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aKR1上游启动子分离及其表达分析

Isolation and Expressional Analysis of the Promoter of CaKR1

中文摘要英文摘要

锚定蛋白是介导蛋白质与蛋白质的相互作用的一类重要蛋白,与植物多种生长发育机制相关,前人研究发现辣椒锚定蛋白CaKR1参与了植物抗氧化和多种逆境胁迫,但其表达调控分子机制还未见报道。本研究运用基因组步移(Genome Walking)技术分离获得了CaKR1基因上游-1594bp的启动子序列,命名为CaKR1p,发现其中含有SA、ABA、低温等信号应答原件以及其它诸如W盒等应答逆境胁迫的调控原件。进一步构建CaKR1p与GUS报告基因融合的植物表达载体,获得了烟草转基因植株及其相应的T1代株系,利用T1代转基因株系分析了CaKR1p在几种外源激素处理下的GUS基因的表达,结果表明外源激素SA,JA和ABA的诱导处理均可激活该启动子下游报告基因GUS的表达,说明CaKR1的表达和作用受到SA、ABA以及JA等信号通路调节。

nchors, a kind of important proteins mediating protein-protein interaction, is closely related to the regulation of plant growth and development as well as stresses responses. CaKR1 isolated from pepper leaves (Capsici annuune L.) is a member of the anchored proteins and involve in pepper response to biotic and abiotic stresses by previous study, but the underlying mechanism is not well understood. In the present study, the -1594 bp upstream promoter sequence of the CaKR1 was isolated by genome walking technology and named CaKR1p and cis-elements such as SARE, ABRE, LTRE were found in this promoter. The promoter was fused to the GUS reporter gene to generate expression vector, which was transformed into tobacco by Agrobacterium mediated method and transgenic plants was acquired and confirmed. With T1 transgenic lines, we analyzed the expression of CaKR1p against the treatment of exogenous hormone, and found that the expression of GUS reporter gene was induced significantly by exogenously applied ABA and SA, suggesting that CaKR1 may involve in pepper response to abiotic and biotic stresses regulated by signaling mediated by ABA and SA, respectively, and the inducible expression of CaKR1 is possibly conferred by the SA and ABA responsive elements in its promoters.

申磊、刘艳艳、黄雪盈、刘志钦、洪水秀、卢蓉、吴杨、梁浩、杨晟、石兰平、何水林、贺俐、王博

植物学生物科学研究方法、生物科学研究技术分子生物学

辣椒锚定蛋白启动子表达

pepperAnchor proteinpromoterexpression

申磊,刘艳艳,黄雪盈,刘志钦,洪水秀,卢蓉,吴杨,梁浩,杨晟,石兰平,何水林,贺俐,王博.aKR1上游启动子分离及其表达分析[EB/OL].(2014-03-10)[2025-08-03].http://www.paper.edu.cn/releasepaper/content/201403-302.点此复制

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