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Nucleic Acids Research 2006 34(7):2067-2076; doi:10.1093/nar/gkl177
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Published online 14 April 2006

© The Author 2006. Published by Oxford University Press. All rights reserved
The online version of this article has been published under an open access model. Users are entitled to use, reproduce, disseminate, or display the open access version of this article for non-commercial purposes provided that: the original authorship is properly and fully attributed; the Journal and Oxford University Press are attributed as the original place of publication with the correct citation details given; if an article is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative work this must be clearly indicated. For commercial re-use, please contact journals.permissions@oxfordjournals.org


Article

Identification and characterization of mitochondrial abasic (AP)-endonuclease in mammalian cells

Ranajoy Chattopadhyay, Lee Wiederhold, Bartosz Szczesny, Istvan Boldogh1, Tapas K. Hazra, Tadahide Izumi and Sankar Mitra*

Sealy Center for Molecular Science, Department of Biochemistry and Molecular Biology, University of Texas Medical Branch Galveston, TX 77555-1079, USA 1 Department of Microbiology and Immunology, University of Texas Medical Branch Galveston, TX 77555-1079, USA

*To whom correspondence should be addressed. Sealy Center for Molecular Science, University of Texas Medical Branch, 6.136 Medical Research Building, Route 1079, Galveston, TX 77555-1079, USA. Tel: +1 409 772 1780; Fax: +1 409 747 8608; Email: samitra{at}utmb.edu

Received December 22, 2005. Revised March 21, 2006. Accepted March 21, 2006.

Abasic (AP)-endonuclease (APE) is responsible for repair of AP sites, and single-strand DNA breaks with 3' blocking groups that are generated either spontaneously or during repair of damaged or abnormal bases via the DNA base excision repair (BER) pathway in both nucleus and mitochondria. Mammalian cells express only one nuclear APE, 36 kDa APE1, which is essential for survival. Mammalian mitochondrial (mt) BER enzymes other than mtAPE have been characterized. In order to identify and characterize mtAPE, we purified the APE activity from beef liver mitochondria to near homogeneity, and showed that the mtAPE which has 3-fold higher specific activity relative to APE1 is derived from the latter with deletion of 33 N-terminal residues which contain the nuclear localization signal. The mtAPE-sized product could be generated by incubating 35S-labeled APE1 with crude mitochondrial extract, but not with cytosolic or nuclear extract, suggesting that cleavage of APE1 by a specific mitochondria-associated N-terminal peptidase is a prerequisite for mitochondrial import. The low abundance of mtAPE, particularly in cultured cells might be the reason for its earlier lack of detection by western analysis.


Present address: Tadahide Izumi, Louisiana State University Health Science Center, 533 Bolivar, New Orleans, LA 70112, USA


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