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Discovery of TBC1D1 as an Insulin-, AICAR-, and Contraction-stimulated Signaling Nexus in Mouse Skeletal Muscle

Taylor, Eric B. ; An, Ding ; Kramer, Henning F. ; Yu, Haiyan ; Fujii, Nobuharu L. ; Roeckl, Katja S.C. ; Bowles, Nicole ; Hirshman, Michael F. ; Xie, Jianxin ; Feener, Edward P. ; Goodyear, Laurie J.

The Journal of biological chemistry, 2008-04, Vol.283 (15), p.9787-9796 [Periódico revisado por pares]

United States: Elsevier Inc

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Título:
Discovery of TBC1D1 as an Insulin-, AICAR-, and Contraction-stimulated Signaling Nexus in Mouse Skeletal Muscle
Autor: Taylor, Eric B. ; An, Ding ; Kramer, Henning F. ; Yu, Haiyan ; Fujii, Nobuharu L. ; Roeckl, Katja S.C. ; Bowles, Nicole ; Hirshman, Michael F. ; Xie, Jianxin ; Feener, Edward P. ; Goodyear, Laurie J.
Assuntos: Adipocytes - metabolism ; Amino Acid Motifs - genetics ; Aminoimidazole Carboxamide - analogs & derivatives ; Aminoimidazole Carboxamide - pharmacology ; Animals ; Cyclic AMP-Dependent Protein Kinases - genetics ; Cyclic AMP-Dependent Protein Kinases - metabolism ; Enzyme Activation - drug effects ; Gene Expression Regulation - drug effects ; Gene Expression Regulation - physiology ; Glucose - metabolism ; Glucose Transporter Type 4 - genetics ; Glucose Transporter Type 4 - metabolism ; GTPase-Activating Proteins - genetics ; GTPase-Activating Proteins - metabolism ; Hypoglycemic Agents - pharmacology ; Insulin - pharmacology ; Male ; Metabolism and Bioenergetics ; Mice ; Mice, Inbred ICR ; Muscle Contraction - drug effects ; Muscle Contraction - physiology ; Muscle Proteins - genetics ; Muscle Proteins - metabolism ; Muscle, Skeletal - metabolism ; Nexus ; Nuclear Proteins - genetics ; Nuclear Proteins - metabolism ; Organ Specificity - physiology ; Phosphorylation - drug effects ; Protein Transport - drug effects ; Protein Transport - physiology ; Proto-Oncogene Proteins c-akt - genetics ; Proto-Oncogene Proteins c-akt - metabolism ; Ribonucleotides - pharmacology
É parte de: The Journal of biological chemistry, 2008-04, Vol.283 (15), p.9787-9796
Notas: ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
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To whom correspondence should be addressed: One Joslin Place, Boston, MA 02215. Tel.: 617-732-2573; Fax: 617-732-2650; E-mail: laurie.goodyear@joslin.harvard.edu.
This research was supported by National Institutes of Health Grants AR42238 and AR45670 (to L. J. G.), Individual Kirschstein National Research Service Award F32 DK075851 (to E. B. T.), Joslin Diabetes Center Diabetes and Endocrinology Research Center Grant DK36836, Canadian Institutes of Health Research Fellowship MFE-83802, and Canadian Diabetes Association Incentive Award PF-3-07-2255-DA (to D. A.). The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.
Descrição: The Akt substrate of 160 kDa (AS160) is phosphorylated on Akt substrate (PAS) motifs in response to insulin and contraction in skeletal muscle, regulating glucose uptake. Here we discovered a dissociation between AS160 protein expression and apparent AS160 PAS phosphorylation among soleus, tibialis anterior, and extensor digitorum longus muscles. Immunodepletion of AS160 in tibialis anterior muscle lysates resulted in minimal depletion of the PAS band at 160 kDa, suggesting the presence of an additional PAS immunoreactive protein. By immunoprecipitation and mass spectrometry, we identified this protein as the AS160 paralog TBC1D1, an obesity candidate gene regulating GLUT4 translocation in adipocytes. TBC1D1 expression was severalfold higher in skeletal muscles compared with all other tissues and was the dominant protein detected by the anti-PAS antibody at 160 kDa in tibialis anterior and extensor digitorum longus but not soleus muscles. In vivo stimulation by insulin, contraction, and the AMP-activated protein kinase (AMPK) activator AICAR increased TBC1D1 PAS phosphorylation. Using mass spectrometry on TBC1D1 from mouse skeletal muscle, we identified several novel phosphorylation sites on TBC1D1 and found the majority were consensus or near consensus sites for AMPK. Semiquantitative analysis of spectra suggested that AICAR caused greater overall phosphorylation of TBC1D1 sites compared with insulin. Purified Akt and AMPK phosphorylated TBC1D1 in vitro, and AMPK, but not Akt, reduced TBC1D1 electrophoretic mobility. TBC1D1 is a major PAS immunoreactive protein in skeletal muscle that is phosphorylated in vivo by insulin, AICAR, and contraction. Both Akt and AMPK phosphorylate TBC1D1, but AMPK may be the more robust regulator.
Editor: United States: Elsevier Inc
Idioma: Inglês

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Discovery of TBC1D1 as an Insulin-, AICAR-, and Contraction-stimulated Signaling Nexus in Mouse Skeletal Muscle

Taylor, Eric B. ; An, Ding ; Kramer, Henning F. ; Yu, Haiyan ; Fujii, Nobuharu L. ; Roeckl, Katja S.C. ; Bowles, Nicole ; Hirshman, Michael F. ; Xie, Jianxin ; Feener, Edward P. ; Goodyear, Laurie J.

United States: Elsevier Inc

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