Structural basis of error-prone replication and stalling at a thymine base by human DNA polymerase iota.

Citation data:

The EMBO journal, ISSN: 1460-2075, Vol: 28, Issue: 11, Page: 1644-54

Publication Year:
2009
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Repository URL:
https://ir.lib.uwo.ca/biochempub/66
PMID:
19440206
DOI:
10.1038/emboj.2009.122
PMCID:
PMC2693154
Author(s):
Kirouac, Kevin N.; Ling, Hong
Publisher(s):
Wiley-Blackwell
Tags:
Neuroscience; Biochemistry, Genetics and Molecular Biology; Immunology and Microbiology; incorporation specificity; mutagenesis; pol i; translesion synthesis; Y family DNA polymerase; Biochemistry
article description
Human DNA polymerase iota (pol iota) is a unique member of Y-family polymerases, which preferentially misincorporates nucleotides opposite thymines (T) and halts replication at T bases. The structural basis of the high error rates remains elusive. We present three crystal structures of pol complexed with DNA containing a thymine base, paired with correct or incorrect incoming nucleotides. A narrowed active site supports a pyrimidine to pyrimidine mismatch and excludes Watson-Crick base pairing by pol. The template thymine remains in an anti conformation irrespective of incoming nucleotides. Incoming ddATP adopts a syn conformation with reduced base stacking, whereas incorrect dGTP and dTTP maintain anti conformations with normal base stacking. Further stabilization of dGTP by H-bonding with Gln59 of the finger domain explains the preferential T to G mismatch. A template 'U-turn' is stabilized by pol and the methyl group of the thymine template, revealing the structural basis of T stalling. Our structural and domain-swapping experiments indicate that the finger domain is responsible for pol's high error rates on pyrimidines and determines the incorporation specificity.