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Originally published In Press as doi:10.1074/jbc.M007311200 on November 14, 2000
J. Biol. Chem., Vol. 276, Issue 8, 5900-5907, February 23, 2001
Diacylglycerol Kinase in Hypothalamus Interacts with Long
Form Leptin Receptor
RELATION TO DIETARY FAT AND BODY WEIGHT REGULATION*
Zhitong
Liu,
Guo-Qing
Chang, and
Sarah F.
Leibowitz
From The Rockefeller University, New York, New York 10021
Leptin and its long form receptor, Ob-Rb, in
hypothalamic nuclei play a key role in regulating energy balance. The
mutation of Ob-Rb into one of its natural variants, Ob-Ra, results in
severe obesity in rodents. We demonstrate here that diacylglycerol
kinase (DGK ) interacts, via its ankyrin repeats, with the
cytoplasmic portion of Ob-Rb in yeast two-hybrid systems, in protein
precipitation experiments in vitro and in vivo.
It does not interact, however, with the short form, Ob-Ra, which
mediates the entry of leptin into the brain. Furthermore, we show by
in situ hybridization that DGK is expressed in neurons
of hypothalamic nuclei known to synthesize Ob-Rb and to participate in
energy homeostasis. The mutant ob-/ob- and
db-/db- mice exhibit increased hypothalamic DGK mRNA level compared with their wild-type controls,
suggesting a role for the leptin/OB-Rb system in regulating DGK
expression. Further experiments show that hypothalamic DGK mRNA
level is stimulated by the consumption of a high-fat diet. In addition, DGK mRNA is statistically significantly lower in rats and inbred mice that become obese on a high-fat diet compared with their lean
counterparts. In fact, it is strongly, negatively correlated with both
body fat and circulating levels of leptin. Taken together, our evidence
suggests that DGK constitutes a downstream component of the leptin
signaling pathway and that reduced hypothalamic DGK mRNA, and
possibly activity, is associated with obesity.
*
The work was supported by National Institutes of Health
Grant MH43422 and the Price Foundation.The costs of publication of this
article were defrayed in part by the
payment of page charges. The article
must therefore be hereby marked
"advertisement" in accordance with 18 U.S.C. Section
1734 solely to indicate this fact.
To whom correspondence should be addressed: The Rockefeller
University, Box 278, 1230 York Ave., New York, NY 10021. Tel.: 212-327-8378; Fax: 212-327-8447; E-mail:
leibow@rockvax.rockefeller.edu.
Copyright © 2001 by The American Society for Biochemistry and Molecular Biology, Inc.

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