Abstract
The 11-gene S10 ribosomal protein operon of Escherichia coli is under the autogenous control of L4, the product of the third gene of the operon. Ribosomal protein L4 inhibits both transcription and translation of the operon. Our in vivo studies indicated that L4 regulates transcription by causing premature termination within the untranslated S10 operon leader. We have now used an in vitro transcription system to study the effect of purified L4 on expression of the S10 operon. We find that the cell-free system reproduces the in vivo observations. Namely, in the absence of L4, most of the RNA polymerases read through the termination site in the S10 attenuator; the addition of L4 results in increased termination at this site. However, RNA polymerase does not terminate at the S10 attenuator, with or without L4, unless an additional factor, protein NusA, is added to the transcription reaction. These results suggest that the attenuator in the S10 operon is a NusA-dependent terminator whose efficiency is regulated by ribosomal protein L4.
MeSH Terms
Bacterial Proteins/genetics
Base Sequence
Cloning, Molecular
Escherichia coli/genetics
Genes, Bacterial
Genes, Regulator
Molecular Sequence Data
Nucleic Acid Conformation
Operon
Protein Sorting Signals/genetics
Restriction Mapping
Ribosomal Proteins/genetics
Terminator Regions, Genetic
Transcription Factors/genetics
Transcription, Genetic
Chemicals
Bacterial Proteins
Protein Sorting Signals
Ribosomal Proteins
Transcription Factors
ribosomal protein L4
ribosomal protein S10
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Zengel J M
Department of Biology, University of Rochester, NY 14627.
Lindahl L
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28 references, click to expand
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