TY - JOUR
T1 - Yeast pol η holds a Cis-Syn thymine dimer loosely in the active site during elongation opposite the 3′-T of the dimer, but tightly opposite the 5′-T
AU - Sun, Liping
AU - Zhang, Kaijiang
AU - Zhou, Lilly
AU - Hohler, Paul
AU - Kool, Eric T.
AU - Yuan, Fenghua
AU - Wang, Zhigang
AU - Taylor, John Stephen
PY - 2003/8/12
Y1 - 2003/8/12
N2 - Polymerase η is a member of the Y family of DNA polymerases which is able to bypass thymine dimers efficiently and in a relatively error-free manner. To elucidate the mechanism of dimer bypass, the efficiency of dAMP and pyrene nucleotide insertion opposite the thymine dimer and its N3-methyl derivatives was determined. Pol η inserts pyrene nucleotide with greater efficiency than dAMP opposite the 3′-T of an undimerized or dimerized T and is an effective inhibitor of DNA synthesis by pol ν. Substitution of the N3H of the 3′-T of an undimerized T or a dimerized T with a methyl group has little effect on the insertion efficiency of pyrene nucleotide but greatly inhibits the insertion of dAMP. Together, these results suggest that the error-free insertion of dAMP opposite the 3′-T of the cis-syn thymine dimer happens by way of a loosely held dimer in the active site which can be displaced from the active site by pyrene nucleotide. In contrast, pol η cannot insert pyrene nucleotide opposite the 5′-T of the dimer, whereas it can insert dAMP with efficiency comparable to that opposite the 3′-T. The inability to insert pyrene nucleotide opposite the 5′-T of the dimer is consistent with the idea that while the polymerase binds loosely to a templating nucleotide, it binds tightly to the nucleotide to its 3′-side. Overall, the results show a marked difference from similar studies on pol I family polymerases, and suggest mechanisms by which this Y family polymerase can process damaged DNA efficiently.
AB - Polymerase η is a member of the Y family of DNA polymerases which is able to bypass thymine dimers efficiently and in a relatively error-free manner. To elucidate the mechanism of dimer bypass, the efficiency of dAMP and pyrene nucleotide insertion opposite the thymine dimer and its N3-methyl derivatives was determined. Pol η inserts pyrene nucleotide with greater efficiency than dAMP opposite the 3′-T of an undimerized or dimerized T and is an effective inhibitor of DNA synthesis by pol ν. Substitution of the N3H of the 3′-T of an undimerized T or a dimerized T with a methyl group has little effect on the insertion efficiency of pyrene nucleotide but greatly inhibits the insertion of dAMP. Together, these results suggest that the error-free insertion of dAMP opposite the 3′-T of the cis-syn thymine dimer happens by way of a loosely held dimer in the active site which can be displaced from the active site by pyrene nucleotide. In contrast, pol η cannot insert pyrene nucleotide opposite the 5′-T of the dimer, whereas it can insert dAMP with efficiency comparable to that opposite the 3′-T. The inability to insert pyrene nucleotide opposite the 5′-T of the dimer is consistent with the idea that while the polymerase binds loosely to a templating nucleotide, it binds tightly to the nucleotide to its 3′-side. Overall, the results show a marked difference from similar studies on pol I family polymerases, and suggest mechanisms by which this Y family polymerase can process damaged DNA efficiently.
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U2 - 10.1021/bi0345687
DO - 10.1021/bi0345687
M3 - Article
C2 - 12899630
AN - SCOPUS:0042572535
SN - 0006-2960
VL - 42
SP - 9431
EP - 9437
JO - Biochemistry
JF - Biochemistry
IS - 31
ER -