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The effect of sequence context on spontaneous Polζ-dependent mutagenesis in Saccharomyces cerevisiae

The Polζ translesion synthesis (TLS) DNA polymerase is responsible for over 50% of spontaneous mutagenesis and virtually all damage-induced mutagenesis in yeast. We previously demonstrated that reversion of the lys2ΔA746 −1 frameshift allele detects a novel type of +1 frameshift that is accompanied...

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Autores principales: Abdulovic, Amy L., Minesinger, Brenda K., Jinks-Robertson, Sue
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2330250/
https://www.ncbi.nlm.nih.gov/pubmed/18276637
http://dx.doi.org/10.1093/nar/gkn054
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author Abdulovic, Amy L.
Minesinger, Brenda K.
Jinks-Robertson, Sue
author_facet Abdulovic, Amy L.
Minesinger, Brenda K.
Jinks-Robertson, Sue
author_sort Abdulovic, Amy L.
collection PubMed
description The Polζ translesion synthesis (TLS) DNA polymerase is responsible for over 50% of spontaneous mutagenesis and virtually all damage-induced mutagenesis in yeast. We previously demonstrated that reversion of the lys2ΔA746 −1 frameshift allele detects a novel type of +1 frameshift that is accompanied by one or more base substitutions and depends completely on the activity of Polζ. These ‘complex’ frameshifts accumulate at two discrete hotspots (HS1 and HS2) in the absence of nucleotide excision repair, and accumulate at a third location (HS3) in the additional absence of the translesion polymerase Polη. The current study investigates the sequence requirements for accumulation of Polζ-dependent complex frameshifts at these hotspots. We observed that transposing 13 bp of identity from HS1 or HS3 to a new location within LYS2 was sufficient to recapitulate these hotspots. In addition, altering the sequence immediately upstream of HS2 had no effect on the activity of the hotspot. These data support a model in which misincorporation opposite a lesion precedes and facilitates the selected slippage event. Finally, analysis of nonsense mutation revertants indicates that Polζ can simultaneously introduce multiple base substitutions in the absence of an accompanying frameshift event.
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spelling pubmed-23302502008-05-05 The effect of sequence context on spontaneous Polζ-dependent mutagenesis in Saccharomyces cerevisiae Abdulovic, Amy L. Minesinger, Brenda K. Jinks-Robertson, Sue Nucleic Acids Res Molecular Biology The Polζ translesion synthesis (TLS) DNA polymerase is responsible for over 50% of spontaneous mutagenesis and virtually all damage-induced mutagenesis in yeast. We previously demonstrated that reversion of the lys2ΔA746 −1 frameshift allele detects a novel type of +1 frameshift that is accompanied by one or more base substitutions and depends completely on the activity of Polζ. These ‘complex’ frameshifts accumulate at two discrete hotspots (HS1 and HS2) in the absence of nucleotide excision repair, and accumulate at a third location (HS3) in the additional absence of the translesion polymerase Polη. The current study investigates the sequence requirements for accumulation of Polζ-dependent complex frameshifts at these hotspots. We observed that transposing 13 bp of identity from HS1 or HS3 to a new location within LYS2 was sufficient to recapitulate these hotspots. In addition, altering the sequence immediately upstream of HS2 had no effect on the activity of the hotspot. These data support a model in which misincorporation opposite a lesion precedes and facilitates the selected slippage event. Finally, analysis of nonsense mutation revertants indicates that Polζ can simultaneously introduce multiple base substitutions in the absence of an accompanying frameshift event. Oxford University Press 2008-04 2008-02-14 /pmc/articles/PMC2330250/ /pubmed/18276637 http://dx.doi.org/10.1093/nar/gkn054 Text en © 2008 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Molecular Biology
Abdulovic, Amy L.
Minesinger, Brenda K.
Jinks-Robertson, Sue
The effect of sequence context on spontaneous Polζ-dependent mutagenesis in Saccharomyces cerevisiae
title The effect of sequence context on spontaneous Polζ-dependent mutagenesis in Saccharomyces cerevisiae
title_full The effect of sequence context on spontaneous Polζ-dependent mutagenesis in Saccharomyces cerevisiae
title_fullStr The effect of sequence context on spontaneous Polζ-dependent mutagenesis in Saccharomyces cerevisiae
title_full_unstemmed The effect of sequence context on spontaneous Polζ-dependent mutagenesis in Saccharomyces cerevisiae
title_short The effect of sequence context on spontaneous Polζ-dependent mutagenesis in Saccharomyces cerevisiae
title_sort effect of sequence context on spontaneous polζ-dependent mutagenesis in saccharomyces cerevisiae
topic Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2330250/
https://www.ncbi.nlm.nih.gov/pubmed/18276637
http://dx.doi.org/10.1093/nar/gkn054
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