help button home button Endocrine Society Endocrinology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Endocrinology, doi:10.1210/en.2005-0282
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplemental Data
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Request Copyright Permission
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Trevaskis, J.
Right arrow Articles by Collier, G. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Trevaskis, J.
Right arrow Articles by Collier, G. R.
Endocrinology Vol. 146, No. 9 3757-3764
Copyright © 2005 by The Endocrine Society

Src Homology 3-Domain Growth Factor Receptor-Bound 2-Like (Endophilin) Interacting Protein 1, a Novel Neuronal Protein that Regulates Energy Balance

James Trevaskis, Ken Walder, Victoria Foletta, Lyndal Kerr-Bayles, Janine McMillan, Adrian Cooper, Scott Lee, Kristy Bolton, Matthew Prior, Richard Fahey, Kate Whitecross, Gregory J. Morton, Michael W. Schwartz and Greg R. Collier

Metabolic Research Unit (J.T., K.W., V.F., L.K.-B., J.M., A.C., S.L., K.B., M.P., R.F., K.W., G.R.C.), School of Exercise and Nutrition Sciences, Deakin University, and ChemGenex Pharmaceuticals Ltd. (K.W., G.R.C.), Waurn Ponds 3217, Victoria, Australia; Department of Medicine (G.J.M., M.W.S.), Harborview Medical Center and University of Washington, Seattle, Washington 98104; and Pennington Biomedical Research Center (J.T.), Baton Rouge, Louisiana 70808

Address all correspondence and requests for reprints to: Ken Walder, Metabolic Research Unit, School of Health Sciences, Deakin University, Geelong 3217, Victoria, Australia. E-mail: walder{at}deakin.edu.au.

To identify genes involved in the central regulation of energy balance, we compared hypothalamic mRNA from lean and obese Psammomys obesus, a polygenic model of obesity, using differential display PCR. One mRNA transcript was observed to be elevated in obese, and obese diabetic, P. obesus compared with lean animals and was subsequently found to be increased 4-fold in the hypothalamus of lethal yellow agouti (Ay/a) mice, a murine model of obesity and diabetes. Intracerebroventricular infusion of antisense oligonucleotide targeted to this transcript selectively suppressed its hypothalamic mRNA levels and resulted in loss of body weight in both P. obesus and Sprague Dawley rats. Reductions in body weight were mediated by profoundly reduced food intake without a concomitant reduction in metabolic rate. Yeast two-hybrid screening, and confirmation in mammalian cells by bioluminescence resonance energy transfer analysis, demonstrated that the protein it encodes interacts with endophilins, mediators of synaptic vesicle recycling and receptor endocytosis in the brain. We therefore named this transcript Src homology 3-domain growth factor receptor-bound 2-like (endophilin) interacting protein 1 (SGIP1). SGIP1 encodes a large proline-rich protein that is expressed predominantly in the brain and is highly conserved between species. Together these data suggest that SGIP1 is an important and novel member of the group of neuronal molecules required for the regulation of energy homeostasis.




This article has been cited by other articles:


Home page
Mol. Cell. ProteomicsHome page
G. E. Craft, M. E. Graham, N. Bache, M. R. Larsen, and P. J. Robinson
The in Vivo Phosphorylation Sites in Multiple Isoforms of Amphiphysin I from Rat Brain Nerve Terminals
Mol. Cell. Proteomics, June 1, 2008; 7(6): 1146 - 1161.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
A. Uezu, A. Horiuchi, K. Kanda, N. Kikuchi, K. Umeda, K. Tsujita, S. Suetsugu, N. Araki, H. Yamamoto, T. Takenawa, et al.
SGIP1{alpha} Is an Endocytic Protein That Directly Interacts with Phospholipids and Eps15
J. Biol. Chem., September 7, 2007; 282(36): 26481 - 26489.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Endocrinology Endocrine Reviews J. Clin. End. & Metab.
Molecular Endocrinology Recent Prog. Horm. Res. All Endocrine Journals
Copyright © 2005 by The Endocrine Society