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PMID: 2563900 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

A membrane form of guanylate cyclase is an atrial natriuretic peptide receptor.

Nature ·Vol. 338 ·No. 6210 ·1989-03-02 ·Pages 78-83

Chinkers M, Garbers DL, Chang MS, Lowe DG, Chin HM, Goeddel DV, Schulz S

Abstract

Atrial natriuretic peptide (ANP) is a polypeptide hormone whose effects include the induction of diuresis, natriuresis and vasorelaxation. One of the earliest events following binding of ANP to receptors on target cells is an increase in cyclic GMP concentration, indicating that this nucleotide might act as a mediator of the physiological effects of the hormone. Guanylate cyclase exists in at least two different molecular forms: a soluble haem-containing enzyme consisting of two subunits and a non-haem-containing transmembrane protein having a single subunit. It is the membrane form of guanylate cyclase that is activated following binding of ANP to target cells. We report here the isolation, sequence and expression of a complementary DNA clone encoding the membrane form of guanylate cyclase from rat brain. Transfection of this cDNA into cultured mammalian cells results in expression of guanylate cyclase activity and ANP-binding activity. The ANP receptor/guanylate cyclase represents a new class of mammalian cell-surface receptors which contain an extracellular ligand-binding domain and an intracellular guanylate cyclase catalytic domain.

MeSH Terms
Amino Acid Sequence Animals Atrial Natriuretic Factor/metabolism Base Sequence Brain/metabolism Cell Membrane/enzymology DNA/genetics Guanylate Cyclase/genetics Mice Molecular Sequence Data Rats Receptors, Atrial Natriuretic Factor Receptors, Cell Surface/genetics Saccharomyces cerevisiae/genetics Sequence Homology, Nucleic Acid Transfection
Chemicals
Receptors, Cell Surface Atrial Natriuretic Factor DNA Guanylate Cyclase Receptors, Atrial Natriuretic Factor
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Chinkers M
Howard Hughes Medical Institute, Vanderbilt University School of Medicine, Nashville, Tennessee 37232.
Garbers D L
Chang M S
Lowe D G
Chin H M
Goeddel D V
Schulz S
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
1989-03-02
Pages
78-83
Language
English
Region
England
NLM ID
0410462
Subset
IM
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