DNA binding properties of the integrase proteins of human immunodeficiency viruses types 1 and 2
Author(s) -
Dik C. van Gent,
Ype Elgersma,
Marian W.J. Bolk,
Cornelis Vink,
Ronald H.A. Plasterk
Publication year - 1991
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/19.14.3821
Subject(s) - biology , integrase , dna , in vitro recombination , circular bacterial chromosome , microbiology and biotechnology , hmg box , viral structural protein , virology , dna polymerase ii , dna binding protein , viral entry , peptide sequence , viral replication , biochemistry , dna replication , virus , gene , rna , reverse transcriptase , molecular cloning , transcription factor
Integration of retroviral DNA into the host chromosome requires the integrase protein (IN). We overexpressed the IN proteins of human immunodeficiency viruses types 1 and 2 (HIV-1 and HIV-2) in E. coli and purified them. Both proteins were found to specifically cut two nucleotides off the ends of linear viral DNA, and to integrate viral DNA into target DNA. This demonstrates that HIV IN is the only protein required for integration of HIV DNA. Although the two types of IN proteins have only 53% amino acid sequence similarity, they act with equal efficiency on both type 1 and type 2 viral DNA. Binding of IN to DNA was tested: purified IN does not bind very specifically to viral DNA ends. Nevertheless, only viral DNA ends are cleaved and integrated. We interpret this as follows: in vitro quick aspecific binding to DNA is followed by slow specific cutting and integration. IN can not find viral DNA ends in the presence of an excess of aspecific DNA; in vivo this is not required since the IN protein is in constant proximity of viral DNA in the viral core particle.
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