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大麦叶绿体psbD-psbC蓝光响应启动子的详细结构

Detailed architecture of the barley chloroplast psbD-psbC blue light-responsive promoter.

作者信息

Kim M, Thum K E, Morishige D T, Mullet J E

机构信息

Department of Biochemistry and Biophysics, Crop Biotechnology Center, Texas A & M University, College Station, Texas 77843, USA.

出版信息

J Biol Chem. 1999 Feb 19;274(8):4684-92. doi: 10.1074/jbc.274.8.4684.

Abstract

The photosystem II reaction center chlorophyll protein D2, is encoded by the chloroplast gene psbD. PsbD is transcribed from at least three different promoters, one which is activated by high fluence blue light. Sequences within 130 base pairs (bp) of the psbD blue light-responsive promoter (BLRP) are highly conserved in higher plants. In this study, the structure of the psbD BLRP was analyzed in detail using deletion and site-directed mutagenesis and in vitro transcription. Deletion analysis showed that a 53-bp DNA region of the psbD BLRP, from -57 to -5, was sufficient for transcription in vitro. Mutation of a putative prokaryotic -10 element (TATTCT) located from -7 to -12 inhibited transcription from the psbD BLRP. In contrast, mutation of a putative prokaryotic -35 element, had no influence on transcription. Mutation of a TATATA sequence located between the barley psbA -10 and -35 elements significantly reduced transcription from this promoter. However, site-directed mutation of sequences located between -35 and -10 had no effect on transcription from the psbD BLRP. Transcription from the psbD BLRP was previously shown to require a 22-bp sequence, termed the AAG-box, located between -36 and -57. The AAG-box specifically binds the protein complex AGF. Site-directed mutagenesis identified two different sequence motifs in the AAG-box that are important for transcription in vitro. Based on these results, we propose that positive factors bind to the AAG-box and interact with the chloroplast-encoded RNA polymerase to promote transcription from the psbD BLRP. Transcription from the psbD BLRP is thus similar to type II bacterial promoters that use activating proteins to stimulate transcription. Transcription of the psbD BLRP was approximately 6. 5-fold greater in plastid extracts from illuminated versus dark-grown plants. This suggests that light-induced activation of this promoter in vivo involves factors interacting with the 53-bp psbD BLRP in vitro.

摘要

光系统II反应中心叶绿素蛋白D2由叶绿体基因psbD编码。PsbD至少从三种不同的启动子转录而来,其中一种由高光通量蓝光激活。在高等植物中,psbD蓝光响应启动子(BLRP)130个碱基对(bp)内的序列高度保守。在本研究中,使用缺失和定点诱变以及体外转录详细分析了psbD BLRP的结构。缺失分析表明,psbD BLRP的一个53 bp DNA区域,从-57到-5,足以进行体外转录。位于-7至-12的假定原核-10元件(TATTCT)的突变抑制了psbD BLRP的转录。相反,假定原核-35元件的突变对转录没有影响。位于大麦psbA -10和-35元件之间的TATATA序列的突变显著降低了该启动子的转录。然而,-35和-10之间序列的定点突变对psbD BLRP的转录没有影响。先前表明,psbD BLRP的转录需要一个位于-36至-57之间的22 bp序列,称为AAG框。AAG框特异性结合蛋白质复合物AGF。定点诱变在AAG框中鉴定出两个不同的序列基序,它们对体外转录很重要。基于这些结果,我们提出正因子与AAG框结合并与叶绿体编码的RNA聚合酶相互作用,以促进psbD BLRP的转录。因此,psbD BLRP的转录类似于使用激活蛋白刺激转录的II型细菌启动子。与黑暗生长的植物相比,光照植物的质体提取物中psbD BLRP的转录大约高6.5倍。这表明该启动子在体内的光诱导激活涉及在体外与53 bp psbD BLRP相互作用的因子。

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