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

被引:40
|
作者
Xiao, Dong [1 ,2 ]
Zhang, Ning-Wen [1 ]
Zhao, Jian-Jun [1 ,3 ]
Bonnema, Guusje [1 ]
Hou, Xi-Lin [2 ]
机构
[1] Wageningen Univ, Lab Plant Breeding, Wageningen, Netherlands
[2] Nanjing Agr Univ, State Key Lab Crop Genet & Germplasm Enhancement, Hort Coll, Nanjing 210095, Jiangsu, Peoples R China
[3] Hebei Agr Univ, Hort Coll, Baoding, Hebei, Peoples R China
关键词
Brassica rapa ssp chinensis; gene expression; qRT-PCR; reference genes; HOUSEKEEPING GENES; INTERNAL CONTROL; BRASSICA-RAPA; EXPRESSION; SELECTION; RICE; IDENTIFICATION; ARABIDOPSIS; STRESS;
D O I
10.1071/FP11246
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
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_alpha, CyP, EF1-alpha, 18SrRNA, 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_alpha and UBC30 are good reference genes when studying different tissues (from flowering to seed set). CyP and Tub_alpha are the most stable reference genes under biotic stress treatments using the fungi Peronospora parasitica and Alternaria brassicicola. UBC30, EF1-alpha 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-alpha and UBQ) are required for accurate qRT-PCR data normalisation when studying gene expression across all tested samples.
引用
收藏
页码:342 / 350
页数:9
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