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J. Biochem, 1982, Vol. 91, No. 6 2057-2065
© 1982 Japanese Biochemical Society


research-article

Action of T4 Endonuclease V on Polydeoxyribonucleotides with Apyrimidinic or Apurinic Sites1

Yoshimichi NAKATSU, Yusaku NAKABEPPU and Mutsuo SEKIGUCHI

Department of Biology, Faculty of Science, Kyushu University 33 Higasbi-ku, Fukuoka, Fukuoka 812

[3H]Thymine-labeled poly(dT) carrying many apyrimidinic (AP) sites has been prepared by treating an enzymatically synthesized poly(dA) poly(dT, dU) with uracil-DNA glycosylase. Incubation of the polymer with a homogeneous preparation of T4 endonuclease V resulted in conversion of the labeled material into acid-soluble forms. Native DNA with apurinic sites was also cleaved by the enzyme. Single-stranded polymers, poly(dT) carrying AP sites or poly(dT) with thymine dimers, were barely attacked by T4 endonuclease V. The polymer whose aldehyde moieties at AP sites were reduced to alcoholic forms was not susceptible to the enzyme. The site of endonucleolytic cleavage was determined by using alternating copolymers whose phosphate groups were differentially labeled. The result is consistent with the view that T4 endonuclease V cleaves a phosphodiester linkage on the 3'-side of AP sites, producing chains terminated at their 3'-ends with base-free deoxyribose and at their 5'-ends with phosphate.

1This work was supported by Scientific Research and Cancer Research Grants from the Ministry of Education, Science and Culture of Japan.


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