Reference gene selection for quantitative real-time PCR normalization in different cherry genotypes, developmental stages and organs

文献类型： 外文期刊

第一作者： Ye, Xia

作者： Ye, Xia;Zhang, Fangming;Tao, Yonghuan;Song, Shangwei;Fang, Jinbao

作者机构：

关键词： Cherry;Reference genes;RNA normalization;qRT-PCR;GeNorm;Norm Finder

期刊名称：SCIENTIA HORTICULTURAE （ 影响因子：3.463； 五年影响因子：3.672 ）

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收录情况： SCI

摘要： Cherry is an important diploid crop species belonging to the Rosaceae family, yet there are limited molecular tools available. For instance, stable reference genes have not yet been defined for use in quantitative real-time PCR across different experiments. Herein, 11 internal control genes were systematically evaluated for usefulness in gene expression normalization. The internal controls were tested across eight cherry genotypes, and tracked temporally, spatially and in response to abiotic stresses. The results indicated that no single reference gene was universally stable across various tissues and organs, in different developmental stages, or under different abiotic stresses in cherry. In eight tested cherry genotypes, candidate reference genes RPL13 and RPII were the most stable according to analysis by the geNorm program, and ACT was the most stable gene by NormFinder. In vegetative tissues and organs, the best normalization was achieved with a combination of CYP2, a-TUB, SAND-2, and RPL13, as determined by geNorm software, or RPL13, as determined by NormFinder. TEF2, CYP2, and ACT were identified as suitable reference genes for fruit and flower development, based on both geNorm and NormFinder analyses. To illustrate the suitability of these reference genes, expression of CHS and MYB10 genes was analyzed in various flower tissues and organs using the most stable and unstable reference genes for normalization. Our results indicated that the selected reference genes were suitable and reliable for cherry gene expression using gRT-PCR. (C) 2014 Elsevier B.V. All rights reserved.

分类号： S6

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