Literature DB >> 6094474

DNA sequence and transcriptional organization of essential cell division genes ftsQ and ftsA of Escherichia coli: evidence for overlapping transcriptional units.

A C Robinson, D J Kenan, G F Hatfull, N F Sullivan, R Spiegelberg, W D Donachie.   

Abstract

The DNA sequence of a cloned segment of the Escherichia coli chromosome containing ftsQ, ftsA, and part of the ftsZ gene was determined and interpreted for genetic complementation and promoter fusion data for the region. The contiguous genes ftsQ, ftsA, and ftsZ were transcribed in the same direction (clockwise on the genetic map) and each had at least one associated promoter which allowed it to be transcribed independently of neighboring genes. ftsA and ftsZ possessed promoters within the coding sequences of the juxtaposed upstream structural genes, and a promoter element for ftsA was surrounded by a region of twofold symmetry which corresponded closely to a symmetrical element in the region of a putative ftsZ promoter. The structural gene of ftsQ consisted of 838 nucleotides, encoding a 276-residue amino acid polypeptide of molecular weight 31,400; the structural gene of ftsA consisted of 1,260 nucleotides, encoding a 420-residue amino acid polypeptide of molecular weight 45,400. The observation that the termination codon of ftsQ overlaps with a potential initiation codon for ftsA suggested that these two genes may be translationally coupled when transcription is initiated upstream of the ftsQ coding sequence.

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Year:  1984        PMID: 6094474      PMCID: PMC214769          DOI: 10.1128/jb.160.2.546-555.1984

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  44 in total

1.  Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I.

Authors:  P W Rigby; M Dieckmann; C Rhodes; P Berg
Journal:  J Mol Biol       Date:  1977-06-15       Impact factor: 5.469

2.  Screening lambdagt recombinant clones by hybridization to single plaques in situ.

Authors:  W D Benton; R W Davis
Journal:  Science       Date:  1977-04-08       Impact factor: 47.728

3.  Measurement of free electrophoretic mobility and retardation coefficient of protein-sodium dodecyl sulfate complexes by gel electrophoresis. A method to validate molecular weight estimates.

Authors:  G A Banker; C W Cotman
Journal:  J Biol Chem       Date:  1972-09-25       Impact factor: 5.157

4.  Supercoiled circular DNA-protein complex in Escherichia coli: purification and induced conversion to an opern circular DNA form.

Authors:  D B Clewell; D R Helinski
Journal:  Proc Natl Acad Sci U S A       Date:  1969-04       Impact factor: 11.205

5.  The construction in vitro of transducing derivatives of phage lambda.

Authors:  K Borck; J D Beggs; W J Brammar; A S Hopkins; N E Murray
Journal:  Mol Gen Genet       Date:  1976-07-23

6.  A simple method for DNA restriction site mapping.

Authors:  H O Smith; M L Birnstiel
Journal:  Nucleic Acids Res       Date:  1976-09       Impact factor: 16.971

7.  Further procedures for sequence analysis by computer.

Authors:  R Staden
Journal:  Nucleic Acids Res       Date:  1978-03       Impact factor: 16.971

8.  Sequence data handling by computer.

Authors:  R Staden
Journal:  Nucleic Acids Res       Date:  1977-11       Impact factor: 16.971

9.  Stimulation by cyclic adenosine monophosphate of plasmid deoxyribonucleic acid replication and catabolite repression of the plasmid deoxyribonucleic acid-protein relaxation complex.

Authors:  L Katz; D T Kingsbury; D R Helinski
Journal:  J Bacteriol       Date:  1973-05       Impact factor: 3.490

10.  DNA sequencing with chain-terminating inhibitors.

Authors:  F Sanger; S Nicklen; A R Coulson
Journal:  Proc Natl Acad Sci U S A       Date:  1977-12       Impact factor: 11.205

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  44 in total

1.  Selected amplification of the cell division genes ftsQ-ftsA-ftsZ in Escherichia coli.

Authors:  D Vinella; M Cashel; R D'Ari
Journal:  Genetics       Date:  2000-12       Impact factor: 4.562

2.  Inhibition of growth of ftsQ, ftsA, and ftsZ mutant cells of Escherichia coli by amplification of a chromosomal region encompassing closely aligned cell division and cell growth genes.

Authors:  H K Jung; F Ishino; M Matsuhashi
Journal:  J Bacteriol       Date:  1989-11       Impact factor: 3.490

3.  FtsL, an essential cytoplasmic membrane protein involved in cell division in Escherichia coli.

Authors:  L M Guzman; J J Barondess; J Beckwith
Journal:  J Bacteriol       Date:  1992-12       Impact factor: 3.490

4.  Inhibition of cell division initiation by an imbalance in the ratio of FtsA to FtsZ.

Authors:  S J Dewar; K J Begg; W D Donachie
Journal:  J Bacteriol       Date:  1992-10       Impact factor: 3.490

5.  Regulation of expression of the ftsA cell division gene by sequences in upstream genes.

Authors:  S J Dewar; W D Donachie
Journal:  J Bacteriol       Date:  1990-11       Impact factor: 3.490

6.  The native form of FtsA, a septal protein of Escherichia coli, is located in the cytoplasmic membrane.

Authors:  J Pla; A Dopazo; M Vicente
Journal:  J Bacteriol       Date:  1990-09       Impact factor: 3.490

7.  The FtsQ protein of Escherichia coli: membrane topology, abundance, and cell division phenotypes due to overproduction and insertion mutations.

Authors:  M J Carson; J Barondess; J Beckwith
Journal:  J Bacteriol       Date:  1991-04       Impact factor: 3.490

8.  Transcription of the ftsZ gene and cell division in Escherichia coli.

Authors:  A Robin; D Joseleau-Petit; R D'Ari
Journal:  J Bacteriol       Date:  1990-03       Impact factor: 3.490

9.  New mre genes mreC and mreD, responsible for formation of the rod shape of Escherichia coli cells.

Authors:  M Wachi; M Doi; Y Okada; M Matsuhashi
Journal:  J Bacteriol       Date:  1989-12       Impact factor: 3.490

10.  Asymmetric constriction of dividing Escherichia coli cells induced by expression of a fusion between two min proteins.

Authors:  Veronica Wells Rowlett; William Margolin
Journal:  J Bacteriol       Date:  2014-03-28       Impact factor: 3.490

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