REV-ERBα influences the stability and nuclear localization of the glucocorticoid receptor

被引:40
|
作者
Okabe, Takashi [1 ]
Chavan, Rohit [1 ]
Costa, Sara S. Fonseca [1 ]
Brenna, Andrea [1 ]
Ripperger, Juergen A. [1 ]
Albrecht, Urs [1 ]
机构
[1] Univ Fribourg, Dept Biol, Dept Biochem, CH-1700 Fribourg, Switzerland
基金
瑞士国家科学基金会;
关键词
Nuclear receptor; Circadian clock; Glucocorticoid receptor; REV-ERB alpha; HSP90; KAPPA-B-ALPHA; MOLECULAR-MECHANISMS; INNATE IMMUNITY; TRANSCRIPTION; ACTIVATION; IMMUNOSUPPRESSION; DEGRADATION; SPECIFICITY; BINDING; HSP90;
D O I
10.1242/jcs.190959
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
REV-ERB alpha (encoded by Nr1d1) is a nuclear receptor that is part of the circadian clock mechanism and regulates metabolism and inflammatory processes. The glucocorticoid receptor (GR, encoded by Nr3c1) influences similar processes, but is not part of the circadian clock, although glucocorticoid signaling affects resetting of the circadian clock in peripheral tissues. Because of their similar impact on physiological processes, we studied the interplay between these two nuclear receptors. We found that REV-ERB alpha binds to the C-terminal portion and GR to the N-terminal portion of HSP90 alpha and HSP90 beta, a chaperone responsible for the activation of proteins to ensure survival of a cell. The presence of REV-ERB alpha influences the stability and nuclear localization of GR by an unknown mechanism, thereby affecting expression of GR target genes, such as I.Ba (Nfkbia) and alcohol dehydrogenase 1 (Adh1). Our findings highlight an important interplay between two nuclear receptors that influence the transcriptional potential of each other. This indicates that the transcriptional landscape is strongly dependent on dynamic processes at the protein level.
引用
收藏
页码:4143 / 4154
页数:12
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