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肠杆菌科中具有异常整合靶位的 IIC 内含子。

Group IIC intron with an unusual target of integration in Enterobacter cloacae.

机构信息

Service de Bactériologie-Virologie, INSERM U914 Emerging Resistance to Antibiotics, Assistance Publique/Hôpital de Paris, and Université Paris-Sud, Hôpital de Bicêtre, K-Bicêtre, France.

出版信息

J Bacteriol. 2012 Jan;194(1):150-60. doi: 10.1128/JB.05786-11. Epub 2011 Oct 21.

Abstract

A potential role of group IIC-attC introns in integron gene cassette formation, that is, the way in which they could provide the attC sequence essential for recombination, has been proposed. Group IIC introns usually target the attC site of gene cassettes and more specifically their inverse core. Here we characterized a novel group IIC intron targeting the core site of the aadA1 gene cassette attC site (aadA1-qacEΔ1 gene cassette junction) from enterobacterial isolates. Intron mobility (retrohoming) was analyzed using a two-plasmid assay performed in Escherichia coli. Intron mobility assays confirmed the mobilization-integration of the group II intron into the core site of the aadA2, bla(VIM-2), bla(CARB-2), aac(6')-Ib, dfrXVb, arr2, cmlA4, and aadB gene cassettes but not into the attI site. This mobility was dependent on maturase activity. Reverse transcriptase PCR showed that this intron was transcriptionally active, and an intermediate circular form was detected by inverse PCR. This element was linked to the bla(VEB-1) extended-spectrum β-lactamase gene in a high number of enterobacterial isolates. A phylogenetic tree showed that the identified element was located in a branch separate from group IIC-attC introns, being an IIC intron possessing the ability to integrate using the core site of the attC sites as target.

摘要

已经提出了 IIC 组内含子在整合子基因盒形成中的潜在作用,即它们提供重组所必需的 attC 序列的方式。IIC 组内含子通常靶向基因盒的 attC 位点,更具体地说是靶向其反向核心。在这里,我们从肠杆菌分离物中鉴定了一种新型靶向 aadA1 基因盒 attC 位点核心位点(aadA1-qacEΔ1 基因盒连接点)的 IIC 组内含子。使用在大肠杆菌中进行的两质粒测定分析了内含子移动性( retrohoming )。内含子移动性测定证实了该 IIC 内含子向 aadA2、bla(VIM-2)、bla(CARB-2)、aac(6')-Ib、dfrXVb、arr2、cmlA4 和 aadB 基因盒的核心位点的移动-整合,但不能整合到 attI 位点。这种移动性依赖于成熟酶活性。逆转录 PCR 显示该内含子具有转录活性,并通过反向 PCR 检测到中间环状形式。该元件与 bla(VEB-1) 超广谱β-内酰胺酶基因在大量肠杆菌分离物中相关。系统发育树表明,鉴定出的元件位于与 IIC-attC 内含子分离的分支上,是一种具有利用 attC 位点核心作为靶标进行整合能力的 IIC 内含子。

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本文引用的文献

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The S.ma.I2 class C group II intron inserts at integron attC sites.S.ma.I2 C类II组内含子插入到整合子attC位点。
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