The ubiquitin ligase Fbxw7 controls adipocyte differentiation by targeting C/EBPα for degradation

被引:67
作者
Bengoechea-Alonso, Maria T. [1 ]
Ericsson, Johan [1 ]
机构
[1] Univ Coll Dublin, Sch Med & Med Sci, Conway Inst, Dublin 4, Ireland
基金
爱尔兰科学基金会;
关键词
adipogenesis; CCAAT/enhancer-binding protein; F-BOX PROTEIN; PHOSPHORYLATION-DEPENDENT DEGRADATION; GENE-EXPRESSION; TRANSCRIPTION FACTORS; TUMOR-SUPPRESSOR; CYCLIN-E; C-MYC; FBW7; ADIPOGENESIS; BINDING;
D O I
10.1073/pnas.0913367107
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Adipose tissue controls body lipid and energy metabolism, as well as food intake, and abnormalities in adipose function play a central role in diseases such as obesity and type-2 diabetes. Adipocyte differentiation is controlled by a transcriptional cascade involving PPAR gamma and members of the C/EBP family of transcription factors. Here, we demonstrate that C/EBP alpha is targeted for degradation by the ubiquitin ligase Fbxw7 in a phosphorylation-dependent manner. Importantly, inactivation of Fbxw7 is sufficient to convert mouse preadipocytes into mature adipocytes in a manner dependent on C/EBP alpha. In addition, inactivation of Fbxw7 promotes adipocyte differentiation of human adult stem cells. Taken together, our results suggest that Fbxw7 is a negative regulator of adipogenesis by targeting C/EBP alpha for degradation. This notion is supported by the observation that the expression of Fbxw7 is down-regulated during adipocyte differentiation, resulting in the accumulation of proadipogenic proteins such as C/EBP alpha. Thus, Fbxw7 could be an important regulator of energy and lipid metabolism.
引用
收藏
页码:11817 / 11822
页数:6
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