A new player in the orchestra of cell growth: SREBP activity is regulated by mTORC1 and contributes to the regulation of cell and organ size

被引:74
|
作者
Porstmann, Thomas [1 ]
Santos, Claudio R. [1 ]
Lewis, Caroline [1 ]
Griffiths, Beatrice [1 ]
Schulze, Almut [1 ]
机构
[1] Canc Res UK London Res Inst, Gene Express Anal Lab, London WC2A 3PX, England
关键词
Akt; cell growth; mammalian target of rapamycin complex 1 (mTORC1); metabolism; sterol-regulatory-element-binding protein (SREBP); ELEMENT-BINDING PROTEINS; ATP CITRATE LYASE; FATTY-ACID; LIPID-SYNTHESIS; ENDOPLASMIC-RETICULUM; TRANSCRIPTION FACTORS; MAMMALIAN TARGET; TRANSGENIC MICE; PATHWAY; KINASE;
D O I
10.1042/BST0370278
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cell growth requires co-ordinated regulation of processes that provide metabolites for the synthesis of macromolecules such as proteins and membrane lipids. In recent years, a lot of emphasis has been placed on the activation of protein synthesis by mTORC1 (mammalian target of rapamycin complex 1). The contribution of anabolic pathways other than protein synthesis has only been considered recently. In the present paper, we discuss recent findings regarding the contribution of transcriptional regulation of lipogenesis genes by the SREBP (sterol-regulatory-element-binding protein) transcription factor, a central regulator of expression of lipogenic genes, to the control of cell size in vitro and cell and organ size in vivo.
引用
收藏
页码:278 / 283
页数:6
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