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Identification and Validation of Reference Genes for RT-qPCR Analysis in Non-Heading Chinese Cabbage Flowers

机译:无标题大白菜花RT-qPCR分析参考基因的鉴定与验证

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摘要

Non-heading Chinese cabbage (Brassica rapa ssp. chinensis Makino) is an important vegetable member of Brassica rapa crops. It exhibits a typical sporophytic self-incompatibility (SI) system and is an ideal model plant to explore the mechanism of SI. Gene expression research are frequently used to unravel the complex genetic mechanism and in such studies appropriate reference selection is vital. Validation of reference genes have neither been conducted in Brassica rapa flowers nor in SI trait. In this study, 13 candidate reference genes were selected and examined systematically in 96 non-heading Chinese cabbage flower samples that represent four strategic groups in compatible and self-incompatible lines of non-heading Chinese cabbage. Two RT-qPCR analysis software, geNorm and NormFinder, were used to evaluate the expression stability of these genes systematically. Results revealed that best-ranked references genes should be selected according to specific sample subsets. DNAJ, UKN1, and PP2A were identified as the most stable reference genes among all samples. Moreover, our research further revealed that the widely used reference genes, CYP and ACP, were the least suitable reference genes in most non-heading Chinese cabbage flower sample sets. To further validate the suitability of the reference genes identified in this study, the expression level of SRK and Exo70A1 genes which play important roles in regulating interaction between pollen and stigma were studied. Our study presented the first systematic study of reference gene(s) selection for SI study and provided guidelines to obtain more accurate RT-qPCR results in non-heading Chinese cabbage.
机译:无头大白菜(Brassica rapa ssp。chinensis Makino)是甘蓝型油菜作物的重要蔬菜成员。它表现出典型的孢子性自我不相容性(SI)系统,是探索SI机理的理想模型植物。基因表达研究经常被用来揭示复杂的遗传机制,在这类研究中,适当的参考选择至关重要。参考基因的验证既未在甘蓝型油菜花中进行,也未在SI性状中进行。在这项研究中,从96个非抽穗大白菜花样品中选择和系统检查了13个候选参考基因,这些样品代表了在非抽穗大白菜的相容和自交不亲和系中的四个策略组。使用两个RT-qPCR分析软件geNorm和NormFinder来系统地评估这些基因的表达稳定性。结果表明,应根据特定的样本子集选择排名最高的参考基因。 DNAJ,UKN1和PP2A被确定为所有样品中最稳定的参考基因。此外,我们的研究进一步揭示,在大多数非抽穗大白菜花样品中,广泛使用的参考基因CYP和ACP是最不适合的参考基因。为了进一步验证本研究中鉴定的参考基因的适用性,研究了在调节花粉和柱头相互作用中起重要作用的SRK和Exo70A1基因的表达水平。我们的研究为SI研究提供了第一个系统的参考基因选择系统研究,并为获得更准确的RT-qPCR结果提供了指导方针。

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