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秀丽隐杆线虫转座元件Tc1的假定转座酶TcA的DNA结合活性的表达及生化特性分析

Expression and biochemical characterization of the DNA binding activity of TcA, the putative transposase of Caenorhabditis elegans transposable element Tc1.

作者信息

Abad P, Cerutti M, Pauron D, Quiles C, Palin B, Devauchelle G, Dalmasso A

机构信息

Laboratoire de Biologie des Invertébrés, INRA, BP 2078, Antibes, France.

出版信息

Biochem Biophys Res Commun. 1993 May 14;192(3):1445-52. doi: 10.1006/bbrc.1993.1578.

Abstract

The TcA protein is one of the proteins essential for Tc1 transposition. In order to study the biochemical parameters of Tc1 transposition mechanism, we used TcA protein overproduced in baculovirus system for DNA binding experiments. We show that, despite its relatively strong non specific affinity for DNA, TcA exhibits a better affinity for its Tc1 specific binding sites. The K0.5 is 3.8 nM for the Tc1 whereas in the same type of experiment the K0.5 is 24 nM for calf thymus DNA. The ratio value between specific and non specific DNA binding activity of the TcA protein was also exhibited by other transposases such as those of the bacteriophage Mu, Tn 10 and the Drosophila P element. This nonspecific DNA binding activity may be involved in determining sites of transposable element insertion.

摘要

TcA蛋白是Tc1转座所必需的蛋白质之一。为了研究Tc1转座机制的生化参数,我们使用在杆状病毒系统中过量表达的TcA蛋白进行DNA结合实验。我们发现,尽管TcA对DNA具有相对较强的非特异性亲和力,但它对其Tc1特异性结合位点表现出更好的亲和力。对于Tc1,K0.5为3.8 nM,而在同一类型实验中,小牛胸腺DNA的K0.5为24 nM。其他转座酶,如噬菌体Mu、Tn 10和果蝇P元件的转座酶,也表现出TcA蛋白特异性和非特异性DNA结合活性之间的比值。这种非特异性DNA结合活性可能参与确定转座元件的插入位点。

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