机构地区:[1]State Key Laboratory far Managing Biotic and Chemical Threats to the Quality and Safety of Agroproducts/Ministry of Agriculture Key Laboratory far Plant Protection and Biotechnology/Zhejiang Provincial Key Laboratory of Plant Virology/Zhejiang Academy of Agricultural Sciences,Hangzhou 310021,China [2]College of Chemistry and Life Sciences,Zhejiang Normal University,Jinhua 321000,China [3]Yueqing Station of Plant Protection,Wenzhou 325600,China [4]College of Plant Protection,Northwest A&F University,Wangling 712100,China [5]Institute of Plant Virology,Ningbo University,Ningbo 315211,China [6]institute of Biotechnology,Ningbo Academy of Agricultural Sciences,Ningbo 315101,China
出 处:《Rice science》2021年第5期442-456,共15页水稻科学(英文版)
基 金:funded by the National Key Research and Development Program of China(Grant No.2016YFD0100601-15);Zhejiang Fundamental Public Welfare Research Program(Grant No.LGN19C140008);Zhejiang Provincial Key Research and Development Plan(Grant No.2019C02006);Major Scientific and Technological Innovation 2025 Project of Ningbo(Grant No.2019B10004);Major Agricultural Science and Technology Project in Ningbo(Grant No.2016C11017).
摘 要:OsPRIOa is one of the well known pathogenesis-related genes in rice,and is induced by multiple plant hormones and pathogens.However,the underlying transcriptional regulation mechanisms in response to differe nt signals and their crosstalks are still largely unknown.In order to find new players participated in the activation of OsPRIOa,we systematically analyzed the basal expression patterns as well as the expression responses of a 2.5 kb OsPRIOa promoter in rice transgenic plants after phytohormone and pathogen stimulations.In agreement with the native gene expression,the OsPRIOa promoter can drive glucuronidase(GUS)gene expressing in spots of leaf cells,leaf trichomes,lemmas and paleae,germinating embryos,calli and root tips.The leaf expression of OsPR10a::GUS was dramatically in creased upon jasm onic acid(JA)and cytoki nin(CK)treatme nts,or challe nges of the pathogen Magnaporthe grisea and Xanthomonas oryzae pv.oryzae.Thus,the OsPRIOa promoter reported here can faithfully reflect its native gene expression.The effects of several JA and CK responsive OsWRKY genes on the regulation of OsPRIOa promoter were then inspected by luciferase transient expression assay,and the JA inducible OsWRKYlO transcription factor was found as a new positive regulator of OsPRIOa.However,the key transcription factors of JA and CK signaling pathways,OsMYC2 and B-type response regulators,were not responsible for the activation of OsPRIOa promote Our findings provided new in sights into the regulation of OsPRIOa expression during plan t-hormone/pathoge n interactions,and the OsPRIOa reporter system can be useful to unravel novel regulators from both pathogen and host.
关 键 词:OsPRIOa promoter Β-GLUCURONIDASE PHYTOHORMONE PATHOGEN OsWRKY10 RICE
分 类 号:S435.11[农业科学—农业昆虫与害虫防治]
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