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PMID: 9545285 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Inhibition of CCAAT/enhancer-binding protein alpha and beta translation by upstream open reading frames.

The Journal of biological chemistry ·Vol. 273 ·No. 16 ·1998-04-17 ·Pages 9552-60

Lincoln AJ, Monczak Y, Williams SC, Johnson PF

Abstract

CCAAT/enhancer-binding protein (C/EBP) alpha is a bZIP transcription factor whose expression is restricted to specific cell types. Analysis of C/EBPalpha mRNA and protein levels in various mammalian cells indicates that expression of this gene is controlled both transcriptionally and post-transcriptionally. We report here that C/EBPalpha translation is repressed in several cell lines by an evolutionarily conserved upstream open reading frame (uORF), which acts in cis to inhibit C/EBPalpha translation. Mutations that disrupt the uORF completely abolished translational repression of C/EBPalpha. The related c/ebpbeta gene also contains an uORF that suppresses translation. The length of the spacer sequence between the uORF terminator and the ORF initiator codon (7 bases in all c/ebpalpha genes and 4 bases in c/ebpbeta homologs) is precisely conserved. The effects of insertions, deletions, and base substitutions in the C/EBPalpha spacer showed that both the length and nucleotide sequence of the spacer are important for efficient translational repression. Our data indicate that the uORFs regulate translation of full-length C/EBPalpha and C/EBPbeta and do not play a role in generating truncated forms of these proteins, as has been suggested by start site multiplicity models.

MeSH Terms
3T3 Cells Amino Acid Sequence Animals Base Sequence CCAAT-Enhancer-Binding Proteins Cattle Cell Line Chickens DNA, Ribosomal/metabolism DNA-Binding Proteins/biosynthesis,genetics Gene Expression Regulation HeLa Cells Humans Male Mice Molecular Sequence Data Nuclear Proteins/biosynthesis,genetics Open Reading Frames Protein Biosynthesis Rats Regulatory Sequences, Nucleic Acid Sequence Alignment Sequence Homology, Amino Acid Transcription Factors/biosynthesis Transfection Xenopus laevis
Chemicals
CCAAT-Enhancer-Binding Proteins DNA, Ribosomal DNA-Binding Proteins Nuclear Proteins Transcription Factors
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Lincoln A J
Advanced BioScience Laboratories-Basic Research Program, NCI-Frederick Cancer Research and Development Center, National Institutes of Health, Frederick, Maryland 21702-1201, USA.
Monczak Y
Williams S C
Johnson P F
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1998-04-17
Pages
9552-60
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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