The ability to associate with activation domains in vitro is not required for the TATA box-binding protein to support activated transcription in vivo.

Details

Serval ID
serval:BIB_7B05E33CCEE8
Type
Article: article from journal or magazin.
Collection
Publications
Title
The ability to associate with activation domains in vitro is not required for the TATA box-binding protein to support activated transcription in vivo.
Journal
Proceedings of the National Academy of Sciences of the United States of America
Author(s)
Tansey W.P., Herr W.
ISSN
0027-8424
Publication state
Published
Issued date
11/1995
Peer-reviewed
Oui
Volume
92
Number
23
Pages
10550-10554
Language
english
Abstract
The TATA box-binding protein (TBP) interacts in vitro with the activation domains of many viral and cellular transcription factors and has been proposed to be a direct target for transcriptional activators. We have examined the functional relevance of activator-TBP association in vitro to transcriptional activation in vivo. We show that alanine substitution mutations in a single loop of TBP can disrupt its association in vitro with the activation domains of the herpes simplex virus activator VP16 and of the human tumor suppressor protein p53; these mutations do not, however, disrupt the transcriptional response of TBP to either activation domain in vivo. Moreover, we show that a region of VP16 distinct from its activation domain can also tightly associate with TBP in vitro, but fails to activate transcription in vivo. These data suggest that the ability of TBP to interact with activation domains in vitro is not directly relevant to its ability to support activated transcription in vivo.
Keywords
DNA-Binding Proteins, Herpes Simplex Virus Protein Vmw65, Humans, Models, Molecular, Point Mutation, Protein Binding, Structure-Activity Relationship, TATA-Box Binding Protein, Transcription Factors, Transcription, Genetic, Tumor Suppressor Protein p53
Pubmed
Web of science
Open Access
Yes
Create date
24/01/2008 15:36
Last modification date
20/08/2019 14:36
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