Abstract
Oligonucleotides containing a specific initiation site for polymerase α- primase (pol α-primase) were used to measure the effects of cytosine arabinoside triphosphate and cytosine arabinoside monophosphate (araCMP) in DNA on RNA-primed DNA synthesis. Primase inserts araCMP at the 3' terminus of a full-length RNA primer with a 400-fold preference over CMP. The araCMP is elongated efficiently by pol α in the primase-coupled reaction. Extension from RNA 3'-araCMP is 50-fold less efficient than from CMP, and extension from DNA 3'-araCMP is 1600-fold less efficient than from dCMP. Using araCMP- containing templates, primer synthesis is reduced 2-3-fold, and RNA-primed DNA synthesis is reduced 2-8-fold. The efficiency of polymerization past a template araCMP by pol α is reduced 180-fold during insertion of dGMP opposite araCMP and 35-fold during extension from the araCMP:dGMP 3' terminus. These results show that the pol α-primase efficiently incorporates araCMP as the border nucleotide between RNA and DNA and suggest that the inhibitory effects of araC most likely result from slowed elongation of pol α and less so from inhibition of primer synthesis by primase.
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CITATION STYLE
Harrington, C., & Perrino, F. W. (1995). The effects of cytosine arabinoside on RNA-primed DNA synthesis by DNA polymerase α-primase. Journal of Biological Chemistry, 270(44), 26664–26669. https://doi.org/10.1074/jbc.270.44.26664
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