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Tn5插入特异性不受靶DNA中IS50末端序列的影响。

Tn5 insertion specificity is not influenced by IS50 end sequences in target DNA.

作者信息

Lodge J K, Weston-Hafer K, Berg D E

机构信息

Department of Molecular Microbiology, Washington University Medical School, St. Louis, MO 63110.

出版信息

Mol Gen Genet. 1991 Aug;228(1-2):312-5. doi: 10.1007/BF00282482.

Abstract

The bacterial transposon Tn5 inserts into dozens of sites in a gene, some of which are used preferentially (hotspots). Features of certain sites and precedents provided by several other transposons had suggested that sequences in target DNA corresponding to the ends of Tn5 or of its component IS50 elements might facilitate transposition to these sites. We tested this possibility using derivatives of plasmid pBR322 carrying IS50 I or O end sequences. Tn5 inserted frequently into an IS50 I end at the major hotspot in pBR322, but not into either an I end or an O end 230 bp away from this hotspot. Adenine (dam) methylation at GATC sequences in the I end segment interferes with its use as the end of a transposon, but a dam- mutation did not affect Tn5 insertion relative to an I end sequence in target DNA. These results support models in which the ability of Tn5 to find its preferred sites depends on several features of DNA sequence and conformation, and in which target selection is distinct from recognition of the element ends during transposition.

摘要

细菌转座子Tn5可插入基因中的数十个位点,其中一些位点被优先使用(热点)。某些位点的特征以及其他几种转座子提供的先例表明,与Tn5或其组成元件IS50元件末端相对应的靶DNA序列可能有助于转座至这些位点。我们使用携带IS50 I或O末端序列的质粒pBR322衍生物来测试这种可能性。Tn5频繁插入pBR322主要热点处的IS50 I末端,但不插入距该热点230 bp处的I末端或O末端。I末端片段中GATC序列处的腺嘌呤(dam)甲基化会干扰其作为转座子末端的使用,但dam突变相对于靶DNA中的I末端序列并不影响Tn5插入。这些结果支持了这样的模型,即Tn5找到其偏好位点的能力取决于DNA序列和构象的几个特征,并且在该模型中,靶标选择与转座过程中元件末端的识别是不同的。

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