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Self-Complementarity of Terminal Sequences Within Plus or Minus Strands of Adenovirus-Associated Virus DNA
Author(s) -
Frank Koczot,
Barrie J. Carter,
Claude F. Garon,
James A. Rose
Publication year - 1973
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.70.1.215
Subject(s) - dna , biology , rolling circle replication , microbiology and biotechnology , virus , adenoviridae , exonuclease , virology , nucleic acid denaturation , dna replication , in vitro recombination , molecule , chemistry , recombinant dna , genetics , dna polymerase , molecular cloning , complementary dna , gene , base sequence , organic chemistry
At least 70% of plus or minus strands of adenovirus-associated virus DNA contain self-complementary sequences at or near their termini. Self-annealing of these sequences generates circular molecules that are closed by duplex, hydrogen-bonded segments. The self-annealed segments are sensitive to exonuclease III and have a thermal stability comparable to that of double-stranded DNA molecules. Length measurements of double-stranded adenovirus-associated virus DNA molecules show a bimodal distribution, with the larger component being 10% shorter than SV40 DNA. The presence of self-complementary terminal sequences in single-stranded molecules of viral DNA has been observed previously only with DNA from adenoviruses. It is thus especially notable that adenovirus-associated virus replication is unconditionally dependent on a helper adenovirus. A possible role for terminal self-complementary sequences in viral DNA replication is suggested.

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