首页|水解酶基因BGIOSGA023826在稻瘟菌侵染过程中的抗病表型效应

水解酶基因BGIOSGA023826在稻瘟菌侵染过程中的抗病表型效应

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[目的]月亮谷(Acuce)是云南重要的地方水稻种质资源,也是目前元阳哈尼梯田的主栽品种,种植历史已逾百年,却未曾有过稻瘟病大流行的发生。探索其对稻瘟病的抗性机制,明确参与抗性反应过程功能基因的种类、数量、表达特征及其表型效应,有助于保护和利用水稻地方品种。[方法]以前期月亮谷-稻瘟菌互作转录组中筛选到与抗病表型高度相关的候选基因BGIOSGA023826为研究对象,首先进行基因克隆及生物信息学分析,然后通过构建过表达载体进行农杆菌遗传转化,获得过表达植株,并进行过表达植株阳性鉴定和抗病表型分析,最后利用实时荧光定量PCR进行过表达植株PR基因表达分析,以及通过酶联免疫测定内源激素含量的变化。[结果]候选基因BGIOSGA023826为一个水解酶基因,编码354个氨基酸,是不稳定疏水蛋白且不存在跨膜域,不属于膜蛋白,为非分泌性蛋白;与日本晴相比,BGIOSGA023826过表达植株对稻瘟病的抗性显著增强;实时荧光定量PCR结果显示,接种后,与日本晴相比,PR基因PR1b、OsNPR1、OsAOS2和转录因子基因WRKY45的相对表达量显著上调,PR1b及茉莉酸合成途径的关键基因OsAOS2在12 hpi表达量持续上调;转录因子基因WRKY45表达量在24 hpi显著上调,至36 hpi时达到峰值,比日本晴上调近2倍;内源激素含量测定结果表明,JA含量在12 hpi升高至263。88 pmol·L-1,到36 hpi时达到高峰304 pmol·L-1;水杨酸(SA)含量在24 hpi升高至186。5 pmol·L-1,36 hpi时达到峰值198。88pmol·L-1;活性氧(ROS)含量也持续上升,且当ROS在36 hpi达到峰值时,丙二醛(MDA)含量也从40。43 nmol·g-1增至53。94 nmol·g-1;而过表达植株的超氧化物歧化酶(SOD)在各接种时段活性差异不大,但在日本晴中呈现上升趋势。[结论]明确了水解酶基因BGIOSGA023826与PR基因及内源激素含量在稻瘟菌侵染初期的时空表达关系,证明其参与了月亮谷对稻瘟菌侵染的抗病过程。
Hydrolase Gene BGIOSGA023826 Involved in Regulation of Resistance Process to Rice Blast
[Objective]Acuce,currently the predominant cultivating rice landrace at Yuanyang Hani terrace,Yunnan Province,has been continuously planted for more than 100 years.Interestingly,there has never been a major outbreak of rice blast during the past decades.Clarifying the types,quantities,expression characteristics,and phenotypic effects of functional genes involved in the resistance response process so as to exploring the molecular mechanism of Acuce resistance to Magnaporthe oryzae will optimize facilitate the conservation and utilization of rice landrace.[Method]The present research focuses on the biological effect of disease resistance-related candidate gene BGIOSGA023826 which screened from Acuce-M.oryzae interaction transcriptome.Initially,biological function of this gene was analyzed by using bioinformatics software and conducted gene cloning.Subsequently,overexpression vector was constructed through Agrobacterium-mediated genetic transformation,then carry out positive identification and disease resistance phenotype analysis of overexpressed plants.Finally,Real-time fluorescence quantitative PCR was used to analyze the expression of PR genes in overexpressed plants,and enzyme-linked immunosorbent assay was used to determine changes in endogenous hormone content.[Result]The candidate gene BGIOSGA023826 encodes 354 amino acids figuring unstable hydrophobic characteristic without transmembrane domains,coding a non-membrane and non-secretory protein,classified as a hydrolase gene.The overexpression of BGIOSGA023826 in transgenic plants significantly enhances resistance to M.oryzae compared to Nipponbare.The results of real-time fluorescent quantitative PCR indicate that the relative expression levels of the PR genes PR1b,OsNPR1,and OsAOS2 as well as transcription factors WRKY45 significantly upregulated.Both of the PR1b gene and the key gene OsAOS2 functioning in the JA synthesis pathway continuously upregulated from 12 hpi.Meanwhile,the expression level of the transcription factor gene WRKY45 drastically increased at 24 hpi and reached its peak at 36 hpi,which were nearly two folds higher than that of Nipponbare.As to the results of endogenous hormone content measurement,the JA increased to 263.88 pmol·L-1 at 12 hpi,reaching peak 304 pmol·L-1 at 36 hpi;Similarly,the SA increased to 186.5 pmol·L-1 at 24 hpi,reaching peak 198.88 pmol·L-1 at 36 hpi;At the same time,the content of ROS also rises continually and reached its peak at 36 hpi,MDA also increased from 40.43 nmol·g-1 to 53.94 nmol·g-1;However,SOD did not exhibit significant differences at individual time points in transgenic plant,but showed an upward trend in Nipponbare.[Conclusion]Preliminary elucidating of the temporal expression relationship between the hydrolase gene BGIOSGA023826 and the PR genes as well as endogenous hormone levels,demonstrating it involved in the landrace Acuce resistance to M.oryzae infection process.

Magnaporthe oryzaerice landracesdisease resistance related genesgenetic transformationreal-time fluorescent quantitative PCR

赵婕、赵龙缘、潘凝辉、管丽蓉、杜云龙、李成云、王云月、谢勇

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云南农业大学植物保护学院,昆明 650201

云南开放大学化学工程学院,昆明 650223

云南生物资源保护与利用国家重点实验室,昆明 650201

稻瘟病 水稻地方品种 抗病相关基因 遗传转化 实时荧光定量PCR

2024

中国农业科学
中国农业科学院

中国农业科学

CSTPCD北大核心
影响因子:1.899
ISSN:0578-1752
年,卷(期):2024.57(23)