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PMID: 1993075 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

The estrogen-regulated destabilization of Xenopus albumin mRNA is independent of translation.

Biochemical and biophysical research communications ·Vol. 174 ·No. 2 ·1991-01-31 ·Pages 825-30

Moskaitis JE, Buzek SW, Pastori RL, Schoenberg DR

Abstract

Protein synthesis inhibitors have been shown to increase the stability of a number of labile mRNAs. In Xenopus laevis serum albumin mRNA is destabilized in the liver cell cytoplasm following estrogen administration. The present study examined the effect of translation inhibitors on this process. The initiation inhibitor 2-(4-methyl-2,6-dinitroanilino)-N-methylpropionamide causes accumulation of albumin mRNA in 20-80S mRNP particles whereas the elongation inhibitor cycloheximide causes albumin mRNA to accumulate in polysomes. Neither inhibitor blocked the disappearance of albumin mRNA from liver cell cytoplasm when added with estradiol to the medium of liver explant cultures. We conclude that unlike a number of labile mRNAs the instability of Xenopus albumin mRNA following estradiol is independent of translation.

MeSH Terms
Animals Cycloheximide/pharmacology Estradiol/pharmacology Liver/drug effects,metabolism Male Organ Culture Techniques Polyribosomes/metabolism Propionates/pharmacology Protein Biosynthesis Protein Synthesis Inhibitors/pharmacology RNA, Messenger/drug effects,genetics Ribonucleoproteins/metabolism Serum Albumin/genetics Xenopus laevis
Chemicals
Propionates Protein Synthesis Inhibitors RNA, Messenger Ribonucleoproteins Serum Albumin messenger ribonucleoprotein 2-(4-methyl-2,6-dinitroanilino)-N-methylpropionamide Estradiol Cycloheximide
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Moskaitis J E
Department of Pharmacology, Uniformed Services University of the Health Sciences, Bethesda, MD 20814-4799.
Buzek S W
Pastori R L
Schoenberg D R
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
1991-01-31
Pages
825-30
Language
English
Region
United States
NLM ID
0372516
Subset
IM
Grants
NIGMS NIH HHS · GM38277 · United States
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