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TnpI 重组酶:Tn5401 中 TnpI 结合和位点特异性重组所需位点的鉴定。

TnpI recombinase: identification of sites within Tn5401 required for TnpI binding and site-specific recombination.

作者信息

Baum J A

机构信息

Ecogen Inc., Langhorne, Pennsylvania 19047-3023, USA.

出版信息

J Bacteriol. 1995 Jul;177(14):4036-42. doi: 10.1128/jb.177.14.4036-4042.1995.

Abstract

The Bacillus thuringiensis class II transposon Tn5401 encodes a recombinase protein, TnpI, that mediates the resolution of cointegrate molecules generated as intermediates during Tn5401 transposition by the TnpA transposase. This recombination event requires a specific target site, or internal resolution site, at which TnpI binds and catalyzes the exchange of DNA strands. Gel mobility shift assays and DNase I footprinting analyses were used to localize the TnpI binding region to the sequence extending from nucleotides 637 to 747 of Tn5401. Deletions within this region blocked TnpI-mediated recombination in vivo. The 12-bp sequence ATGTCC RCTAAY, present in four copies within the TnpI binding region, is proposed to be the recognition sequence for TnpI binding. TnpI also binds to a single copy of this sequence located within the 53-bp terminal inverted repeats of Tn5401. The unique juxtaposition of recombinase and transposase binding sites at the terminal inverted repeats of Tn5401 suggests that TnpI regulates the binding and/or catalytic activity of TnpA transposase.

摘要

苏云金芽孢杆菌II类转座子Tn5401编码一种重组酶蛋白TnpI,它介导由TnpA转座酶在Tn5401转座过程中作为中间体产生的共整合分子的拆分。这种重组事件需要一个特定的靶位点,即内部拆分位点,TnpI在该位点结合并催化DNA链的交换。凝胶迁移率变动分析和DNase I足迹分析被用于将TnpI结合区域定位到Tn5401从核苷酸637延伸至747的序列。该区域内的缺失在体内阻断了TnpI介导的重组。在TnpI结合区域内以四个拷贝存在的12碱基序列ATGTCC RCTAAY被认为是TnpI结合的识别序列。TnpI也结合位于Tn5401 53碱基对末端反向重复序列内的该序列的单拷贝。TnpI和转座酶结合位点在Tn5401末端反向重复序列处的独特并列表明TnpI调节TnpA转座酶的结合和/或催化活性。

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