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J Biol Chem, Vol. 273, Issue 33, 21332-21341, August 14, 1998
From the Department of Biochemistry and Molecular Biology, Research
Institute for Microbial Diseases, Osaka University, 3-1 Yamada-oka,
Suita, Osaka 565-0871, Japan
Two forms of DNA polymerase II (
DNA Polymerase II (
) of Saccharomyces cerevisiae
Dissociates from the DNA Template by Sensing Single-stranded
DNA
) of
Saccharomyces cerevisiae, Pol II* and Pol II, were purified
to near homogeneity from yeast cells. Pol II* is a four-subunit complex
containing a 256-kDa catalytic polypeptide, whereas Pol II consists
solely of a 145-kDa polypeptide derived from the N-terminal half of the
256-kDa polypeptide of Pol II*. We show that Pol II* and Pol II are
indistinguishable with respect to the processivity and rate of
DNA-chain elongation. The equilibrium dissociation constants of the
complexes of Pol II* and Pol II with the DNA template showed that the
stability of these complexes is almost the same. However, when the
rates of dissociation of the Pol II* and Pol II from the DNA template were measured using single-stranded DNA as a trap for the dissociated polymerase, Pol II* dissociated 75-fold faster than Pol II.
Furthermore, the rate of dissociation of Pol II* from the DNA template
became faster as the concentration of the single-stranded DNA was
increased. These results indicate that the rapid dissociation of Pol
II* from the DNA template is actively promoted by single-stranded DNA.
The dissociation of Pol II from the DNA template was also shown to be
promoted by single-stranded DNA, although at a much slower rate. These
results suggest that the site for sensing single-stranded DNA resides
within the 145-kDa N-terminal portion of the catalytic subunit and that
the efficiency for sensing single-stranded DNA by this site is
positively modulated by either the C-terminal half of the catalytic
subunit and/or the other subunits.
Copyright © 1998 by The American Society for Biochemistry and Molecular Biology, Inc.
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