MMBR Figure table search 04
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Hindmarsh, P.
Right arrow Articles by Leis, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Hindmarsh, P.
Right arrow Articles by Leis, J.

 Previous Article  |  Next Article 

Microbiology and Molecular Biology Reviews, December 1999, p. 836-843, Vol. 63, No. 4
1092-2172/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Retroviral DNA Integration

Patrick Hindmarsh1 and Jonathan Leis2,*

Department of Biochemistry, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106,1 and Department of Microbiology and Immunology, Northwestern University School of Medicine, Chicago, Illinois 606112

DNA integration is a unique enzymatic process shared by all retroviruses and retrotransposons. During integration, double-stranded linear viral DNA is inserted into the host genome in a process catalyzed by the virus-encoded integrase (IN). The mechanism involves a series of nucleophillic attacks, the first of which removes the terminal 2 bases from the 3' ends of the long terminal repeats and of the second which inserts the viral DNA into the host genome. IN specifically recognizes the DNA sequences at the termini of the viral DNA, juxtaposing both ends in an enzyme complex that inserts the viral DNA into a single site in a concerted manner. Small duplications of the host DNA, characteristic of the viral IN, are found at the sites of insertion. At least two host proteins, HMG-I(Y) and BAF, have been shown to increase the efficiency of the integration reaction.


* Corresponding author. Mailing address: Department of Microbiology and Immunology, Northwestern University School of Medicine, Chicago, IL 60611. Phone: (312) 503-1166. Fax: (312) 503-1339. E-mail: j-leis{at}nwu.edu.


Microbiology and Molecular Biology Reviews, December 1999, p. 836-843, Vol. 63, No. 4
1092-2172/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
Appl. Environ. Microbiol. Infect. Immun. Eukaryot. Cell
Mol. Cell. Biol. J. Virol. J. Bacteriol.
ALL ASM JOURNALS

Copyright © 1999 by the American Society for Microbiology. All rights reserved.