Assessment of suitable reference genes for quantitative gene expression studies in melon fruits

Melon (Cucumis melo. L) is an attractive model plant for investigating fruit development because of its morphological, physiological, and biochemical diversity. Quantification of gene expression by quantitative reverse transcription PCR (qRT-PCR) with stably expressed reference genes for normalizati...

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Main Authors: Qiusheng Kong, Lingyun Gao, Lei Cao, Yue Liu, Saba Hameed, Yuan Huang, Zhilong Bie
Format: Article
Language:English
Published: Frontiers Media S.A. 2016-08-01
Series:Frontiers in Plant Science
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fpls.2016.01178/full
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spelling doaj-b49b139c63194dd9b923f2c432ff5c5f2020-11-25T00:13:51ZengFrontiers Media S.A.Frontiers in Plant Science1664-462X2016-08-01710.3389/fpls.2016.01178214397Assessment of suitable reference genes for quantitative gene expression studies in melon fruitsQiusheng Kong0Lingyun Gao1Lei Cao2Yue Liu3Saba Hameed4Yuan Huang5Zhilong Bie6Huazhong Agricultural UniversityHuazhong Agricultural UniversityHuazhong Agricultural UniversityHuazhong Agricultural UniversityHuazhong Agricultural UniversityHuazhong Agricultural UniversityHuazhong Agricultural UniversityMelon (Cucumis melo. L) is an attractive model plant for investigating fruit development because of its morphological, physiological, and biochemical diversity. Quantification of gene expression by quantitative reverse transcription PCR (qRT-PCR) with stably expressed reference genes for normalization can effectively elucidate the biological functions of genes regulating fruit development. However, the reference genes for data normalization in melon fruits have not yet been systematically validated. In this study, 20 candidate reference genes were assessed for their potential use as reference genes in melon fruits. GeNorm and NormFinder analyses showed that Cytosolic ribosomal protein S15 (CmRPS15) was the preferred single reference gene. While, CmRPS15 and Ribosomal protein L (CmRPL), or RAN GTPase (CmRAN) and TATA-box binding protein (CmTBP2) were the suitable reference gene combinations in melon fruits. Reliabilities of these identified genes was further validated by the parallel analyses of sucrose contents, activities of soluble acid invertase (AI) and sucrose phosphate synthase (SPS), and expression profiles of their respective encoding genes CmAIN2 and CmSPS1 during melon fruit ripening. These validated reference genes will help to improve the accuracy of gene expression quantification in melon fruits.http://journal.frontiersin.org/Journal/10.3389/fpls.2016.01178/fullCucumis meloGene ExpressionqRT-PCRnormalizationFruit developmentreference gene
collection DOAJ
language English
format Article
sources DOAJ
author Qiusheng Kong
Lingyun Gao
Lei Cao
Yue Liu
Saba Hameed
Yuan Huang
Zhilong Bie
spellingShingle Qiusheng Kong
Lingyun Gao
Lei Cao
Yue Liu
Saba Hameed
Yuan Huang
Zhilong Bie
Assessment of suitable reference genes for quantitative gene expression studies in melon fruits
Frontiers in Plant Science
Cucumis melo
Gene Expression
qRT-PCR
normalization
Fruit development
reference gene
author_facet Qiusheng Kong
Lingyun Gao
Lei Cao
Yue Liu
Saba Hameed
Yuan Huang
Zhilong Bie
author_sort Qiusheng Kong
title Assessment of suitable reference genes for quantitative gene expression studies in melon fruits
title_short Assessment of suitable reference genes for quantitative gene expression studies in melon fruits
title_full Assessment of suitable reference genes for quantitative gene expression studies in melon fruits
title_fullStr Assessment of suitable reference genes for quantitative gene expression studies in melon fruits
title_full_unstemmed Assessment of suitable reference genes for quantitative gene expression studies in melon fruits
title_sort assessment of suitable reference genes for quantitative gene expression studies in melon fruits
publisher Frontiers Media S.A.
series Frontiers in Plant Science
issn 1664-462X
publishDate 2016-08-01
description Melon (Cucumis melo. L) is an attractive model plant for investigating fruit development because of its morphological, physiological, and biochemical diversity. Quantification of gene expression by quantitative reverse transcription PCR (qRT-PCR) with stably expressed reference genes for normalization can effectively elucidate the biological functions of genes regulating fruit development. However, the reference genes for data normalization in melon fruits have not yet been systematically validated. In this study, 20 candidate reference genes were assessed for their potential use as reference genes in melon fruits. GeNorm and NormFinder analyses showed that Cytosolic ribosomal protein S15 (CmRPS15) was the preferred single reference gene. While, CmRPS15 and Ribosomal protein L (CmRPL), or RAN GTPase (CmRAN) and TATA-box binding protein (CmTBP2) were the suitable reference gene combinations in melon fruits. Reliabilities of these identified genes was further validated by the parallel analyses of sucrose contents, activities of soluble acid invertase (AI) and sucrose phosphate synthase (SPS), and expression profiles of their respective encoding genes CmAIN2 and CmSPS1 during melon fruit ripening. These validated reference genes will help to improve the accuracy of gene expression quantification in melon fruits.
topic Cucumis melo
Gene Expression
qRT-PCR
normalization
Fruit development
reference gene
url http://journal.frontiersin.org/Journal/10.3389/fpls.2016.01178/full
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AT sabahameed assessmentofsuitablereferencegenesforquantitativegeneexpressionstudiesinmelonfruits
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