Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow Print PDF (102K) 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 Huang, W
Right arrow Articles by Bateman, E
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Huang, W
Right arrow Articles by Bateman, E
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, Vol 24, Issue 6 1158-1163, Copyright © 1996 by Oxford University Press


ARTICLES

TATA elements direct bi-directional transcription by RNA polymerases II and III

W Huang, JM Wong and E Bateman
Department of Microbiology, University of Vermont, Burlington 05405 USA.

Eukaryotic promoter elements specify the direction and efficiency of transcription, as well as the type of RNA polymerase to be used. One such element, the TATA box, is thought to participate in determining the direction of transcription and can function within promoters for RNA polymerase II or III, depending on the sequence context. In this report the ability of four different TATA boxes to support transcription in vitro was determined. It was found that TATA elements are not directional. However, they support transcription by RNA polymerases II and III. An upstream activating sequence was found to stimulate downstream transcription by RNA polymerase II and to inhibit upstream transcription by RNA polymerases II and III. Thus a promoter necessarily consists of a TATA element and upstream sequences in order to specify the direction of transcription and the type of polymerase to be used.
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
Genes Dev.Home page
L. Schramm and N. Hernandez
Recruitment of RNA polymerase III to its target promoters
Genes & Dev., October 15, 2002; 16(20): 2593 - 2620.
[Full Text] [PDF]


Home page
J. Biol. Chem.Home page
L. Chen and E. Bateman
Linker Scanning Analysis of TBP Promoter Binding Factor DNA Binding, Activation, and Repression Domains
J. Biol. Chem., January 28, 2000; 275(4): 2771 - 2776.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
M. D. Librizzi, M. Brenowitz, and I. M. Willis
The TATA Element and Its Context Affect the Cooperative Interaction of TATA-binding Protein with the TFIIB-related Factor, TFIIIB70
J. Biol. Chem., February 20, 1998; 273(8): 4563 - 4568.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
J. M. Cox, M. M. Hayward, J. F. Sanchez, L. D. Gegnas, S. van der Zee, J. H. Dennis, P. B. Sigler, and A. Schepartz
Bidirectional binding of the TATA box binding protein to the TATA box
PNAS, December 9, 1997; 94(25): 13475 - 13480.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
W. Huang and E. Bateman
Transcription of the Acanthamoeba TATA-binding Protein Gene. A SINGLE TRANSCRIPTION FACTOR ACTS BOTH AS AN ACTIVATOR AND A REPRESSOR
J. Biol. Chem., February 7, 1997; 272(6): 3852 - 3859.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
M. D. Librizzi, R. D. Moir, M. Brenowitz, and I. M. Willis
Expression and Purification of the RNA Polymerase III Transcription Specificity Factor IIIB70 from Saccharomyces cerevisiae and Its Cooperative Binding with TATA-binding Protein
J. Biol. Chem., December 20, 1996; 271(51): 32695 - 32701.
[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.