Selection of reliable reference genes for gene expression studies in Rhododendron micranthum Turcz

被引:26
作者
Yi, Shanjun [1 ]
Qian, Yongqiang [1 ]
Han, Lei [1 ]
Sun, Zhenyuan [1 ]
Fan, Chengming [2 ]
Liu, Junxiang [1 ]
Ju, Guansheng [1 ]
机构
[1] Chinese Acad Forestry, State Key Lab Forest Genet & Tree Breeding, Beijing 100091, Peoples R China
[2] Chinese Acad Agr Sci, Inst Crop Sci, Beijing 100081, Peoples R China
基金
国家高技术研究发展计划(863计划);
关键词
Quantitative real-time PCR; Reference gene; geNorm; NormFinder; Rhododendron micranthum Turcz; TIME RT-PCR; POLYMERASE CHAIN-REACTION; REAL-TIME; HOUSEKEEPING GENES; INTERNAL CONTROL; GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE; QUANTITATIVE-PCR; RNA; NORMALIZATION; VALIDATION;
D O I
10.1016/j.scienta.2012.02.013
中图分类号
S6 [园艺];
学科分类号
0902 ;
摘要
Selection of reliable reference genes is a prerequisite for accurate normalization of gene expression in quantitative real-time polymerase chain reaction (qRT-PCR). The present study is the first report of a systematic evaluation of potential reference genes in Rhododendron micranthum Turcz. The expression stabilities of 6 candidate reference genes (185, ACT, CYP, UBQ TUA, and EF1 alpha) in different tissues and the same tissue at different developmental stages were assessed in Rh. micranthum Turcz, using two analysis software packages, geNorm and NormFinder. The results indicated that EF1 alpha and UBQ were the most stable reference genes for different tissues (leaf, root, stem and flower) at the same developmental stage, whereas 18S should be avoided. During leaf development. EF1 alpha and 185 can be used as the most reliable reference genes, but CYP was the most variable one. During flower development, the most stable genes were CYP and EF1 alpha, while 18S was the least stable one. In order to demonstrate the importance of using suitable reference genes for obtaining an accurate and reliable results in gene expression studies, the expression pattern of an independent target gene, RhMDH gene was analyzed in parallel, the RhMDH showed an expression difference of 58-fold in stem when normalized with the most stable gene (EF1 alpha)or the least stable gene (185) act as reference, respectively. Our results support that the selection of suitable reference genes is necessary to achieve accurate results in qRT-PCR. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:128 / 133
页数:6
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