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Mol Cell Biol, May 1998, p. 2668-2676, Vol. 18, No. 5
Laboratory of Molecular Pathology, Department
of Pathology, University of Texas Southwestern Medical Center,
Dallas, Texas 75235
Received 22 December 1997/Returned for modification 6 February
1998/Accepted 20 February 1998
The Saccharomyces cerevisiae transcription factor IIH
(TFIIH) is essential both for transcription by RNA polymerase II (RNAP II) and for nucleotide excision repair (NER) of damaged DNA. We have
established cell extracts which support RNAP II transcription from the
yeast CYC1 promoter or NER of transcriptionally silent damaged DNA on independent plasmid templates and substrates. When plasmid templates and substrates for both processes are simultaneously incubated with these extracts, transcription is significantly inhibited. This inhibition is strictly dependent on active NER and can
be complemented with purified holo-TFIIH. These results suggest that in
the presence of active NER, TFIIH is preferentially mobilized from the
basal transcription machinery for use in NER. Inhibition of
transcription in the presence of active NER requires the
RAD26 gene, the yeast homolog of the human Cockayne
syndrome group B gene (CSB).
0270-7306/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Yeast RNA Polymerase II Transcription In Vitro Is Inhibited in
the Presence of Nucleotide Excision Repair: Complementation of
Inhibition by Holo-TFIIH and Requirement for RAD26
*
Corresponding author. Mailing address: Laboratory of
Molecular Pathology, Department of Pathology, University of Texas
Southwestern Medical Center, Dallas, TX 75235. Phone: (214) 648-4020. Fax: (214) 648-4067. E-mail:
friedberg.errol{at}pathology.swmed.edu.
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