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关于[具体物种]果实发育的参考基因的综合转录组分析

Comprehensive transcriptome analysis of reference genes for fruit development of .

作者信息

Yang Cheng-Long, Yuan Xue-Yan, Zhang Jie, Sun Wei-Hong, Liu Zhong-Jian, Zou Shuang-Quan

机构信息

Biotechnology Institute, Fujian Academy of Agricultural Sciences, Fuzhou, Fujian, China.

Fujian Colleges and Universities Engineering Research Institute of Conservation and Utilization of Natural Bioresources at College of Forestry, Fujian Agriculture and Forestry University, Fujian, Fuzhou, China.

出版信息

PeerJ. 2020 Feb 11;8:e8474. doi: 10.7717/peerj.8474. eCollection 2020.

Abstract

BACKGROUND

Quantitativereal-time reverse transcriptase polymerase chain reaction is the common method to quantify relative gene expression. Normalizating using reliable genes is critical in correctly interpreting expression data from qRT-PCR. is a medicinal plant with a long history in China, which has various chemical compounds in fruit. However, there is no report describing the selection of reference genes in fruit development of .

METHODS

We selected eight candidate reference genes based on RNA-seq database analysis, and ranked expression stability using statistical algorithms GeNorm, NormFinder, BestKeeper and ReFinder. Finally, The nine genes related to the anthocyanin synthesis pathway of Euscaphis konishii were used to verify the suitability of reference gene.

RESULTS

The results showed that the stability of EkUBC23, EkCYP38 and EkGAPDH2 was better, and the low expression reference genes (EkUBC23 and EkCYP38) were favourable for quantifying low expression target genes, while the high expression reference gene (EkGAPDH2) was beneficial for quantifying high expression genes. In this study, we present the suitable reference genes for fruit development of Euscaphis konishii based on transcriptome data, our study will contribute to further studies in molecular biology and gene function on and other closely related species.

摘要

背景

定量实时逆转录聚合酶链反应是定量相对基因表达的常用方法。使用可靠的基因进行标准化对于正确解释qRT-PCR的表达数据至关重要。栲树是一种在中国有着悠久历史的药用植物,其果实中含有多种化合物。然而,尚无关于栲树果实发育过程中内参基因选择的报道。

方法

基于RNA-seq数据库分析选择了8个候选内参基因,并使用统计算法GeNorm、NormFinder、BestKeeper和ReFinder对表达稳定性进行排序。最后,利用与台湾野桐花青素合成途径相关的9个基因来验证内参基因的适用性。

结果

结果表明,EkUBC23、EkCYP38和EkGAPDH2的稳定性较好,低表达内参基因(EkUBC23和EkCYP38)有利于定量低表达靶基因,而高表达内参基因(EkGAPDH2)有利于定量高表达基因。在本研究中,我们基于转录组数据给出了栲树果实发育合适的内参基因,我们的研究将有助于对栲树及其他近缘物种进行进一步的分子生物学和基因功能研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2388/7020815/bbcebf9b5b6c/peerj-08-8474-g001.jpg

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