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鉴定一个对水杨酸有响应的水稻病程相关蛋白10a(OsPR10a)启动子区域。

Identification of an OsPR10a promoter region responsive to salicylic acid.

作者信息

Hwang Seon-Hee, Lee In Ah, Yie Se Won, Hwang Duk-Ju

机构信息

National Institute of Agricultural Biotechnology, Rural Development Administration, Suwon, South Korea.

出版信息

Planta. 2008 Apr;227(5):1141-50. doi: 10.1007/s00425-007-0687-8. Epub 2008 Jan 12.

Abstract

Orysa sativa pathogenesis-related protein 10a (OsPR10a) was induced by pathogens, salicylic acid (SA), jasmonic acid (JA), ethephon, abscisic acid (ABA), and NaCl. We tried to analyze the OsPR10a promoter to investigate the transcriptional regulation of OsPR10a by SA. We demonstrated the inducibility of OsPR10a promoter by SA using transgenic Arabidopsis carrying OsPR10a:GFP as well as by transient expression assays in rice. To further identify the promoter region responsible for its induction by SA, four different deletions of the OsPR10a promoter were made, and their activities were measured by transient assays. The construct containing 687-bp OsPR10a promoter from its start codon exhibited a six-fold increase of induction compared to the control in response to SA. Mutation in the W-box like element 1 (WLE 1) between 687 and 637-bp from TGACA to TGAAA completely abolished induction of the OsPR10a promoter by SA, indicating that the WLE 1 between -687 and -637 of OsPR10a promoter is important in SA-mediated OsPR10a expression. We show for the first time that the W-box like element plays a role in SA mediated PR gene expression.

摘要

水稻病程相关蛋白10a(OsPR10a)受病原体、水杨酸(SA)、茉莉酸(JA)、乙烯利、脱落酸(ABA)和NaCl诱导。我们试图分析OsPR10a启动子,以研究SA对OsPR10a的转录调控。我们通过携带OsPR10a:GFP的转基因拟南芥以及水稻中的瞬时表达试验,证明了SA对OsPR10a启动子的诱导性。为了进一步确定负责SA诱导的启动子区域,我们对OsPR10a启动子进行了四种不同的缺失,并通过瞬时试验测量了它们的活性。与对照相比,含有从起始密码子起687 bp的OsPR10a启动子的构建体在响应SA时诱导增加了六倍。从TGACA到TGAAA的687至637 bp之间的类W盒元件1(WLE 1)中的突变完全消除了SA对OsPR10a启动子的诱导,表明OsPR10a启动子-687至-637之间的WLE 1在SA介导的OsPR10a表达中很重要。我们首次表明类W盒元件在SA介导的PR基因表达中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8946/2270913/f95142abed32/425_2007_687_Fig1_HTML.jpg

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