Craigen W J, Lee C C, Caskey C T
Institute for Molecular Genetics, Howard Hughes Medical Institute, Baylor College of Medicine, Houston, Texas 77030.
Mol Microbiol. 1990 Jun;4(6):861-5. doi: 10.1111/j.1365-2958.1990.tb00658.x.
Peptide chain termination occurs when a stop codon is decoded by a release factor. In Escherichia coli two codon-specific release factors (RF1 and RF2) direct the termination of protein synthesis, while in eukaryotes a single factor is required. The E. coli factors have been purified and their genes isolated. A combination of protein and DNA sequence data reveal that the RFs are structurally similar and that RF2 is encoded in two reading frames. Frame-shifting from one reading frame to the next occurs at a rate of 50%, is regulated by the RF2-specific stop codon UGA, and involves the direct interaction of the RF2 mRNA with the 3' end of the 16S rRNA. The RF genes are located in two separate operons, with the RF1 gene located at 26.7 min and the RF2 gene at 62.3 min on the chromosome map. Ribosomal binding studies place the RF-binding region at the interface between the ribosomal subunits. A possible mechanism of stop-codon recognition is reviewed.
当终止密码子被释放因子解码时,肽链终止就会发生。在大肠杆菌中,两种密码子特异性释放因子(RF1和RF2)指导蛋白质合成的终止,而在真核生物中则需要单一因子。大肠杆菌的这些因子已被纯化,其基因也已分离出来。蛋白质和DNA序列数据相结合表明,这些释放因子在结构上相似,并且RF2由两个阅读框编码。从一个阅读框到另一个阅读框的移码以50%的速率发生,受RF2特异性终止密码子UGA调控,并且涉及RF2 mRNA与16S rRNA 3'端的直接相互作用。RF基因位于两个独立的操纵子中,在染色体图谱上,RF1基因位于26.7分钟处,RF2基因位于62.3分钟处。核糖体结合研究将RF结合区域定位在核糖体亚基之间的界面处。本文综述了一种可能的终止密码子识别机制。