Kollmar Martin, Mühlhausen Stefanie
a Group Systems Biology of Motor Proteins , Department of NMR-based Structural Biology, Max-Planck-Institute for Biophysical Chemistry , Göttingen , Germany.
b Milner Centre for Evolution, Department of Biology and Biochemistry , University of Bath, Milner Centre for Evolution , Bath , UK.
RNA Biol. 2017 Mar 4;14(3):293-299. doi: 10.1080/15476286.2017.1279785. Epub 2017 Jan 17.
mRNA decoding by tRNAs and tRNA charging by aminoacyl-tRNA synthetases are biochemically separated processes that nevertheless in general involve the same nucleotides. The combination of charging and decoding determines the genetic code. Codon reassignment happens when a differently charged tRNA replaces a former cognate tRNA. The recent discovery of the polyphyly of the yeast CUG sense codon reassignment challenged previous mechanistic considerations and led to the proposal of the so-called tRNA loss driven codon reassignment hypothesis. Accordingly, codon capture is caused by loss of a tRNA or by mutations in the translation termination factor, subsequent reduction of the codon frequency through reduced translation fidelity and final appearance of a new cognate tRNA. Critical for codon capture are sequence and structure of the new tRNA, which must be compatible with recognition regions of aminoacyl-tRNA synthetases. The proposed hypothesis applies to all reported nuclear and organellar codon reassignments.
tRNA对mRNA的解码以及氨酰tRNA合成酶对tRNA的负载是两个生化分离的过程,但通常涉及相同的核苷酸。负载与解码的组合决定了遗传密码。当一个负载不同的tRNA取代先前的同源tRNA时,就会发生密码子重新分配。酵母CUG有义密码子重新分配的多系性的最新发现对先前的机制考量提出了挑战,并导致了所谓的tRNA缺失驱动的密码子重新分配假说的提出。因此,密码子捕获是由tRNA的缺失或翻译终止因子中的突变引起的,随后通过降低翻译保真度来降低密码子频率,并最终出现新的同源tRNA。对密码子捕获至关重要的是新tRNA的序列和结构,其必须与氨酰tRNA合成酶的识别区域兼容。所提出的假说适用于所有已报道的核和细胞器密码子重新分配。