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确定 qPCR 归一化的参考基因,以研究绿豆应对生物和非生物胁迫的反应。

Defining reference genes for qPCR normalization to study biotic and abiotic stress responses in Vigna mungo.

机构信息

Division of Plant Biology, Bose Institute, Kolkata, 700054, West Bengal, India.

出版信息

Plant Cell Rep. 2013 Oct;32(10):1647-58. doi: 10.1007/s00299-013-1478-2. Epub 2013 Jul 19.

Abstract

Expression of ACT, EF1A; H2A, EF1A, ACT and 18S, TUB showed stability under MYMIV, salinity and drought stress, respectively; these are recommended as reference genes for qPCR normalization in Vigna mungo. Accurate gene expression profiling through qPCR depends on selection of appropriate reference gene(s) for normalization. Due to lack of unanimous internal standard, suitable constitutively expressed reference genes are selected that exhibit stable expression under diverse experimental conditions. In this communication, a comparative evaluation of stability among seven V. mungo genes encoding actin (ACT), histone H2A (H2A), elongation factor 1-alpha (EF1A), 18S rRNA (18S), glyceraldehyde 3-phosphate dehydrogenase (GAPDH), cyclophilin (CYP) and tubulin (TUB) under biotic (MYMIV) and abiotic (drought and salinity) stress conditions has been attempted. Specificity and amplification efficiency for each primer pair were verified; however, cumulative assessment of their accumulated transcripts revealed no uniformity. Therefore, individual stability and suitability of these seven candidates have been assessed in silico, by two widely used algorithms, geNorm and Normfinder. Based on the computed results, high stability was obtained for ACT and EF1A during MYMIV stress, while H2A, EFIA and ACT were found to be most suitable in salinity stress experiments and TUB and 18S during drought treatments. Combinations of ACT/TUB or ACT/EFIA were recommended for their use in the pooled analysis, while expression of 18S and CYP showed greater variations and therefore considered unsuitable as reference genes. Additionally, precise quantification of the target gene VmPRX under these stresses was shown to be a function of reference genes' stability, which tends to get affected when normalized with the least stable genes. Hence, use of these normalizers will facilitate accurate and reliable analyses of gene expression in V. mungo.

摘要

ACT、EF1A、H2A、EF1A、ACT 和 18S、TUB 的表达在 MYMIV、盐度和干旱胁迫下分别稳定;这些基因被推荐为 Vigna mungo qPCR 归一化的参考基因。通过 qPCR 进行准确的基因表达谱分析取决于选择合适的参考基因进行归一化。由于缺乏一致的内参,因此选择稳定表达的合适组成型表达参考基因,这些基因在不同的实验条件下表现出稳定的表达。在本通讯中,尝试比较了生物胁迫(MYMIV)和非生物胁迫(干旱和盐度)条件下编码肌动蛋白(ACT)、组蛋白 H2A(H2A)、延伸因子 1-α(EF1A)、18S rRNA(18S)、甘油醛 3-磷酸脱氢酶(GAPDH)、环孢素(CYP)和微管蛋白(TUB)的 7 个 V. mungo 基因在稳定性方面的差异。验证了每个引物对的特异性和扩增效率;然而,对其累积转录物的综合评估显示没有一致性。因此,通过两种广泛使用的算法 geNorm 和 Normfinder,对这 7 个候选物的个体稳定性和适用性进行了计算机评估。根据计算结果,在 MYMIV 胁迫下,ACT 和 EF1A 的稳定性较高,而在盐胁迫实验中,H2A、EF1A 和 ACT 是最适合的,在干旱处理中,TUB 和 18S 是最适合的。建议使用 ACT/TUB 或 ACT/EFIA 组合进行汇总分析,而 18S 和 CYP 的表达变化较大,因此不适合作为参考基因。此外,这些胁迫下目标基因 VmPRX 的精确定量是参考基因稳定性的函数,当与最不稳定的基因归一化时,其稳定性往往会受到影响。因此,使用这些归一化因子将有助于在 V. mungo 中准确可靠地分析基因表达。

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