首页 | 官方网站   微博 | 高级检索  
     

灰葡萄孢BcPDR1基因与PKA编码基因的关系研究
引用本文:张强,李白,袁雪梅,刘晓颖,藏金萍,曹宏哲,张康,邢继红,董金皋.灰葡萄孢BcPDR1基因与PKA编码基因的关系研究[J].植物病理学报,2021,51(2):184-191.
作者姓名:张强  李白  袁雪梅  刘晓颖  藏金萍  曹宏哲  张康  邢继红  董金皋
作者单位:河北省植物生理与分子病理学重点实验室/河北农业大学真菌毒素与植物分子病理学实验室,保定 071000
基金项目:国家自然科学基金资助项目(31972217);河北省自然科学基金资助项目(C2018204045);河北省高等学校科学技术研究项目(ZD2016001);河北省引进留学人员资助项目(0316012)
摘    要: 为明确灰葡萄孢BcPDR1基因与病菌cAMP信号途径中PKA编码基因BcPKA1BcPKA2BcPKAR之间的关系,利用Real-time PCR技术分析了BcPDR1基因突变对PKA编码基因BcPKA1BcPKA2BcPKAR表达的影响,以及PKA编码基因突变对BcPDR1基因表达的影响。结果发现,BcPDR1基因突变体中BcPKA1BcPKA2BcPKAR的表达水平均显著高于野生型和回复菌株,BcPKA1BcPKA2BcPKAR基因的RNAi突变体中BcPDR1基因表达水平显著低于野生型。我们分别构建了PKA编码基因BcPKA1BcPKA2BcPKAR在敲除突变体ΔBcpdr1中过表达的菌株ΔBcpdr1/BcPKA1-OE、ΔBcpdr1/BcPKA2-OE、ΔBcpdr1/BcPKAR-OE;对过表达菌株的表型和致病力进行分析发现,过表达菌株的菌落形态、菌核形成、菌丝形态、生长速率、产孢量和致病力均与突变体ΔBcpdr1表现显著的差异,而更接近野生型BC22的表型和致病力。结果表明,灰葡萄孢BcPDR1基因与PKA亚基基因BcPKA1BcPKA2BcPKAR的表达水平密切相关,BcPDR1基因负调控这3个基因的表达,而这3个基因对BcPDR1基因表达有正调控作用。本研究为进一步阐明灰葡萄孢BcPDR1基因调控病菌生长发育和致病力的分子机制奠定了基础。

关 键 词:灰葡萄孢    BcPDR1  PKA编码基因  生长发育  致病力  
收稿时间:2020-03-18

A cross-regulation between BcPDR1 and PKA coding genes in Botrytis cinerea
ZHANG Qiang,LI Bai,YUAN Xue-mei,LIU Xiao-ying,ZANG Jin-ping,CAO Hong-zhe,ZHANG Kang,XING Ji-hong,DONG Jin-gao.A cross-regulation between BcPDR1 and PKA coding genes in Botrytis cinerea [J].Acta Phytopathologica Sinica,2021,51(2):184-191.
Authors:ZHANG Qiang  LI Bai  YUAN Xue-mei  LIU Xiao-ying  ZANG Jin-ping  CAO Hong-zhe  ZHANG Kang  XING Ji-hong  DONG Jin-gao
Affiliation:Key Laboratory of Hebei Province for Plant Physiology and Molecular Pathology/Mycotoxin and Molecular Plant Pathology Laboratory of Hebei Agricultural University, Baoding 071000,China
Abstract:To clarify the relationship between BcPDR1 gene and PKA coding genes of the cAMP signaling pathway in Botrytis cinerea. Real-time PCR was used to analyze the expression levels of BcPKA1, BcPKA2 and BcPKAR in BcPDR1 gene mutants and the expression levels of BcPDR1 in mutants of BcPKA1, BcPKA2 and BcPKAR. It was found that the expression levels of PKA coding genes BcPKA1, BcPKA2 and BcPKAR in BcPDR1 gene mutations were significantly higher than those in wild-type BC22 and the BcPDR1 complementing strain. The expression levels of BcPDR1 gene in RNAi mutations of BcPKA1, BcPKA2 and BcPKAR genes were significantly lower than those in wild-type BC22. We constructed the over-expression isolates of BcPKA1, BcPKA2 and BcPKAR in ΔBcpdr1 background, respectively. The colony morphology, sclerotium forming, mycelial morphology, growth rate, conidiation, and pathogenicity of the over-expression isolates significantly different from ΔBcpdr1, and closer to the wild-type BC22. These results suggest that the expression of BcPDR1 was closely related to BcPKA1, BcPKA2 and BcPKAR in B. cinerea. The BcPDR1 gene negatively regulates the expression of BcPKA1, BcPKA2 and BcPKAR, while BcPKA1, BcPKA2 and BcPKAR genes positively regulate the expression of the BcPDR1. In a summary, our findings would increase understanding the molecular mechanism of the BcPDR1 gene in growth, development and pathogenicity in B. cinerea.
Keywords:Botrytis cinerea  BcPDR1  PKA coding gene  growth and development  pathogenicity  
点击此处可从《植物病理学报》浏览原始摘要信息
点击此处可从《植物病理学报》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司    京ICP备09084417号-23

京公网安备 11010802026262号