Abstract
Integration of the viral genome into the nuclear DNA of a host cell plays a pivotal role in the replication of retroviruses. We have developed an in vitro method for studying the biochemistry of human immunodeficiency virus (HIV) integration by using extracts from HIV-infected cells. Analysis of the reaction products showed that HIV integration in vitro accurately reproduces the in vivo process. Integration occurred without apparent specificity for the target sequence, and the integrated provirus was directly flanked by a 5-base-pair duplication of DNA from the target site. HIV integration did not require a high-energy cofactor, and the enzymatic activities required for integration were recovered with the viral DNA when cell extracts were fractionated by gel exclusion chromatography.
MeSH Terms
Base Sequence
CD4 Antigens/analysis
Cell Line
Cell Transformation, Viral
Cell-Free System
Cloning, Molecular
DNA, Neoplasm/genetics
DNA, Viral/genetics
Genes, Viral
HIV/genetics
Humans
Lysogeny
Molecular Sequence Data
Oligonucleotide Probes
Proviruses/genetics
T-Lymphocytes
Chemicals
CD4 Antigens
DNA, Neoplasm
DNA, Viral
Oligonucleotide Probes
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Ellison V
Department of Pediatrics, Stanford University Medical Center, California 94305-5428.
Abrams H
Roe T
Lifson J
Brown P
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