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[大肠杆菌K12中的复合转座子Tn5和Tn10:精确切除与重组]

[Composite transposons Tn5 and Tn10 in Escherichia coli K12: precise excision and recombination].

作者信息

Goryshin I Iu, Tamm S E, Lantsov V A

出版信息

Mol Gen Mikrobiol Virusol. 1987 Jun(6):17-23.

PMID:3041201
Abstract

The number of exconjugants having the transposon Tn5 excised precisely during the crosses of the Escherichia coli proA::Tn5 donor with the recipients F- rec+ or F- recA441 (tif) was 20-30 times higher for the crosses involving the latter recipient. The high recombinogenic activity is characteristic of the tif recipient. Precise excision from a tandem duplication is more efficient than from nonduplicated region of the genome. It is four orders higher, if a transposon is localized in an arm of a duplication. The effect is recA-dependent. The presented data permit us to suggest the participation of RecA protein (its synaptic function) in the formation of the intermediate "stem-loop" structure. The latter is predicted by the three mechanisms of transposon excision: "slippage", "correctional" and "recombinational". The latter two mechanisms were formulated in the paper. The experimental proof of the postexcision transposition presented in the paper, is a good support to the version of "recombinational" excision.

摘要

在大肠杆菌proA::Tn5供体与受体F- rec+或F- recA441(tif)杂交过程中,精确切除转座子Tn5的接合后体数量,对于涉及后一种受体的杂交而言,比涉及前一种受体的杂交高20 - 30倍。高重组活性是tif受体的特征。从串联重复序列中精确切除比从基因组的非重复区域更有效。如果转座子位于重复序列的一个臂中,效率要高四个数量级。这种效应是recA依赖性的。所呈现的数据使我们能够推测RecA蛋白(其突触功能)参与了中间“茎环”结构的形成。后者是由转座子切除的三种机制预测的:“滑动”、“校正”和“重组”。后两种机制是在本文中提出的。本文中给出的切除后转座的实验证据,有力支持了“重组”切除的观点。

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