Home LiteratureArticle Details
PMID: 8394362 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Molecular cloning and expression of a 5-hydroxytryptamine7 serotonin receptor subtype.

The Journal of biological chemistry ·Vol. 268 ·No. 24 ·1993-08-25 ·Pages 18200-4

Shen Y, Monsma FJ, Metcalf MA, Jose PA, Hamblin MW, Sibley DR

Abstract

We have utilized the polymerase chain reaction technique to selectively amplify a G protein-coupled receptor cDNA from rat kidney proximal convoluted tubule mRNA, which exhibits high homology with previously cloned serotonin receptors. Sequencing of a full-length clone isolated from a rat hippocampal cDNA library revealed an open reading frame of 1,212 base pairs encoding a 404-residue protein with seven hydrophobic regions predicted to represent transmembrane-spanning domains. Within the transmembrane regions, this receptor was found to be 44-50% identical with various members of the 5-HT1, 5-HT5, and 5-HT6 subfamilies with lower (37-40%) homology to the 5-HT2-like receptors. Northern blots revealed a approximately 3.6-kilobase transcript localized in various brain regions with the following rank order of abundance: hypothalamus > hippocampus = mesencephalon > cerebral cortex = olfactory bulb > olfactory tubercle. Expression of this clone in COS-7 cells resulted in the appearance of high affinity, saturable binding of [3H]lysergic acid diethylamide ([3H]LSD; KD = 5 nM) and [3H]serotonin ([3H]5-HT; KD = 1 nM). Among endogenous biogenic amines, only 5-HT completely inhibited radioligand binding. The inhibition of radioligand binding by other serotonergic agents revealed a pharmacological profile that does not correlate with any previously described serotonin receptor subtype. In addition, this receptor exhibits high affinity for a number of tricyclic antipsychotic and antidepressant drugs including clozapine, loxapine, and amitriptyline. In HEK-293 cells stably transfected with this receptor, serotonin elicits a potent stimulation of adenylylcyclase activity. The distinct structural and pharmacological properties of this receptor suggests that it represents a completely novel serotonin receptor subtype, which we propose to designate 5-HT7. Based on its pharmacology and its localization to limbic and cortical regions of the brain, it is likely that this receptor may play a role in several neuropsychiatric disorders that involve serotonergic systems.

MeSH Terms
Amino Acid Sequence Animals Base Sequence Binding, Competitive Cell Line Cell Membrane/metabolism Cloning, Molecular/methods Cyclic AMP/metabolism Gene Expression Kidney Tubules, Proximal/metabolism Lysergic Acid Diethylamide/metabolism Molecular Sequence Data Oligodeoxyribonucleotides Polymerase Chain Reaction/methods Radioligand Assay Rats Receptors, Serotonin/biosynthesis,genetics,metabolism Recombinant Proteins/biosynthesis,metabolism Serotonin/metabolism,pharmacology Transfection
Chemicals
Oligodeoxyribonucleotides Receptors, Serotonin Recombinant Proteins Serotonin Lysergic Acid Diethylamide Cyclic AMP
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Shen Y
Molecular Neuropharmacology Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892.
Monsma F J
Metcalf M A
Jose P A
Hamblin M W
Sibley D R
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1993-08-25
Pages
18200-4
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Databases
GENBANK
L15228
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]