Adhin M R, van Duin J
Department of Biochemistry, Leiden University, The Netherlands.
J Mol Biol. 1990 Jun 20;213(4):811-8. doi: 10.1016/S0022-2836(05)80265-7.
Premature termination of translation in eubacteria, like Escherichia coli, often leads to reinitiation at nearby start codons. Restarts also occur in response to termination at the end of natural coding regions, where they serve to enforce translational coupling between adjacent cistrons. Here, we present a model in which the terminated but not released ribosome reaches neighboring initiation codons by lateral diffusion along the mRNA. The model is based on the finding that introduction of an additional start codon between the termination and the reinitiation site consistently obstructs ribosomes to reach the authentic restart site. Instead, the ribosome now begins protein synthesis at this newly introduced AUG codon. This ribosomal scanning-like movement is bidirectional, has a radius of action of more than 40 nucleotides in the model system used, and activates the first encountered restart site. The ribosomal reach in the upstream direction is less than in the downstream one, probably due to dislodging by elongating ribosomes. The proposed model has parallels with the scanning mechanism postulated for eukaryotic translational initiation and reinitiation.
在真细菌(如大肠杆菌)中,翻译的提前终止常常导致在附近的起始密码子处重新起始。重新起始也会在天然编码区末端的终止处发生,在那里它们用于加强相邻顺反子之间的翻译偶联。在此,我们提出一个模型,其中已终止但未释放的核糖体通过沿着mRNA的侧向扩散到达相邻的起始密码子。该模型基于这样一个发现:在终止位点和重新起始位点之间引入一个额外的起始密码子会持续阻碍核糖体到达真正的重新起始位点。相反,核糖体现在会在这个新引入的AUG密码子处开始蛋白质合成。这种类似核糖体扫描的移动是双向的,在所使用的模型系统中作用半径超过40个核苷酸,并激活第一个遇到的重新起始位点。核糖体在上游方向的覆盖范围小于下游方向,这可能是由于延伸的核糖体将其挤离所致。所提出的模型与真核生物翻译起始和重新起始所假定的扫描机制有相似之处。