Mahadevan S, Wright A
Cell. 1987 Jul 31;50(3):485-94. doi: 10.1016/0092-8674(87)90502-2.
We have investigated the mechanism of regulation of the bgl operon in Escherichia coli K-12. A regulatory region has been located downstream of the bgl promoter, revealing a 130 base leader containing a sequence from +64 to +112 characteristic of a rho-independent terminator. In vitro, over 90% of the transcripts initiated at the bgl promoter terminate within the leader, at the 3' end of the terminator. Transcriptional fusions containing the terminator require the bglC gene in trans for expression; fusions deleted for the sequence show bglC-independent expression. A mutation resulting in partially constitutive expression of the fusion maps within the terminator. We propose that the bglC gene product mediates positive regulation of the bgl operon by functioning as an antiterminator at the rho-independent terminator located within the leader.
我们研究了大肠杆菌K-12中bgl操纵子的调控机制。一个调控区域位于bgl启动子的下游,发现了一个130个碱基的前导序列,其中包含一段从+64到+112的序列,具有不依赖ρ因子的终止子特征。在体外,超过90%从bgl启动子起始的转录本在该前导序列内、终止子的3'端终止。含有该终止子的转录融合体需要反式的bglC基因来进行表达;缺失该序列的融合体表现出不依赖bglC的表达。一个导致融合体部分组成型表达的突变定位在终止子内。我们提出,bglC基因产物通过在位于前导序列内的不依赖ρ因子的终止子处作为抗终止子发挥作用,介导bgl操纵子的正调控。