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The 14-3-3 proteins in regulation of cellular metabolism

期刊

SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY
卷 22, 期 7, 页码 713-719

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.semcdb.2011.08.008

关键词

14-3-3 Proteins; Metabolism; Tyrosine hydroxylase; Membrane association; Cell signaling

资金

  1. Research Council of Norway
  2. Kristian Gerhard Jebsen Foundation
  3. Norwegian Cancer Society
  4. Western Norway Health Authorities

向作者/读者索取更多资源

Thirty years ago, it was discovered that 14-3-3 proteins could activate enzymes involved in amino acid metabolism. In the following decades, 14-3-3s have been shown to be involved in many different signaling pathways that modulate cellular and whole body energy and nutrient homeostasis. Large scale screening for cellular binding partners of 14-3-3 has identified numerous proteins that participate in regulation of metabolic pathways, although only a minority of these targets have yet been subject to detailed studies. Because of the wide distribution of potential 14-3-3 targets and the resurging interest in metabolic pathway control in diseases like cancer, diabetes, obesity and cardiovascular disease, we review the role of 14-3-3 proteins in the regulation of core and specialized cellular metabolic functions. We cite illustrative examples of 14-3-3 action through their direct modulation of individual enzymes and through regulation of master switches in cellular pathways, such as insulin signaling, mTOR- and AMP dependent kinase signaling pathways, as well as regulation of autophagy. We further illustrate the quantitative impact of 14-3-3 association on signal response at the target protein level and we discuss implications of recent findings showing 14-3-3 protein membrane binding of target proteins. (C) 2011 Elsevier Ltd. All rights reserved.

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