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大肠杆菌K-12的ruv区域的核苷酸测序揭示了一个由LexA调控的操纵子,该操纵子编码两个基因。

Nucleotide sequencing of the ruv region of Escherichia coli K-12 reveals a LexA regulated operon encoding two genes.

作者信息

Benson F E, Illing G T, Sharples G J, Lloyd R G

机构信息

Department of Genetics, Queen's Medical Centre, University of Nottingham, UK.

出版信息

Nucleic Acids Res. 1988 Feb 25;16(4):1541-9. doi: 10.1093/nar/16.4.1541.

DOI:10.1093/nar/16.4.1541
PMID:3279394
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC336333/
Abstract

The nucleotide sequence of a 2505 bp region of the Escherichia coli chromosome containing the LexA regulated ruv gene has been determined. A sequence of 1631 bp encoding two non-overlapping open reading frames that constitute a single operon and which specify polypeptides with predicted molecular weights of 22172 daltons and 37177 daltons respectively, was identified as the most probable sequence for ruv. Each of the two open reading frames, designated ruvA and ruvB, is preceded by a reasonable Shine-Dalgarno sequence. Two 16 bp sequences (SOS boxes) that match the consensus sequence for binding LexA protein are located 5' to ruvA in a region that provides a possible single promoter for expression of both ruvA and ruvB, with the second SOS box overlapping the putative -35 region. A possible transcriptional terminator is located 137 bp downstream of ruvB. The amino acid sequence predicted for RuvB contains a region that matches a highly conserved sequence found in several DNA repair and recombination proteins that bind ATP.

摘要

已确定大肠杆菌染色体中包含受LexA调控的ruv基因的2505 bp区域的核苷酸序列。一段1631 bp的序列编码两个不重叠的开放阅读框,它们构成一个单一操纵子,并分别指定预测分子量为22172道尔顿和37177道尔顿的多肽,该序列被确定为ruv最可能的序列。两个开放阅读框分别命名为ruvA和ruvB,每个阅读框之前都有一个合理的Shine-Dalgarno序列。两个与LexA蛋白结合的共有序列匹配的16 bp序列(SOS框)位于ruvA的5'端,该区域可能为ruvA和ruvB的表达提供单一启动子,第二个SOS框与推定的-35区域重叠。一个可能的转录终止子位于ruvB下游137 bp处。预测的RuvB氨基酸序列包含一个与几种结合ATP的DNA修复和重组蛋白中发现的高度保守序列相匹配的区域。

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1
Nucleotide sequencing of the ruv region of Escherichia coli K-12 reveals a LexA regulated operon encoding two genes.大肠杆菌K-12的ruv区域的核苷酸测序揭示了一个由LexA调控的操纵子,该操纵子编码两个基因。
Nucleic Acids Res. 1988 Feb 25;16(4):1541-9. doi: 10.1093/nar/16.4.1541.
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本文引用的文献

1
Damage to DNA induces expression of the ruv gene of Escherichia coli.DNA损伤会诱导大肠杆菌ruv基因的表达。
Mol Gen Genet. 1982;185(2):352-5. doi: 10.1007/BF00330811.
2
Mechanism of action of the lexA gene product.lexA基因产物的作用机制。
Proc Natl Acad Sci U S A. 1981 Jul;78(7):4204-8. doi: 10.1073/pnas.78.7.4204.
3
Purified lexA protein is a repressor of the recA and lexA genes.纯化的LexA蛋白是recA和LexA基因的阻遏物。
Proc Natl Acad Sci U S A. 1981 Jul;78(7):4199-203. doi: 10.1073/pnas.78.7.4199.
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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.
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Sequences of the recA gene and protein.recA基因和蛋白质的序列。
Proc Natl Acad Sci U S A. 1980 May;77(5):2611-5. doi: 10.1073/pnas.77.5.2611.
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Genetic analysis and regulation of inducible recombination in Escherichia coli K-12.大肠杆菌K-12中诱导重组的遗传分析与调控
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The nucleotide sequence of the uvrD gene of E. coli.大肠杆菌uvrD基因的核苷酸序列。
Nucleic Acids Res. 1984 Jul 25;12(14):5789-99. doi: 10.1093/nar/12.14.5789.
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Effect of ruv mutations on recombination and DNA repair in Escherichia coli K12.鲁夫突变对大肠杆菌K12中重组和DNA修复的影响。
Mol Gen Genet. 1984;194(1-2):303-9. doi: 10.1007/BF00383532.
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Mutagenesis and inducible responses to deoxyribonucleic acid damage in Escherichia coli.大肠杆菌中的诱变作用及对脱氧核糖核酸损伤的诱导反应
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Recognition of messenger RNA during translational initiation in Escherichia coli.大肠杆菌翻译起始过程中信使核糖核酸的识别
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