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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:照明刺激来自含有I类和II类启动子元素的CAMP受体蛋白依赖性转录激活,在SyneChocystis sp中。 PCC 6803.

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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, chlAIIand 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)是与营地相关时结合序列特异性启动子元素的全局转录调节剂。在动机蓝绿杆菌综合症Sp。菌株PCC 6803,细胞内阵营增加时,当暗适应的细胞照明时增加。以前的工作已经确定CRP在体外结合SLR1351(Murf),SLL1874(Chlaii),SLL1708(Nar1),SLR0442和SLL1268的上游的CRP靶位点,并且在光学营养生长期间在CRP突变体中下调SLR0442。为了鉴定综合症中的额外CRP靶基因,对先前的计算调查中提出的11种不同的CRP结合位点进行了体外序列特异性结合和CRP依赖性转录。结果表明,Murf,Chlaiiand SLR0442可以在SyneChocystis中作为“Sycrp1”的“靶基因”。靶标的启动子映射揭示了RNA聚合酶和CRP的相同密切关联,因为在大肠杆菌类I和II类CRP调节启动子中发现,强烈表明了转录活化的类似机制。

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