Cloning of a Xenopus laevis muscarinic receptor encoded by an intronless gene.

Abstract:

:The Xenopus laevis oocyte has endogenous sites that bind muscarinic agonists, which have been pharmacologically characterized as M3 and/or M1 receptor subtypes. In order to define the molecular identify of the receptor protein we have analyzed a Xenopus oocyte cDNA library and cloned a 2.9 kb cDNA fragment encoding a muscarinic receptor (xMR). The deduced amino acid sequence reveals a protein of 484 residues with an apparent molecular weight of 54,188 Da. Amino acid comparison with previously cloned mammalian muscarinic receptors showed a 78% identity with the human m4 subtype, presenting at the same time clustered differences within the amino-terminal region and third intracellular loop Genomic Southern analysis displayed the presence of one main gene belonging to this subtype, and the PCR analysis revealed an intronless gene.

journal_name

FEBS Lett

journal_title

FEBS letters

authors

Herrera L,Carvallo P,Antonelli M,Olate J

doi

10.1016/0014-5793(94)00957-0

subject

Has Abstract

pub_date

1994-09-26 00:00:00

pages

175-9

issue

2

eissn

0014-5793

issn

1873-3468

pii

0014-5793(94)00957-0

journal_volume

352

pub_type

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