Literature DB >> 8190068

The NlaIV restriction and modification genes of Neisseria lactamica are flanked by leucine biosynthesis genes.

P C Lau1, F Forghani, D Labbé, H Bergeron, R Brousseau, H J Höltke.   

Abstract

The genes encoding the Neisseria lactamica restriction endonuclease IV (R.NlaIV) and its cognate DNA methyltransferase (M.NlaIV), both of which recognize the sequence GGNNCC, have been cloned in Escherichia coli and overexpressed using the T7 polymerase/promoter system. Analysis of a sequenced 3.58 kb fragment established the gene order, leuD-M.NlaIV-R.NlaIV-leuB. The predicted primary sequence of M.NlaIV (423 amino acids) shows the highest degree of identity to a pair of cytosine-specific methyltransferases, M.BanI (44.9%) and M.HgiCI (44.3%), which recognize the sequence GGYRCC (Y, pyrimidines; R, purines). In contrast, the R.NlaIV protein sequence (243 amino acids) is unique in the existing data-base, a situation that holds for most endonucleases. Flanking the NlaIV modification and restriction genes are homologues of the leuD and leuB genes of enteric bacteria, which code for enzymes in the leucine biosynthesis pathway. This gene context implies a possible new mode of gene regulation for the RM.NlaIV system, which would involve a mechanism similar to the recently discovered leucine/Lrp regulon in E. coli.

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Year:  1994        PMID: 8190068     DOI: 10.1007/bf00283872

Source DB:  PubMed          Journal:  Mol Gen Genet        ISSN: 0026-8925


  33 in total

1.  Cloning and nucleotide sequence of the genes coding for the Sau96I restriction and modification enzymes.

Authors:  L Szilák; P Venetianer; A Kiss
Journal:  Nucleic Acids Res       Date:  1990-08-25       Impact factor: 16.971

2.  Characterization of Lrp, and Escherichia coli regulatory protein that mediates a global response to leucine.

Authors:  D A Willins; C W Ryan; J V Platko; J M Calvo
Journal:  J Biol Chem       Date:  1991-06-15       Impact factor: 5.157

3.  Stepwise cloning and genetic organization of the seemingly unclonable HgiCII restriction-modification system from Herpetosiphon giganteus strain Hpg9, using PCR technique.

Authors:  D Erdmann; G Horst; A Düsterhöft; M Kröger
Journal:  Gene       Date:  1992-08-01       Impact factor: 3.688

4.  Characterization of the cloned BamHI restriction modification system: its nucleotide sequence, properties of the methylase, and expression in heterologous hosts.

Authors:  J E Brooks; P D Nathan; D Landry; L A Sznyter; P Waite-Rees; C L Ives; L S Moran; B E Slatko; J S Benner
Journal:  Nucleic Acids Res       Date:  1991-02-25       Impact factor: 16.971

5.  Two unique restriction endonucleases from Neisseria lactamica.

Authors:  B Q Qiang; I Schildkraut
Journal:  Nucleic Acids Res       Date:  1986-03-11       Impact factor: 16.971

6.  Sequence motifs characteristic of DNA[cytosine-N4]methyltransferases: similarity to adenine and cytosine-C5 DNA-methylases.

Authors:  S Klimasauskas; A Timinskas; S Menkevicius; D Butkienè; V Butkus; A Janulaitis
Journal:  Nucleic Acids Res       Date:  1989-12-11       Impact factor: 16.971

7.  The nucleotide sequence of 3-isopropylmalate dehydrogenase gene from Bacillus subtilis.

Authors:  R Imai; T Sekiguchi; Y Nosoh; K Tsuda
Journal:  Nucleic Acids Res       Date:  1987-06-25       Impact factor: 16.971

8.  The cysteine conserved among DNA cytosine methylases is required for methyl transfer, but not for specific DNA binding.

Authors:  M W Wyszynski; S Gabbara; E A Kubareva; E A Romanova; T S Oretskaya; E S Gromova; Z A Shabarova; A S Bhagwat
Journal:  Nucleic Acids Res       Date:  1993-01-25       Impact factor: 16.971

9.  Cloning and characterization of two tandemly arranged DNA methyltransferase genes of Neisseria lactamica: an adenine-specific M.NlaIII and a cytosine-type methylase.

Authors:  D Labbé; H J Höltke; P C Lau
Journal:  Mol Gen Genet       Date:  1990-10

10.  Directed mutagenesis in an asporogenous methylotrophic yeast: cloning, sequencing, and one-step gene disruption of the 3-isopropylmalate dehydrogenase gene (LEU2) of Candida boidinii to derive doubly auxotrophic marker strains.

Authors:  Y Sakai; Y Tani
Journal:  J Bacteriol       Date:  1992-09       Impact factor: 3.490

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  3 in total

1.  Use of a non-selective transformation technique to construct a multiply restriction/modification-deficient mutant of Neisseria gonorrhoeae.

Authors:  J S Gunn; D C Stein
Journal:  Mol Gen Genet       Date:  1996-07-19

2.  BplI, a new BcgI-like restriction endonuclease, which recognizes a symmetric sequence.

Authors:  J Vitkute; Z Maneliene; M Petrusyte; A Janulaitis
Journal:  Nucleic Acids Res       Date:  1997-11-15       Impact factor: 16.971

3.  Restriction and sequence alterations affect DNA uptake sequence-dependent transformation in Neisseria meningitidis.

Authors:  Ole Herman Ambur; Stephan A Frye; Mariann Nilsen; Eirik Hovland; Tone Tønjum
Journal:  PLoS One       Date:  2012-07-02       Impact factor: 3.240

  3 in total

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