Cargando…

Selection and validation of reference genes for quantitative expression analysis of miRNAs and mRNAs in Poplar

BACKGROUND: Quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) is a rapid and sensitive approach to identify miRNA and protein-coding gene expression in plants. However, because of the specially designated reverse transcription and shorter PCR products, very few reference genes h...

Descripción completa

Detalles Bibliográficos
Autores principales: Tang, Fang, Chu, Liwei, Shu, Wenbo, He, Xuejiao, Wang, Lijuan, Lu, Mengzhu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6451301/
https://www.ncbi.nlm.nih.gov/pubmed/30996729
http://dx.doi.org/10.1186/s13007-019-0420-1
_version_ 1783409172211040256
author Tang, Fang
Chu, Liwei
Shu, Wenbo
He, Xuejiao
Wang, Lijuan
Lu, Mengzhu
author_facet Tang, Fang
Chu, Liwei
Shu, Wenbo
He, Xuejiao
Wang, Lijuan
Lu, Mengzhu
author_sort Tang, Fang
collection PubMed
description BACKGROUND: Quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) is a rapid and sensitive approach to identify miRNA and protein-coding gene expression in plants. However, because of the specially designated reverse transcription and shorter PCR products, very few reference genes have been identified for the quantitative analysis of miRNA expression in plants, and different internal reference genes are needed to normalize the expression of miRNAs and mRNA genes respectively. Therefore, it is particularly important to select the suitable common reference genes for normalization of quantitative PCR of miRNA and mRNA. RESULTS: In this study, a modified reverse transcription PCR protocol was adopted for selecting and validating universal internal reference genes of mRNAs and miRNAs. Eight commonly used reference genes, four stably expressed novel genes in Populus tremula, three small noncoding RNAs and three conserved miRNAs were selected as candidate genes, and the stability of their expression was examined across a set of 38 tissue samples from four developmental stages of poplar clone 84K (Populus alba × Populus glandulosa). The expression stability of these candidate genes was evaluated systematically by four algorithms: geNorm, NormFinder, Bestkeeper and DeltaCt. The results showed that Eukaryotic initiation factor 4A III (EIF4A) and U6-2 were suitable for samples of the callus stage; U6-1 and U6-2 were best for the seedling stage; Protein phosphatase 2A-2 (PP2A-2) and U6-1 were best for the plant stage; and Protein phosphatase 2A-2 (PP2A-2) and Oligouridylate binding protein 1B (UBP) were the best reference genes in the adventitious root (AR) regeneration stage. CONCLUSIONS: The purpose of this study was to identify the most appropriate reference genes for qRT-PCR of miRNAs and mRNAs in different tissues at several developmental stages in poplar. U6-1, EIF4A and PP2A-2 were the three most appropriate reference genes for qRT-PCR normalization of miRNAs and mRNAs during the plant regeneration process, and PP2A-2 and UBP represent the best reference genes in the AR regeneration stage of poplar. This work will benefit future studies of expression and function analysis of miRNAs and their target genes in poplar. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13007-019-0420-1) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6451301
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-64513012019-04-17 Selection and validation of reference genes for quantitative expression analysis of miRNAs and mRNAs in Poplar Tang, Fang Chu, Liwei Shu, Wenbo He, Xuejiao Wang, Lijuan Lu, Mengzhu Plant Methods Research BACKGROUND: Quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) is a rapid and sensitive approach to identify miRNA and protein-coding gene expression in plants. However, because of the specially designated reverse transcription and shorter PCR products, very few reference genes have been identified for the quantitative analysis of miRNA expression in plants, and different internal reference genes are needed to normalize the expression of miRNAs and mRNA genes respectively. Therefore, it is particularly important to select the suitable common reference genes for normalization of quantitative PCR of miRNA and mRNA. RESULTS: In this study, a modified reverse transcription PCR protocol was adopted for selecting and validating universal internal reference genes of mRNAs and miRNAs. Eight commonly used reference genes, four stably expressed novel genes in Populus tremula, three small noncoding RNAs and three conserved miRNAs were selected as candidate genes, and the stability of their expression was examined across a set of 38 tissue samples from four developmental stages of poplar clone 84K (Populus alba × Populus glandulosa). The expression stability of these candidate genes was evaluated systematically by four algorithms: geNorm, NormFinder, Bestkeeper and DeltaCt. The results showed that Eukaryotic initiation factor 4A III (EIF4A) and U6-2 were suitable for samples of the callus stage; U6-1 and U6-2 were best for the seedling stage; Protein phosphatase 2A-2 (PP2A-2) and U6-1 were best for the plant stage; and Protein phosphatase 2A-2 (PP2A-2) and Oligouridylate binding protein 1B (UBP) were the best reference genes in the adventitious root (AR) regeneration stage. CONCLUSIONS: The purpose of this study was to identify the most appropriate reference genes for qRT-PCR of miRNAs and mRNAs in different tissues at several developmental stages in poplar. U6-1, EIF4A and PP2A-2 were the three most appropriate reference genes for qRT-PCR normalization of miRNAs and mRNAs during the plant regeneration process, and PP2A-2 and UBP represent the best reference genes in the AR regeneration stage of poplar. This work will benefit future studies of expression and function analysis of miRNAs and their target genes in poplar. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13007-019-0420-1) contains supplementary material, which is available to authorized users. BioMed Central 2019-04-06 /pmc/articles/PMC6451301/ /pubmed/30996729 http://dx.doi.org/10.1186/s13007-019-0420-1 Text en © The Author(s) 2019 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
Tang, Fang
Chu, Liwei
Shu, Wenbo
He, Xuejiao
Wang, Lijuan
Lu, Mengzhu
Selection and validation of reference genes for quantitative expression analysis of miRNAs and mRNAs in Poplar
title Selection and validation of reference genes for quantitative expression analysis of miRNAs and mRNAs in Poplar
title_full Selection and validation of reference genes for quantitative expression analysis of miRNAs and mRNAs in Poplar
title_fullStr Selection and validation of reference genes for quantitative expression analysis of miRNAs and mRNAs in Poplar
title_full_unstemmed Selection and validation of reference genes for quantitative expression analysis of miRNAs and mRNAs in Poplar
title_short Selection and validation of reference genes for quantitative expression analysis of miRNAs and mRNAs in Poplar
title_sort selection and validation of reference genes for quantitative expression analysis of mirnas and mrnas in poplar
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6451301/
https://www.ncbi.nlm.nih.gov/pubmed/30996729
http://dx.doi.org/10.1186/s13007-019-0420-1
work_keys_str_mv AT tangfang selectionandvalidationofreferencegenesforquantitativeexpressionanalysisofmirnasandmrnasinpoplar
AT chuliwei selectionandvalidationofreferencegenesforquantitativeexpressionanalysisofmirnasandmrnasinpoplar
AT shuwenbo selectionandvalidationofreferencegenesforquantitativeexpressionanalysisofmirnasandmrnasinpoplar
AT hexuejiao selectionandvalidationofreferencegenesforquantitativeexpressionanalysisofmirnasandmrnasinpoplar
AT wanglijuan selectionandvalidationofreferencegenesforquantitativeexpressionanalysisofmirnasandmrnasinpoplar
AT lumengzhu selectionandvalidationofreferencegenesforquantitativeexpressionanalysisofmirnasandmrnasinpoplar