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Illumination stimulates cAMP receptor protein-dependent transcriptional activation from regulatory regions containing class I and class II promoter elements in Synechocystis sp. PCC 6803

机译:照明刺激突触藻属中含有I类和II类启动子元件的调节区的cAMP受体蛋白依赖性转录激活。 PCC 6803

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摘要

The cAMP receptor protein (Crp) is a global transcriptional regulator that binds sequence-specific promoter elements when associated with cAMP. In the motile cyanobacterium Synechocystis sp. strain PCC 6803, intracellular cAMP increases when dark-adapted cells are illuminated. Previous work has established that Crp binds proposed Crp target sites upstream of slr1351 (murF), sll1874 (chlAII), sll1708 (narL), slr0442 and sll1268 in vitro, and that slr0442 is downregulated in a crp mutant during photoautotrophic growth. To identify additional Crp target genes in Synechocystis, 11 different Crp binding sites proposed during a previous computational survey were tested for in vitro sequence-specific binding and crp-dependent transcription. The results indicate that murF, chlAII and slr0442 can be added as ‘target genes of Sycrp1’ in Synechocystis. Promoter mapping of the targets revealed the same close association of RNA polymerase and Crp as that found in Escherichia coli class I and class II Crp-regulated promoters, thereby strongly suggesting similar mechanisms of transcriptional activation.
机译:cAMP受体蛋白(Crp)是一种全局转录调节剂,与cAMP结合时可结合序列特异性启动子元件。在能动的蓝藻中,Synechocystis sp.。菌株PCC 6803,当照亮适应黑暗的细胞时,细胞内cAMP增加。先前的工作已经确定,Crp在体外与slr1351(murF),sll1874(chlAII),sll1708(narL),slr0442和sll1268上游的拟议Crp靶位点结合,并且在光养植物生长过程中,在crp突变体中slr0442下调。为了鉴定集胞藻中的其他Crp靶基因,对先前计算调查中提出的11个不同的Crp结合位点进行了体外序列特异性结合和crp依赖性转录测试。结果表明,可以将murF,chlAII和slr0442添加为 Synechocystis 中的“ Sycrp1的靶基因”。靶标的启动子作图揭示了RNA聚合酶和Crp的紧密联系与在大肠杆菌 I和II类Crp调节的启动子中发现的相同,从而强烈暗示了类似的转录激活机制。

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