首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Specificity determinants and structural features in the RNA target of the bacterial antiterminator proteins of the BglG/SacY family.
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Specificity determinants and structural features in the RNA target of the bacterial antiterminator proteins of the BglG/SacY family.

机译:BglG / SacY家族的细菌抗终止剂蛋白的RNA靶标中的特异性决定子和结构特征。

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摘要

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.
机译:枯草芽孢杆菌sacB基因和sacPA操纵子和大肠杆菌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剂介导。激活后,这些蛋白质可阻止位于三个操纵子前导区的终止子的早期转录终止。先前显示,BglG在体外与不完全回文的29核苷酸RNA序列结合,该序列位于终止子的上游并与其部分重叠[Houman,F.,Diaz-Torres,MR&Wright,A.(1990)Cell 62,1153 -1163]。在sacB和sacPA的前导序列中都发现了类似的基序,在这里被称为核糖核酸抗终止剂(RAT),在序列和位置上都非常保守。在sacB RAT中创建了突变,并在枯草芽孢杆菌中进行了测试;这表明sacB RAT是SacY介导的sacB诱导的靶标,并且mRNA中的茎环结构是调节功能所必需的。分别增加了sacB RAT与sacPA或bgl的相似性的突变使sacB可以被SacT或BglG诱导;这些变化中的大多数并没有强烈影响SacY的诱导,表明这些可变位置上的核苷酸起着负特异性决定子的作用。

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