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Uracil excision repair pathway activities are not intrinsic to nucleoside diphosphate kinases from Mycobacterium tuberculosis and Escherichia coli.

Kumar, Pradeep and Krishna, Kurthkoti and Srinivasan, Ramanujam and kumar, Parthasarathi Ajit and Varshney, Umesh (2004) Uracil excision repair pathway activities are not intrinsic to nucleoside diphosphate kinases from Mycobacterium tuberculosis and Escherichia coli. In: DNA Repair, 3 (11). pp. 1483-1492.

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Abstract

E. coli nucleoside diphosphate kinase (EcoNDK) is an important cellular enzyme required to maintain balanced nucleotide pools in the cells.Recently, it was reported that EcoNDK is also a multifunctional base excision repair enzyme, possessing uracil-DNA glycosylase (UDG) and AP-DNA processing activities. We investigated for the presence of such activities in M. tuberculosis NDK (MtuNDK), which shares 45.2% identity, and 52.6% similarity with EcoNDK. In contrast to the robust uracil excision activity reported for EcoNDK, MtuNDK preparation exhibited very poor excision of uracil from DNA. However, this activity was undetectable when MtuNDK was purified from an ung(-) strain of Ecoli, or when the assays were performed in the presence of extremely low amounts of a highly specific proteinaceous inhibitor, Ugi which forms an extremely tight complex with the host Ung (UDG), showing that MtuNDK preparation was contaminated with UDG. Reinvestigation of uracil processing activity of EcoNDK, showed that even this protein lacked UDGactivity. All preparations of NDK were shown to be active by their autophosphorylation activity. Ugi neither displayed a physical interaction with EcoNDK nor did it affect autophosphorylation of NDKs.Further, neither of the NDK preparations processed the AP-DNA generatedby UDG treatment of the uracil containing DNA duplexes. However,partially purified preparations of NDK did process such DNA substrates.

Item Type: Journal Article
Additional Information: Copyright for this article belongs to Elsevier.
Keywords: UDG;Ung;Ugi;NDK;AP-endonuclease
Department/Centre: Division of Biological Sciences > Microbiology & Cell Biology
Date Deposited: 21 Feb 2005
Last Modified: 19 Sep 2010 04:18
URI: http://eprints.iisc.ernet.in/id/eprint/2826

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