Opinion: alternative views of AMP-activated protein kinase

被引:0
|
作者
Jay E. Brenman
Brenda R. S. Temple
机构
[1] University of North Carolina at Chapel Hill School of Medicine,Department of Cell and Developmental Biology and Neuroscience Center
[2] University of North Carolina at Chapel Hill School of Medicine,The Juliano Structural Bioinformatics Core Facility
来源
Cell Biochemistry and Biophysics | 2007年 / 47卷
关键词
AMPK; AMP-activated protein kinase; LKB1; Diabetes; Polarity; KA-1 domain;
D O I
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中图分类号
学科分类号
摘要
Genes most closely related to adenosine monophosphate (AMP)-activated protein kinase, including SAD kinases and Par-1 regulate cell polarity, although AMP-activated protein kinase (AMPK) modulates cellular energy status. LKB1 (Par-4) is required for normal activation of AMPK in the liver and also regulates cell polarity. AMPK is proposed to inhibit energy consuming activity while initiating energy producing activity during energy limitation. Demonstration that metformin, a common drug for Type 2 diabetes, requires LKB1 for full therapeutic benefit has increased interest in AMPK signaling. Despite the potential importance of AMPK signaling for diabetes, metabolic syndrome and even cancer, the developmental processes regulated by AMPK in genetically mutant animals require further elucidation. Mouse conditional null mutants for AMPK activity will allow genetic elucidation of AMPK function in vivo. This perspective focuses on sequence and structural moieties of AMPK and genetic analysis of AMPK mutations. Interestingly, the predicted protein structure of the carboxy-terminus of AMPKα resembles the carboxy-terminal KA-1 domain of MARK3, a Par-1 orthologue.
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页码:321 / 331
页数:10
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