The 14-3-3 proteins in regulation of cellular metabolism
[Display omitted] ► 14-3-3 Proteins are abundant and have hundreds of binding partners in eukaryotic cells. ► Many of these target phosphoproteins are involved in metabolic control. ► 14-3-3 Binding can amplify and modulate the effects of phosphorylation events. ► 14-3-3 Targets include insulin, mTO...
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Veröffentlicht in: | Seminars in cell & developmental biology 2011-09, Vol.22 (7), p.713-719 |
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Sprache: | eng |
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► 14-3-3 Proteins are abundant and have hundreds of binding partners in eukaryotic cells. ► Many of these target phosphoproteins are involved in metabolic control. ► 14-3-3 Binding can amplify and modulate the effects of phosphorylation events. ► 14-3-3 Targets include insulin, mTOR- and AMP dependent kinase signaling pathways. ► 14-3-3 Proteins can direct metabolic activities at different cellular locations.
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. |
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ISSN: | 1084-9521 1096-3634 |
DOI: | 10.1016/j.semcdb.2011.08.008 |