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TRB3 Links the E3 Ubiquitin Ligase COP1 to Lipid Metabolism
Ling Qi,1*Jose E. Heredia,1*Judith Y. Altarejos,1Robert Screaton,1Naomi Goebel,1Sherry Niessen,2Ian X. MacLeod,2Chong Wee Liew,3Rohit N. Kulkarni,3James Bain,4Christopher Newgard,4Michael Nelson,1Ronald M. Evans,1John Yates,2Marc Montminy1
During fasting, increased concentrations of circulating catecholaminespromote the mobilization of lipid stores from adipose tissuein part by phosphorylating and inactivating acetylcoenzymeA carboxylase (ACC), the rate-limiting enzyme in fatty acidsynthesis. Here, we describe a parallel pathway, in which thepseudokinase Tribbles 3 (TRB3), whose abundance is increasedduring fasting, stimulates lipolysis by triggering the degradationof ACC in adipose tissue. TRB3 promoted ACC ubiquitination throughan association with the E3 ubiquitin ligase constitutive photomorphogenicprotein 1 (COP1). Indeed, adipocytes deficient in TRB3 accumulatedlarger amounts of ACC protein than did wild-type cells. Becausetransgenic mice expressing TRB3 in adipose tissue are protectedfrom diet-induced obesity due to enhanced fatty acid oxidation,these results demonstrate how phosphorylation and ubiquitinationpathways converge on a key regulator of lipid metabolism tomaintain energy homeostasis.
1 Peptide Biology Laboratories and Gene Expression Laboratories, Salk Institute for Biological Studies, La Jolla, CA 92037, USA. 2 The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA. 3 Joslin Diabetes Center, One Joslin Place, Boston, MA 02215, USA. 4 Sarah W. Stedman Nutrition and Metabolism Center, Duke University Medical Center, 4321 Medical Park Drive, Suite 200, Durham, NC 27704, USA.
* These authors contributed equally to this work.
To whom correspondence should be addressed. E-mail: montminy{at}salk.edu
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