Wu H Y, Tan J, Fang M
Department of Pharmacology, School of Medicine, Wayne State University, Detroit, Michigan 48201, USA.
Cell. 1995 Aug 11;82(3):445-51. doi: 10.1016/0092-8674(95)90433-6.
The leu-500 mutation can be suppressed in S. typhimurium topA. Previous studies have demonstrated that the plasmid-borne leu-500 minimal promoter cannot be activated in topA mutants unless adjacent (< 250 bp) transcription occurs away from the leu-500 promoter (short-range promoter interaction). To search for a potential upstream promoter responsible for activation of leu-500 in the chromosomal context, we have identified the ilvlH promoter, located 1.9 kb upstream of leu-500 (long-range promoter interaction). Different from short-range promoter interaction, which is abolished by DNA sequence insertions, the long-range promoter interaction is mediated by the intervening DNA sequence. These studies suggest that the long-range interaction between a pair of divergently arrayed promoters is probably mediated by a complex process involving relay of DNA supercoiling by the DNA sequence located between the two promoters.
亮氨酸-500(leu-500)突变在鼠伤寒沙门氏菌topA中可以被抑制。先前的研究表明,质粒携带的leu-500最小启动子在topA突变体中无法被激活,除非相邻(<250 bp)的转录远离leu-500启动子发生(短程启动子相互作用)。为了寻找在染色体环境中负责激活leu-500的潜在上游启动子,我们鉴定出了位于leu-500上游1.9 kb处的ilvIH启动子(长程启动子相互作用)。与被DNA序列插入消除的短程启动子相互作用不同,长程启动子相互作用是由中间的DNA序列介导的。这些研究表明,一对反向排列的启动子之间的长程相互作用可能是由一个复杂的过程介导的,该过程涉及两个启动子之间的DNA序列对DNA超螺旋的传递。