Weak Palindromic Consensus Sequences Are a Common Feature Found at the Integration Target Sites of Many Retroviruses
Open Access
- 15 April 2005
- journal article
- research article
- Published by American Society for Microbiology in Journal of Virology
- Vol. 79 (8) , 5211-5214
- https://doi.org/10.1128/jvi.79.8.5211-5214.2005
Abstract
Integration into the host genome is one of the hallmarks of the retroviral life cycle and is catalyzed by virus-encoded integrases. While integrase has strict sequence requirements for the viral DNA ends, target site sequences have been shown to be very diverse. We carefully examined a large number of integration target site sequences from several retroviruses, including human immunodeficiency virus type 1, simian immunodeficiency virus, murine leukemia virus, and avian sarcoma-leukosis virus, and found that a statistical palindromic consensus, centered on the virus-specific duplicated target site sequence, was a common feature at integration target sites for these retroviruses.Keywords
This publication has 41 references indexed in Scilit:
- Genome-Wide Analyses of Avian Sarcoma Virus Integration SitesJournal of Virology, 2004
- Retroviral DNA Integration: ASLV, HIV, and MLV Show Distinct Target Site PreferencesPLoS Biology, 2004
- Integrase-Specific Enhancement and Suppression of Retroviral DNA Integration by Compacted Chromatin Structure In VitroJournal of Virology, 2004
- Targeting SurvivalCell, 2003
- Transcription Start Regions in the Human Genome Are Favored Targets for MLV IntegrationScience, 2003
- HIV-1 Integration in the Human Genome Favors Active Genes and Local HotspotsCell, 2002
- A-form Conformational Motifs in Ligand-bound DNA StructuresJournal of Molecular Biology, 2000
- Rod models of DNA: sequence-dependent anisotropic elastic modelling of local bending phenomenaTrends in Biochemical Sciences, 1998
- Target-Sequence Preferences of HIV-1 Integration Complexesin VitroVirology, 1996
- Nucleosomes, DNA-binding proteins, and DNA sequence modulate retroviral integration target site selectionCell, 1992