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PMID: 1707871 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Deadenylation and turnover of interferon-beta mRNA.

The Journal of biological chemistry ·Vol. 266 ·No. 11 ·1991-04-15 ·Pages 6663-6

Peppel K, Baglioni C

Abstract

The pathway of degradation of human interferon-beta (IFN-beta) mRNA was examined in murine C127 cells that carry an expression vector for this mRNA. The IFN-beta mRNA decayed with a half-life of approximately 45 min in actinomycin D-treated cells and became gradually shorter. This mRNA was superinduced in cycloheximide-treated cells, but it also became gradually shorter. However, apparently full-length species of IFN-beta mRNA accumulated after prolonged incubation with cycloheximide. The shortened IFN-beta mRNA species were partially deadenylated and less stable than full-length species. These findings suggest that at least two nuclease activities are involved in degrading IFN-beta mRNA; one deadenylates this mRNA and decays in cycloheximide-treated cells, while the other apparently breaks down deadenylated mRNA.

MeSH Terms
Animals Cell Line Cycloheximide/pharmacology Dactinomycin/pharmacology Humans Interferon-gamma/genetics Mice Poly A/metabolism RNA/metabolism RNA, Messenger/drug effects,genetics,metabolism Transfection
Chemicals
RNA, Messenger Dactinomycin Poly A RNA Interferon-gamma Cycloheximide
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Peppel K
Department of Biological Sciences, State University of New York, Albany 12222.
Baglioni C
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1991-04-15
Pages
6663-6
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Grants
NCI NIH HHS · CA-29895 · United States
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