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HERO ID
7047254
Reference Type
Journal Article
Title
Polymerization of 2 '-fluoro-and 2 '-O-methyl-dNTPs by human DNA polymerase alpha, polymerase gamma, and primase
Author(s)
Richardson, FC; Kuchta, RD; Mazurkiewicz, A; Richardson, KA; ,
Year
2000
Is Peer Reviewed?
Yes
Journal
Biochemical Pharmacology
ISSN:
0006-2952
EISSN:
1873-2968
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Location
OXFORD
Page Numbers
1045-1052
Language
English
PMID
10704933
DOI
10.1016/s0006-2952(99)00414-1
Web of Science Id
WOS:000085835600003
Abstract
Studies were undertaken to assess the ability of human polymerase alpha (pol alpha) and polymerase gamma (pol gamma) to incorporate 2'-fluoro- and 2'-O-methyldeoxynucleotides into DNA. In vitro DNA synthesis systems were used to detect incorporation and determine K-m and V-max for 2'-FdATP, 2'-FdUTP, 2'-FdCTP, 2'-FdGTP, 2'-O-MedATP, 2'-O-MedCTP, 2'-O-MedGTP, 2'-O-MedUTP, dUTP, UTP, and FIAUTP, in addition to normal deoxynucleotides. Pol alpha incorporated all 2'-FdNTPs except 2'-FdATP, but not 2'-O-MedNTPs. Pol gamma incorporated all 2'-FdNTPs, but not 2'-O-MedNTPs. In general, 2'-fluorine substitution decreased V-max/K-m; however, the magnitude of the changes was nucleotide dependent, with dATP and dUTP being the most affected. Misinsertion frequencies for pol alpha and pol gamma of 2'-FdNTPs compared with their normal nucleotides were: FIAUTP > 2'-FdCTP > 2'-FdGTP > 2'-FdATP (pol gamma only) > 2'-FdUTP. Because kinetics of insertion of pol alpha can be affected by the nature of the primer, we examined the ability of pol alpha to polymerize 2'-fluoro- and 2'-O-MedATP and dGTP when elongating a primer synthesized by DNA primase. Under these conditions, both 2'-FdATP and 2'-FdCTP were polymerized, but 2'-O-MedATP and 2'-O-MedGTP were not. Primase alone could not readily polymerize these analogs into RNA primers. Previous studies showed that 2'-deoxy-2'-fluorocytosine (2'-FdC) is incorporated by several non-human DNA polymerases. The current studies showed that human polymerases can polymerize numerous 2'-FdNTPs but cannot polymerize 2'-O-MedNTPs. (C) 2000 Elsevier Science Inc.
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