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构建ColE1 RNA1突变体并分析其体内功能。

Construction of Co1E1 RNA1 mutants and analysis of their function in vivo.

作者信息

Polisky B, Tamm J, Fitzwater T

出版信息

Basic Life Sci. 1985;30:321-33. doi: 10.1007/978-1-4613-2447-8_25.

Abstract

We have carried out experiments designed to investigate the relationship between structure and function for the Co1E1 RNA1 species. RNA1 is a small RNA (108 nucleotides) that has been implicated in copy number control of the multicopy plasmid Co1E1. In vitro, RNA1 inhibits the processing of the primer precursor required for initiation of DNA replication. The RNA1 gene is entirely complementary to the 5'-terminal region of the primer. We have functionally separated these 2 RNA species by cloning the RNA1 gene downstream from the S. marcescens trp promoter. When cloned in a Co1E1-compatible plasmid, a trp-RNA1 fusion has been shown to mediate Co1E1-type incompatibility in vivo. The construction scheme described here also generates mutant RNA1 species with altered sequences at the 5' terminus of RNA1 which have been assayed for function in vivo. These experiments have indicated that sequences at the 5' terminus play a critical role in RNA1 function.

摘要

我们开展了旨在研究ColE1 RNA1物种结构与功能关系的实验。RNA1是一种小RNA(108个核苷酸),与多拷贝质粒ColE1的拷贝数控制有关。在体外,RNA1抑制DNA复制起始所需引物前体的加工。RNA1基因与引物的5'末端区域完全互补。我们通过将RNA1基因克隆到粘质沙雷氏菌trp启动子下游,从功能上分离了这两种RNA物种。当克隆到与ColE1兼容的质粒中时,trp-RNA1融合体已被证明在体内介导ColE1型不相容性。这里描述的构建方案还产生了在RNA1的5'末端具有改变序列的突变RNA1物种,并已在体内对其功能进行了测定。这些实验表明,5'末端的序列在RNA1功能中起关键作用。

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