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In-depth analysis of internal control genes for quantitative real-time PCR in Brassica oleracea var. botrytis

文献类型: 外文期刊

作者: Sheng, X. G. 1 ; Zhao, Z. Q. 1 ; Yu, H. F. 1 ; Wang, J. S. 1 ; Zheng, C. F. 2 ; Gu, H. H. 1 ;

作者机构: 1.Zhejiang Acad Agr Sci, Inst Vegetables, Hangzhou, Zhejiang, Peoples R China

2.Zhejiang Mariculture Res Inst, Wenzhou, Peoples R China

关键词: Cauliflower;Reference genes;geNorm;NormFinder

期刊名称:GENETICS AND MOLECULAR RESEARCH ( 影响因子:0.764; 五年影响因子:0.912 )

ISSN: 1676-5680

年卷期: 2016 年 15 卷 3 期

页码:

收录情况: SCI

摘要: Quantitative reverse-transcription PCR (qRT-PCR) is a versatile technique for the analysis of gene expression. The selection of stable reference genes is essential for the application of this technique. Cauliflower (Brassica oleracea L. var. botrytis) is a commonly consumed vegetable that is rich in vitamin, calcium, and iron. Thus far, to our knowledge, there have been no reports on the validation of suitable reference genes for the data normalization of qRT-PCR in cauliflower. In the present study, we analyzed 12 candidate housekeeping genes in cauliflower subjected to different abiotic stresses, hormone treatment conditions, and accessions. geNorm and NormFinder algorithms were used to assess the expression stability of these genes. ACT2 and TIP41 were selected as suitable reference genes across all experimental samples in this study. When different accessions were compared, ACT2 and UNK3 were found to be the most suitable reference genes. In the hormone and abiotic stress treatments, ACT2, TIP41, and UNK2 were the most stably expressed. Our study also provided guidelines for selecting the best reference genes under various experimental conditions.

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