Sprengart M L, Porter A G
Institute of Molecular and Cell Biology, National University of Singapore, Republic of Singapore.
Mol Microbiol. 1997 Apr;24(1):19-28. doi: 10.1046/j.1365-2958.1997.3161684.x.
RNA base pairing between the initiation codon and anticodon loop of initiator tRNA is essential but not sufficient for the selection of the 'correct' mRNA translational start site by ribosomes. In prokaryotes, additional RNA interactions between small ribosomal subunit RNA and mRNA sequences just upstream of the start codon can efficiently direct the ribosome to the initiation site. Although there is presently no proof for a similar important ribosomal RNA interaction in eukaryotes, the 5' non-coding regions of their mRNAs and 'consensus sequences' surrounding initiation codons have been shown to be strong determinants for initiation-site selection, but the exact mechanisms are not yet understood. Intramolecular base pairing in mRNA and participation of translation initiation factors can strongly influence the formation of mRNA-small ribosomal subunit-initiator tRNA complexes and modulate translational activities in both prokaryotes and eukaryotes. Only recently has it been appreciated that alternative mechanisms may also contribute to the selection of initiation codons in all organisms. Although direct proof is currently lacking, there is accumulating evidence that additional cis-acting mRNA elements and trans-acting proteins may form specific 'bridging' interactions with ribosomes during translation initiation.
起始密码子与起始tRNA的反密码子环之间的RNA碱基配对对于核糖体选择“正确的”mRNA翻译起始位点至关重要,但并不充分。在原核生物中,小核糖体亚基RNA与起始密码子上游的mRNA序列之间的额外RNA相互作用可以有效地将核糖体引导至起始位点。尽管目前尚无证据表明真核生物中存在类似的重要核糖体RNA相互作用,但已表明其mRNA的5'非编码区和起始密码子周围的“共有序列”是起始位点选择的重要决定因素,但其确切机制尚不清楚。mRNA中的分子内碱基配对以及翻译起始因子的参与可以强烈影响mRNA-小核糖体亚基-起始tRNA复合物的形成,并调节原核生物和真核生物中的翻译活性。直到最近人们才认识到,替代机制也可能有助于所有生物体中起始密码子的选择。尽管目前缺乏直接证据,但越来越多的证据表明,额外的顺式作用mRNA元件和反式作用蛋白可能在翻译起始过程中与核糖体形成特定的“桥接”相互作用。