{"title":"RNA Determinants of Picornavirus Cap-Independent Translation Initiation","authors":"Stacey R. Stewart, Bert L. Semler","doi":"10.1006/smvy.1997.0127","DOIUrl":null,"url":null,"abstract":"<div><p>Internal ribosome entry was first identified as a translation mechanism used by picornavirus RNAs and has since been shown to be used by other viral and eukaryotic RNAs as well. Cap-independent translation is dependent on complex interactions between eukaryotic factors and picornavirus RNAs in the cytoplasm of the host cell. Determinants for ribosome association lie in the 5′-noncoding region of viral RNAs and consist of several levels of structure including primary sequence, stem-loop structures, and perhaps tertiary folding. Host cell factors involved in this process include some canonical translation factors and additional RNA-binding proteins, of which only a few have been identified. Recent advances in reconstituting translation<em>in vitro</em>have provided a useful means for deciphering the roles of protein and RNA factors and the steps leading to end-independent protein synthesis.</p></div>","PeriodicalId":92955,"journal":{"name":"Seminars in virology","volume":"8 3","pages":"Pages 242-255"},"PeriodicalIF":0.0000,"publicationDate":"1997-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1006/smvy.1997.0127","citationCount":"63","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Seminars in virology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S104457739790127X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 63
Abstract
Internal ribosome entry was first identified as a translation mechanism used by picornavirus RNAs and has since been shown to be used by other viral and eukaryotic RNAs as well. Cap-independent translation is dependent on complex interactions between eukaryotic factors and picornavirus RNAs in the cytoplasm of the host cell. Determinants for ribosome association lie in the 5′-noncoding region of viral RNAs and consist of several levels of structure including primary sequence, stem-loop structures, and perhaps tertiary folding. Host cell factors involved in this process include some canonical translation factors and additional RNA-binding proteins, of which only a few have been identified. Recent advances in reconstituting translationin vitrohave provided a useful means for deciphering the roles of protein and RNA factors and the steps leading to end-independent protein synthesis.