Abstract
UV-induced DNA damage causes cells to repress RNA synthesis and to initiate nucleotide excision repair (NER). NER and transcription are intimately linked processes. Evidence has been presented that, in addition to damaged genes, undamaged loci are transcriptionally inhibited. We investigated whether RNA synthesis from undamaged genes is affected by the presence of UV damage elsewhere in the same nucleus, using a novel technique to UV irradiate only part of a nucleus. We show that the basal transcription/repair factor TFIIH is recruited to the damaged nuclear area, partially depleting the undamaged nuclear area. Remarkably, this sequestration has no effect on RNA synthesis. This result was obtained for cells that are able to carry out NER and for cells deficient in NER. We conclude that cross talk between NER and transcription occurs only over short distances in nuclei of living cells.
MeSH Terms
Cell Nucleus/radiation effects
Cells, Cultured
DNA Damage
DNA Repair
Fibroblasts/radiation effects
Humans
Microscopy, Fluorescence
Plasmids/metabolism
Time Factors
Transcription Factor TFIIH
Transcription Factors/metabolism
Transcription Factors, TFII
Transcription, Genetic/radiation effects
Ultraviolet Rays
Chemicals
Transcription Factors
Transcription Factors, TFII
Transcription Factor TFIIH
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Moné M J
Swammerdam Institute for Life Sciences, BioCentrum Amsterdam, University of Amsterdam, Plantage Muidergracht 12, 1018 TV Amsterdam, The Netherlands.
Volker M
Nikaido O
Mullenders L H
van Zeeland A A
Verschure P J
Manders E M
van Driel R
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