Differential utilization of 2',3'-dideoxyguanosine 5'-triphosphate as a substrate for various DNA polymerases.

Abstract

2',3'-dideoxyguanosine 5'-triphosphate (ddGTP) was found to be an efficient substrate for DNA polymerase beta when activated DNA was used as the template.primer. Under the optimized reaction conditions with activated DNA, the rate of the incorporation of ddGTP into DNA was almost equal to that of the corresponding normal substrate dGTP. The Km value for ddGTP (1.8 microM) was smaller than that for dGTP (7.8 microM). In contrast, ddGTP was not utilized as a substrate for DNA polymerase gamma with any of the activated DNA and (dC)n.(dG)12-18 as the template primer. Other DNA polymerases such as DNA polymerase alpha, E coli DNA polymerase I and retroviral reverse transcriptase could poorly utilize ddGTP as a substrate. Some of the kinetic properties of DNA polymerase beta revealed toward ddGTP are also described. Since DNA polymerase beta plays a role in DNA repair, the present results predict possible appearance of cytotoxicity or clinical side effect(s) of 2',3'-dideoxyguanosine (ddG), known as a potent inhibitor of human immunodeficiency virus, when ddG is administered to the patients with acquired immune deficiency syndrome (AIDS) or AIDS-related complex.

• Authors: K Ono, H Nakane
• Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie (Biomed Pharmacother) Vol. 45 Issue 4-5 Pg. 179-85 ( 1991) ISSN: 0753-3322 [Print] France
• PMID: 1932601 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Deoxyguanine Nucleotides
• Dideoxynucleotides
• 2',3'-dideoxyguanosine 5'-triphosphate
• DNA Polymerase I
• DNA-Directed DNA Polymerase

Topics

• DNA Polymerase I (pharmacokinetics)
• DNA-Directed DNA Polymerase (metabolism)
• Deoxyguanine Nucleotides (metabolism)
• Dideoxynucleotides
• Substrate Specificity