Springer M, Graffe M, Dondon J, Grunberg-Manago M, Romby P, Ehresmann B, Ehresmann C, Ebel J P
Institut de Biologie Physico-Chimique, Paris, France.
Biosci Rep. 1988 Dec;8(6):619-32. doi: 10.1007/BF01117341.
Genetic studies have shown that expression of the E. coli threonyl-tRNA synthetase (thrS) gene is negatively auto-regulated at the translational level. A region called the operator, located 110 nucleotides downstream of the 5' end of the mRNA and between 10 and 50 bp upstream of the translational initiation codon in the thrS gene, is directly involved in that control. The conformation of an in vitro RNA fragment extending over the thrS regulatory region has been investigated with chemical and enzymatic probes. The operator locus displays structural similarities to the anti-codon arm of threonyl tRNA. The conformation of 3 constituent mutants containing single base changes in the operator region shows that replacement of a base in the anti-codon-like loop does not induce any conformational change, suggesting that the residue concerned is directly involved in regulation. However mutation in or close to the anti-codon-like stem results in a partial or complete rearrangement of the structure of the operator region. Further experiments indicate that there is a clear correlation between the way the synthetase recognises each operator, causing translational repression, and threonyl-tRNA.
遗传学研究表明,大肠杆菌苏氨酰 - tRNA合成酶(thrS)基因的表达在翻译水平上受到负向自我调控。一个被称为操纵子的区域,位于mRNA 5'端下游110个核苷酸处,且在thrS基因翻译起始密码子上游10至50个碱基对之间,直接参与了这种调控。利用化学和酶促探针研究了延伸至thrS调控区域的体外RNA片段的构象。操纵子位点与苏氨酰tRNA的反密码子臂具有结构相似性。在操纵子区域含有单碱基变化的3个组成型突变体的构象表明,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。然而,反密码子样茎或其附近的突变会导致操纵子区域结构的部分或完全重排。进一步的实验表明,合成酶识别每个操纵子从而导致翻译抑制的方式与苏氨酰 - tRNA之间存在明显的相关性。