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pMB1 拷贝数突变体的表征与互补:RNA I 基因剂量对质粒拷贝数和不相容性的影响

Characterization and complementation of pMB1 copy number mutant: effect of RNA I gene dosage on plasmid copy number and incompatibility.

作者信息

Moser D R, Campbell J L

出版信息

J Bacteriol. 1983 May;154(2):809-18. doi: 10.1128/jb.154.2.809-818.1983.

Abstract

A 16-base-pair insertion has been identified as the mutation responsible for the high-copy-number phenotype of the plasmid copy number mutant pFH118. The mutation is located near the plasmid origin of replication in a region of the genome that encodes two overlapping RNA transcripts. One of these transcripts, RNA I, acts as a negative regulator of plasmid replication. The second transcript is the precursor to the primer for the initiation of DNA synthesis. We demonstrate through complementation that the pFH118 DNA overproduction phenotype is a consequence of the reduced effectiveness of the mutant RNA I at inhibiting plasmid replication and not a consequence of an altered target site on the primer precursor. In addition, a series of plasmids containing multiple RNA I-coding genes was constructed for investigating the effects of RNA I gene dosage on plasmid copy number and incompatibility. The results of this study strongly support the inhibitor dilution model of plasmid copy control with RNA I as the plasmid-specified inhibitor responsible for both copy number control and incompatibility.

摘要

一个16个碱基对的插入已被确定为导致质粒拷贝数突变体pFH118高拷贝数表型的突变。该突变位于基因组中编码两个重叠RNA转录本的区域内,靠近质粒复制起点。这些转录本之一,即RNA I,作为质粒复制的负调控因子。第二个转录本是DNA合成起始引物的前体。我们通过互补实验证明,pFH118 DNA过量产生表型是突变型RNA I抑制质粒复制有效性降低的结果,而不是引物前体上靶位点改变的结果。此外,构建了一系列含有多个RNA I编码基因的质粒,以研究RNA I基因剂量对质粒拷贝数和不相容性的影响。本研究结果有力地支持了以RNA I作为负责拷贝数控制和不相容性的质粒特异性抑制剂的质粒拷贝控制抑制剂稀释模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed5/217533/5996c263f274/jbacter00246-0284-a.jpg

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