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能源作物柳枝稷在非生物胁迫下 qPCR 数据归一化的内参基因的选择

Selection of reference genes suitable for normalization of qPCR data under abiotic stresses in bioenergy crop Arundo donax L.

机构信息

Department of Biodiversity and Molecular Ecology, Research and Innovation Centre, Fondazione Edmund Mach, Via E. Mach 1, 38010, S. Michele all'Adige (TN), Italy.

Department of Agricultural Sciences, University of Bologna, Bologna, Italy.

出版信息

Sci Rep. 2017 Sep 6;7(1):10719. doi: 10.1038/s41598-017-11019-0.

Abstract

Suitable reference gene selection in qRT-PCR is a key pre-requisite to produce reliable data in gene expression analyses. In this study, novel primers for six commonly used reference genes (AC1, TLF, Act2, TUB α, EF-1α and GAPDH) plus two new candidates (pDUF221 and RPN6) were designed and comparatively tested for expression stability under abiotic stresses (osmotic, heavy metal and heat shock) in shoot, root and their combination of Arundo donax L., a raising non-food energy crop. Expression stability rankings from the most to the least stable gene in each condition and in two tissues (young shoots and roots) were generated with geNorm, NormFinder and BestKeeper programs. All programs provided similar rankings and, strikingly, in most cases identified one of the new candidates, RPN6, as the most suitable reference gene. This novel set of reliable references allows to choose either the best combination of reference genes across multiple stress/organ conditions or to select condition-specific genes that can improve the quality of qRT-PCR analysis. This work provides a solid basis for the functional characterization of A. donax, by enabling accurate quantification of the transcriptional responsiveness under a series of common stress conditions of any gene of interest in this promising biomass/bioenergy species.

摘要

在 qRT-PCR 中选择合适的参考基因是产生可靠基因表达分析数据的关键前提。在这项研究中,为六种常用的参考基因(AC1、TLF、Act2、TUBα、EF-1α和 GAPDH)加上两个新候选基因(pDUF221 和 RPN6)设计了新的引物,并在 shoot、root 及其组合中比较测试了它们在非生物胁迫(渗透、重金属和热休克)下的表达稳定性。geNorm、NormFinder 和 BestKeeper 程序生成了每种条件和两种组织(幼嫩的 shoot 和根)中从最稳定到最不稳定的基因的表达稳定性排名。所有程序都提供了类似的排名,而且在大多数情况下,都将一个新候选基因 RPN6 鉴定为最适合的参考基因。这组新的可靠参考基因允许选择在多种胁迫/器官条件下最佳的参考基因组合,或者选择特定条件下的基因,从而提高 qRT-PCR 分析的质量。这项工作为 A. donax 的功能特征提供了坚实的基础,通过在这个有前途的生物质/生物能源物种的任何感兴趣基因的一系列常见胁迫条件下实现转录应答的准确定量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c902/5587670/a9bbd94b5ac2/41598_2017_11019_Fig1_HTML.jpg

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