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3´-5´ Exonuclease Activity of Human Apurinic/Apyrimidinic Endonuclease 1 towards DNAs Containing dNMP and Their Modified Analogs at the 3´ End of Single Strand DNA Break

N. S. Dyrkheeva1,2, S. N. Khodyreva1, M. V. Sukhanova1, I. V. Safronov1, S. V. Dezhurov1, and O. I. Lavrik1*

1Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, pr. Lavrent'eva 8, 630090 Novosibirsk, Russia; fax: (3832) 333-677; E-mail: lavrik@niboch.nsc.ru

2Novosibirsk State University, ul. Pirogova 2, 630090 Novosibirsk, Russia

* To whom correspondence should be addressed.

Received February 16, 2005; Revision received April 4, 2005
Human DNA apurinic/apyrimidinic (AP-) endonuclease 1 (APE1) is involved in the base excision repair (BER) pathway. The enzyme hydrolyzes DNA from the 5´ side of the AP site. In addition to endonuclease activity, APE1 also possesses other slight activities including 3´-5´ exonuclease activity. The latter is preferentially exhibited towards mispaired (non-canonical) nucleotides, this being the reason why APE1 is considered as a proofreading enzyme correcting the misincorporations introduced by DNA polymerase beta. We have studied 3´-5´ exonuclease activity of APE1 towards dCMP and dTMP residues and modified dCMP analogs with photoreactive groups at the 3´ end of the nicked DNA. Photoreactive dNMP residues were incorporated at the 3´ end of the lesion using DNA polymerase beta and photoreactive dNTPs. The dependence of exonuclease activity on the “canonicity” of the base pair formed by dNMP flanking the nick at the 3´ end, on the nature of the group flanking the nick at the 5´ end, and on the reaction conditions has been determined. Optimal reaction conditions for the 3´-5´ exonuclease hydrolysis reaction catalyzed by APE1 in vitro have been established, and conditions when photoreactive residues are not removed by APE1 have been chosen. These reaction conditions are suitable for using photoreactive nicked DNAs bearing 3´-photoreactive dNMP residues for photoaffinity labeling of proteins in cellular/nuclear extracts and model APE1-containing systems. We recommend using FAPdCTP for photoaffinity modification in APE1-containing systems because the FAPdCMP residue is less prone to exonuclease degradation, in contrast to FABOdCTP, which is not recommended.
KEY WORDS: APE1 exonuclease activity, modified photoreactive dNTP analog

DOI: 10.1134/S0006297906020131