Tortosa P, Le Coq D
Laboratoire de Génétique Moléculaire et Cellulaire, Centre National de la Recherche Scientifique URA 537, Institut National Agronomique Paris-Grignon, Thiverval-Grignon, France.
Microbiology (Reading). 1995 Nov;141 ( Pt 11):2921-7. doi: 10.1099/13500872-141-11-2921.
The Bacillus subtilis sacXY regulatory operon is involved in sucrose induction of the levansucrase sacB gene by an antitermination mechanism. In the presence of sucrose, the activated SacY antiterminator protein stabilizes the secondary structure of a ribonucleic antiterminator sequence (RAT) located in the leader region of the sacB transcript, and overlapping a rho-independent transcription terminator. Formation of the SacY-RAT complex prevents alternative formation of the terminator, allowing transcription of the downstream sequences. In the absence of sucrose, inhibition of SacY activity by SacX leads to termination of transcription. Expression of sacXY is also sucrose-inducible. This induction was previously shown to be mediated by SacY itself and/or SacT, another antiterminator involved in induction of genes belonging to a distinct sucrose pathway. These antiterminators are not activated at the same concentration of sucrose. We show here that sacXY induction occurs through activation of either SacY or SacT antiterminators, at their respective sucrose activation concentration. This result demonstrates a link between SacY- and SacT-mediated metabolic pathways. In addition, the sacXY leader region carries a RAT-like sequence, which however does not appear to overlap any apparent rho-independent transcription terminator. Site-directed mutagenesis experiments on this RAT-like sequence demonstrated its involvement in sucrose induction. Deletions generated in the sacXY leader region showed that a palindrome, located 100 nt downstream from the RAT-like sequence, also acts as a cis-acting element. Computer analysis of the leader RNA suggested that formation of the secondary structure of the RAT-like sequence and the palindrome could be mutually exclusive.
枯草芽孢杆菌的sacXY调控操纵子通过抗终止机制参与蔗糖对果聚糖蔗糖酶sacB基因的诱导。在蔗糖存在的情况下,被激活的SacY抗终止蛋白稳定位于sacB转录本前导区且与一个不依赖ρ因子的转录终止子重叠的核糖核酸抗终止序列(RAT)的二级结构。SacY-RAT复合物的形成阻止了终止子的另一种形成方式,使下游序列得以转录。在没有蔗糖的情况下,SacX对SacY活性的抑制导致转录终止。sacXY的表达也是蔗糖可诱导的。先前已表明这种诱导是由SacY自身和/或SacT介导的,SacT是另一种参与诱导属于不同蔗糖途径的基因的抗终止子。这些抗终止子在不同的蔗糖浓度下被激活。我们在此表明,sacXY的诱导是通过SacY或SacT抗终止子在其各自的蔗糖激活浓度下被激活而发生的。这一结果证明了SacY和SacT介导的代谢途径之间的联系。此外,sacXY前导区携带一个类似RAT的序列,然而它似乎并不与任何明显的不依赖ρ因子的转录终止子重叠。对这个类似RAT的序列进行的定点诱变实验证明了它参与蔗糖诱导。在sacXY前导区产生的缺失表明,位于类似RAT序列下游100个核苷酸处的一个回文结构也作为一个顺式作用元件起作用。对前导RNA的计算机分析表明,类似RAT的序列和回文结构的二级结构形成可能是相互排斥的。