| Literature DB >> 1826903 |
G Johnson1, W Widner, W N Xin, M Feiss.
Abstract
Bacteriophage lambda development is blocked in cells carrying a plasmid that expresses the terminase genes of phage 21. The interference is caused by the small subunit of phage 21 terminase, gp1. Mutants of lambda able to form plaques in the presence of gp1 include sti mutants. One such mutation, sti30, is an A. T-to-G.C transition mutation at base pair 184 on the lambda chromosome. The sti30 mutation extends the length of the ribosome-binding sequence of the Nul gene that is complementary to the 3' end of the 16S rRNA from GGA to GGAG. The sti30 mutation causes a approximately 50-fold increase in the level of expression of a Nul-lacZ reporter gene, indicating that the sti30 mutation overcomes the gp1 inhibition by increasing the level of expression of gpNul. Although the Nul and A genes of lambda overlap, the sti30 mutation has little effect on the level of gpA expression, indicating that translational coupling does not occur.Entities:
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Year: 1991 PMID: 1826903 PMCID: PMC207852 DOI: 10.1128/jb.173.9.2733-2738.1991
Source DB: PubMed Journal: J Bacteriol ISSN: 0021-9193 Impact factor: 3.490