Selection and validation of reference genes for quantitative real-time PCR in Cymbidium sinense

Author:

Tian Yunfang12ORCID,Chu Zhigang12,Wang Huiyu12,Wang Guoxia12,Wu Si12,Yang Yuzhen12

Affiliation:

1. College of Life Sciences, Zhengzhou Normal University, Zhengzhou, 450044, People's Republic of China

2. Zhengzhou Key Laboratory of Ornamental & Medicinal Resources Plants, Zhengzhou, 450044, People's Republic of China

Abstract

Selection of reference genes (RGs) is important for the accurate analysis of real-time quantitative PCR (RT-qPCR) results. This study screened RGs of Cymbidium sinense for more accurate quantification of target genes. The two most stable RGs for all tissues were ACT and EF1α, those for vegetative organs were UBQ3 and ACT, while those for reproductive organs as well as organs in the full flowering stage were EF1α and ACT. The AGAMOUS ( CsAG1) expression level was verified using EF1α, ACT, GAPDH, UBQ2 and UBQ3 as RG. The expression profile of CsAG1 was consistent when normalized with EF1α, ACT and UBQ3. The results have practical value for the expression of key genes during the development of C. sinense.

Publisher

Future Science Ltd

Subject

General Biochemistry, Genetics and Molecular Biology,Biotechnology

Reference28 articles.

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2. Selection of suitable reference genes for qRT-PCR analysis of Begonia semperflorens under stress conditions

3. Evaluation of Internal Control for Gene Expression in Phalaenopsis by Quantitative Real-Time PCR

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