Cruz Edwin, Vargas-Rodriguez Oscar
Department of Molecular Biology and Biophysics, University of Connecticut School of Medicine, Farmington, CT, United States.
Front Microbiol. 2024 Jul 18;15:1437528. doi: 10.3389/fmicb.2024.1437528. eCollection 2024.
The rules of the genetic code are implemented by the unique features that define the amino acid identity of each transfer RNA (tRNA). These features, known as "identity elements," mark tRNAs for recognition by aminoacyl-tRNA synthetases (ARSs), the enzymes responsible for ligating amino acids to tRNAs. While tRNA identity elements enable stringent substrate selectivity of ARSs, these enzymes are prone to errors during amino acid selection, leading to the synthesis of incorrect aminoacyl-tRNAs that jeopardize the fidelity of protein synthesis. Many error-prone ARSs have evolved specialized domains that hydrolyze incorrectly synthesized aminoacyl-tRNAs. These domains, known as editing domains, also exist as free-standing enzymes and, together with ARSs, safeguard protein synthesis fidelity. Here, we discuss how the same identity elements that define tRNA aminoacylation play an integral role in aminoacyl-tRNA editing, synergistically ensuring the correct translation of genetic information into proteins. Moreover, we review the distinct strategies of tRNA selection used by editing enzymes and ARSs to avoid undesired hydrolysis of correctly aminoacylated tRNAs.
遗传密码规则是通过定义每个转运RNA(tRNA)氨基酸特性的独特特征来实现的。这些特征被称为“识别元件”,用于标记tRNA以便被氨酰-tRNA合成酶(ARS)识别,氨酰-tRNA合成酶是负责将氨基酸连接到tRNA上的酶。虽然tRNA识别元件能够使ARS具有严格的底物选择性,但这些酶在氨基酸选择过程中容易出错,导致合成错误的氨酰-tRNA,从而危及蛋白质合成的保真度。许多易出错的ARS已经进化出专门的结构域,能够水解错误合成的氨酰-tRNA。这些结构域被称为编辑结构域,也以独立酶的形式存在,并且与ARS一起保障蛋白质合成的保真度。在这里,我们讨论定义tRNA氨酰化的相同识别元件如何在氨酰-tRNA编辑中发挥不可或缺的作用,协同确保遗传信息正确翻译成蛋白质。此外,我们回顾了编辑酶和ARS用于避免正确氨酰化的tRNA发生不必要水解的不同tRNA选择策略。