Site-specific hydrolysis and alcoholysis of human immunodeficiency virus DNa termini mediated by the viral integrase protein
- 1 January 1991
- journal article
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 19 (24) , 6691-6698
- https://doi.org/10.1093/nar/19.24.6691
Abstract
Before integration of the human immunodeficiency virus (HIV) DNA, two nucleotides are removed from the 3' ends of the viral DNA by the integrase (IN) protein. We studied the chemistry of this reaction, and found that IN mediates site-specific hydrolysis of a phosphodiester bond, resulting in release of a dinucleotide. A class of alcohols (including glycerol, 1,2-propanediol, but not 1,3-propanediol) can also act as nucleophile in this reaction, and likewise the alcoholic amino acids L-serine and L-threonine can be covalently linked to the dinucleotide. No evidence was found for a covalent linkage between the IN protein and this dinucleotide, suggesting that IN directs a single nucleophilic attack of water at the specific phosphodiester bond.Keywords
This publication has 18 references indexed in Scilit:
- Inversion of the phosphate chirality at the target site of Mu DNA strand transfer: Evidence for a one-step transesterification mechanismCell, 1991
- Activities of human immunodeficiency virus (HIV) integration protein in vitro: specific cleavage and integration of HIV DNA.Proceedings of the National Academy of Sciences, 1991
- DNA binding properties of the integrase proteins of human immunodeficiency viruses types 1 and 2Nucleic Acids Research, 1991
- Host sequences flanking the HIV provirusNucleic Acids Research, 1990
- The avian retroviral IN protein is both necessary and sufficient for integrative recombination in vitroCell, 1990
- Retroviral DNA Integration Directed by HIV Integration Protein in VitroScience, 1990
- Retroviral DNA integration: Structure of an integration intermediateCell, 1988
- Nucleotide sequence of the AIDS virus, LAVCell, 1985
- Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Nature, 1970
- SOME PROPERTIES OF ALKALINE PHOSPHATASE FROM ESCHERICHIA COLI - TRANSPHOSPHORYLATION1964