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用于核盘菌诱导下粉红粘帚霉67-1基因表达研究的可靠内参基因的筛选

Selection of reliable reference genes for gene expression studies in Clonostachys rosea 67-1 under sclerotial induction.

作者信息

Sun Zhan-Bin, Li Shi-Dong, Sun Man-Hong

机构信息

Key Laboratory of Integrated Pest Management in Crops, Ministry of Agriculture, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, China.

Key Laboratory of Integrated Pest Management in Crops, Ministry of Agriculture, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, China.

出版信息

J Microbiol Methods. 2015 Jul;114:62-5. doi: 10.1016/j.mimet.2015.05.009. Epub 2015 May 8.

Abstract

Reference genes are important to precisely quantify gene expression by real-time PCR. In order to identify stable and reliable expressed genes in mycoparasite Clonostachys rosea in different modes of nutrition, seven commonly used housekeeping genes, 18S rRNA, actin, β-tubulin, elongation factor 1, ubiquitin, ubiquitin-conjugating enzyme and glyceraldehyde-3-phosphate dehydrogenase, from the effective biocontrol isolate C. rosea 67-1 were tested for their expression under sclerotial induction and during vegetative growth on PDA medium. Analysis by three software programs showed that differences existed among the candidates. Elongation factor 1 was most stable; the M value in geNorm, SD value in Bestkeeper and stability value in Normfinder analysis were 0.405, 0.450 and 0.442, respectively, indicating that the gene elongation factor 1 could be used to normalize gene expression in C. rosea in both vegetative growth and parasitic process. By using elongation factor 1, the expression of a serine protease gene, sep, in different conditions was assessed, which was consistent with the transcriptomic data. This research provides an effective method to quantitate expression changes of target genes in C. rosea, and will assist in further investigation of parasitism-related genes of this fungus.

摘要

内参基因对于通过实时定量PCR精确量化基因表达非常重要。为了鉴定在不同营养模式下的真菌寄生菌粉红粘帚霉中稳定且可靠表达的基因,对来自有效的生防菌株粉红粘帚霉67-1的7个常用管家基因,即18S rRNA、肌动蛋白、β-微管蛋白、延伸因子1、泛素、泛素结合酶和甘油醛-3-磷酸脱氢酶,在菌核诱导下以及在PDA培养基上营养生长期间的表达情况进行了检测。通过三个软件程序进行的分析表明,候选基因之间存在差异。延伸因子1最为稳定;geNorm中的M值、Bestkeeper中的SD值以及Normfinder分析中的稳定性值分别为0.405、0.450和0.442,这表明延伸因子1基因可用于在粉红粘帚霉的营养生长和寄生过程中对基因表达进行标准化。通过使用延伸因子1,评估了丝氨酸蛋白酶基因sep在不同条件下的表达,其与转录组数据一致。本研究提供了一种有效方法来定量粉红粘帚霉中靶基因的表达变化,并将有助于进一步研究该真菌的寄生相关基因。

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