Suppr超能文献

评价在针叶树病原菌(粗皮侧耳)基因表达研究中使用的潜在内参基因。

Evaluation of potential reference genes for use in gene expression studies in the conifer pathogen (Heterobasidion annosum).

机构信息

Department of Forest Sciences, University of Helsinki, Helsinki, Finland.

出版信息

Mol Biol Rep. 2013 Jul;40(7):4605-11. doi: 10.1007/s11033-013-2553-z. Epub 2013 May 5.

Abstract

The basidiomycete Heterobasidion annosum is the causative agent of butt and root rot disease of conifer trees and it's one of the most destructive conifer pathogen in the northern hemisphere. Because of the intrinsic difficulties in genome manipulation in this fungus, most studies have been focused on gene expression analysis using quantitative real time polymerase chain reaction (qPCR). qPCR is a powerful technique but its reliability resides in the correct selection of a set of reference genes used in the data normalization. In this study, we determined the expression stability of 11 selected reference genes in H. annosum. Almost nothing has so far been published about validation of a set of reference genes to be used in gene expression experiments in this fungus. Eleven reference genes were validated in H. annosum which was grown on three different substrates: pine bark, pine heartwood, and pine sapwood. Bestkeeper and NormFinder Excel-based software were used to evaluate the reference gene transcripts' stability. The results from these two programs indicated that three reference genes namely Tryp metab, RNA Pol3 TF, and Actin were stable in H. annosum in the conditions studied. Interestingly, the GAPDH transcript which has been extensively used in qPCR data normalization is not the best choice when a wide reference gene selection is available. This work represents the first extensive validation of reference genes in H. annosum providing support for gene expression studies and benefits for the wider forest pathology community.

摘要

担子菌 Heterobasidion annosum 是针叶树枯梢和根腐病的病原体,也是北半球最具破坏性的针叶树病原菌之一。由于该真菌在基因组操作方面存在固有困难,因此大多数研究都集中在使用定量实时聚合酶链反应 (qPCR) 进行基因表达分析上。qPCR 是一种强大的技术,但它的可靠性取决于在数据归一化中正确选择一组参考基因。在这项研究中,我们确定了 11 个选定的参考基因在 H. annosum 中的表达稳定性。迄今为止,关于在该真菌中用于基因表达实验的一组参考基因的验证,几乎没有任何出版物。在 H. annosum 中验证了 11 个参考基因,这些基因在三种不同的基质上生长:松树皮、松心材和松边材。Bestkeeper 和 NormFinder Excel 软件用于评估参考基因转录本的稳定性。这两个程序的结果表明,在研究条件下,Tryp metab、RNA Pol3 TF 和 Actin 这三个参考基因在 H. annosum 中稳定。有趣的是,当有广泛的参考基因选择时,广泛用于 qPCR 数据归一化的 GAPDH 转录本并不是最佳选择。这项工作代表了对 H. annosum 中参考基因的首次广泛验证,为基因表达研究提供了支持,并为更广泛的森林病理学社区带来了益处。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验