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大肠杆菌recR基因座的序列与表达

Sequence and expression of the Escherichia coli recR locus.

作者信息

Yeung T, Mullin D A, Chen K S, Craig E A, Bardwell J C, Walker J R

机构信息

Department of Microbiology, University of Texas, Austin 78712.

出版信息

J Bacteriol. 1990 Oct;172(10):6042-7. doi: 10.1128/jb.172.10.6042-6047.1990.

Abstract

The Escherichia coli RecR protein participates in a recombinational DNA repair process. Its gene is located in a region of chromosome that extends from 502 to 509 kilobases on the physical map and that contains apt, dnaX, orf12-recR, htpG, and adk. Most, if not all, of these are involved in nucleic acid metabolism. The orf12-recR reading frames consist of 935 base pairs and overlap by one nucleotide, with the 3' A of the orf12 termination codon forming the 5' nucleotide of the recR initiation codon. The orf12-recR promoter was located upstream of orf12 by sequence analysis, promoter cloning, and S1 nuclease protection analysis. The start point of transcription was determined by primer extension. The transcript 5' end contained a long, apparently untranslated region of 199 nucleotides. Absence of a detectable promoter specific for recR and the overlap of the orf12 and recR reading frames suggest that translation of recR is coupled to that of orf12. By maxicell analysis, it was determined that both orf12 and recR are translated.

摘要

大肠杆菌RecR蛋白参与重组DNA修复过程。其基因位于染色体上一个区域,在物理图谱上该区域从502千碱基延伸至509千碱基,其中包含apt、dnaX、orf12 - recR、htpG和adk。这些基因中大部分(如果不是全部的话)都参与核酸代谢。orf12 - recR阅读框由935个碱基对组成,且有一个核苷酸重叠,orf12终止密码子的3'A构成recR起始密码子的5'核苷酸。通过序列分析、启动子克隆和S1核酸酶保护分析,确定orf12 - recR启动子位于orf12上游。转录起始点通过引物延伸法确定。转录本的5'端包含一个199个核苷酸的长的、明显未翻译的区域。未检测到recR特异性启动子以及orf12和recR阅读框的重叠表明recR的翻译与orf12的翻译相关联。通过大细胞分析确定orf12和recR都能被翻译。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e290/526927/514a3f95a31e/jbacter00164-0536-a.jpg

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