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体外转运RNA合成

Transfer RNA synthesis in vitro.

作者信息

Nierlich D P, Lamfrom H, Sarabhai A, Abelson J

出版信息

Proc Natl Acad Sci U S A. 1973 Jan;70(1):179-82. doi: 10.1073/pnas.70.1.179.

Abstract

During infection of Escherichia coli, bacteriophage T4 directs the synthesis of at least eight transfer RNAs and of two stable RNA species of low molecular weight, of unknown function. When T4 DNA is incubated with purified RNA polymerase and the appropriate substrates, a high molecular weight RNA is produced. This RNA, on further incubation with a supernatant fraction prepared from E. coli, is cleaved to several species of RNA. These cleaved RNAs were analyzed by gel electrophoresis and fingerprint techniques, and were found to be similar or identical to those made in vivo. The fingerprint analysis of one of these, a tRNA(Gly), is presented. The molecule made in vitro, except for the absence of modified bases, appears to be identical to the RNA made by T4-infected cells. Therefore, in this system the tRNA genes are transcribed with fidelity, the transcript is cleaved correctly, and the tRNAs are made in good yield.

摘要

在大肠杆菌感染过程中,噬菌体T4指导合成至少八种转移RNA以及两种功能未知的低分子量稳定RNA。当T4 DNA与纯化的RNA聚合酶及合适的底物一起温育时,会产生一种高分子量RNA。这种RNA在与从大肠杆菌制备的上清液部分进一步温育后,会被切割成几种RNA。通过凝胶电泳和指纹技术对这些切割后的RNA进行分析,发现它们与体内产生的RNA相似或相同。本文展示了其中一种tRNA(甘氨酸)的指纹分析。体外合成的分子,除了没有修饰碱基外,似乎与T4感染细胞产生的RNA相同。因此,在这个系统中,tRNA基因被准确转录,转录本被正确切割,并且tRNA的产量很高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a58/433210/b9ea301f20fc/pnas00064-0186-a.jpg

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