Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow Print PDF (131K) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Satoh, M.
Right arrow Articles by Hanawalt, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Satoh, M.
Right arrow Articles by Hanawalt, P.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, Vol 24, Issue 18 3576-3582, Copyright © 1996 by Oxford University Press


ARTICLES

TFIIH-mediated nucleotide excision repair and initiation of mRNA transcription in an optimized cell-free DNA repair and RNA transcription assay

MS Satoh and PC Hanawalt
Department of Biological Sciences, Stanford University, CA 94305-5020, USA.

In mammalian cells, mRNA transcription is initiated with the aid of transcription initiation factors. Of these, TFIIH has also been shown to play an essential role in nucleotide excision repair (NER), which is a versatile biochemical pathway that corrects a broad range of DNA damage. Since the dual role of TFIIH is conserved among eukaryotes, including yeast and mammalian cells, the sharing of TFIIH between NER and RNA transcription initiation might provide some survival advantage. However, the functional relationship between NER and RNA transcription initiation through TFIIH is not yet understood. We have developed an optimized cell-free assay which allows us to analyze NER and RNA transcription under identical conditions. In this assay, NER did not compete with RNA transcription, probably because the extracts contained sufficient amounts of TFIIH to support both processes. Thus, NER can be considered functionally independent of RNA transcription initiation despite the fact that both processes use the same factor.
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
D. A. P. Rockx, R. Mason, A. van Hoffen, M. C. Barton, E. Citterio, D. B. Bregman, A. A. van Zeeland, H. Vrieling, and L. H. F. Mullenders
UV-induced inhibition of transcription involves repression of transcription initiation and phosphorylation of RNA polymerase II
PNAS, September 5, 2000; (2000) 180169797.
[Abstract] [Full Text]


Home page
Proc. Natl. Acad. Sci. USAHome page
S. Vispé, T. M. C. Yung, J. Ritchot, H. Serizawa, and M. S. Satoh
A cellular defense pathway regulating transcription through poly(ADP-ribosyl)ation in response to DNA damage
PNAS, August 10, 2000; (2000) 170280397.
[Abstract] [Full Text]


Home page
CarcinogenesisHome page
B. C. McKay, M. Ljungman, and A. J. Rainbow1
Potential roles for p53 in nucleotide excision repair
Carcinogenesis, August 1, 1999; 20(8): 1389 - 1396.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
P. Calsou, P. Frit, O. Humbert, C. Muller, D. J. Chen, and B. Salles
The DNA-dependent Protein Kinase Catalytic Activity Regulates DNA End Processing by Means of Ku Entry into DNA
J. Biol. Chem., March 19, 1999; 274(12): 7848 - 7856.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
Z. You, W. J. Feaver, and E. C. Friedberg
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
Mol. Cell. Biol., May 1, 1998; 18(5): 2668 - 2676.
[Abstract] [Full Text]


Home page
J. Biol. Chem.Home page
C. P. Selby and A. Sancar
Human Transcription-Repair Coupling Factor CSB/ERCC6 Is a DNA-stimulated ATPase but Is Not a Helicase and Does Not Disrupt the Ternary Transcription Complex of Stalled RNA Polymerase II
J. Biol. Chem., January 17, 1997; 272(3): 1885 - 1890.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
P. Frit, R.-Y. Li, D. Arzel, B. Salles, and P. Calsou
Ku Entry into DNA Inhibits Inward DNA Transactions in Vitro
J. Biol. Chem., November 10, 2000; 275(46): 35684 - 35691.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
T. M. C. Yung and M. S. Satoh
Functional Competition between Poly(ADP-ribose) Polymerase and Its 24-kDa Apoptotic Fragment in DNA Repair and Transcription
J. Biol. Chem., March 30, 2001; 276(14): 11279 - 11286.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
S. Vispe, T. M. C. Yung, J. Ritchot, H. Serizawa, and M. S. Satoh
A cellular defense pathway regulating transcription through poly(ADP-ribosyl)ation in response to DNA damage
PNAS, August 29, 2000; 97(18): 9886 - 9891.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
D. A. P. Rockx, R. Mason, A. van Hoffen, M. C. Barton, E. Citterio, D. B. Bregman, A. A. van Zeeland, H. Vrieling, and L. H. F. Mullenders
UV-induced inhibition of transcription involves repression of transcription initiation and phosphorylation of RNA polymerase II
PNAS, September 12, 2000; 97(19): 10503 - 10508.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.