Mutagenesis during plant responses to UVB radiation
Language English Country France Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
25542779
DOI
10.1016/j.plaphy.2014.12.013
PII: S0981-9428(14)00383-0
Knihovny.cz E-resources
- Keywords
- APT mutagenesis, Comet assay, DNA repair, Error-prone bypass, UV dimers,
- MeSH
- Bryopsida genetics metabolism MeSH
- Mutation * MeSH
- DNA Repair radiation effects MeSH
- Plant Proteins genetics metabolism MeSH
- Ultraviolet Rays * MeSH
- DNA Breaks * MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Plant Proteins MeSH
We tested an idea that induced mutagenesis due to unrepaired DNA lesions, here the UV photoproducts, underlies the impact of UVB irradiation on plant phenotype. For this purpose we used protonemal culture of the moss Physcomitrella patens with 50% of apical cells, which mimics actively growing tissue, the most vulnerable stage for the induction of mutations. We measured the UVB mutation rate of various moss lines with defects in DNA repair (pplig4, ppku70, pprad50, ppmre11), and in selected clones resistant to 2-Fluoroadenine, which were mutated in the adenosine phosphotrasferase gene (APT), we analysed induced mutations by sequencing. In parallel we followed DNA break repair and removal of cyclobutane pyrimidine dimers with a half-life τ = 4 h 14 min determined by comet assay combined with UV dimer specific T4 endonuclease V. We show that UVB induces massive, sequence specific, error-prone bypass repair that is responsible for a high mutation rate owing to relatively slow, though error-free, removal of photoproducts by nucleotide excision repair (NER).
References provided by Crossref.org
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