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1
DNA sequence analysis of five genes; tnsA, B, C, D and E, required for Tn7 transposition.Tn7转座所需的五个基因tnsA、B、C、D和E的DNA序列分析。
Nucleic Acids Res. 1990 Feb 25;18(4):901-11. doi: 10.1093/nar/18.4.901.
2
Identification of transposition proteins encoded by the bacterial transposon Tn7.细菌转座子Tn7编码的转座蛋白的鉴定
Gene. 1991 Jul 31;104(1):125-31. doi: 10.1016/0378-1119(91)90478-t.
3
Analysis of Tn7 transposition.Tn7转座分析。
Mol Gen Genet. 1986 Dec;205(3):550-6. doi: 10.1007/BF00338097.
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Tn7 transposition: two transposition pathways directed by five Tn7-encoded genes.Tn7转座:由五个Tn7编码基因指导的两条转座途径。
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Formation of a nucleoprotein complex containing Tn7 and its target DNA regulates transposition initiation.包含Tn7及其靶DNA的核蛋白复合物的形成调节转座起始。
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7
A minimal system for Tn7 transposition: the transposon-encoded proteins TnsA and TnsB can execute DNA breakage and joining reactions that generate circularized Tn7 species.Tn7转座的最小系统:转座子编码的蛋白质TnsA和TnsB可执行DNA断裂和连接反应,从而产生环化的Tn7分子。
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Tn7.Tn7.
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A Tn7-like transposon is present in the glmUS region of the obligately chemoautolithotrophic bacterium Thiobacillus ferrooxidans.一种类Tn7转座子存在于专性化能自养细菌氧化亚铁硫杆菌的glmUS区域。
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DNA damage differentially activates regional chromosomal loci for Tn7 transposition in Escherichia coli.DNA损伤以不同方式激活大肠杆菌中用于Tn7转座的区域染色体位点。
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9
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10
Tn7 recognizes transposition target structures associated with DNA replication using the DNA-binding protein TnsE.Tn7利用DNA结合蛋白TnsE识别与DNA复制相关的转座靶结构。
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本文引用的文献

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Gin-mediated site-specific recombination in bacteriophage Mu DNA: overproduction of the protein and inversion in vitro.噬菌体 Mu DNA 的金介导的位点特异性重组:蛋白质的过表达和体外反转。
EMBO J. 1984 Oct;3(10):2415-21. doi: 10.1002/j.1460-2075.1984.tb02148.x.
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Homology among DNA-binding proteins suggests use of a conserved super-secondary structure.DNA结合蛋白之间的同源性表明存在保守的超二级结构。
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The bacteriophage P1 site-specific recombinase cin: recombination events and DNA recognition sequences.噬菌体P1位点特异性重组酶cin:重组事件与DNA识别序列
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5
Many gene-regulatory proteins appear to have a similar alpha-helical fold that binds DNA and evolved from a common precursor.许多基因调控蛋白似乎具有相似的结合DNA的α螺旋结构,并且由一个共同的前体进化而来。
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Distantly related sequences in the alpha- and beta-subunits of ATP synthase, myosin, kinases and other ATP-requiring enzymes and a common nucleotide binding fold.ATP合酶、肌球蛋白、激酶及其他需ATP的酶的α亚基和β亚基中关系较远的序列以及一个共同的核苷酸结合结构域。
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Tn7转座所需的五个基因tnsA、B、C、D和E的DNA序列分析。

DNA sequence analysis of five genes; tnsA, B, C, D and E, required for Tn7 transposition.

作者信息

Flores C, Qadri M I, Lichtenstein C

机构信息

Imperial College of Science, Technology and Medicine, Centre for Biotechnology, London, UK.

出版信息

Nucleic Acids Res. 1990 Feb 25;18(4):901-11. doi: 10.1093/nar/18.4.901.

DOI:10.1093/nar/18.4.901
PMID:2156235
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC330344/
Abstract

A region of DNA sequence of the bacterial transposon Tn7, which is required for transposition, has been determined. This DNA sequence completes an 8351 base pair (bp) region containing five long open reading frames (ORF's) that correspond to the genetically defined genes, tnsA, B, C, D and E, required for Tn7 transposition. All of the ORF's are oriented in the same direction, ie. inward from the element's right end. The genes are in a very compact arrangement with the presumed initiation codons never more than two bases beyond the preceding termination codon. Domains with similarity to the helix-turn-helix genre of Cro-like, sequence specific DNA binding sites occur within the deduced amino acid (a.a.) sequence of the TnsA, TnsB, TnsD and TnsE proteins. Translation of the tnsC ORF reveals strong homology to a consensus sequence for nucleotide binding sites as well as a region of similarity to a transcriptional activator (MalT). No striking a.a. sequence similarity to other DNA recombinases is observed. The possible roles of these proteins in Tn7 transposition is discussed in light of the analysis presented.

摘要

已确定细菌转座子Tn7转座所需的一段DNA序列区域。该DNA序列完善了一个8351碱基对(bp)的区域,该区域包含五个长开放阅读框(ORF),它们对应于Tn7转座所需的基因tnsA、B、C、D和E,这些基因已通过遗传学方法确定。所有的ORF都按相同方向排列,即从元件右端向内。这些基因排列非常紧密,推测的起始密码子与前一个终止密码子之间的距离从不超过两个碱基。在TnsA、TnsB、TnsD和TnsE蛋白的推导氨基酸(a.a.)序列中存在与Cro样螺旋-转角-螺旋类型的序列特异性DNA结合位点相似的结构域。tnsC ORF的翻译显示与核苷酸结合位点的共有序列有很强的同源性,以及与转录激活因子(MalT)相似的区域。未观察到与其他DNA重组酶有明显的氨基酸序列相似性。根据所提供的分析讨论了这些蛋白在Tn7转座中的可能作用。