McPheeters D S, Stormo G D, Gold L
Department of Molecular, Cellular, and Developmental Biology, University of Colorado, Boulder 80309.
J Mol Biol. 1988 Jun 5;201(3):517-35. doi: 10.1016/0022-2836(88)90634-1.
We have identified the binding site on the bacteriophage T4 gene 32 mRNA responsible for autogenous translational regulation. We demonstrate that this site is largely unstructured and overlaps the initiation codon of gene 32 as previously predicted. Co-operative binding of gene 32 protein to this site specifically blocks the formation of 30 S-tRNA(fMet)-gene 32 mRNA ternary complexes and initiation of translation. The translational operator is bound co-operatively by gene 32 protein and this binding is facilitated by a nucleation site far upstream from the initiation codon. A similar unstructured mRNA lacking this nucleation site is also bound co-operatively, but only at concentrations of gene 32 protein higher than those needed to repress binding of ribosomes to the gene 32 mRNA. Some sequence-specific interactions may also influence this binding. Comparison of the bacteriophage T2, T4 and T6 gene 32 operator sequences leads us to propose that the nucleation site is a pseudoknot.
我们已经确定了噬菌体T4基因32 mRNA上负责自身翻译调控的结合位点。我们证明,该位点在很大程度上是无结构的,并且如先前预测的那样与基因32的起始密码子重叠。基因32蛋白与该位点的协同结合特异性地阻断了30 S-起始tRNA(fMet)-基因32 mRNA三元复合物的形成以及翻译起始。翻译操纵子由基因32蛋白协同结合,并且起始密码子上游远处的一个成核位点促进了这种结合。一种缺乏该成核位点的类似无结构mRNA也能被协同结合,但仅在基因32蛋白浓度高于抑制核糖体与基因32 mRNA结合所需浓度时才能结合。一些序列特异性相互作用也可能影响这种结合。对噬菌体T2、T4和T6基因32操纵子序列的比较使我们提出,成核位点是一个假结。