Abstract
A series of 6-anilinouracils, dGTP analogues which selectively inhibit specific bacterial DNA polymerases, were examined for their capacity to inhibit purified DNA polymerases from HeLa cells. The p-n-butyl derivative (BuAU) was found to inhibit DNA polymerase alpha with a Ki of approximately 60 microM. The inhibitory effect of BuAU was reversed specifically by dGTP and was observed only for DNA polymerase alpha; polymerases beta and lambda were not inhibited by drug at concentrations as high as 1 mM. BuAU also was inhibitory in vivo in HeLa cell culture; at 100 microM it reversibly inhibited cell division and selectively depressed DNA synthesis. The results of these studies indicate that BuAU is an inhibitor with considerable potential as a specific probe with which to dissect the structure of mammalian polymerase alpha and its putative role in cellular DNA replication.
MeSH Terms
Avian Myeloblastosis Virus/enzymology
Bacillus subtilis/enzymology
DNA Polymerase I/metabolism
DNA Polymerase II/antagonists & inhibitors
DNA Polymerase III/metabolism
DNA Replication/drug effects
DNA, Neoplasm/biosynthesis
Escherichia coli/enzymology
HeLa Cells/drug effects,metabolism
Humans
Kinetics
Nucleic Acid Synthesis Inhibitors
RNA-Directed DNA Polymerase/metabolism
Structure-Activity Relationship
Uracil/analogs & derivatives,pharmacology
Chemicals
DNA, Neoplasm
Nucleic Acid Synthesis Inhibitors
Uracil
butylanilinouracil
RNA-Directed DNA Polymerase
DNA Polymerase I
DNA Polymerase II
DNA Polymerase III
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Wright G E
Baril E F
Brown N C
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21 references, click to expand
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