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Inhibition of CCAAT/enhancer-binding protein alpha and beta translation by upstream open reading frames.
- Source :
-
The Journal of biological chemistry [J Biol Chem] 1998 Apr 17; Vol. 273 (16), pp. 9552-60. - Publication Year :
- 1998
-
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.
- Subjects :
- 3T3 Cells
Amino Acid Sequence
Animals
Base Sequence
CCAAT-Enhancer-Binding Proteins
Cattle
Cell Line
Chickens
DNA, Ribosomal metabolism
DNA-Binding Proteins genetics
HeLa Cells
Humans
Male
Mice
Molecular Sequence Data
Nuclear Proteins genetics
Rats
Regulatory Sequences, Nucleic Acid
Sequence Alignment
Sequence Homology, Amino Acid
Transcription Factors biosynthesis
Transfection
Xenopus laevis
DNA-Binding Proteins biosynthesis
Gene Expression Regulation
Nuclear Proteins biosynthesis
Open Reading Frames
Protein Biosynthesis
Subjects
Details
- Language :
- English
- ISSN :
- 0021-9258
- Volume :
- 273
- Issue :
- 16
- Database :
- MEDLINE
- Journal :
- The Journal of biological chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 9545285
- Full Text :
- https://doi.org/10.1074/jbc.273.16.9552