Translation is Enhanced After Silent Nucleotide Substitutions in A+T‐Rich Sequences of the Coding Region of CD46 cDNA
- 1 May 1996
- journal article
- Published by Wiley in European Journal of Biochemistry
- Vol. 238 (1) , 221-230
- https://doi.org/10.1111/j.1432-1033.1996.0221q.x
Abstract
Specific sequences in the coding region of CD46 (membrane cofactor protein) transcripts have been shown to have a marked effect on translation. Two A+T-rich regions of CD46 cDNA were altered by mutation without changing the CD46 amino acid sequence (silent nucleotide substitution). In one region, the A+T content was reduced from 78% to 55% and in the other a putative polyadenylation addition sequence was disrupted. In each example, mutated sequences transfected into COS-7 cells produced significantly more soluble or cell surface protein (up to a 20-fold increase) than wild-type sequences. The amount of cellular plasmid DNA and CD46 mRNA was not increased, suggesting that the effect was not due to increased transfection efficiency, or transcript synthesis or stability. Biosynthetically labelled transfected cells showed an increase in translation rate but cell-free in vitro translation studies demonstrated that wild-type and mutated transcripts were translated with similar efficiency. The data show that translation of CD46 is affected by specific mRNA coding sequences, 400-540 bases from the initiation codon, and suggest that these sequences require the structural integrity of the cell to exert their effect.Keywords
This publication has 61 references indexed in Scilit:
- Engineering hybrid genes without the use of restriction enzymes: gene splicing by overlap extensionPublished by Elsevier ,2003
- Translation factors as effectors of cell growth and tumorigenesisCurrent Opinion in Cell Biology, 1993
- Different membrane cofactor protein (CD46) isoforms protect transfected cells against antibody and complement mediated lysisTransplant Immunology, 1993
- Effect of growth hormone on levels of differentially processed insulin- like growth factor I mRNAs in total and polysomal mRNA populationsMolecular Endocrinology, 1992
- Tissue‐specific and allelic expression of the complement regulator CD46 is controlled by alternative splicingEuropean Journal of Immunology, 1992
- Membrane Cofactor Protein (MCP or CD46): Newest Member of the Regulators of Complement Activation Gene ClusterAnnual Review of Immunology, 1991
- A special repressor/activator system controls distribution of mRNA between translationally active and inactive mRNPs in rabbit reticulocytesFEBS Letters, 1989
- 3′ cleavage and polyadenylation of mRNA precursors in vitro requires a poly(A) polymerase, a cleavage factor, and a snRNPCell, 1988
- Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomesCell, 1986
- Hu Ly-m5: A unique antigen physically associated with HLA moleculesHuman Immunology, 1983