Giegé R, Sissler M, Florentz C
Unité Propre de Recherche 9002, 'Structure des Macromolécules Biologiques et Mécanismes de Reconnaissance', Scientifique, 15 rue René Descartes, F-67084, Strasbourg Cedex, France.
Nucleic Acids Res. 1998 Nov 15;26(22):5017-35. doi: 10.1093/nar/26.22.5017.
Correct expression of the genetic code at translation is directly correlated with tRNA identity. This survey describes the molecular signals in tRNAs that trigger specific aminoacylations. For most tRNAs, determinants are located at the two distal extremities: the anticodon loop and the amino acid accepting stem. In a few tRNAs, however, major identity signals are found in the core of the molecule. Identity elements have different strengths, often depend more on k cat effects than on K m effects and exhibit additive, cooperative or anti-cooperative interplay. Most determinants are in direct contact with cognate synthetases, and chemical groups on bases or ribose moieties that make functional interactions have been identified in several systems. Major determinants are conserved in evolution; however, the mechanisms by which they are expressed are species dependent. Recent studies show that alternate identity sets can be recognized by a single synthetase, and emphasize the importance of tRNA architecture and anti-determinants preventing false recognition. Identity rules apply to tRNA-like molecules and to minimalist tRNAs. Knowledge of these rules allows the manipulation of identity elements and engineering of tRNAs with switched, altered or multiple specificities.
翻译过程中遗传密码的正确表达与tRNA的身份直接相关。本综述描述了tRNA中触发特定氨酰化作用的分子信号。对于大多数tRNA而言,决定因素位于两个远端:反密码子环和氨基酸接受茎。然而,在少数tRNA中,主要的身份信号存在于分子的核心部位。身份元件具有不同的强度,通常更多地取决于催化常数(kcat)效应而非米氏常数(Km)效应,并表现出加性、协同或反协同相互作用。大多数决定因素与同源合成酶直接接触,并且在几个系统中已经确定了碱基或核糖部分上进行功能相互作用的化学基团。主要决定因素在进化过程中是保守的;然而,它们的表达机制因物种而异。最近的研究表明,单个合成酶可以识别交替的身份集,并强调了tRNA结构和反决定因素防止错误识别的重要性。身份规则适用于tRNA样分子和简约tRNA。了解这些规则有助于对身份元件进行操作,并对具有转换、改变或多种特异性的tRNA进行工程改造。