeeper, and ΔCt, for comparisons and rankings. Finally, by using RefFinder, a comprehensive and comparative ranking of the four methods was achieved. The results highlight that the expression stability of candidate reference genes fluctuates depending on tissue type, fruit stage, and hormonal treatment. As reference genes, the use of and is recommended for vegetative tissues; and for fruit ripening stages; and for fruit subjected to ABA and NDGA treatments; and for fruit under AUXIN and TIBA treatments; and and when all fruit stages and hormonal treatments are compared. If just one reference gene is employed as a normalizer, should be chosen as it is the most stable internal control in most conditions. Therefore, the present study delivers a set of reliable reference genes for RT-qPCR expression analysis in tissues and fruits subjected to several hormonal treatments.
The online version contains supplementary material available at 10.1007/s12298-022-01227-y.
定量实时PCR(RT-qPCR)在基因表达研究中被广泛应用。为了进行充分的比较,识别和使用可靠的内参基因至关重要。然而,草莓物种中此类基因的可用性有限,智利草莓的相关基因尚未见报道。在本研究中,分析了一组10个候选内参基因在不同营养组织(根、匍匐茎、茎、叶和花)以及不同成熟阶段或接受不同激素处理(脱落酸、生长素)的果实中的表达动态。通过一系列算法,如geNorm、NormFinder、BestKeeper和ΔCt,检测候选基因的表达稳定性,以进行比较和排名。最后,通过使用RefFinder,实现了四种方法的综合比较排名。结果表明,候选内参基因的表达稳定性因组织类型、果实阶段和激素处理而异。作为内参基因,建议在营养组织中使用 和 ;在果实成熟阶段使用 和 ;在接受脱落酸和去甲二氢愈创木酸处理的果实中使用 和 ;在接受生长素和三碘苯甲酸处理的果实中使用 和 ;在比较所有果实阶段和激素处理时使用 和 。如果仅使用一个内参基因作为标准化因子,应选择 ,因为它在大多数情况下是最稳定的内参。因此,本研究为在多种激素处理下的 组织和果实的RT-qPCR表达分析提供了一组可靠的内参基因。
在线版本包含可在10.1007/s12298-022-01227-y获取的补充材料。