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大肠杆菌lexA基因的核苷酸序列。

Nucleotide sequence of the lexA gene of E. coli.

作者信息

Horii T, Ogawa T, Ogawa H

出版信息

Cell. 1981 Mar;23(3):689-97. doi: 10.1016/0092-8674(81)90432-3.

DOI:10.1016/0092-8674(81)90432-3
PMID:7013987
Abstract

Using a cloned fragment containing the lexA gene of E. coli, the entire nucleotide sequence of the lexA gene has been determined. The probable coding region of the lexA gene contains 606 nucleotide residues and encodes a single protein of 202 amino acids. The initiation site of in vitro transcription of the lexA messenger RNA has been determined by analysis of the 5' nucleotide sequence. Comparison of the DNA sequence of the promoter region of the lexA gene with that of the recA gene reveals the presence of sequences that are common to both. There is some similarity between the amino acid sequences of the lexA and the lambda repressor proteins.

摘要

利用包含大肠杆菌lexA基因的克隆片段,已确定lexA基因的完整核苷酸序列。lexA基因的可能编码区包含606个核苷酸残基,编码一种由202个氨基酸组成的单一蛋白质。通过对5'核苷酸序列的分析,已确定lexA信使核糖核酸的体外转录起始位点。将lexA基因启动子区域的DNA序列与recA基因的DNA序列进行比较,发现两者存在共同序列。lexA蛋白与λ阻遏蛋白的氨基酸序列之间存在一些相似性。

相似文献

1
Nucleotide sequence of the lexA gene of E. coli.大肠杆菌lexA基因的核苷酸序列。
Cell. 1981 Mar;23(3):689-97. doi: 10.1016/0092-8674(81)90432-3.
2
Transcription of the uvrD gene of Escherichia coli is controlled by the lexA repressor and by attenuation.大肠杆菌uvrD基因的转录受lexA阻遏物和衰减作用的控制。
Nucleic Acids Res. 1983 Dec 20;11(24):8625-40. doi: 10.1093/nar/11.24.8625.
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Isolation and characterization of noncleavable (Ind-) mutants of the LexA repressor of Escherichia coli K-12.大肠杆菌K-12 LexA阻遏物不可裂解(Ind-)突变体的分离与鉴定。
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Regulation of SOS functions: purification of E. coli LexA protein and determination of its specific site cleaved by the RecA protein.
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Nucleotide sequence of the lexA gene of Escherichia coli K-12.大肠杆菌K-12的lexA基因的核苷酸序列。
Nucleic Acids Res. 1981 Aug 25;9(16):4149-61. doi: 10.1093/nar/9.16.4149.
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Nucleotide sequence and LexA regulation of the Escherichia coli recN gene.大肠杆菌recN基因的核苷酸序列及LexA调控
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Cloned truncated recA genes in E. coli. I. Effect on radiosensitivity and recA+ dependent processes.大肠杆菌中克隆的截短recA基因。I. 对辐射敏感性和recA+依赖过程的影响。
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Plasmid vectors designed for high-efficiency expression controlled by the portable recA promoter-operator of Escherichia coli.设计用于由大肠杆菌便携式recA启动子-操纵子控制的高效表达的质粒载体。
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Organization of the lexA gene of Escherichia coli and nucleotide sequence of the regulatory region.
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