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PMID: 1358887 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Beta-adrenergic agonists that down-regulate receptor mRNA up-regulate a M(r) 35,000 protein(s) that selectively binds to beta-adrenergic receptor mRNAs.

The Journal of biological chemistry ·Vol. 267 ·No. 33 ·1992-11-25 ·Pages 24103-8

Port JD, Huang LY, Malbon CC

Abstract

In an effort to explore the molecular basis for agonist-induced destabilization of beta-adrenergic receptor mRNA, we investigated the nature of RNA-binding proteins both in untreated and agonist-treated DDT1-MF2 smooth muscle cells. Messenger RNAs for the alpha 1b-, beta 1-, and beta 2-adrenergic receptors as well as for beta-globin were transcribed in vitro, incubated with cytosolic fractions, covalently cross-linked by short-wave UV light, and analyzed by SDS-polyacrylamide gel electrophoresis. A prominent M(r) 35,000 radiolabeled protein(s) with the following characteristics was identified: (i) binds selectively to beta 1- and beta 2-adrenergic receptor mRNAs, both of which undergo agonist-induced down-regulation; (ii) does not bind to either alpha 1b-adrenergic receptor mRNA, which does not undergo agonist induced down-regulation, or to beta-globin mRNA; (iii) displays binding to beta 2-adrenergic receptor mRNA that is selectively competed by poly(U) RNA, but not poly(A), -(C), or -(G) RNA; and (iv) displays binding to receptor mRNA that can be competed by RNA harboring destabilizer sequences that are AU-rich and AUUUA pentamer-rich. The abundance of the M(r) 35,000 RNA-binding protein selective for beta-adrenergic receptor message, a factor we term beta ARB protein, varies inversely with the level of receptor mRNA, being induced by agonists that down-regulate receptor mRNA.

MeSH Terms
Adrenergic beta-Agonists/pharmacology Animals Base Sequence Binding, Competitive Cell Line Cytosol/metabolism Dexamethasone/pharmacology Down-Regulation/drug effects Insulin/pharmacology Isoproterenol/pharmacology Male Molecular Weight Polyribonucleotides/pharmacology Polyribosomes/metabolism RNA, Messenger/genetics,metabolism RNA-Binding Proteins/biosynthesis,isolation & purification,metabolism Receptors, Adrenergic, beta/biosynthesis,drug effects,genetics Structure-Activity Relationship Vas Deferens/metabolism
Chemicals
Adrenergic beta-Agonists Insulin Polyribonucleotides RNA, Messenger RNA-Binding Proteins Receptors, Adrenergic, beta Dexamethasone Isoproterenol
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Port J D
Department of Pharmacology, School of Medicine, State University of New York, Stony Brook 11794-8651.
Huang L Y
Malbon C C
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1992-11-25
Pages
24103-8
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NIDDK NIH HHS · DK25410 · United States
NIDDK NIH HHS · DK30111 · United States
NIADDK NIH HHS · K04 AM00786 · United States
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