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Acta Academiae Medicinae Sinicae ; (6): 756-759, 2009.
Article in Chinese | WPRIM | ID: wpr-301613

ABSTRACT

<p><b>OBJECTIVE</b>To explore the effects of PIH1D1 on its binding protein SNF5, a core subunit of the SWI/SNF chromatin remodeling complex.</p><p><b>METHOD</b>The degradation pathway of SNF5 was identified with protein synthesis inhibitor cycloheximide (CHX) and a potent proteasome inhibitor MG132, and then the PIH1D1 eukaryotic expression plasmid was transfected to explore its effect on the stability of SNF5.</p><p><b>RESULTS</b>HEK293T cells were effectively treated with CHX (optimal concentration: 400 microg/ml) and MG132 (optimal concentration: 20 mmol/L). The degradation of SNF5 was mediated by the proteasome pathway. PIH1D1 regulated the protein level of SNF5 by attenuating its proteasome degradation.</p><p><b>CONCLUSION</b>PIH1D1 may stabilize SNF5 by attenuating its proteasome degradation pathway.</p>


Subject(s)
Humans , Apoptosis Regulatory Proteins , Genetics , Metabolism , Chromosomal Proteins, Non-Histone , Metabolism , DNA-Binding Proteins , Metabolism , Genetic Vectors , HEK293 Cells , Plasmids , Genetics , Proteasome Endopeptidase Complex , Metabolism , SMARCB1 Protein , Transcription Factors , Metabolism , Transfection
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