The gef gene from Escherichia coli is regulated at the level of translation
- 1 July 1991
- journal article
- Published by Wiley in Molecular Microbiology
- Vol. 5 (7) , 1639-1648
- https://doi.org/10.1111/j.1365-2958.1991.tb01911.x
Abstract
We describe post‐transcriptional regulation of the chromosomal gene, gef, from Escherichia coli. The gef gene is a member of a gene family consisting of the chromosomal gef and relF genes from Escherichia coli and the hok, flmA, smB, and pndA genes, which are situated on conjugative plasmids. All the genes encode small, toxic proteins of approximately 50 amino acids which are functionally and structurally homologous. Furthermore, the gene family shares post‐transcriptional regulation of expression, albeit by different mechanisms. We demonstrate here that translation of gef is coupled to an upstream open reading frame which, in turn, is regulated by a transacting factor, probably an antisense RNA.Keywords
This publication has 24 references indexed in Scilit:
- Topographic analysis of the toxic Gef protein from Escherichia coliMolecular Microbiology, 1991
- Mechanism of post‐segregational killing by the hoklsok system of plasmid R1: sok antisense RNA regulates formation of a hok mRNA species correlated with killing of plasmid‐free cellsMolecular Microbiology, 1990
- A family of genes encoding a cell‐killing function may be conserved in all Gram‐negative bacteriaMolecular Microbiology, 1989
- Translational control and differential RNA decay are key elements regulating postsegregational expression of the killer protein encoded by the parB locus of plasmid R1Journal of Molecular Biology, 1988
- Nucleotide sequence and transcriptional analysis of a third function (Flm) involved in F-plasmid maintenanceGene, 1988
- Nucleotide sequence of the F plasmid genesrnBthat promotes degradation of stable RNA inEscherichia coliFEMS Microbiology Letters, 1986
- Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mpl8 and pUC19 vectorsGene, 1985
- High-copy-number derivatives of the plasmid cloning vector pBR322Gene, 1984
- New versatile plasmid vectors for expression of hybrid proteins coded by a cloned gene fused to lacA gene sequences encoding an enzymatically active carboxy-terminal portion of β-galactosidaseGene, 1983
- Analysis of gene control signals by DNA fusion and cloning in Escherichia coliJournal of Molecular Biology, 1980