Elsen S, Ponnampalam S N, Bauer C E
Department of Biology, Department of Chemistry, Indiana University, Bloomington, Indiana 47405, USA.
J Biol Chem. 1998 Nov 13;273(46):30762-9. doi: 10.1074/jbc.273.46.30762.
Expression of light harvesting II genes and of bacteriochlorophyll and carotenoid biosynthesis genes in Rhodobacter capsulatus is repressed under aerobic growth conditions by the transcription factor CrtJ. In this study, we demonstrate that the crtA-crtI intergenic region contains divergent promoters that initiate transcription 116 base pairs apart, based on primer extension analyses. DNase I protection assays demonstrate that purified CrtJ binds to one palindrome that overlaps the crtA -10 promoter recognition sequence as well as to a second palindrome that overlaps the -35 crtI promoter recognition sequence. Similar analyses also show that the puc promoter region contains two distant CrtJ palindromes, with one near the -35 promoter recognition sequence and the other located 240 base pairs upstream. Gel mobility shift and filter retention assays indicate that CrtJ binds in a cooperative manner to these distantly separated palindromes. In vivo expression assays with puc and crtI promoter reporter plasmids further demonstrate that aerobic repression of puc and crtI expression requires both CrtJ palindromes. These in vitro and in vivo results indicate that aerobic repression of puc, crtA, and crtI expression involves cooperative interactions between CrtJ bound to distant palindromes. A DNA looping model is discussed.
在需氧生长条件下,红假单胞菌中捕光II基因以及细菌叶绿素和类胡萝卜素生物合成基因的表达受到转录因子CrtJ的抑制。在本研究中,基于引物延伸分析,我们证明crtA - crtI基因间区域包含两个反向排列的启动子,它们起始转录的位置相隔116个碱基对。DNA酶I保护试验表明,纯化的CrtJ与一个与crtA -10启动子识别序列重叠的回文序列结合,同时也与另一个与crtI启动子 -35识别序列重叠的回文序列结合。类似分析还表明,puc启动子区域包含两个相距较远的CrtJ回文序列,一个靠近 -35启动子识别序列,另一个位于上游240个碱基对处。凝胶迁移率变动分析和滤膜滞留试验表明,CrtJ以协同方式结合到这些相距较远的回文序列上。用puc和crtI启动子报告质粒进行的体内表达试验进一步证明,puc和crtI表达的需氧抑制需要两个CrtJ回文序列。这些体外和体内结果表明,puc、crtA和crtI表达的需氧抑制涉及与相距较远的回文序列结合的CrtJ之间的协同相互作用。本文讨论了一种DNA环化模型。