Literature DB >> 33467497

Selection and Validation of Reference Genes for Quantitative RT-PCR Analysis in Corylus heterophylla Fisch. × Corylus avellana L.

Sihao Hou1,2,3, Tiantian Zhao1,2,3, Dan Yang1,2,3, Qing Li1,2,3, Lisong Liang1,2,3, Guixi Wang1,2,3, Qinghua Ma1,2,3.   

Abstract

(1) Background: the species of Corylus have sporophytic type of self-incompatibility. Several genes related to recognition reaction between pollen and stigma have been identified in hazelnuts. To better understand the self-incompatibility (SI) response, we screened the suitable reference genes by using quantitative real-time reverse transcription PCR (qRT-PCR) analysis in hazelnut for the first time. (2)
Methods: the major cultivar "Dawei" was used as material. A total of 12 candidate genes were identified and their expression profiles were compared among different tissues and in response to various treatments (different times after self- and cross-pollination) by RT-qPCR. The expression stability of these 12 candidate reference genes was evaluated using geNorm, NormFinder, BestKeeper, Delta Ct, and RefFinder programs. (3)
Results: the comprehensive ranking of RefFinder indicated that ChaActin, VvActin, ChaUBQ14, and ChaEF1-α were the most suitable reference genes. According to the stability analysis of 12 candidate reference genes for each sample group based on four software packages, ChaActin and ChaEF1-α were most stable in different times after self-pollination and 4 h after self- and cross-pollination, respectively. To further validate the suitability of the reference genes identified in this study, CavPrx, which the expression profiles in Corylus have been reported, was quantified by using ChaActin and ChaEF1-α as reference genes. (4) Conclusions: our study of reference genes selection in hazelnut shows that the two reference genes, ChaActin and ChaEF1-α, are suitable for the evaluation of gene expression, and can be used for the analysis of pollen-pistil interaction in Corylus. The results supply a reliable foundation for accurate gene quantifications in Corylus species, which will facilitate the studies related to the reproductive biology in Corylus.

Entities:  

Keywords:  Ping’ou hybrid hazelnut (C. heterophylla Fisch. × C. avellana L.); real-time quantitative PCR; reference gene; self-incompatibility; stability of gene expression

Year:  2021        PMID: 33467497      PMCID: PMC7830083          DOI: 10.3390/plants10010159

Source DB:  PubMed          Journal:  Plants (Basel)        ISSN: 2223-7747


  39 in total

1.  Quantification of splice variants using real-time PCR.

Authors:  I I Vandenbroucke; J Vandesompele; A D Paepe; L Messiaen
Journal:  Nucleic Acids Res       Date:  2001-07-01       Impact factor: 16.971

2.  Molecular cloning and expression analysis of hybrid hazelnut (Corylus heterophylla × Corylus avellana) ChaSRK1/2 genes and their homologs from other cultivars and species.

Authors:  Qing Li; Tiantian Zhao; Lisong Liang; Sihao Hou; Guixi Wang; Qinghua Ma
Journal:  Gene       Date:  2020-06-23       Impact factor: 3.688

3.  RAPD markers linked to eastern filbert blight resistance in Corylus avellana.

Authors:  S A Mehlenbacher; R N Brown; J W Davis; H Chen; N V Bassil; D C Smith; T L Kubisiak
Journal:  Theor Appl Genet       Date:  2003-10-21       Impact factor: 5.699

4.  The implications of using an inappropriate reference gene for real-time reverse transcription PCR data normalization.

Authors:  K Dheda; J F Huggett; J S Chang; L U Kim; S A Bustin; M A Johnson; G A W Rook; A Zumla
Journal:  Anal Biochem       Date:  2005-09-01       Impact factor: 3.365

5.  Genetics of incompatibility inCorylus avellana L.

Authors:  M M Thompson
Journal:  Theor Appl Genet       Date:  1979-05       Impact factor: 5.699

6.  miRDeepFinder: a miRNA analysis tool for deep sequencing of plant small RNAs.

Authors:  Fuliang Xie; Peng Xiao; Dongliang Chen; Lei Xu; Baohong Zhang
Journal:  Plant Mol Biol       Date:  2012-01-31       Impact factor: 4.076

7.  Validation of reference genes for gene expression studies in virus-infected Nicotiana benthamiana using quantitative real-time PCR.

Authors:  Deshui Liu; Lindan Shi; Chenggui Han; Jialin Yu; Dawei Li; Yongliang Zhang
Journal:  PLoS One       Date:  2012-09-28       Impact factor: 3.240

8.  Reference gene selection for quantitative real-time PCR normalization in Reaumuria soongorica.

Authors:  Xia Yan; Xicun Dong; Wen Zhang; Hengxia Yin; Honglang Xiao; Peng Chen; Xiao-Fei Ma
Journal:  PLoS One       Date:  2014-08-12       Impact factor: 3.240

9.  Exploring valid reference genes for gene expression studies in Brachypodium distachyon by real-time PCR.

Authors:  Shin-Young Hong; Pil Joon Seo; Moon-Sik Yang; Fengning Xiang; Chung-Mo Park
Journal:  BMC Plant Biol       Date:  2008-11-07       Impact factor: 4.215

10.  Assessment of reference gene stability in Rice stripe virus and Rice black streaked dwarf virus infection rice by quantitative Real-time PCR.

Authors:  Peng Fang; Rongfei Lu; Feng Sun; Ying Lan; Wenbiao Shen; Linlin Du; Yijun Zhou; Tong Zhou
Journal:  Virol J       Date:  2015-10-24       Impact factor: 4.099

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  2 in total

1.  Stigmatic Transcriptome Analysis of Self-Incompatible and Compatible Pollination in Corylus heterophylla Fisch. × Corylus avellana L.

Authors:  Sihao Hou; Tiantian Zhao; Zhen Yang; Lisong Liang; Wenxu Ma; Guixi Wang; Qinghua Ma
Journal:  Front Plant Sci       Date:  2022-03-01       Impact factor: 5.753

2.  Selection of Suitable Reference Genes for Gene Expression Normalization Studies in Dendrobium huoshanense.

Authors:  Shanyong Yi; Haibo Lu; Chuanjun Tian; Tao Xu; Cheng Song; Wei Wang; Peipei Wei; Fangli Gu; Dong Liu; Yongping Cai; Bangxing Han
Journal:  Genes (Basel)       Date:  2022-08-19       Impact factor: 4.141

  2 in total

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