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转座酶基因的一个拟议超家族:纤毛原生动物中的类转座子元件及一个常见的“D35E”基序

A proposed superfamily of transposase genes: transposon-like elements in ciliated protozoa and a common "D35E" motif.

作者信息

Doak T G, Doerder F P, Jahn C L, Herrick G

机构信息

Department of Cellular, Viral and Molecular Biology, University of Utah School of Medicine, Salt Lake City 84132.

出版信息

Proc Natl Acad Sci U S A. 1994 Feb 1;91(3):942-6. doi: 10.1073/pnas.91.3.942.

Abstract

The transposon-like elements TBE1, Tec1, and Tec2 of hypotrichous ciliated protozoa appear to encode a protein that belongs to the IS630-Tc1 family of transposases. The Anabaena IS895 transposase also is placed in this family. We note that most family members transpose into the dinucleotide target, TA, and that members with eukaryotic hosts have a tendency for somatic excision that is carried to an extreme by the ciliate elements. Alignments including the additional members, and also mariner elements, show that transposases of this family share strongly conserved residues in a large C-terminal portion, including a fully conserved dipeptide, Asp-Glu (DE), and a block consisting of a fully conserved Asp and highly conserved Glu, separated by 34 or 35 residues (D35E). This D35E motif likely is homologous to the previously characterized D35E motif of the family of retroviral-retrotransposon integrases and IS3-like transposases. Because it is known that the IS3-retroposon D35E region is a critical portion of a domain capable of various in vitro transposition-related reactions, the results suggest that the two families share homologous catalytic transposase domains and that members of both families may share a common transposition mechanism.

摘要

纤毛类纤毛虫的转座子样元件TBE1、Tec1和Tec2似乎编码一种属于转座酶IS630-Tc1家族的蛋白质。鱼腥藻IS895转座酶也属于这个家族。我们注意到,该家族的大多数成员会转座到二核苷酸靶标TA中,而且具有真核宿主的成员有体细胞切除的倾向,纤毛虫元件将这种倾向发挥到了极致。包含其他成员以及水手元件的比对结果显示,该家族的转座酶在一个大的C末端部分共享高度保守的残基,包括一个完全保守的二肽Asp-Glu(DE),以及一个由一个完全保守的Asp和一个高度保守的Glu组成的模块,二者相隔34或35个残基(D35E)。这个D35E基序可能与先前鉴定的逆转录病毒-逆转座子整合酶家族和IS3样转座酶的D35E基序同源。由于已知IS3-逆转座子的D35E区域是一个能够进行各种体外转座相关反应的结构域的关键部分,因此结果表明这两个家族共享同源的催化转座酶结构域,且两个家族的成员可能共享一种共同的转座机制。

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