Back to Search
Start Over
Translation initiation controls the relative rates of expression of the bacteriophage lambda late genes.
- Source :
-
Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 1988 Aug; Vol. 85 (15), pp. 5439-43. - Publication Year :
- 1988
-
Abstract
- The late operon of bacteriophage lambda contains the genes encoding the morphogenetic proteins of the phage. These genes are transcribed equally from the single late promoter. Although the functional half-lives of the mRNA for the various genes of this operon vary less than 2-fold, their relative rates of expression have been shown to vary by nearly 1000-fold. This variation could result from differing rates of translation initiation, from overlapping upstream translation, or from differential elongation rates due to the presence of codons for which the corresponding tRNAs are rare. To distinguish between these possibilities, we have cloned sequences surrounding the initiator codons of several of these genes and measured their ability to drive synthesis of hybrid lambda-beta-galactosidase proteins. The rates of expression of the hybrid genes thus produced correlate very well with the natural rates of expression of the corresponding phage genes, suggesting that the rate of initiation of translation controls the relative expression rates of these genes.
- Subjects :
- Base Sequence
Cloning, Molecular
DNA, Viral genetics
Electrophoresis, Polyacrylamide Gel
Genes, Viral
Molecular Sequence Data
Operon
Promoter Regions, Genetic
Recombinant Fusion Proteins analysis
Bacteriophage lambda genetics
Gene Expression Regulation
Protein Biosynthesis
Recombinant Fusion Proteins genetics
Recombinant Proteins genetics
Viral Proteins genetics
Subjects
Details
- Language :
- English
- ISSN :
- 0027-8424
- Volume :
- 85
- Issue :
- 15
- Database :
- MEDLINE
- Journal :
- Proceedings of the National Academy of Sciences of the United States of America
- Publication Type :
- Academic Journal
- Accession number :
- 2969591
- Full Text :
- https://doi.org/10.1073/pnas.85.15.5439