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草酸胁迫下哈茨木霉LTR-2基因表达研究中可靠内参基因的筛选

Selection of reliable reference genes for gene expression studies in Trichoderma afroharzianum LTR-2 under oxalic acid stress.

作者信息

Lyu Yuping, Wu Xiaoqing, Ren He, Zhou Fangyuan, Zhou Hongzi, Zhang Xinjian, Yang Hetong

机构信息

College of Life Science, Shandong University of Technology, Zibo 255000, Shandong Province, People's Republic of China; Shandong Provincial Key Laboratory of Applied Microbiology, Ecology Institute, Shandong Academy of Sciences, Jinan 250014, Shandong Province, People's Republic of China.

Shandong Provincial Key Laboratory of Applied Microbiology, Ecology Institute, Shandong Academy of Sciences, Jinan 250014, Shandong Province, People's Republic of China.

出版信息

J Microbiol Methods. 2017 Oct;141:28-31. doi: 10.1016/j.mimet.2017.07.011. Epub 2017 Jul 25.

Abstract

An appropriate reference gene is required to get reliable results from gene expression analysis by quantitative real-time reverse transcription PCR (qRT-PCR). In order to identify stable and reliable reference genes in Trichoderma afroharzianum under oxalic acid (OA) stress, six commonly used housekeeping genes, i.e., elongation factor 1, ubiquitin, ubiquitin-conjugating enzyme, glyceraldehyde-3-phosphate dehydrogenase, α-tubulin, actin, from the effective biocontrol isolate T. afroharzianum strain LTR-2 were tested for their expression during growth in liquid culture amended with OA. Four in silico programs (comparative ΔCt, NormFinder, geNorm and BestKeeper) were used to evaluate the expression stabilities of six candidate reference genes. The elongation factor 1 gene EF-1 was identified as the most stably expressed reference gene, and was used as the normalizer to quantify the expression level of the oxalate decarboxylase coding gene OXDC in T. afroharzianum strain LTR-2 under OA stress. The result showed that the expression of OXDC was significantly up-regulated as expected. This study provides an effective method to quantify expression changes of target genes in T. afroharzianum under OA stress.

摘要

为了通过定量实时逆转录PCR(qRT-PCR)从基因表达分析中获得可靠结果,需要一个合适的内参基因。为了鉴定草酸(OA)胁迫下哈茨木霉中稳定可靠的内参基因,对有效生物防治菌株哈茨木霉LTR-2中的六个常用管家基因,即延伸因子1、泛素、泛素结合酶、甘油醛-3-磷酸脱氢酶、α-微管蛋白、肌动蛋白,在添加OA的液体培养物生长过程中的表达进行了检测。使用四个计算机程序(比较ΔCt、NormFinder、geNorm和BestKeeper)评估六个候选内参基因的表达稳定性。延伸因子1基因EF-1被鉴定为表达最稳定的内参基因,并用作标准化物来定量哈茨木霉LTR-2菌株在OA胁迫下草酸脱羧酶编码基因OXDC的表达水平。结果表明,OXDC的表达如预期的那样显著上调。本研究提供了一种有效方法来定量哈茨木霉在OA胁迫下靶基因的表达变化。

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