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Selection and evaluation of reference genes for qRT-PCR analysis in Euscaphis konishii Hayata based on transcriptome data

BACKGROUND: Quantitative real-time reverse transcription-polymerase chain reaction has been widely used in gene expression analysis, however, to have reliable and accurate results, reference genes are necessary to normalize gene expression under different experimental conditions. Several reliable re...

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Autores principales: Liang, Wenxian, Zou, Xiaoxing, Carballar-Lejarazú, Rebeca, Wu, Lingjiao, Sun, Weihong, Yuan, Xueyuan, Wu, Songqing, Li, Pengfei, Ding, Hui, Ni, Lin, Huang, Wei, Zou, Shuangquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5985561/
https://www.ncbi.nlm.nih.gov/pubmed/29881443
http://dx.doi.org/10.1186/s13007-018-0311-x
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author Liang, Wenxian
Zou, Xiaoxing
Carballar-Lejarazú, Rebeca
Wu, Lingjiao
Sun, Weihong
Yuan, Xueyuan
Wu, Songqing
Li, Pengfei
Ding, Hui
Ni, Lin
Huang, Wei
Zou, Shuangquan
author_facet Liang, Wenxian
Zou, Xiaoxing
Carballar-Lejarazú, Rebeca
Wu, Lingjiao
Sun, Weihong
Yuan, Xueyuan
Wu, Songqing
Li, Pengfei
Ding, Hui
Ni, Lin
Huang, Wei
Zou, Shuangquan
author_sort Liang, Wenxian
collection PubMed
description BACKGROUND: Quantitative real-time reverse transcription-polymerase chain reaction has been widely used in gene expression analysis, however, to have reliable and accurate results, reference genes are necessary to normalize gene expression under different experimental conditions. Several reliable reference genes have been reported in plants of Traditional Chinese Medicine, but none have been identified for Euscaphis konishii Hayata. RESULTS: In this study, 12 candidate reference genes, including 3 common housekeeping genes and 9 novel genes based on E. konishii Hayata transcriptome data were selected and analyzed in different tissues (root, branch, leaf, capsule and seed), capsule and seed development stages. Expression stability was calculated using geNorm and NormFinder, the minimal number of reference genes required for accurate normalization was calculated by Vn/Vn + 1 using geNorm. EkEEF-5A-1 and EkADF2 were the two most stable reference genes for all samples, while EkGSTU1 and EkGAPDH were the most stable reference genes for tissue samples. For seed development stages, EkGAPDH and EkEEF-5A-1 were the most stable genes, whereas EkGSTU1 and EkGAPDH were identified as the two most stable genes in the capsule development stages. Two reference genes were sufficient to normalize gene expression across all sample sets. CONCLUSION: Results of this study revealed that suitable reference genes should be selected for different experimental samples, and not all the common reference genes are suitable for different tissue samples and/or experimental conditions. In this study, we present the first data of reference genes selection for E. konishii Hayata based on transcriptome data, our data will facilitate further studies in molecular biology and gene function on E. konishii Hayata and other closely related species. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13007-018-0311-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-59855612018-06-07 Selection and evaluation of reference genes for qRT-PCR analysis in Euscaphis konishii Hayata based on transcriptome data Liang, Wenxian Zou, Xiaoxing Carballar-Lejarazú, Rebeca Wu, Lingjiao Sun, Weihong Yuan, Xueyuan Wu, Songqing Li, Pengfei Ding, Hui Ni, Lin Huang, Wei Zou, Shuangquan Plant Methods Research BACKGROUND: Quantitative real-time reverse transcription-polymerase chain reaction has been widely used in gene expression analysis, however, to have reliable and accurate results, reference genes are necessary to normalize gene expression under different experimental conditions. Several reliable reference genes have been reported in plants of Traditional Chinese Medicine, but none have been identified for Euscaphis konishii Hayata. RESULTS: In this study, 12 candidate reference genes, including 3 common housekeeping genes and 9 novel genes based on E. konishii Hayata transcriptome data were selected and analyzed in different tissues (root, branch, leaf, capsule and seed), capsule and seed development stages. Expression stability was calculated using geNorm and NormFinder, the minimal number of reference genes required for accurate normalization was calculated by Vn/Vn + 1 using geNorm. EkEEF-5A-1 and EkADF2 were the two most stable reference genes for all samples, while EkGSTU1 and EkGAPDH were the most stable reference genes for tissue samples. For seed development stages, EkGAPDH and EkEEF-5A-1 were the most stable genes, whereas EkGSTU1 and EkGAPDH were identified as the two most stable genes in the capsule development stages. Two reference genes were sufficient to normalize gene expression across all sample sets. CONCLUSION: Results of this study revealed that suitable reference genes should be selected for different experimental samples, and not all the common reference genes are suitable for different tissue samples and/or experimental conditions. In this study, we present the first data of reference genes selection for E. konishii Hayata based on transcriptome data, our data will facilitate further studies in molecular biology and gene function on E. konishii Hayata and other closely related species. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13007-018-0311-x) contains supplementary material, which is available to authorized users. BioMed Central 2018-06-04 /pmc/articles/PMC5985561/ /pubmed/29881443 http://dx.doi.org/10.1186/s13007-018-0311-x Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Liang, Wenxian
Zou, Xiaoxing
Carballar-Lejarazú, Rebeca
Wu, Lingjiao
Sun, Weihong
Yuan, Xueyuan
Wu, Songqing
Li, Pengfei
Ding, Hui
Ni, Lin
Huang, Wei
Zou, Shuangquan
Selection and evaluation of reference genes for qRT-PCR analysis in Euscaphis konishii Hayata based on transcriptome data
title Selection and evaluation of reference genes for qRT-PCR analysis in Euscaphis konishii Hayata based on transcriptome data
title_full Selection and evaluation of reference genes for qRT-PCR analysis in Euscaphis konishii Hayata based on transcriptome data
title_fullStr Selection and evaluation of reference genes for qRT-PCR analysis in Euscaphis konishii Hayata based on transcriptome data
title_full_unstemmed Selection and evaluation of reference genes for qRT-PCR analysis in Euscaphis konishii Hayata based on transcriptome data
title_short Selection and evaluation of reference genes for qRT-PCR analysis in Euscaphis konishii Hayata based on transcriptome data
title_sort selection and evaluation of reference genes for qrt-pcr analysis in euscaphis konishii hayata based on transcriptome data
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5985561/
https://www.ncbi.nlm.nih.gov/pubmed/29881443
http://dx.doi.org/10.1186/s13007-018-0311-x
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