Document Detail


Dual modification of BMAL1 by SUMO2/3 and ubiquitin promotes circadian activation of the CLOCK/BMAL1 complex.
MedLine Citation:
PMID:  18644859     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Heterodimers of BMAL1 and CLOCK drive rhythmic expression of clock-controlled genes, thereby generating circadian physiology and behavior. Posttranslational modifications of BMAL1 play a key role in modulating the transcriptional activity of the CLOCK/BMAL1 complex during the circadian cycle. Recently, we demonstrated that circadian activation of the heterodimeric transcription factor is accompanied by ubiquitin-dependent proteolysis of BMAL1. Here we show that modification by SUMO localizes BMAL1 exclusively to the promyelocytic leukemia nuclear body (NB) and simultaneously promotes its transactivation and ubiquitin-dependent degradation. Under physiological conditions, BMAL1 was predominantly conjugated to poly-SUMO2/3 rather than SUMO1, and the level of these conjugates underwent rhythmic variation, peaking at times of maximum E-box-mediated circadian transcription. Interestingly, mutation of the sumoylation site (Lys(259)) of BMAL1 markedly inhibited both its ubiquitination and its proteasome-mediated proteolysis, and these effects were reversed by covalent attachment of SUMO3 to the C terminus of the mutant BMAL1. Consistent with this, SUSP1, a SUMO protease highly specific for SUMO2/3, abolished ubiquitination, as well as sumoylation of BMAL1, while the ubiquitin protease UBP41 blocked BMAL1 ubiquitination but induced accumulation of polysumoylated BMAL1 and its localization to the NB. Furthermore, inhibition of proteasome with MG132 elicited robust nuclear accumulation of SUMO2/3- and ubiquitin-modified BMAL1 that was restricted to the transcriptionally active stage of the circadian cycle. These results indicate that dual modification of BMAL1 by SUMO2/3 and ubiquitin is essential for circadian activation and degradation of the CLOCK/BMAL1 complex.
Authors:
Jiwon Lee; Yool Lee; Min Joo Lee; Eonyoung Park; Sung Hwan Kang; Chin Ha Chung; Kun Ho Lee; Kyungjin Kim
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2008-07-21
Journal Detail:
Title:  Molecular and cellular biology     Volume:  28     ISSN:  1098-5549     ISO Abbreviation:  Mol. Cell. Biol.     Publication Date:  2008 Oct 
Date Detail:
Created Date:  2008-09-23     Completed Date:  2008-10-20     Revised Date:  2013-06-05    
Medline Journal Info:
Nlm Unique ID:  8109087     Medline TA:  Mol Cell Biol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  6056-65     Citation Subset:  IM    
Affiliation:
School of Biological Sciences, Seoul National University, Seoul 151-742, Republic of Korea.
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MeSH Terms
Descriptor/Qualifier:
ARNTL Transcription Factors
Animals
Basic Helix-Loop-Helix Transcription Factors / metabolism*
CLOCK Proteins
COS Cells
Cercopithecus aethiops
Circadian Rhythm
Dimerization
HeLa Cells
Humans
Mice
NIH 3T3 Cells
Protein Processing, Post-Translational*
Small Ubiquitin-Related Modifier Proteins / metabolism*
Trans-Activators / metabolism*
Ubiquitins / metabolism*
Chemical
Reg. No./Substance:
0/ARNTL Transcription Factors; 0/ARNTL protein, human; 0/Arntl protein, mouse; 0/Basic Helix-Loop-Helix Transcription Factors; 0/Small Ubiquitin-Related Modifier Proteins; 0/Trans-Activators; 0/Ubiquitins; EC 2.3.1.48/CLOCK Proteins; EC 2.3.1.48/CLOCK protein, human; EC 2.3.1.48/Clock protein, mouse
Comments/Corrections

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