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脊髓灰质炎病毒的病毒体和复制中间体RNA的5'-末端,蛋白质与特定核苷酸序列的共价连接。

Covalent linkage of a protein to a defined nucleotide sequence at the 5'-terminus of virion and replicative intermediate RNAs of poliovirus.

作者信息

Flanegan J B, Petterson R F, Ambros V, Hewlett N J, Baltimore D

出版信息

Proc Natl Acad Sci U S A. 1977 Mar;74(3):961-5. doi: 10.1073/pnas.74.3.961.

Abstract

The 5'-terminus of poliovirus polyribosomal RNA is pUp. A candidate for the 5'-terminus of poliovirion RNA was recovered as a compound migrating toward the cathode when 32P-labeled virion RNA was completely digested with ribonucleases T1, T2 and A and analyzed by paper ionophoresis at pH 3.5. Treatment with proteinase K reversed its direction of migration, indicating the presence of protein. Treatment with venom phosphodiesterase liberated all of the radioactivity as pUp, suggesting that poliovirion RNA has a protein-pUp 5'-terminus. Treatment of virion RNA with T1 ribonuclease alone generated a proteinase K-sensitive oligoribonucleotide. Analysis of the oligoribonucleotide using ribonucleases A and U2 showed its structure to be protein-pU-U-A-A-A-A-C-A-G. Digests of replicative intermediate RNA contained sufficient protein-pUp to suggest that this structure is at the 5'-end of most nascent poliovirus RNA molecules. We suggest that a protein-nucleotide structure acts as a primer for initiating synthesis of poliovirus RNA.

摘要

脊髓灰质炎病毒多核糖体RNA的5'端是pUp。当用核糖核酸酶T1、T2和A将32P标记的病毒体RNA完全消化并在pH 3.5条件下进行纸电泳分析时,一种脊髓灰质炎病毒体RNA 5'端的候选物作为一种向阴极迁移的复合物被回收。用蛋白酶K处理可使其迁移方向逆转,表明存在蛋白质。用蛇毒磷酸二酯酶处理可将所有放射性释放为pUp,这表明脊髓灰质炎病毒体RNA具有蛋白质-pUp 5'端。单独用T1核糖核酸酶处理病毒体RNA可产生一种对蛋白酶K敏感的寡核糖核苷酸。使用核糖核酸酶A和U2对该寡核糖核苷酸进行分析表明其结构为蛋白质-pU-U-A-A-A-A-C-A-G。复制中间体RNA的消化产物中含有足够的蛋白质-pUp,这表明该结构位于大多数新生脊髓灰质炎病毒RNA分子的5'端。我们认为蛋白质-核苷酸结构作为启动脊髓灰质炎病毒RNA合成的引物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95ba/430548/9344e546d7d7/pnas00025-0168-a.jpg

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