CREB and ChREBP oppositely regulate SIRT1 expression in response to energy availability

被引:134
作者
Noriega, Lilia G. [1 ,2 ]
Feige, Jerome N. [1 ,2 ]
Canto, Carles [1 ,2 ]
Yamamoto, Hiroyasu [1 ,2 ]
Yu, Jiujiu [1 ,2 ]
Herman, Mark A. [3 ,4 ]
Mataki, Chikage [1 ,2 ]
Kahn, Barbara B. [3 ,4 ]
Auwerx, Johan [1 ,2 ]
机构
[1] Ecole Polytech Fed Lausanne, Lab Integrat & Syst Physiol, CH-1015 Lausanne, Switzerland
[2] Ecole Polytech Fed Lausanne, Nestle Chair Energy Metab, CH-1015 Lausanne, Switzerland
[3] Beth Israel Deaconess Med Ctr, Dept Med, Div Endocrinol Diabet & Metab, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Boston, MA 02115 USA
基金
美国国家卫生研究院; 瑞士国家科学基金会;
关键词
SIRT1; CREB; ChREBP; glucagon; nutrient availability; ELEMENT-BINDING PROTEIN; METABOLIC-REGULATION; GLUCOSE; TRANSCRIPTION; LIVER; MOUSE; DEACETYLASE; PATHWAYS; SIRTUINS; COMPLEX;
D O I
10.1038/embor.2011.151
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
The nicotinamide adenine dinucleotide (NAD(+))-dependent deacetylase SIRT1 is a major metabolic regulator activated by energy stresses such as fasting or calorie restriction. SIRT1 activation during fasting not only relies on the increase in the NAD(+)/NADH ratio caused by energy deprivation but also involves an upregulation of SIRT1 mRNA and protein levels in various metabolic tissues. We demonstrate that SIRT1 expression is controlled systemically by the activation of the cyclic AMP response-element-binding protein upon low nutrient availability. Conversely, in the absence of energetic stress, the carbohydrate response-element-binding protein represses the expression of SIRT1. Altogether, these results demonstrate that SIRT1 expression is tightly controlled at the transcriptional level by nutrient availability and further underscore that SIRT1 is a crucial metabolic checkpoint connecting the energetic status with transcriptional programmes.
引用
收藏
页码:1069 / 1076
页数:8
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