The State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, Hubei, China.
J Bacteriol. 2012 May;194(9):2297-306. doi: 10.1128/JB.00119-12. Epub 2012 Mar 2.
HetR is the master regulator of heterocyst differentiation in Anabaena sp. strain PCC 7120 and has been found to specifically bind to an inverted-repeat-containing region upstream of hetP, a heterocyst differentiation gene. However, no such inverted-repeat sequence can be found in promoters of other genes in the genome. hetZ is a gene involved in early heterocyst differentiation. As shown with the gfp reporter gene, transcription from P(hetZ) was correlated to the expression level of hetR and inhibition by RGSGR, the pentapeptide derived from the C terminus of PatS. As detected by electrophoretic mobility shift assay, a recombinant HetR showed specific binding to the region upstream of hetZ, and the binding was inhibited by RGSGR. Tests of a series of the upstream fragments delimited the HetR-binding site to a 40-bp region that shows similarity to that upstream of hetP. The introduction of substitutions of bases conserved in the two HetR-binding sites showed that at least 12 bases are required for recognition by HetR. Deletion of a 51-bp region containing the HetR-binding site completely eliminated the transcription activity of P(hetZ). Based on the HetR recognition sequence of hetZ, those upstream of hetR and patA are proposed.
HetR 是集胞藻 PCC 7120 中异形胞分化的主要调控因子,已被发现特异性结合到 hetP(一个异形胞分化基因)上游含有反向重复序列的区域。然而,在基因组中其他基因的启动子中没有发现这样的反向重复序列。hetZ 是一个参与早期异形胞分化的基因。如用 gfp 报告基因所示,从 P(hetZ)转录与 hetR 的表达水平相关,并受到 RGSGR(来自 PatS C 端的五肽)的抑制。电泳迁移率变动分析检测到重组 HetR 特异性结合到 hetZ 上游区域,且 RGSGR 抑制了这种结合。一系列上游片段的测试将 HetR 结合位点限定在一个 40 碱基对的区域,该区域与 hetP 上游的序列相似。HetR 结合位点的碱基取代试验表明,HetR 的识别至少需要 12 个碱基。包含 HetR 结合位点的 51 碱基对缺失区域完全消除了 P(hetZ)的转录活性。基于 hetZ、hetR 和 patA 的 HetR 识别序列被提出。