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Journal ArticleDOI

Characterization of broadly pleiotropic phenotypes caused by an hfq insertion mutation in Escherichia coli K‐12

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TLDR
Hfq function plays a fundamental role in Escherichia coli physiology and that hfq and the hflA region are in the amiB‐mutL‐miaA‐hfq‐hflX superoperon.
Abstract
The region immediately downstream from the miaA tRNA modification gene at 94.8 min contains the hfq gene and the hflA region, which are important in the bacteriophage Q beta and lambda life cycles. The roles of these genes in bacteria remain largely unknown. We report here the characterization of two chromosomal hfq insertion mutations. An omega (omega) cassette insertion near the end of hfq resulted in phenotypes only slightly different from the parent, although transcript mapping demonstrated that the insertion was completely polar on hflX expression. In contrast, an equally polar omega cassette insertion near the beginning of hfq caused pronounced pleiotropic phenotypes, including decreased growth rates and yields, decreased negative supercoiling of plasmids in stationary phase, increased cell size, osmosensitivity, increased oxidation of carbon sources, increased sensitivity to ultraviolet light, and suppression of bgl activation by hns mutations. hfq::omega mutant phenotypes were distinct from those caused by omega insertions early in the miaA tRNA modification gene. On the other hand, both hfq insertions interfered with lambda phage plaque formation, probably by means of polarity at the hflA region. Together, these results show that hfq function plays a fundamental role in Escherichia coli physiology and that hfq and the hflA-region are in the amiB-mutL-miaA-hfq-hflX superoperon.

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Signal transduction and regulatory mechanisms involved in control of the sigma(S) (RpoS) subunit of RNA polymerase.

TL;DR: This review summarizes the current knowledge about the molecular functions and interactions of the σS subunit of RNA polymerase and tries to establish a framework for further research on the mode of multiple signal input into this complex regulatory system.
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Hfq and its constellation of RNA

TL;DR: The salient structural and functional features of Hfq are described and possible mechanisms by which this protein can promote RNA interactions to catalyse specific and rapid regulatory responses in vivo are discussed.
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Proteases and their targets in Escherichia coli.

TL;DR: Many of the specific proteases found in E. coli are well-conserved in both prokaryotes and eukaryotes, and serve critical functions in developmental systems.
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Coupled degradation of a small regulatory RNA and its mRNA targets in Escherichia coli

TL;DR: Two other Hfq-dependent small RNAs, DsrA and OxyS, are also stable when overall transcription is off, and unstable when it is not, suggesting that they, too, are degraded when their target mRNAs are available for pairing.
Journal ArticleDOI

The Small RNA Regulators of Escherichia coli: Roles and Mechanisms*

TL;DR: The most exhaustive searches have taken place in E. coli, resulting in identification of more than 50 small RNAs, or 1%-2% of the number of protein-coding genes.
References
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Book

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TL;DR: Methodology for General and Molecular Microbiology Morphology Light microscopy Determinative and cytological light microscopy Electron microscopy Cell fractionation Antigen-antibody reactions Growth: Physicochemical factors in growth Nutrition and media Enrichment and isolation Solid, liquid/solid and semisolid culture Liquid culture Growth measurement Culture preservation Molecular Genetics: Gene mutation Gene transfer in Gram-negative bacteria Gene transferIn Gram-positive bacteria Plasmids Transposon mutagenesis
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A short course in bacterial genetics

TL;DR: This second edition of Molecular Cloning reflects more comprehensive coverage of topics previously included in the first edition as well as the addition of new chapters, such as those on oligonucleotide probes and mutagenesis, in vitro amplification by the polymerase chain reaction, expression of cloned genes in Escherichia coli and mammalian cells, and analysis of proteins ex­ pressed from cloning genes.
Journal ArticleDOI

Transposition and fusion of the lac genes to selected promoters in Escherichia coli using bacteriophage lambda and Mu.

TL;DR: Fusions of lac genes to selected locations on the Escherichia coli chromosome are useful in discovering new types of regulation of gene expression, as was found in the case of the araC gene.
Journal ArticleDOI

In vitro insertional mutagenesis with a selectable DNA fragment

TL;DR: A new method for in vitro insertional mutagenesis of genes cloned in Escherichia coli that makes use of the omega fragment, a 2.0-kb DNA segment consisting of an antibiotic resistance gene flanked by short inverted repeats carrying transcription and translation termination signals and synthetic polylinkers.
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