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来自噬菌体P1的一个克隆DNA片段增强了IS2插入。

A cloned DNA fragment from bacteriophage P1 enhances IS2 insertion.

作者信息

Sengstag C, Arber W

出版信息

Mol Gen Genet. 1987 Feb;206(2):344-51. doi: 10.1007/BF00333593.

DOI:10.1007/BF00333593
PMID:3035338
Abstract

A 1.75 kb DNA segment of the bacteriophage P1 genome is known to serve as a preferred target for IS2 insertions. The presence of this fragment in a plasmid expressing the galK gene dramatically increases the proportion of IS2 insertions among spontaneous galK- mutants. Subfragments from two different parts of the 1.75 kb segment independently stimulate IS2 insertion, while another subfragment does not. In the plasmids studied IS2 elements not only insert into the cloned P1 fragment but also into parts of the galK gene with similar probability and mostly in one orientation. Many insertion sites are unique but several specific sites within the preferred target are repeatedly used for IS2 integration. The experimental data are compatible with a proposed cooperative mechanism, according to which more than one attracting sequence on the same plasmid might significantly enhance the probability of a particular target region to attract IS2.

摘要

已知噬菌体P1基因组的一段1.75 kb DNA片段是IS2插入的首选靶点。在表达galK基因的质粒中存在该片段会显著增加自发galK -突变体中IS2插入的比例。来自1.75 kb片段两个不同部分的亚片段可独立刺激IS2插入,而另一个亚片段则不能。在所研究的质粒中,IS2元件不仅插入到克隆的P1片段中,而且以相似的概率插入到galK基因的部分区域,且大多为一个方向。许多插入位点是独特的,但首选靶点内的几个特定位点会被反复用于IS2整合。实验数据与提出的协同机制相符,根据该机制,同一质粒上的多个吸引序列可能会显著提高特定靶区域吸引IS2的概率。

相似文献

1
A cloned DNA fragment from bacteriophage P1 enhances IS2 insertion.来自噬菌体P1的一个克隆DNA片段增强了IS2插入。
Mol Gen Genet. 1987 Feb;206(2):344-51. doi: 10.1007/BF00333593.
2
The sequence of the bacteriophage P1 genome region serving as hot target for IS2 insertion.作为IS2插入热点靶点的噬菌体P1基因组区域的序列。
EMBO J. 1983;2(10):1777-81. doi: 10.1002/j.1460-2075.1983.tb01657.x.
3
IS2 insertion is a major cause of spontaneous mutagenesis of the bacteriophage P1: non-random distribution of target sites.IS2插入是噬菌体P1自发诱变的主要原因:靶位点的非随机分布。
EMBO J. 1983;2(1):67-71. doi: 10.1002/j.1460-2075.1983.tb01382.x.
4
Transcription initiation sites within an IS2 insertion in a Gal-constitutive mutant of Escherichia coli.大肠杆菌半乳糖组成型突变体中IS2插入片段内的转录起始位点。
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Orientation and sequence analysis of right ends and target sites of bacteriophage mu and D108 insertions in the plasmid pSC101.噬菌体μ和D108在质粒pSC101中的右端及靶位点的定位与序列分析
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Integration specificity of an artificial kanamycin transposon constructed by the in vitro insertion of an internal Tn5 fragment into IS2.通过将Tn5内部片段体外插入IS2构建的人工卡那霉素转座子的整合特异性。
Mol Gen Genet. 1981;183(1):45-50. doi: 10.1007/BF00270136.
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引用本文的文献

1
Insertion sequences.插入序列
Microbiol Mol Biol Rev. 1998 Sep;62(3):725-74. doi: 10.1128/MMBR.62.3.725-774.1998.
2
Isolation, characterization and transposition of an (IS2)2 intermediate.一种(IS2)2中间体的分离、特性鉴定及转座
Mol Gen Genet. 1996 Jun 12;251(3):281-9. doi: 10.1007/BF02172518.
3
Transposition of IS2 into the hemB gene of Escherichia coli K-12.IS2转座至大肠杆菌K-12的hemB基因中。

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作为IS2插入热点靶点的噬菌体P1基因组区域的序列。
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Improved plasmid vectors with a thermoinducible expression and temperature-regulated runaway replication.具有热诱导表达和温度调节失控复制功能的改良质粒载体。
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Integration specificity of an artificial kanamycin transposon constructed by the in vitro insertion of an internal Tn5 fragment into IS2.通过将Tn5内部片段体外插入IS2构建的人工卡那霉素转座子的整合特异性。
Mol Gen Genet. 1981;183(1):45-50. doi: 10.1007/BF00270136.
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Studies on transposition mechanisms and specificity of IS4.IS4转座机制及特异性的研究。
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