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PMID: 7566093 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Growth-dependent translation of IGF-II mRNA by a rapamycin-sensitive pathway.

Nature ·Vol. 377 ·No. 6547 ·1995-09-28 ·Pages 358-62

Nielsen FC, Ostergaard L, Nielsen J, Christiansen J

Abstract

Insulin-like growth factor (IGF)-II is important for fetal growth and development. The human IGF-II gene generates multiple mature transcripts with different 5' untranslated regions (5'UTRs) but identical coding regions and 3'UTRs. We have previously shown that a minor 4.8-kilobase messenger RNA was engaged in the synthesis of preproIGF-II, and a major 6.0-kb mRNA was untranslated and stored in a 100S ribonucleoprotein particle. Here we demonstrate that the 6.0-kb mRNA is selectively mobilized and translated in dispersed exponentially growing cells. Translational activation is prevented by rapamycin and mimicked by anisomycin, which suggests that translation of the 6.0-kb mRNA is regulated by the p70S6k/85S6k kinase signalling pathway. Therefore, the minor 4.8-kb mRNA generates a constitutive production of prepro-IGF-II, whereas the major 6.0-kb mRNA provides a post-transcriptionally regulated species.

MeSH Terms
Anisomycin/pharmacology Cell Division/physiology Humans Insulin-Like Growth Factor II/genetics Polyenes/pharmacology Protein Biosynthesis/drug effects Protein Synthesis Inhibitors/pharmacology RNA, Messenger/genetics Ribosomal Protein S6 Ribosomal Proteins/metabolism Sirolimus Transfection Tumor Cells, Cultured
Chemicals
Polyenes Protein Synthesis Inhibitors RNA, Messenger Ribosomal Protein S6 Ribosomal Proteins Insulin-Like Growth Factor II Anisomycin Sirolimus
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Nielsen F C
Department of Clinical Biochemistry, Rigshospitalet, Copenhagen O, Denmark.
Ostergaard L
Nielsen J
Christiansen J
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
1995-09-28
Pages
358-62
Language
English
Region
England
NLM ID
0410462
Subset
IM
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