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插入序列

Insertion sequences.

作者信息

Mahillon J, Chandler M

机构信息

Laboratoire de Génétique Microbienne, Université catholique de Louvain, B-1348 Louvain-la-Neuve, Belgium.

出版信息

Microbiol Mol Biol Rev. 1998 Sep;62(3):725-74. doi: 10.1128/MMBR.62.3.725-774.1998.

Abstract

Insertion sequences (ISs) constitute an important component of most bacterial genomes. Over 500 individual ISs have been described in the literature to date, and many more are being discovered in the ongoing prokaryotic and eukaryotic genome-sequencing projects. The last 10 years have also seen some striking advances in our understanding of the transposition process itself. Not least of these has been the development of various in vitro transposition systems for both prokaryotic and eukaryotic elements and, for several of these, a detailed understanding of the transposition process at the chemical level. This review presents a general overview of the organization and function of insertion sequences of eubacterial, archaebacterial, and eukaryotic origins with particular emphasis on bacterial elements and on different aspects of the transposition mechanism. It also attempts to provide a framework for classification of these elements by assigning them to various families or groups. A total of 443 members of the collection have been grouped in 17 families based on combinations of the following criteria: (i) similarities in genetic organization (arrangement of open reading frames); (ii) marked identities or similarities in the enzymes which mediate the transposition reactions, the recombinases/transposases (Tpases); (iii) similar features of their ends (terminal IRs); and (iv) fate of the nucleotide sequence of their target sites (generation of a direct target duplication of determined length). A brief description of the mechanism(s) involved in the mobility of individual ISs in each family and of the structure-function relationships of the individual Tpases is included where available.

摘要

插入序列(ISs)是大多数细菌基因组的重要组成部分。迄今为止,文献中已描述了500多种不同的插入序列,并且在正在进行的原核生物和真核生物基因组测序项目中还发现了更多。在过去十年中,我们对转座过程本身的理解也取得了一些显著进展。其中最主要的是开发了针对原核和真核元件的各种体外转座系统,并且对于其中一些系统,在化学层面上对转座过程有了详细的了解。本综述概述了真细菌、古细菌和真核生物来源的插入序列的组织和功能,特别强调细菌元件以及转座机制的不同方面。它还试图通过将这些元件归类到不同的家族或组中,为其分类提供一个框架。根据以下标准的组合,该集合中的443个成员被分为17个家族:(i)遗传组织的相似性(开放阅读框的排列);(ii)介导转座反应的酶,即重组酶/转座酶(Tpases)的显著同一性或相似性;(iii)其末端的相似特征(末端反向重复序列);(iv)其靶位点核苷酸序列的命运(产生确定长度的直接靶标重复序列)。如有可用信息,还包括对每个家族中单个ISs移动性所涉及的机制以及单个Tpases的结构-功能关系的简要描述。

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