Literature DB >> 8883359

Identification of the gene encoding the DNA (cytosine-5) methyltransferase of lymphocystis disease virus.

C A Tidona1, P Schnitzler, R Kehm, G Darai.   

Abstract

The gene encoding the DNA (cytosine-5) methyltransferase (m5C-MTase) of lymphocystis disease virus (flounder isolate, LCDV-1) has been identified by polymerase chain reaction (PCR) using oligonucleotide primers synthesized corresponding to different regions of the m5C-MTase gene of frog virus 3 (FV3). A DNA fragment of 487 bp was amplified using oligonucleotide primers L3 and R4 which correspond to the nucleotide positions 87 to 109 and 530 to 550 of the m5C-MTase gene of FV3, respectively. The DNA nucleotide sequence of the PCR product was determined by direct cycle sequencing. The alignment of the deduced amino acid sequence derived from the PCR product and the m5C-MTase protein of FV3 revealed a homology of 55.4% identity and 29.1% similarity. The amino acid sequence which was found to be significantly homologous to the amino acid sequence deduced from the nucleotide sequence of the PCR product was located at the amino acid position 37 to 175 of the m5C-MTase of FV3 indicating the specificity of the amplified PCR product. The DNA nucleotide sequence of the LCDV-1 genome corresponding to the 5' and 3' termini of the m5C-MTase gene was determined by primer walking. The locus of the m5C-MTase gene of LCDV-1 was identified within the EcoRI DNA fragment G of LCDV-1 (7.9 kbp; 0.947 to 0.034 map units). The m5C-MTase gene of LCDV-1 comprises 684 nucleotides coding for a putative protein of 228 amino acid residues. A high degree of amino acid sequence homology (53.3% identity and 25.8% similarity) was detected between the m5C-MTase of LCDV-1 and FV3.

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Year:  1996        PMID: 8883359     DOI: 10.1007/bf00284642

Source DB:  PubMed          Journal:  Virus Genes        ISSN: 0920-8569            Impact factor:   2.332


  33 in total

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Authors:  P Schnitzler; J B Soltau; M Fischer; H Reisner; J Scholz; H Delius; G Darai
Journal:  Virology       Date:  1987-09       Impact factor: 3.616

2.  DNA methyltransferase genes of Bacillus subtilis phages: comparison of their nucleotide sequences.

Authors:  A Tran-Betcke; B Behrens; M Noyer-Weidner; T A Trautner
Journal:  Gene       Date:  1986       Impact factor: 3.688

3.  Fast and sensitive multiple sequence alignments on a microcomputer.

Authors:  D G Higgins; P M Sharp
Journal:  Comput Appl Biosci       Date:  1989-04

4.  Methylation pattern of fish lymphocystis disease virus DNA.

Authors:  H Wagner; D Simon; E Werner; H Gelderblom; C Darai; R M Flügel
Journal:  J Virol       Date:  1985-03       Impact factor: 5.103

5.  The M.AluI DNA-(cytosine C5)-methyltransferase has an unusually large, partially dispensable, variable region.

Authors:  B Zhang; T Tao; G G Wilson; R M Blumenthal
Journal:  Nucleic Acids Res       Date:  1993-02-25       Impact factor: 16.971

6.  DNA methyltransferase induced by frog virus 3.

Authors:  D B Willis; R Goorha; A Granoff
Journal:  J Virol       Date:  1984-01       Impact factor: 5.103

7.  Identification of the gene encoding the major capsid protein of insect iridescent virus type 6 by polymerase chain reaction.

Authors:  R Stohwasser; K Raab; P Schnitzler; W Janssen; G Darai
Journal:  J Gen Virol       Date:  1993-05       Impact factor: 3.891

8.  Analysis of the genome of fish lymphocystis disease virus isolated directly from epidermal tumours of pleuronectes.

Authors:  G Darai; K Anders; H G Koch; H Delius; H Gelderblom; C Samalecos; R M Flügel
Journal:  Virology       Date:  1983-04-30       Impact factor: 3.616

9.  Patterns of frog virus 3 DNA methylation and DNA methyltransferase activity in nuclei of infected cells.

Authors:  C Schetter; B Grünemann; I Hölker; W Doerfler
Journal:  J Virol       Date:  1993-12       Impact factor: 5.103

10.  Characterization of the repetitive DNA elements in the genome of fish lymphocystis disease viruses.

Authors:  P Schnitzler; G Darai
Journal:  Virology       Date:  1989-09       Impact factor: 3.616

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5.  Systematic CpT (ApG) depletion and CpG excess are unique genomic signatures of large DNA viruses infecting invertebrates.

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