A stop codon-dependent internal secondary translation initiation region in Escherichia coli rpoS
Author(s) -
Pochi R. Subbarayan,
Malancha Sarkar
Publication year - 2004
Publication title -
rna
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.037
H-Index - 171
eISSN - 1469-9001
pISSN - 1355-8382
DOI - 10.1261/rna.7500604
Subject(s) - biology , rpos , escherichia coli , translation (biology) , start codon , genetics , escherichia coli proteins , eukaryotic translation , stop codon , computational biology , gene , base sequence , messenger rna , gene expression , promoter
Sigma S (σ s ) encoded by rpoS is a stationary phase-specific σ subunit of the Escherichia coli RNA polymerase holoenzyme. In many E. coli strains, rpoS has an amber stop as codon 33 ( rpoSAm ), resulting in a 32-amino-acid-long peptide. Nevertheless, suppressor-free rpoSAm strains have functional σ S . This led us to hypothesize the presence of an intracistronic secondary translational initiation region (STIR) in the E. coli rpoS gene. Here, we demonstrate that the STIR is functional and is controlled by the upstream amber stop codon 33. Removal of the primary translational initiation region did not abolish translation from STIR, ruling out translational coupling. Importantly, the functional STIR conferred survival advantage. Taken together, our results reveal a hitherto unknown physiologically significant post-transcriptional process in E. coli rpoSAm strains.
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