Aymerich S, Steinmetz M
Laboratoire de Génétique, Institut National de la Recherche Agronomique, Thiverval-Grignon, France.
Proc Natl Acad Sci U S A. 1992 Nov 1;89(21):10410-4. doi: 10.1073/pnas.89.21.10410.
Induction of the Bacillus subtilis sacB gene and sacPA operon and Escherichia coli bgl operon is mediated by structurally homologous antiterminators encoded by the sacY, sacT, and bglG genes, respectively. When activated, these proteins prevent early transcription termination at terminators located in the leader regions of the three operons. BglG was previously shown to bind in vitro to an imperfectly palindromic 29-nucleotide RNA sequence located upstream of the terminator and partially overlapping with it [Houman, F., Diaz-Torres, M.R. & Wright, A. (1990) Cell 62, 1153-1163]. Similar motifs, here termed ribonucleic antiterminators (RATs), strongly conserved in sequence and in position, are found in the leader of both sacB and sacPA. Mutations were created in sacB RAT and tested in B. subtilis; this showed that sacB RAT is the target for SacY-mediated induction of sacB and that a stem-loop structure in the mRNA is required for regulatory function. Mutations increasing the similarity of the sacB RAT with those of sacPA or bgl rendered sacB inducible by SacT or BglG, respectively; most of these changes did not strongly affect induction by SacY, suggesting that the nucleotides at these variable positions act as negative specificity determinants.
枯草芽孢杆菌sacB基因和sacPA操纵子以及大肠杆菌bgl操纵子的诱导分别由sacY、sacT和bglG基因编码的结构同源抗终止子介导。激活后,这些蛋白质可防止在位于这三个操纵子前导区的终止子处发生早期转录终止。之前研究表明,BglG在体外可与位于终止子上游且部分与其重叠的一段29个核苷酸的不完全回文RNA序列结合[胡曼,F.,迪亚兹 - 托雷斯,M.R. & 赖特,A.(1990年)《细胞》62卷,1153 - 1163页]。在sacB和sacPA的前导区中发现了在序列和位置上都高度保守的类似基序,这里称为核糖核酸抗终止子(RATs)。在sacB RAT中产生突变并在枯草芽孢杆菌中进行测试;结果表明sacB RAT是SacY介导的sacB诱导作用的靶点,并且mRNA中的茎环结构对于调节功能是必需的。增加sacB RAT与sacPA或bgl的RAT相似性的突变分别使sacB可被SacT或BglG诱导;这些变化中的大多数对SacY的诱导作用影响不大,这表明这些可变位置的核苷酸充当负性特异性决定因素。