Effects of alterations in the translation control region on bacterial gene expression: use of cat gene constructs transcribed from the lac promoter as a model system

Janet L. Schottel, John J. Sninsky, Stanley N. Cohen

Research output: Contribution to journalArticlepeer-review

37 Scopus citations

Abstract

The region controlling translation of the cat gene, which codes for chloramphenicol acetyltransferase, has been varied structurally in a series of plasmids that place the gene under control of the lac promoter. These plasmid constructs have enabled study of the structural features that affect the efficiency of mRNA translation. Altering the potential for secondary structure formation within the translation control region caused a tenfold variation in the synthesis of CAT enzyme, whereas varying the distance between the Shine-Dalgarno sequence (SD) and the translation start codon from 7 to 13 bases did not significantly affect the yield of CAT. If the SD was situated in a region of mRNA that is capable of base pairing, the efficiency of translation was decreased; however, the translation start codon, AUG, can initiate translation efficiently even when located in a segment capable of duplex formation. Overlapping of the cat translation control region by translation initiated upstream markedly affected initiation of translation within the cat gene: out-of-frame overlapping translation reduced CAT production by 90%; in-frame overlapping translation prevented detectable initiation of protein synthesis at the cat gene translation start codon, and yielded only fusion proteins. The enzymatic activity of such proteins was influenced by the length of the adventitious peptide segment added to the amino-terminus of the CAT polypeptide.

Original languageEnglish (US)
Pages (from-to)177-193
Number of pages17
JournalGene
Volume28
Issue number2
DOIs
StatePublished - May 1984

Bibliographical note

Funding Information:
The authors thank Mr. Ezra Abrams and Dr. Julius Marmur for the antibodyt o the CAT enzyme, and Mr. Zvi Loewy for the data shown in Fig. 2. These studiesw ere supportedb y NIH grant GM 27241t o S.N.C.J.J.S. acknowledgessu pportf rom NIH grant AI08295.

Keywords

  • Recombinant DNA
  • mRNA
  • plasmid vectors
  • protein start signals
  • ribosome binding site

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