Moine H, Romby P, Springer M, Grunberg-Manago M, Ebel J P, Ehresmann C, Ehresmann B
Laboratoire de Biochimie, Institut de Biologie Moléculaire et Cellulaire du Centre National de la Recherche Scientifique, Strasbourg, France.
Proc Natl Acad Sci U S A. 1988 Nov;85(21):7892-6. doi: 10.1073/pnas.85.21.7892.
Previous work showed that the expression of the Escherichia coli threonine:tRNAThr ligase (EC 6.1.1.3)-encoding gene (thrS) is negatively autoregulated at the translational level and that a region called the operator that is located between 10 and 50 base pairs upstream of the translation initiation codon of the thrS gene is directly involved in that control. The conformation of an in vitro synthesized RNA fragment extending over the thrS regulatory region has been investigated using chemical and enzymatic probes. This study shows that the RNA folds into four well-defined secondary-structure domains, one of them displaying structural similarities to the anticodon arm of tRNAThr. The conformation of three constitutive mutants containing single base changes in the operator region leading to the loss of the regulatory control was also investigated. The replacement of a base in the anticodon-like loop does not induce any conformational change, suggesting that the residue concerned is directly involved in the regulatory process. However, single mutations in or close to the anticodon-like stem result in a partial or complete reorganization of the structure of the operator region. These rearrangements should affect the binding of the ligase to the operator, leading to loss of the regulatory process.
先前的研究表明,大肠杆菌苏氨酸:tRNAThr连接酶(EC 6.1.1.3)编码基因(thrS)的表达在翻译水平上受到负向自动调节,并且在thrS基因翻译起始密码子上游10至50个碱基对之间的一个称为操纵子的区域直接参与该调控。使用化学和酶促探针研究了延伸至thrS调控区域的体外合成RNA片段的构象。这项研究表明,该RNA折叠成四个明确的二级结构域,其中一个与tRNAThr的反密码子臂具有结构相似性。还研究了在操纵子区域中包含单个碱基变化导致调控控制丧失的三个组成型突变体的构象。反密码子样环中一个碱基的替换不会引起任何构象变化,这表明相关残基直接参与调控过程。然而,反密码子样茎中或其附近的单个突变会导致操纵子区域结构的部分或完全重组。这些重排应会影响连接酶与操纵子的结合,从而导致调控过程丧失。