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Selection of reference genes for quantitative real-time PCR in Cocos nucifera during abiotic stress.

机译:非生物胁迫过程中椰子实时定量PCR参考基因的选择。

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Reverse transcription quantitative real-time polymerase chain reaction (PCR) is a widely used and reproducible method for studying gene expression changes. However, its accuracy and reliability is highly dependent on the normalization step. Cocos nucifera L., a perennial palm with a long productive life span, is frequently exposed to soil and atmospheric drought and other stresses. In applying gene expression analysis to understand coconut stress responses, validation of suitable reference genes is an important first step. In this study, seven putative reference genes were identified from coconut transcriptome data. The stability of these putative reference genes was assessed in a diverse set of 18 coconut samples subject to cold, drought, and high-salinity treatment and representing different endosperm developmental stages. Using statistical algorithms geNorm, NormFinder, and BestKeeper, eEF1- alpha and UBC10 genes were identified as stable reference genes in all stress treatments and endosperm development stages, consistent with validated reference genes in rice (Oryza sativa L.), potato (Solanum tuberosum L.), and other species. Further validation of analyzed reference genes by normalization of a C-repeat binding factor (CBF)-like gene in cold-treatment samples indicated that the less stable reference genes produced different results from the more stable reference genes, with weaker variation or higher expression levels of a target gene. Our results will be beneficial for further research on molecular mechanisms of stress resistance.
机译:逆转录定量实时聚合酶链反应(PCR)是研究基因表达变化的一种广泛使用且可重现的方法。但是,其准确性和可靠性高度依赖于标准化步骤。 Cocos nucifera L.是多年生的棕榈树,具有长的使用寿命,经常暴露于土壤和大气干旱以及其他压力下。在应用基因表达分析来了解椰子胁迫反应时,验证合适的参考基因是重要的第一步。在这项研究中,从椰子转录组数据中鉴定出七个推定的参考基因。这些假定的参考基因的稳定性在接受冷,旱和高盐度处理并代表不同胚乳发育阶段的18种椰子样品中进行了评估。使用统计算法geNorm,NormFinder和BestKeeper,eEF1- alpha和UBC10基因在所有胁迫处理和胚乳发育阶段均被鉴定为稳定的参考基因,与水稻(Oryza sativa L.),马铃薯(Solanum tuberosum L)的有效参考基因一致。 。)和其他物种。通过对冷处理样品中的C-重复结合因子(CBF)样基因进行归一化来进一步验证分析的参考基因,表明稳定性较差的参考基因与稳定性较差的参考基因产生的结果不同,变异较小或表达水平较高靶基因。我们的研究结果将有助于进一步研究抗逆性的分子机制。

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