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不结球白菜实时定量PCR标准化中内参基因的验证

Validation of reference genes for real-time quantitative PCR normalisation in non-heading Chinese cabbage.

作者信息

Xiao Dong, Zhang Ning-Wen, Zhao Jian-Jun, Bonnema Guusje, Hou Xi-Lin

机构信息

State Key Laboratory of Crop Genetics and Germplasm Enhancement; Horticultural College, Nanjing Agricultural University, Nanjing, Jiangsu 210095, China.

Laboratory of Plant Breeding, Wageningen University, The Netherlands.

出版信息

Funct Plant Biol. 2012 May;39(4):342-350. doi: 10.1071/FP11246.

Abstract

Non-heading Chinese cabbage is an important vegetable crop that includes pak choi, caixin and several Japanese vegetables like mizuna, mibuna and komatsuna. Gene expression studies are frequently used to unravel the genetics of complex traits and in such studies the proper selection of reference genes for normalisation is crucial. We assessed the expression of 13 candidate reference genes including ACTIN, ACTIN-1, ACTIN-2, GAPDH, Tub_α, CyP, EF1-α, 18S rRNA, UBQ, UBC30, PPR, PP2A and MDH. Their expression stabilities were analysed using two programs, geNorm and NormFinder, in 20 different samples that represent four strategic groups. Results showed that no single gene was uniformly expressed in all tested samples. ACTIN and CyP are proposed as good reference genes when studying developmental stages. CyP, Tub_α and UBC30 are good reference genes when studying different tissues (from flowering to seed set). CyP and Tub_α are the most stable reference genes under biotic stress treatments using the fungi Peronospora parasitica and Alternaria brassicicola. UBC30, EF1-α and ACTIN are recommended for normalisation in abiotic stress studies, including hormone, salt, drought, cold and heath treatments. Moreover, at least five reference genes (ACTIN, CyP, UBC30, EF1-α and UBQ) are required for accurate qRT-PCR data normalisation when studying gene expression across all tested samples.

摘要

小白菜是一种重要的蔬菜作物,包括白菜、菜心以及几种日本蔬菜,如水菜、三叶芹和小松菜。基因表达研究经常用于揭示复杂性状的遗传学,在这类研究中,正确选择用于标准化的参考基因至关重要。我们评估了13个候选参考基因的表达,包括肌动蛋白(ACTIN)、肌动蛋白-1(ACTIN-1)、肌动蛋白-2(ACTIN-2)、甘油醛-3-磷酸脱氢酶(GAPDH)、α-微管蛋白(Tub_α)、环孢素(CyP)、延伸因子1-α(EF1-α)、18S核糖体RNA(18S rRNA)、泛素(UBQ)、泛素结合酶30(UBC30)、五肽重复序列蛋白(PPR)、蛋白磷酸酶2A(PP2A)和苹果酸脱氢酶(MDH)。使用geNorm和NormFinder两个程序,在代表四个策略组的20个不同样本中分析了它们的表达稳定性。结果表明,没有一个基因在所有测试样本中都均匀表达。在研究发育阶段时,建议将ACTIN和CyP作为良好的参考基因。在研究不同组织(从开花到结实)时,CyP、Tub_α和UBC30是良好的参考基因。在使用寄生霜霉和芸苔链格孢进行生物胁迫处理时,CyP和Tub_α是最稳定的参考基因。在非生物胁迫研究中,包括激素、盐、干旱、寒冷和热处理,建议使用UBC30、EF1-α和ACTIN进行标准化。此外,在研究所有测试样本中的基因表达时,准确的qRT-PCR数据标准化至少需要五个参考基因(ACTIN、CyP、UBC30、EF1-α和UBQ)。

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