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分离和鉴定受除草剂和激素调控的水稻谷胱甘肽 S-转移酶基因启动子。

Isolation and characterization of a rice glutathione S-transferase gene promoter regulated by herbicides and hormones.

机构信息

Key Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Chongqing University, 400044 Chongqing, People's Republic of China.

出版信息

Plant Cell Rep. 2011 Apr;30(4):539-49. doi: 10.1007/s00299-010-0964-z. Epub 2010 Dec 9.

Abstract

OsGSTL2, encoding glutathione S-transferase, is a lambda class gene on chromosome 3 of rice (Oryza sativa L.). RNA blot analysis and semi-quantitative RT-PCR assays demonstrated that the transcription of OsGSTL2 in rice roots treated with chlorsulfuron increased significantly. To further understand OsGSTL2 promoter activity, a DNA fragment (GST2171) of 2,171 bp upstream of the OsGSTL2 coding region was isolated. In silico sequence analysis revealed that this fragment contains stress-regulated regulatory elements, hormone-responsive elements and three transposable elements. To define the core promoter sequence, a series of 5' truncation derivatives of GST2171 were fused to uidA gene. The chimeric genes were introduced into rice plants via Agrobacterium-mediated transformation. The expression of the GST2171::GUS transgene varied considerably. GUS staining indicated that the uidA gene is expressed in young seedlings, older leaves, flowering glumes and seeds, but not in older roots. Quantitative fluorescence assays revealed that the expression of the uidA gene is strong in young seedlings and decreases gradually over a period of 25 days. To our surprise, among the 5' truncation derivatives, the shortest promoter GST525 showed the highest GUS expression, and the second shortest promoter GST962 showed the lowest GUS expression. The uidA gene expression in the roots of transgenic rice seedlings is upregulated by chlorsulfuron, glyphosate, salicylic acid (SA) and naphthalene acetic acid (NAA). The possible roles of the repetitive elements on the OsGSTL2 promoter were discussed in terms of transcription repression and promoter induction by herbicides and hormones.

摘要

OsGSTL2 编码谷胱甘肽 S-转移酶,是水稻(Oryza sativa L.)第 3 号染色体上的一个 lambda 类基因。RNA 印迹分析和半定量 RT-PCR 检测表明,氯磺隆处理的水稻根中 OsGSTL2 的转录显著增加。为了进一步了解 OsGSTL2 启动子的活性,分离了 OsGSTL2 编码区上游 2171bp 的 DNA 片段(GST2171)。计算机序列分析表明,该片段包含受胁迫调控的调控元件、激素响应元件和三个转座元件。为了定义核心启动子序列,对 GST2171 的一系列 5' 截短衍生物进行了融合到 uidA 基因。通过农杆菌介导的转化将嵌合基因导入水稻植株。GST2171::GUS 转基因的表达变化很大。GUS 染色表明,uidA 基因在幼苗、老叶、颖花和种子中表达,但在老根中不表达。定量荧光分析表明,在幼苗中 uidA 基因的表达很强,并在 25 天的时间内逐渐下降。令我们惊讶的是,在 5' 截短衍生物中,最短的启动子 GST525 表现出最高的 GUS 表达,而第二短的启动子 GST962 表现出最低的 GUS 表达。氯磺隆、草甘膦、水杨酸(SA)和萘乙酸(NAA)可上调转基因水稻幼苗根中 uidA 基因的表达。从除草剂和激素对转录抑制和启动子诱导的角度讨论了 OsGSTL2 启动子上重复元件的可能作用。

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