Source:http://linkedlifedata.com/resource/pubmed/id/16987992
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2007-1-12
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pubmed:abstractText |
The role of the proteasome in the regulation of cellular levels of the transcription factor CCAAT/enhancer-binding protein beta (C/EBPbeta) is poorly understood. We tested the hypothesis that C/EBPbeta levels in cultured myotubes are regulated, at least in part, by proteasome activity. Treatment of cultured L6 myotubes, a rat skeletal muscle cell line, with the specific proteasome inhibitor beta-lactone resulted in increased nuclear levels of C/EBPbeta as determined by Western blotting and immunofluorescent detection. This effect of beta-lactone reflected inhibited degradation of C/EBPbeta. Surprisingly, the increased C/EBPbeta levels in beta-lactone-treated myotubes did not result in increased DNA-binding activity. In additional experiments, treatment of the myotubes with beta-lactone resulted in increased nuclear levels of growth arrest DNA damage/C/EBP homologous protein (Gadd153/CHOP), a dominant-negative member of the C/EBP family that can form heterodimers with other members of the C/EBP family and block DNA binding. Coimmunoprecipitation and immunofluorescent detection provided evidence that C/EBPbeta and Gadd153/CHOP interacted and colocalized in the nuclei of the beta-lactone-treated myotubes. When Gadd153/CHOP expression was downregulated by transfection of myotubes with siRNA targeting Gadd153/CHOP, C/EBPbeta DNA-binding activity was restored in beta-lactone-treated myotubes. The results suggest that C/EBPbeta is degraded by a proteasome-dependent mechanism in skeletal muscle cells and that Gadd153/CHOP can interact with C/EBPbeta and block its DNA-binding activity. The observations are important because they increase the understanding of the complex regulation of the expression and activity of C/EBPbeta in skeletal muscle.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/CCAAT-Enhancer-Binding Protein-beta,
http://linkedlifedata.com/resource/pubmed/chemical/DNA,
http://linkedlifedata.com/resource/pubmed/chemical/Lactones,
http://linkedlifedata.com/resource/pubmed/chemical/Proteasome Endopeptidase Complex,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Small Interfering,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factor CHOP,
http://linkedlifedata.com/resource/pubmed/chemical/clasto-lactacystin beta-lactone
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0363-6143
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
292
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
C216-26
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:16987992-Animals,
pubmed-meshheading:16987992-Blotting, Western,
pubmed-meshheading:16987992-CCAAT-Enhancer-Binding Protein-beta,
pubmed-meshheading:16987992-Cell Line,
pubmed-meshheading:16987992-Cell Nucleus,
pubmed-meshheading:16987992-DNA,
pubmed-meshheading:16987992-DNA Damage,
pubmed-meshheading:16987992-Down-Regulation,
pubmed-meshheading:16987992-Fluorescent Antibody Technique,
pubmed-meshheading:16987992-Lactones,
pubmed-meshheading:16987992-Muscle Fibers, Skeletal,
pubmed-meshheading:16987992-Proteasome Endopeptidase Complex,
pubmed-meshheading:16987992-RNA, Small Interfering,
pubmed-meshheading:16987992-Rats,
pubmed-meshheading:16987992-Tissue Distribution,
pubmed-meshheading:16987992-Transcription Factor CHOP
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pubmed:year |
2007
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pubmed:articleTitle |
Treatment of cultured myotubes with the proteasome inhibitor beta-lactone increases the expression of the transcription factor C/EBPbeta.
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pubmed:affiliation |
Department of Surgery, Beth Israel Deaconess Medical Center, 330 Brookline Avenue ST 919, Boston, MA 02215, USA.
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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