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

Liping Sun, Kaijiang Zhang, Lilly Zhou, Paul Hohler, Eric T. Kool, Fenghua Yuan, Zhigang Wang, John Stephen Taylor

Research output: Contribution to journalArticlepeer-review

19 Scopus citations

Abstract

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.

Original languageEnglish (US)
Pages (from-to)9431-9437
Number of pages7
JournalBiochemistry
Volume42
Issue number31
DOIs
StatePublished - Aug 12 2003
Externally publishedYes

ASJC Scopus subject areas

  • Biochemistry

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