Article
- The EMBO Journal (2004) 23, 3408 - 3420
- doi:10.1038/sj.emboj.7600344
Published online: 29 July 2004
Subject Category:
True reversal of Mu integration
T K Au, Shailja Pathaniaa and Rasika M Harshey
- Section of Molecular Genetics and Microbiology, Institute of Cellular and Molecular Biology, University of Texas at Austin, Austin, TX, USA
Correspondence to:
Rasika M Harshey, Department of Microbiology, Section of Molecular Genetics and Microbiology, Institute of Cellular and Molecular Biology, University of Texas at Austin, Austin, TX 78712-1095, USA. Tel.: +1 512 471 6881; Fax: +1 512 471 7088; E-mail: rasika@uts.cc.utexas.edu
aPresent address: Dana Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, USA
Received 6 May 2004; Accepted 5 July 2004
Abstract
We describe a high-temperature (75°C) transition in the Mu integration complex that causes efficient and true reversal of the integration reaction. A second reversal pathway, first described as 'foldback' reversal for the HIV integrase, was also observed upon disassembly/reassembly of the Mu complex at normal temperatures. Both true and foldback reversal severed only one or the other of the two integrated Mu ends, and each exhibited distinct metal ion specificities. Our results directly implicate an altered transposase configuration in the Mu strand transfer complex that inhibits reversal, thereby regulating the directionality of transposition.
Keywords:
- directionality of transposition,
- disintegration,
- hairpin formation,
- target conformation,
- transposase
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