Kappell Anthony D, Bhaya Devaki, van Waasbergen Lorraine G
Department of Biology, The University of Texas at Arlington, Arlington, TX 76019, USA.
Arch Microbiol. 2006 Nov;186(5):403-13. doi: 10.1007/s00203-006-0154-0. Epub 2006 Aug 9.
The hliA gene of the cyanobacterium Synechococcus elongatus PCC 7942 is known to be upregulated by high-intensity light through the activity of the NblS sensor kinase. In this work it was found that, within the hliA upstream region, changes to the sequence around -30 to -25 (relative to the transcriptional start site) resulted in elevated hliA expression, implicating this region in negative regulation of the gene. Electrophoretic mobility shift assays performed were consistent with a protein binding this region that acts to keep the gene off in lower light. A reduction in gene dosage of nblS in vivo resulted in enhanced hliA expression, suggesting that negative control of hliA is mediated through NblS. An extended version of the high light regulatory 1 (HLR1) motif (previously described in Synechocystis PCC 6803) was identified within the sequence surrounding -30 to -25 of hliA. The extended HLR1 sequence was found upstream of other NblS-controlled genes from S. elongatus and Synechocystis PCC 6803 and upstream of hli genes from a variety of cyanobacterial and related genomes. These results point to the evolutionary conservation of the HLR1 element and its importance in NblS-mediated signaling and yield new insight into NblS-mediated control of gene expression.
已知通过NblS传感器激酶的活性,高强度光可上调细长聚球藻PCC 7942的hliA基因。在这项研究中发现,在hliA上游区域,-30至-25(相对于转录起始位点)周围序列的变化导致hliA表达升高,这表明该区域对该基因具有负调控作用。进行的电泳迁移率变动分析结果表明,有一种蛋白质结合该区域,在低光照条件下使该基因处于关闭状态。体内nblS基因剂量的减少导致hliA表达增强,这表明hliA的负调控是通过NblS介导的。在hliA基因-30至-25周围的序列中鉴定出了高光调节1(HLR1)基序的扩展版本(先前在集胞藻PCC 6803中描述过)。在细长聚球藻和集胞藻PCC 6803的其他NblS控制基因的上游以及各种蓝细菌和相关基因组的hli基因的上游都发现了扩展的HLR1序列。这些结果表明HLR1元件在进化上具有保守性,及其在NblS介导的信号传导中的重要性,并为NblS介导的基因表达调控提供了新的见解。