Bénard L, Philippe C, Ehresmann B, Ehresmann C, Portier C
UPR 9073 CNRS, IBPC, Paris, France.
Biochimie. 1996;78(7):568-76. doi: 10.1016/s0300-9084(96)80003-4.
Translational autocontrol of the expression of the ribosomal protein S15 proceeds through the transitory formation of a pseudoknot. A synopsis of the known data is used to propose a molecular model of the mechanism involved and for the role of the pseudoknot. This latter structure is able to recruit 30S ribosomal subunits to initiate translation, but also to bind S15 and to stop translation by trapping the ribosome on its loading site. Information on the S15 protein recognition of the messenger RNA site was deduced from mutational analyses and chemical probing. A comparison of this messenger site with the S15 ribosomal binding site was conducted by analysing hydroxyl radical footprintings of these two sites. The existence of two subsites in 16S RNA suggests that the ribosomal protein S15 might present either two different binding sites or at least one common subsite. Clues for the presence of a common site between the messenger and 16S RNA are given which cannot rule out that recognition specificity is linked to a few other determinants. Whether these determinants are different or not remains an open question.
核糖体蛋白S15表达的翻译自调控通过假结的瞬时形成进行。利用已知数据的概要提出了所涉及机制及其假结作用的分子模型。后一种结构能够募集30S核糖体亚基来启动翻译,但也能结合S15并通过将核糖体困在其加载位点来终止翻译。通过突变分析和化学探针推导了S15蛋白对信使RNA位点的识别信息。通过分析这两个位点的羟基自由基足迹,对该信使位点与S15核糖体结合位点进行了比较。16S RNA中存在两个亚位点表明核糖体蛋白S15可能具有两个不同的结合位点或至少一个共同的亚位点。给出了信使RNA与16S RNA之间存在共同位点的线索,但不能排除识别特异性与其他一些决定因素有关。这些决定因素是否不同仍然是一个悬而未决的问题。