Literature DB >> 15023344

Snapshots of replication through an abasic lesion; structural basis for base substitutions and frameshifts.

Hong Ling1, François Boudsocq, Roger Woodgate, Wei Yang.   

Abstract

Dpo4 from S. Solfataricus, a DinB-like Y family polymerase, efficiently replicates DNA past an abasic lesion. We have determined crystal structures of Dpo4 complexed with five different abasic site-containing DNA substrates and find that translesion synthesis is template directed with the abasic site looped out and the incoming nucleotide is opposite the base 5' to the lesion. The ensuing DNA synthesis generates a -1 frameshift when the abasic site remains extrahelical. Template realignment during primer extension is also observed, resulting in base substitutions or even +1 frameshifts. In the case of a +1 frameshift, the extra nucleotide is accommodated in the solvent-exposed minor groove. In addition, the structure of an unproductive Dpo4 ternary complex suggests that the flexible little finger domain facilitates DNA orientation and translocation during translesion synthesis.

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Year:  2004        PMID: 15023344     DOI: 10.1016/s1097-2765(04)00101-7

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


  94 in total

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2.  Amino acid templating mechanisms in selection of nucleotides opposite abasic sites by a family a DNA polymerase.

Authors:  Samra Obeid; Wolfram Welte; Kay Diederichs; Andreas Marx
Journal:  J Biol Chem       Date:  2012-02-07       Impact factor: 5.157

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.  Roles of the Y-family DNA polymerase Dbh in accurate replication of the Sulfolobus genome at high temperature.

Authors:  Cynthia J Sakofsky; Patricia L Foster; Dennis W Grogan
Journal:  DNA Repair (Amst)       Date:  2012-02-04

5.  Translesion synthesis past the C8- and N2-deoxyguanosine adducts of the dietary mutagen 2-Amino-3-methylimidazo[4,5-f]quinoline in the NarI recognition sequence by prokaryotic DNA polymerases.

Authors:  James S Stover; Goutam Chowdhury; Hong Zang; F Peter Guengerich; Carmelo J Rizzo
Journal:  Chem Res Toxicol       Date:  2006-11       Impact factor: 3.739

6.  Subtle but variable conformational rearrangements in the replication cycle of Sulfolobus solfataricus P2 DNA polymerase IV (Dpo4) may accommodate lesion bypass.

Authors:  Yanli Wang; Karunesh Arora; Tamar Schlick
Journal:  Protein Sci       Date:  2005-12-01       Impact factor: 6.725

7.  Controlling the subcellular localization of DNA polymerases iota and eta via interactions with ubiquitin.

Authors:  Brian S Plosky; Antonio E Vidal; Antonio R Fernández de Henestrosa; Mary P McLenigan; John P McDonald; Samantha Mead; Roger Woodgate
Journal:  EMBO J       Date:  2006-06-08       Impact factor: 11.598

8.  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

9.  Fidelity of Dpo4: effect of metal ions, nucleotide selection and pyrophosphorolysis.

Authors:  Alexandra Vaisman; Hong Ling; Roger Woodgate; Wei Yang
Journal:  EMBO J       Date:  2005-08-18       Impact factor: 11.598

10.  Biochemical analysis of active site mutations of human polymerase η.

Authors:  Samuel C Suarez; Renee A Beardslee; Shannon M Toffton; Scott D McCulloch
Journal:  Mutat Res       Date:  2013-03-13       Impact factor: 2.433

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