Lee J K, Kaplan S
Department of Microbiology and Molecular Genetics, University of Texas Medical School, P.O. Box 20708, Houston 77225.
J Bacteriol. 1992 Feb;174(4):1146-57. doi: 10.1128/jb.174.4.1146-1157.1992.
Transcriptional expression of the puc operon in Rhodobacter sphaeroides is highly regulated by both oxygen and light. The approximately 600 bp of DNA upstream of the 5' ends of the two puc-specific transcripts encompasses two functionally separable cis-acting domains. The upstream regulatory region (URS) (-629 to -150) is responsible for enhanced transcriptional regulation of puc operon expression by oxygen and light. The more proximal upstream region (downstream regulatory region [DRS]), containing putative promoter(s), operator(s), and factor binding sites (-150 to -1), is involved in unenhanced transcriptional expression of the puc operon under aerobic and anaerobic conditions. Thus, the DRS shows normal derepression of puc operon expression when cells are shifted from aerobic to photosynthetic growth conditions in terms of percent change but does not show the potential range of expression that is only observed when elements of the URS are present. Because of these observations, we have made a distinction between anaerobic control (describing the shift) and oxygen control (describing the magnitude of derepression). Promoter(s) and/or activator function(s) of the puc operon is associated with a 35-bp DNA region between -92 and -57. Homologous sequences at -10 to -27 and -35 to -52 appear to involve additional regulatory elements: mutations at -12 (A to C) and -26 (G to A) result in partial derepression of puc operon expression under conditions of high aeration. Both point mutations require the upstream regulatory region (-629 to -150) to be present in cis for partial derepression of puc operon transcription under aerobic conditions. Immediately upstream of the promoter and/or activator region are overlapping consensus sequences for IHF (integratin host factor) and FNR (fumarate nitrate reductase) (-105 to -129). This region appears to be essential for enhanced expression of the puc operon. Thus, these two regulatory domains (URS and DRS) appear to involve approximately seven unique regulatory elements. In addition, the data reveal a direct interaction between the URS (-629 to -150) and the DRS (-150 to -1).
球形红细菌中puc操纵子的转录表达受到氧气和光的高度调控。两个puc特异性转录本5'端上游约600 bp的DNA包含两个功能上可分离的顺式作用结构域。上游调控区(URS)(-629至-150)负责通过氧气和光增强puc操纵子表达的转录调控。更靠近近端的上游区域(下游调控区[DRS]),包含假定的启动子、操纵子和因子结合位点(-150至-1),参与puc操纵子在需氧和厌氧条件下的非增强转录表达。因此,当细胞从需氧生长条件转变为光合生长条件时,DRS在百分比变化方面显示出puc操纵子表达的正常去阻遏,但没有显示出只有当URS元件存在时才观察到的潜在表达范围。基于这些观察结果,我们区分了厌氧控制(描述转变)和氧气控制(描述去阻遏的程度)。puc操纵子的启动子和/或激活功能与-92至-57之间的一个35 bp DNA区域相关。-10至-27和-35至-52处的同源序列似乎涉及额外的调控元件:-12(A到C)和-26(G到A)处的突变导致在高通气条件下puc操纵子表达的部分去阻遏。这两个点突变都需要上游调控区(-629至-150)顺式存在,以便在需氧条件下部分去阻遏puc操纵子转录。在启动子和/或激活区的紧邻上游是整合宿主因子(IHF)和延胡索酸硝酸还原酶(FNR)的重叠共有序列(-105至-129)。该区域似乎对增强puc操纵子的表达至关重要。因此,这两个调控结构域(URS和DRS)似乎涉及大约七个独特的调控元件。此外,数据揭示了URS(-629至-150)和DRS(-150至-1)之间的直接相互作用。