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Identification of suitable reference genes for studying gene expression in cucumber plants subjected to abiotic stress and growth regulators

机译:鉴定合适的参考基因以研究受到非生物胁迫和生长调节剂的黄瓜植物中的基因表达

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It has been shown that genes considered to be valid reference genes using semi-quantitative techniques (e.g. northern blot) appear to be less reliable when highly sensitive real-time PCR (qPCR) or microarrays are used. Therefore, the validation of expression stability of reference genes has become an important component of any study using such types of assay. No reference genes have been validated for expression studies of cucumber genes to date. Since the genome of this widely cultivated crop has been recently sequenced, the availability of suitable reference genes for expression analyses of the new cucumber genes is urgently required. For the purpose of normalization in studying expression of cucumber target genes, the stability of twelve reference genes in different cucumber tissues and under various stresses and growth regulators were determined in this study. These included commonly used cucumber reference genes, such as actin, EF, cyclophilin, ubiquitin and tubulin and the newly identified candidates for reference genes that encode clathrin adaptor complex subunit (CACS), F-box protein, PPA2 activator (tonoplast intrinsic protein, TIP41), mitosis protein (YSL8), protein phosphatase 2 (PDF2), helicase (HEL) and protein homolog of At4g33380. Analyses of quantitative real-time PCR data by three commonly used Excel-based applets, BestKeeper, geNorm and NormFinder, confirmed that expression stability of reference genes depends on the experimental parameters. In addition, they revealed that, except for EF, the most stable cucumber genes included mainly the new reference genes: CACS, F-box and TIP41, whereas the commonly used internal controls demonstrated various (actin, cyclophilin, ubiquitin) or much lower stability (tubulin). Hence, the authors of this study assume that the novel cucumber reference genes will enable better normalization and quantification of transcript levels in future expression studies on cucumber plants.
机译:已经表明,当使用高度敏感的实时PCR(qPCR)或微阵列时,使用半定量技术(例如northern blot)被视为有效参考基因的基因似乎不太可靠。因此,参考基因表达稳定性的验证已成为使用此类检测方法的任何研究的重要组成部分。迄今为止,尚未验证参考基因用于黄瓜基因的表达研究。由于最近已经对该广泛种植的农作物的基因组进行了测序,因此迫切需要合适的参考基因来进行新黄瓜基因的表达分析。为了标准化研究黄瓜靶基因的表达,本研究确定了十二种参考基因在不同黄瓜组织中以及在各种胁迫和生长调节剂下的稳定性。这些包括常用的黄瓜参考基因,如肌动蛋白,EF,亲环蛋白,泛素和微管蛋白,以及新鉴定的参考基因候选物,这些参考基因编码网格蛋白衔接子复合物亚基(CACS),F-box蛋白,PPA2激活剂(液泡内在蛋白,TIP41 ),有丝分裂蛋白(YSL8),蛋白磷酸酶2(PDF2),解旋酶(HEL)和At4g33380的蛋白同源物。通过三种常用的基于Excel的小程序,BestKeeper,geNorm和NormFinder对定量实时PCR数据进行的分析证实,参考基因的表达稳定性取决于实验参数。此外,他们还发现,除EF外,最稳定的黄瓜基因主要包括新的参考基因:CACS,F-box和TIP41,而常用的内部对照表现出多种(肌动蛋白,亲环蛋白,泛素)或更低的稳定性。 (微管蛋白)。因此,这项研究的作者认为,新的黄瓜参考基因将能够在今后对黄瓜植物的表达研究中更好地标准化和量化转录本水平。

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