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SUMO modification negatively modulates the transcriptional activity of CREB-binding protein via the recruitment of Daxx.


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.

SUBMITTER: Kuo HY 

PROVIDER: S-EPMC1287974 | biostudies-literature | 2005 Nov

REPOSITORIES: biostudies-literature

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SUMO modification negatively modulates the transcriptional activity of CREB-binding protein via the recruitment of Daxx.

Kuo Hong-Yi HY   Chang Che-Chang CC   Jeng Jen-Chong JC   Hu Hui-Mei HM   Lin Ding-Yen DY   Maul Gerd G GG   Kwok Roland P S RP   Shih Hsiu-Ming HM  

Proceedings of the National Academy of Sciences of the United States of America 20051115 47


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 exp  ...[more]

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