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PMID: 8227010 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Expression cloning of type 2 angiotensin II receptor reveals a unique class of seven-transmembrane receptors.

The Journal of biological chemistry ·Vol. 268 ·No. 33 ·1993-11-25 ·Pages 24539-42

Mukoyama M, Nakajima M, Horiuchi M, Sasamura H, Pratt RE, Dzau VJ

Abstract

Angiotensin II acts on at least two distinct receptor subtypes (AT1 and AT2). Most known effects of angiotensin II in adult tissues are attributable to the AT1 receptor. The function of AT2 receptor is undefined, but its abundant expressions in fetal tissues, immature brain, skin wound, and atretic ovarian follicles suggest a role in growth and development. Previous studies suggested that AT2 receptor may not be G protein-coupled. Here, from a rat fetus expression library, we cloned a cDNA encoding a unique 363-amino acid protein with pharmacological specificity, tissue distribution, and developmental pattern of the AT2 receptor. It is 34% identical in sequence to the AT1 receptor, sharing a seven-transmembrane domain topology. A review of prior data on other receptors suggests that this receptor may belong to a unique class of seven-transmembrane receptors (including somatostatin SSTR1, dopamine D3, and frizzled protein Fz) for which G protein coupling has not been demonstrated. All members of this class exhibit fetal and developmental and/or neuronal-specific expression. A conserved motif in the third intracellular loop, distinguishing this class from "classical" G protein-coupled receptors, may mediate novel intracellular effects.

MeSH Terms
Amino Acid Sequence Animals Base Sequence Cell Line Cell Membrane/metabolism Cloning, Molecular DNA, Complementary GTP-Binding Proteins/metabolism Molecular Sequence Data RNA, Messenger/metabolism Rats Rats, Sprague-Dawley Receptors, Angiotensin/classification,genetics,metabolism Sequence Homology, Amino Acid
Chemicals
DNA, Complementary RNA, Messenger Receptors, Angiotensin GTP-Binding Proteins
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Mukoyama M
Falk Cardiovascular Research Center, Stanford University School of Medicine, California 94305-5246.
Nakajima M
Horiuchi M
Sasamura H
Pratt R E
Dzau V J
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1993-11-25
Pages
24539-42
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NHLBI NIH HHS · HL35252 · United States
NHLBI NIH HHS · HL35610 · United States
NHLBI NIH HHS · HL46631 · United States
Databases
GENBANK
U01908
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