Suppr超能文献

秀丽隐杆线虫Tc1转座酶的体内和体外特性研究

Characterization of the Caenorhabditis elegans Tc1 transposase in vivo and in vitro.

作者信息

Vos J C, van Luenen H G, Plasterk R H

机构信息

The Netherlands Cancer Institute, Division of Molecular Biology, Amsterdam.

出版信息

Genes Dev. 1993 Jul;7(7A):1244-53. doi: 10.1101/gad.7.7a.1244.

Abstract

We have investigated the function of the Tc1A gene of the mobile element Tc1 of Caenorhabditis elegans. Tc1 is a member of a family of transposons found in several animal phyla, such as nematodes, insects, and vertebrates. Two lines of evidence show that Tc1A encodes the transposase of Tc1. First, forced expression of the Tc1A protein in transgenic nematodes results in an enhanced level of transposition of endogenous Tc1 elements. Second, DNase I footprinting and gel retardation assays show that Tc1A binds specifically to the inverted repeats at the ends of the element and that the Tc1A recognition site is located between base pairs 5 and 26 from the ends of Tc1. Functional dissection of the transposase shows the presence of two distinct DNA-binding domains. A site-specific DNA-binding domain is contained within the amino-terminal 63 residues of Tc1A; this region shows sequence similarity to the prokaryotic IS30 transposase. A second, general DNA-binding domain is located between amino acids 71 and 207. Our results suggest that Tc1 is more similar to prokaryotic insertion elements than to eukaryotic transposons such as P elements in Drosophila or Ac and En-1 in plants.

摘要

我们研究了秀丽隐杆线虫移动元件Tc1的Tc1A基因的功能。Tc1是在多个动物门中发现的转座子家族的成员,如线虫、昆虫和脊椎动物。有两条证据表明Tc1A编码Tc1的转座酶。首先,在转基因线虫中强制表达Tc1A蛋白会导致内源性Tc1元件的转座水平提高。其次,DNA酶I足迹法和凝胶阻滞分析表明,Tc1A特异性结合元件末端的反向重复序列,且Tc1A识别位点位于距离Tc1末端碱基对5至26之间。对转座酶的功能剖析显示存在两个不同的DNA结合结构域。一个位点特异性DNA结合结构域包含在Tc1A的氨基末端63个残基内;该区域与原核IS30转座酶具有序列相似性。第二个一般DNA结合结构域位于氨基酸71至207之间。我们的结果表明,Tc1与原核插入元件比与真核转座子(如果蝇中的P元件或植物中的Ac和En-1)更相似。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验