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泰勒氏鼠脑脊髓炎病毒5'非翻译区介导的不依赖帽结构的翻译

Cap-independent translation by the 5' untranslated region of Theiler's murine encephalomyelitis virus.

作者信息

Bandyopadhyay P K, Wang C, Lipton H L

机构信息

Department of Neurology, University of Colorado Health Sciences Center, Denver 80262.

出版信息

J Virol. 1992 Nov;66(11):6249-56. doi: 10.1128/JVI.66.11.6249-6256.1992.

Abstract

The RNA genome of Theiler's murine encephalomyelitis viruses, a picornavirus belonging to the genus Cardiovirus, is translated in infected cells to a polyprotein. Unlike cellular messages, the 5' end of the RNA is not capped, and the untranslated region (UTR) is quite long (1,064 nucleotides in size). In poliovirus and encephalomyocarditis virus, the 5'UTR is thought to mediate cap-independent translation. We report here experiments to determine the role of the Theiler's murine encephalomyelitis virus 5'UTR in translation. Recombinant DNAs were constructed that were transcribed into bicistronic mRNAs encoding 5' chloramphenicol acetyltransferase intercistronic sequences linked to luciferase and a poly(A) 3' tail. The sequences of the 5'UTR, either complete or with sequential 5' deletions, were inserted into the intercistronic region. Bicistronic RNA transcripts were translated in a rabbit reticulocyte lysate or used to transfect BHK-21 cells, and chloramphenicol acetyltransferase and luciferase synthesis was quantitated. The results strongly suggest that the Theiler's virus 5'UTR promotes cap-independent translation and that the 5' boundary of the relevant signals resides 3' to nucleotide 500. Monocistronic mRNAs were synthesized by using an expression vector in which the 5'UTR containing deletions at the 3' terminus was inserted 5' to the coding sequences for luciferase. Analysis of luciferase translation in a rabbit reticulocyte lysate suggests that the 3' end of the translation initiation signal lies between nucleotides 1043 and 1053.

摘要

泰勒氏鼠脑脊髓炎病毒属于心病毒属的微小核糖核酸病毒,其RNA基因组在受感染细胞中被翻译为一种多聚蛋白。与细胞信使不同,该RNA的5'端没有帽结构,且非翻译区(UTR)相当长(大小为1064个核苷酸)。在脊髓灰质炎病毒和脑心肌炎病毒中,5'UTR被认为介导不依赖帽结构的翻译。我们在此报告了一些实验,以确定泰勒氏鼠脑脊髓炎病毒5'UTR在翻译中的作用。构建了重组DNA,将其转录为双顺反子mRNA,该mRNA编码与荧光素酶和聚腺苷酸3'尾相连的5'氯霉素乙酰转移酶顺反子间序列。将完整的或带有连续5'端缺失的5'UTR序列插入顺反子间区域。双顺反子RNA转录本在兔网织红细胞裂解物中进行翻译,或用于转染BHK - 21细胞,并对氯霉素乙酰转移酶和荧光素酶的合成进行定量分析。结果强烈表明,泰勒氏病毒5'UTR促进不依赖帽结构的翻译,且相关信号的5'边界位于核苷酸500的3'端。通过使用一种表达载体合成单顺反子mRNA,其中在3'末端含有缺失的5'UTR被插入到荧光素酶编码序列的5'端。对兔网织红细胞裂解物中荧光素酶翻译的分析表明,翻译起始信号的3'端位于核苷酸1043和1053之间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6cad/240115/aaebe913388f/jvirol00042-0021-a.jpg

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