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Cleavage of phi X174 single-stranded DNA by gene A protein and formation of a tight protein-DNA complex
Author(s) -
S Eisenberg
Publication year - 1980
Publication title -
journal of virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.617
H-Index - 292
eISSN - 1070-6321
pISSN - 0022-538X
DOI - 10.1128/jvi.35.2.409-413.1980
Subject(s) - micrococcal nuclease , biology , microbiology and biotechnology , dna , nuclease , phosphodiester bond , biochemistry , ddb1 , gene , single stranded binding protein , cleavage (geology) , deoxyribonuclease i , dna clamp , hmg box , polynucleotide , dna binding protein , chromatin , rna , nucleosome , transcription factor , paleontology , reverse transcriptase , fracture (geology) , base sequence
The gene A protein cleaves phi X174 single-stranded DNA (ssDNA). The cleavage appears to be stoichiometric, whereby a gene A protein molecule breaks a phosphodiester bond and binds to the 5' end. The enzyme introduces mostly a single break in a circular ssDNA molecule. However, at high enzyme-to-DNA ratios, more than one break in the DNA could be observed. The cleavage of the ssDNA by gene A protein renders the DNA sensitive to the action of terminal transferase to incorporate [alpha -32P]ATP. Thus, the 3'OH end is free. All attempts to label the 5' end by T4-induced polynucleotide kinase and [gamma-32P]ATP failed. The formation of a gene A-ssDNA complex was demonstrated directly by using 3H-labeled gene A protein and 32P-labeled ssDNA in the reaction. Such a complex is resistant to treatments with 0.2 M NaOH, banding in CsCl, and boiling in 2.5% sodium dodecyl sulfate. Only treatment with a nuclease released the bound protein. Also, after cleaving [32P]ssDNA by gene A protein, followed by either DNase I or micrococcal nuclease digestion, a fraction of the 32P label remained resistant to nuclease treatment and comigrated with gene A protein on polyacrylamide gels.

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