Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1972 Jan;9(1):116-29.
doi: 10.1128/JVI.9.1.116-129.1972.

RNA-dependent DNA polymerase activity of RNA tumor viruses. I. Directing influence of DNA in the reaction

RNA-dependent DNA polymerase activity of RNA tumor viruses. I. Directing influence of DNA in the reaction

J Hurwitz et al. J Virol. 1972 Jan.

Abstract

The template requirements and deoxyribonucleic acid (DNA) products of the DNA polymerases isolated from Rauscher leukemia and avian myeloblastosis viruses have been examined. All DNA preparations or synthetic polydeoxynucleotides which are active as primers possess a duplex structure containing single-stranded regions with a 3'-hydroxyl terminus. Native DNA and fully single-stranded DNA are inactive; moreover, their activity is not enhanced by sonic oscillation or treatment with micrococcal nuclease, Neurospora nuclease, or low levels of deoxyribonuclease I. Poor DNA templates are activated by treatment with exonuclease III, large amounts of deoxyribonuclease I, or an endonuclease isolated from Rauscher viral preparations. In reactions primed with deoxyadenylate-deoxythymidylate copolymer, the product formed is covalently attached to primer strands, indicating that no new strands are initiated. DNA polymerase products formed with exonuclease III- or deoxyribonuclase I-treated DNA are duplex structures. Short single-stranded regions are completely filled in, whereas long single-stranded regions are only partly repaired. DNA preparations containing extensive single-stranded regions are poorly utilized as templates.

PubMed Disclaimer

References

    1. Biochem J. 1964 Jan;90(1):147-9 - PubMed
    1. Proc Natl Acad Sci U S A. 1965 Sep;54(3):794-800 - PubMed
    1. J Biol Chem. 1966 Jun 25;241(12):2923-32 - PubMed
    1. Cancer Res. 1967 Jun;27(6):1138-57 - PubMed
    1. J Biol Chem. 1967 Jun 10;242(11):2780-9 - PubMed

MeSH terms

LinkOut - more resources