Literature DB >> 11919199

Low fidelity DNA synthesis by a y family DNA polymerase due to misalignment in the active site.

Robert J Kokoska1, Katarzyna Bebenek, Francois Boudsocq, Roger Woodgate, Thomas A Kunkel.   

Abstract

Sulfolobus solfataricus DNA polymerase IV (Dpo4) is a member of the Y family of DNA polymerases whose crystal structure has recently been solved. As a model for other evolutionarily conserved Y family members that perform translesion DNA synthesis and have low fidelity, we describe here the base substitution and frameshift fidelity of DNA synthesis by Dpo4. Dpo4 generates all 12 base-base mismatches at high rates, 11 of which are similar to those of its human homolog, DNA polymerase kappa. This result is consistent with the Dpo4 structure, implying lower geometric selection for correct base pairs. Surprisingly, Dpo4 generates C.dCMP mismatches at an unusually high average rate and preferentially at cytosine flanked by 5'-template guanine. Dpo4 also has very low frameshift fidelity and frequently generates deletions of even noniterated nucleotides, especially cytosine flanked by a 5'-template guanine. Both unusual features of error specificity suggest that Dpo4 can incorporate dNTP precursors when two template nucleotides are present in the active site binding pocket. These results have implications for mutagenesis resulting from DNA synthesis by Y family polymerases.

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Year:  2002        PMID: 11919199     DOI: 10.1074/jbc.M202021200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  44 in total

1.  Identification of an unfolding intermediate for a DNA lesion bypass polymerase.

Authors:  Shanen M Sherrer; Brian A Maxwell; Lindsey R Pack; Kevin A Fiala; Jason D Fowler; Jun Zhang; Zucai Suo
Journal:  Chem Res Toxicol       Date:  2012-06-15       Impact factor: 3.739

2.  Processing of DNA lesions by archaeal DNA polymerases from Sulfolobus solfataricus.

Authors:  Petr Grúz; Masatomi Shimizu; Francesca M Pisani; Mariarita De Felice; Yusuke Kanke; Takehiko Nohmi
Journal:  Nucleic Acids Res       Date:  2003-07-15       Impact factor: 16.971

3.  UmuD(2) inhibits a non-covalent step during DinB-mediated template slippage on homopolymeric nucleotide runs.

Authors:  James J Foti; Angela M Delucia; Catherine M Joyce; Graham C Walker
Journal:  J Biol Chem       Date:  2010-05-13       Impact factor: 5.157

4.  Multiple solutions to inefficient lesion bypass by T7 DNA polymerase.

Authors:  Scott D McCulloch; Thomas A Kunkel
Journal:  DNA Repair (Amst)       Date:  2006-07-28

5.  Mechanism of template-independent nucleotide incorporation catalyzed by a template-dependent DNA polymerase.

Authors:  Kevin A Fiala; Jessica A Brown; Hong Ling; Ajay K Kshetry; Jun Zhang; John-Stephen Taylor; Wei Yang; Zucai Suo
Journal:  J Mol Biol       Date:  2006-10-07       Impact factor: 5.469

6.  A mechanism of nucleotide misincorporation during transcription due to template-strand misalignment.

Authors:  Richard T Pomerantz; Dmitry Temiakov; Michael Anikin; Dmitry G Vassylyev; William T McAllister
Journal:  Mol Cell       Date:  2006-10-20       Impact factor: 17.970

7.  Frameshift deletion by Sulfolobus solfataricus P2 DNA polymerase Dpo4 T239W is selective for purines and involves normal conformational change followed by slow phosphodiester bond formation.

Authors:  Huidong Zhang; Jeff W Beckman; F Peter Guengerich
Journal:  J Biol Chem       Date:  2009-10-16       Impact factor: 5.157

Review 8.  Half-Intercalation Stabilizes Slipped Mispairing and Explains Genome Vulnerability to Frameshift Mutagenesis by Endogenous "Molecular Bookmarks".

Authors:  Andrei Kuzminov
Journal:  Bioessays       Date:  2019-08-05       Impact factor: 4.345

9.  Differential temperature-dependent multimeric assemblies of replication and repair polymerases on DNA increase processivity.

Authors:  Hsiang-Kai Lin; Susan F Chase; Thomas M Laue; Linda Jen-Jacobson; Michael A Trakselis
Journal:  Biochemistry       Date:  2012-09-06       Impact factor: 3.162

10.  Kinetic analysis of correct nucleotide insertion by a Y-family DNA polymerase reveals conformational changes both prior to and following phosphodiester bond formation as detected by tryptophan fluorescence.

Authors:  Jeff W Beckman; Qixin Wang; F Peter Guengerich
Journal:  J Biol Chem       Date:  2008-11-04       Impact factor: 5.157

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