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Open Access Research article

Reference genes for quantitative reverse transcription-polymerase chain reaction expression studies in wild and cultivated peanut

Carolina V Morgante12, Patricia M Guimarães1, Andressa CQ Martins13, Ana CG Araújo1, Soraya CM Leal-Bertioli1, David J Bertioli34 and Ana CM Brasileiro1*

Author Affiliations

1 EMBRAPA Recursos Genéticos e Biotecnologia. Parque Estação Biológica, CP 02372. Final W5 Norte, Brasília, DF - Brazil

2 EMBRAPA Semiárido, CP 23, Petrolina, PE - Brazil

3 Universidade de Brasília, Campus I, Brasília, DF - Brazil

4 Universidade Católica de Brasília, Campus II, 916 Norte, Brasília, DF - Brazil

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BMC Research Notes 2011, 4:339  doi:10.1186/1756-0500-4-339

Published: 9 September 2011

Abstract

Background

Wild peanut species (Arachis spp.) are a rich source of new alleles for peanut improvement. Plant transcriptome analysis under specific experimental conditions helps the understanding of cellular processes related, for instance, to development, stress response, and crop yield. The validation of these studies has been generally accomplished by quantitative reverse transcription-polymerase chain reaction (qRT-PCR) which requires normalization of mRNA levels among samples. This can be achieved by comparing the expression ratio between a gene of interest and a reference gene which is constitutively expressed. Nowadays there is a lack of appropriate reference genes for both wild and cultivated Arachis. The identification of such genes would allow a consistent analysis of qRT-PCR data and speed up candidate gene validation in peanut.

Results

A set of ten reference genes were analyzed in four Arachis species (A. magna; A. duranensis; A. stenosperma and A. hypogaea) subjected to biotic (root-knot nematode and leaf spot fungus) and abiotic (drought) stresses, in two distinct plant organs (roots and leaves). By the use of three programs (GeNorm, NormFinder and BestKeeper) and taking into account the entire dataset, five of these ten genes, ACT1 (actin depolymerizing factor-like protein), UBI1 (polyubiquitin), GAPDH (glyceraldehyde-3-phosphate dehydrogenase), 60S (60S ribosomal protein L10) and UBI2 (ubiquitin/ribosomal protein S27a) emerged as top reference genes, with their stability varying in eight subsets. The former three genes were the most stable across all species, organs and treatments studied.

Conclusions

This first in-depth study of reference genes validation in wild Arachis species will allow the use of specific combinations of secure and stable reference genes in qRT-PCR assays. The use of these appropriate references characterized here should improve the accuracy and reliability of gene expression analysis in both wild and cultivated Arachis and contribute for the better understanding of gene expression in, for instance, stress tolerance/resistance mechanisms in plants.