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串联插入序列二聚体在IS911转座中的作用。

The role of tandem IS dimers in IS911 transposition.

作者信息

Turlan C, Ton-Hoang B, Chandler M

机构信息

Laboratoire de Microbiologie et Génétique Moléculaires, CNRS UPR9007, 118 Rte de Narbonne, F31062 Toulouse Cedex, France.

出版信息

Mol Microbiol. 2000 Mar;35(6):1312-25. doi: 10.1046/j.1365-2958.2000.01800.x.

DOI:10.1046/j.1365-2958.2000.01800.x
PMID:10760133
Abstract

Using a combined in vivo and in vitro approach, we demonstrated that the transposition products generated by IS911 from a dimeric donor plasmid are different from those generated from a plasmid monomer. When carried by a monomeric plasmid donor, free IS911 transposon circles are generated by intra-IS recombination in which one IS end undergoes attack by the other. These represent transposition intermediates that undergo integration using the abutted left (IRL) and right (IRR) ends of the element, the active IRR-IRL junction, to generate simple insertions. In contrast, the two IS911 copies carried by a dimeric donor plasmid not only underwent intra-IS recombination to generate transposon circles but additionally participated in inter-IS recombination. This also creates an active IRR-IRL junction by generating a head-to-tail IS tandem dimer ([IS]2) in which one of the original plasmid backbone copies is eliminated in the formation of the junction. Both transposon circles and IS tandem dimers are generated from an intermediate in which two transposon ends are retained by a single strand joint to generate a figure 8 molecule. Inter-IS figure 8 molecules generated in vitro could be resolved into the [IS]2 form following introduction into a host strain by transformation. Resolution did not require IS911 transposase. The [IS]2 structure was stable in the absence of transposase but was highly unstable in its presence both in vivo and in vitro. Previous studies had demonstrated that the IRR-IRL junction promotes efficient intermolecular integration and intramolecular deletions both in vivo and in vitro. Integration of the [IS]2 derivative would result in a product that resembles a co-integrate structure. It is also shown here that the IRR-IRL junction of the [IS]2 form and derivative structures can specifically target one of the other ends in an intramolecular transposition reaction to generate transposon circles in vitro. These results not only demonstrate that IS911 (and presumably other members of the IS3 family) is capable of generating a range of transposition products, it also provides a mechanistic framework which explains the formation and activity of such structures previously observed for several other unrelated IS elements. This behaviour is probably characteristic of a large number of IS elements.

摘要

通过体内和体外相结合的方法,我们证明了由IS911从二聚体供体质粒产生的转座产物与从质粒单体产生的转座产物不同。当由单体性质粒供体携带时,游离的IS911转座子环通过IS内部重组产生,其中一个IS末端受到另一个末端的攻击。这些代表转座中间体,它们利用元件相邻的左(IRL)端和右(IRR)端(活性IRR-IRL连接)进行整合,以产生简单插入。相比之下,由二聚体供体质粒携带的两个IS911拷贝不仅进行IS内部重组以产生转座子环,还参与IS间重组。这也通过产生头对头的IS串联二聚体([IS]2)形成活性IRR-IRL连接,其中在连接形成过程中一个原始质粒骨架拷贝被消除。转座子环和IS串联二聚体均由一个中间体产生,在该中间体中,两个转座子末端通过单链连接保留,形成一个8字形分子。体外产生的IS间8字形分子通过转化导入宿主菌株后可解析为[IS]2形式。解析不需要IS911转座酶。[IS]2结构在没有转座酶的情况下是稳定的,但在体内和体外存在转座酶时都高度不稳定。先前的研究表明,IRR-IRL连接在体内和体外均促进有效的分子间整合和分子内缺失。[IS]2衍生物的整合将产生一个类似于共整合结构的产物。本文还表明,[IS]2形式及其衍生物结构的IRR-IRL连接可在分子内转座反应中特异性靶向另一端之一,以在体外产生转座子环。这些结果不仅证明了IS911(可能还有IS3家族的其他成员)能够产生一系列转座产物,还提供了一个机制框架,解释了先前在其他几个不相关的IS元件中观察到的此类结构的形成和活性。这种行为可能是大量IS元件的特征。

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