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Characterization of Chlorella virus PBCV-1 CviAII restriction and modification system

A second DNA site-specific (restriction) endonuclease (R.CviAII) and its cognate adenine DNA methyltransferase (M.CviAII) were isolated from virus PBCV-1 infected Chlorella strain NC64A cells. R.CviAII, a heteroschizomer of the bacterial restriction endonuclease NlaIII, recognizes the sequence CATG,...

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Bibliographic Details
Published in:Nucleic acids research 1992-10, Vol.20 (20), p.5351-5356
Main Authors: Zhang, Y, Nelson, M, Nietfeldt, J.W, Burbank, D.E, Van Etten, J.L
Format: Article
Language:English
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Summary:A second DNA site-specific (restriction) endonuclease (R.CviAII) and its cognate adenine DNA methyltransferase (M.CviAII) were isolated from virus PBCV-1 infected Chlorella strain NC64A cells. R.CviAII, a heteroschizomer of the bacterial restriction endonuclease NlaIII, recognizes the sequence CATG, and does not cleave C(m)ATG sequences. However, unlike NlaIII, which cleaves after the G and does not cleave either C(m)ATG or (m)CATG sequences, CviAII cleaves between the C and A and is unaffected by (m)CATG methylation. The M.CviAII and R.CviAII genes were cloned and their DNA sequences were determined. These genes are tandemly arranged head-to-tail such that the TAA termination codon of the M.CviAII methyltransferase gene overlaps the ATG translational start site of R.CviAII endonuclease. R.CviAII is the first chlorella virus site-specific endonuclease gene to be cloned and sequenced.
ISSN:0305-1048
1362-4962
DOI:10.1093/nar/20.20.5351