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PMID: 9192681 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Anatomic localization of alternatively spliced leptin receptors (Ob-R) in mouse brain and other tissues.

Fei H, Okano HJ, Li C, Lee GH, Zhao C, Darnell R, Friedman JM

Abstract

Leptin's effects are mediated by interactions with a receptor that is alternatively spliced, resulting in at least five different murine forms: Ob-Ra, Ob-Rb, Ob-Rc, Ob-Rd, and Ob-Re. A mutation in one splice form, Ob-Rb, results in obesity in mice. Northern blots, RNase protection assays, and PCR indicate that Ob-Rb is expressed at a relatively high level in hypothalamus and low level in several other tissues. Ob-Ra is expressed ubiquitously, whereas Ob-Rc, -Rd, and -Re RNAs are only detectable using PCR. In hypothalamus, Ob-Rb is present in the arcuate, ventromedial, dorsomedial, and lateral hypothalamic nuclei but is not detectable in other brain regions. These nuclei are known to regulate food intake and body weight. The level of Ob-Rb in hypothalamus is reduced in mice rendered obese by gold thioglucose (GTG), which causes hypothalamic lesions. The obesity in GTG-treated mice is likely to be caused by ablation of Ob-Rb-expressing neurons, which results in leptin resistance.

MeSH Terms
Alternative Splicing Animals Blotting, Northern Brain/metabolism Carrier Proteins/genetics,metabolism In Situ Hybridization Mice Molecular Sequence Data Mutation Organ Specificity Receptors, Cell Surface Receptors, Leptin
Chemicals
Carrier Proteins Receptors, Cell Surface Receptors, Leptin leptin receptor, mouse
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Fei H
Laboratory of Molecular Genetics, Rockefeller University, 1230 York Avenue, New York, NY 10021, USA.
Okano H J
Li C
Lee G H
Zhao C
Darnell R
Friedman J M
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1997-06-24
Pages
7001-5
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC21274
Subset
IM
Grants
NIDDK NIH HHS · DK41096 · United States
NCI NIH HHS · CA09673-18 · United States
NIDDK NIH HHS · R01 DK041096 · United States
NINDS NIH HHS · R01 NS034389 · United States
NCI NIH HHS · T32 CA009673 · United States
NINDS NIH HHS · R01NS34389 · United States
Databases
GENBANK
U97032, U97034
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