Cytoplasmic Polyadenylation Element Binding Protein Deficiency Stimulates PTEN and Stat3 mRNA Translation and Induces Hepatic Insulin Resistance

被引:54
作者
Alexandrov, Ilya M. [1 ]
Ivshina, Maria [1 ]
Jung, Dae Young [1 ]
Friedline, Randall [1 ]
Ko, Hwi Jin [1 ]
Xu, Mei [2 ]
O'Sullivan-Murphy, Bryan [1 ,3 ]
Bortell, Rita [1 ]
Huang, Yen-Tsung [4 ,5 ]
Urano, Fumihiko [1 ,3 ]
Kim, Jason K. [1 ,6 ]
Richter, Joel D. [1 ]
机构
[1] Univ Massachusetts, Sch Med, Program Mol Med, Worcester, MA 01605 USA
[2] Univ Massachusetts, Sch Med, Informat Serv Dept, Worcester, MA USA
[3] Univ Massachusetts, Sch Med, Program Gene Funct & Express, Worcester, MA USA
[4] Harvard Univ, Dept Epidemiol, Boston, MA 02115 USA
[5] Harvard Univ, Dept Biostat, Boston, MA 02115 USA
[6] Univ Massachusetts, Sch Med, Dept Med, Div Endocrinol Diabet & Metab, Worcester, MA USA
关键词
LARGE GENE LISTS; CELLULAR SENESCENCE; CPEB; PHOSPHORYLATION; MECHANISMS; MATURATION; PATHWAY; MUSCLE; MICE;
D O I
10.1371/journal.pgen.1002457
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
The cytoplasmic polyadenylation element binding protein CPEB1 (CPEB) regulates germ cell development, synaptic plasticity, and cellular senescence. A microarray analysis of mRNAs regulated by CPEB unexpectedly showed that several encoded proteins are involved in insulin signaling. An investigation of Cpeb1 knockout mice revealed that the expression of two particular negative regulators of insulin action, PTEN and Stat3, were aberrantly increased. Insulin signaling to Akt was attenuated in livers of CPEB-deficient mice, suggesting that they might be defective in regulating glucose homeostasis. Indeed, when the Cpeb1 knockout mice were fed a high-fat diet, their livers became insulin-resistant. Analysis of HepG2 cells, a human liver cell line, depleted of CPEB demonstrated that this protein directly regulates the translation of PTEN and Stat3 mRNAs. Our results show that CPEB regulated translation is a key process involved in insulin signaling.
引用
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页数:11
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