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SUMO modification negatively modulates the transcriptional activity of CREB-binding protein via the recruitment of Daxx
- Publication Year :
- 2005
- Publisher :
- National Academy of Sciences, 2005.
-
Abstract
- Small ubiquitin-like modifier (SUMO) modification is emerging as an important control in transcription regulation. Here, we show that CREB-binding protein (CBP), a versatile transcriptional coactivator for numerous transcription factors in response to diverse signaling events, can be modified by SUMO-1 at lysine residues 999, 1034, and 1057 both in vitro and in vivo . Mutation of the SUMO acceptor lysine residues either individually or in combination enhanced CBP transcriptional activity, and expression of a SUMO protease SENP2 potentiated the transcriptional activity of CBP wild-type but not its sumoylation mutant, indicating that SUMO modification negatively regulates CBP transcriptional activity. Furthermore, we demonstrated an interaction of SUMO-1-modified CBP with the transcriptional corepressor Daxx and an essential role of Daxx in mediating SUMO-dependent transcriptional regulation of CBP through histone deacetylase 2 recruitment. Together, our findings indicate that SUMO modification and subsequent recruitment of Daxx represent a previously undescribed mechanism in modulating CBP transcriptional potential.
- Subjects :
- Co-Repressor Proteins
Transcription, Genetic
genetic processes
SUMO-1 Protein
SUMO protein
Down-Regulation
macromolecular substances
environment and public health
Mice
Death-associated protein 6
Chlorocebus aethiops
Transcriptional regulation
Animals
Humans
Nuclear protein
CREB-binding protein
Transcription factor
Multidisciplinary
biology
Histone deacetylase 2
Lysine
Intracellular Signaling Peptides and Proteins
Nuclear Proteins
Biological Sciences
Molecular biology
CREB-Binding Protein
Cell biology
enzymes and coenzymes (carbohydrates)
COS Cells
biology.protein
health occupations
Carrier Proteins
HeLa Cells
Molecular Chaperones
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....fb74fb442a22585494cd3747d72c05a9