ePrints@IIScePrints@IISc Home | About | Browse | Latest Additions | Advanced Search | Contact | Help

Characterization of the restriction enzyme-like endonuclease encoded by the Entamoeba histolytica non-long terminal repeat retrotransposon EhLINE1

Yadav, Vijay Pal and Mandal, Prabhat Kumar and Rao, Desirazu N and Bhattacharya, Sudha (2009) Characterization of the restriction enzyme-like endonuclease encoded by the Entamoeba histolytica non-long terminal repeat retrotransposon EhLINE1. In: Febs journal, 276 (23). pp. 7070-7082.

[img] PDF
2.pdf - Published Version
Restricted to Registered users only

Download (1MB) | Request a copy
Official URL: http://www3.interscience.wiley.com/journal/1226854...

Abstract

The genome of the human pathogen Entamoeba histolytica, a primitive protist, contains non-long terminal repeat retrotransposable elements called EhLINEs. These encode reverse transcriptase and endonuclease required for retrotransposition. The endonuclease shows sequence similarity with bacterial restriction endonucleases. Here we report the salient enzymatic features of one such endonuclease. The kinetics of an EhLINE1-encoded endonuclease catalyzed reaction, determined under steady-state and single-turnover conditions, revealed a significant burst phase followed by a slower steady-state phase, indicating that release of product could be the slower step in this reaction. For circular supercoiled DNA the K-m was 2.6 x 10-8 m and the k(cat) was 1.6 x 10-2 sec-1. For linear E. histolytica DNA substrate the K-m and k(cat) values were 1.3 x 10-8 m and 2.2 x 10-4 sec-1 respectively. Single-turnover reaction kinetics suggested a noncooperative mode of hydrolysis. The enzyme behaved as a monomer. While Mg2+ was required for activity, 60% activity was seen with Mn2+ and none with other divalent metal ions. Substitution of PDX12-14D (a metal-binding motif) with PAX(12-14)D caused local conformational change in the protein tertiary structure, which could contribute to reduced enzyme activity in the mutated protein. The protein underwent conformational change upon the addition of DNA, which is consistent with the known behavior of restriction endonucleases. The similarities with bacterial restriction endonucleases suggest that the EhLINE1-encoded endonuclease was possibly acquired from bacteria through horizontal gene transfer. The loss of strict sequence specificity for nicking may have been subsequently selected to facilitate spread of the retrotransposon to intergenic regions of the E. histolytica genome.

Item Type: Journal Article
Additional Information: copyright of this article belongs to Wiley-blackwell publishing, inc.
Keywords: EhLINE; Entamoeba histolytica; nicking endonuclease; restriction endonuclease-like endonuclease (RE-like endonuclease); retrotransposon-encoded endonuclease
Department/Centre: Division of Biological Sciences > Biochemistry
Depositing User: Users 920 not found.
Date Deposited: 04 Jan 2010 09:02
Last Modified: 16 Jan 2013 11:53
URI: http://eprints.iisc.ac.in/id/eprint/25163

Actions (login required)

View Item View Item