Yokobori S, Suzuki T, Watanabe K
Department of Molecular Biology, School of Life Science, Tokyo University of Pharmacy and Life Science, 1432 Horinouchi, Hachioji, Tokyo 192-0392, Japan.
J Mol Evol. 2001 Oct-Nov;53(4-5):314-26. doi: 10.1007/s002390010221.
Characteristic features of tRNA such as the anticodon sequence and modified nucleotides in the anticodon loop are thought to be crucial effectors for promoting or restricting codon reassignment. Our recent findings on basepairing rules between anticodon and codon in various metazoan mitochondria suggest that the complete loss of a codon is not necessarily essential for codon reassignment to take place. We postulate that a possible competition between two tRNAs with cognate anticodon sequences towards the relevant codon to be varied has a potential role in codon reassignment. Our proposition can be viewed as an expanded version of the codon capture theory proposed by Osawa and Jukes (J Mol Evol 28: 271-278, 1989).
转运RNA的特征,如反密码子序列和反密码子环中的修饰核苷酸,被认为是促进或限制密码子重新分配的关键因素。我们最近关于各种后生动物线粒体中反密码子与密码子之间碱基配对规则的研究结果表明,密码子的完全缺失对于密码子重新分配的发生不一定是必不可少的。我们推测,具有同源反密码子序列的两种转运RNA对相关可变密码子的潜在竞争在密码子重新分配中具有潜在作用。我们的观点可以看作是大泽和朱克斯提出的密码子捕获理论的扩展版本(《分子进化杂志》28:271 - 278, 1989)。