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Reference gene selection for quantitative real-time polymerase chain reaction in Populus.

Identifieur interne : 002D34 ( Main/Exploration ); précédent : 002D33; suivant : 002D35

Reference gene selection for quantitative real-time polymerase chain reaction in Populus.

Auteurs : Meng Xu [République populaire de Chine] ; Bo Zhang ; Xiaohua Su ; Shougong Zhang ; Minren Huang

Source :

RBID : pubmed:20816740

Descripteurs français

English descriptors

Abstract

Accurate quantification of gene expression with quantitative real-time polymerase chain reaction (qRT-PCR) relies on the choice of an appropriate reference gene. In this study, nine candidate reference genes were selected to study the expression stability for qRT-PCR normalization in adventitious rooting of Populus hardwood cuttings. geNorm, NormFinder, and BestKeeper analysis revealed that actin isoform B (ACT) was the most unstable gene across developmental stages, whereas elongation factor 1 alpha (EF1a) and 18S recombinant RNA (18S) emerged as the most appropriate reference genes for qRT-PCR analysis in this complex developmental process.

DOI: 10.1016/j.ab.2010.08.044
PubMed: 20816740


Affiliations:


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Le document en format XML

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<name sortKey="Zhang, Shougong" sort="Zhang, Shougong" uniqKey="Zhang S" first="Shougong" last="Zhang">Shougong Zhang</name>
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<term>Peptide Elongation Factor 1 (genetics)</term>
<term>Peptide Elongation Factor 1 (standards)</term>
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<term>RNA, Ribosomal, 18S (genetics)</term>
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<div type="abstract" xml:lang="en">Accurate quantification of gene expression with quantitative real-time polymerase chain reaction (qRT-PCR) relies on the choice of an appropriate reference gene. In this study, nine candidate reference genes were selected to study the expression stability for qRT-PCR normalization in adventitious rooting of Populus hardwood cuttings. geNorm, NormFinder, and BestKeeper analysis revealed that actin isoform B (ACT) was the most unstable gene across developmental stages, whereas elongation factor 1 alpha (EF1a) and 18S recombinant RNA (18S) emerged as the most appropriate reference genes for qRT-PCR analysis in this complex developmental process.</div>
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