GTC
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE ADVANCED SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
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 Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Fukuda, A
Right arrow Articles by Hisatake, K
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Fukuda, A
Right arrow Articles by Hisatake, K
GENES CELLS (2001) 6, 707-719.
Copyright © 2001 Blackwell Publishing or its licensors



Original Article

Reconstitution of recombinant TFIIH that can mediate activator-dependent transcription

A Fukuda, J Yamauchi, SY Wu, CM Chiang, M Muramatsu, and K Hisatake

BACKGROUND: TFIIH is one of the general transcription factors required for accurate transcription of protein-coding genes by RNA polymerase II. TFIIH has helicase and kinase activities, plays a role in promoter opening and promoter escape, and is also implicated in efficient activator-dependent transcription. RESULTS: We have established a reconstitution system of recombinant TFIIH using a three-virus baculovirus expression system. The recombinant TFIIH was active in CTD kinase and DNA helicase assays, and showed both basal and activator-dependent transcriptional activities that were indistinguishable from those of HeLa cell-derived TFIIH. Further analyses using recombinant TFIIH confirmed a critical role of TFIIH in activator-dependent transcription. The dose response of TFIIH in activator-dependent transcription suggested that mere recruitment of TFIIH is not sufficient for transcriptional activation. The sensitivity of activator-dependent transcription to nonhydrolysable ATP analogues indicated the importance of the enzymatic activities of TFIIH in transcriptional activation. CONCLUSIONS: Our results raise a possibility that transcriptional activation by GAL4-VP16 requires enzymatic activities. Recombinant TFIIH reconstituted from this baculovirus system should be useful for analysis of the mechanisms of activation by GAL4-VP16.


This article has been cited by other articles:


Home page
Mol. Cell. Biol.Home page
A. Fukuda, T. Nakadai, M. Shimada, T. Tsukui, M. Matsumoto, Y. Nogi, M. Meisterernst, and K. Hisatake
Transcriptional Coactivator PC4 Stimulates Promoter Escape and Facilitates Transcriptional Synergy by GAL4-VP16
Mol. Cell. Biol., July 15, 2004; 24(14): 6525 - 6535.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
A. Fukuda, S. Tokonabe, M. Hamada, M. Matsumoto, T. Tsukui, Y. Nogi, and K. Hisatake
Alleviation of PC4-mediated Transcriptional Repression by the ERCC3 Helicase Activity of General Transcription Factor TFIIH
J. Biol. Chem., April 18, 2003; 278(17): 14827 - 14831.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
E. Botta, T. Nardo, A. R. Lehmann, J.-M. Egly, A. M. Pedrini, and M. Stefanini
Reduced level of the repair/transcription factor TFIIH in trichothiodystrophy
Hum. Mol. Genet., November 1, 2002; 11(23): 2919 - 2928.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
A. Fukuda, Y. Nogi, and K. Hisatake
The regulatory role for the ERCC3 helicase of general transcription factor TFIIH during promoter escape in transcriptional activation
PNAS, February 5, 2002; 99(3): 1206 - 1211.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE ADVANCED SEARCH TABLE OF CONTENTS
Copyright © 2001 by Wiley-Blackwell Publishing.