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An exonuclease I-sensitive DNA repair pathway in Deinococcus radiodurans: a major determinant of radiation resistance
Author(s): Misra HS, Khairnar NP, Kota S, Shrivastava S, Joshi VP, Apte SK
Source: MOLECULAR MICROBIOLOGY    Volume: 59    Issue: 4    Pages: 1308-1316    Published: FEB 2006  
Times Cited: 17     References: 36     
Abstract: Deinococcus radiodurans R1 recovering from acute dose of gamma radiation shows a biphasic mechanism of DNA double-strand break repair. The possible involvement of microsequence homology-dependent, or non-homologous end joining type mechanisms during initial period followed by RecA-dependent homologous recombination pathways has been suggested for the reconstruction of complete genomes in this microbe. We have exploited the known roles of exonuclease I in DNA recombination to elucidate the nature of recombination involved in DNA double-strand break repair during post-irradiation recovery of D. radiodurans. Transgenic Deinococcus cells expressing exonuclease I functions of Escherichia coli showed significant reduction in gamma radiation radioresistance, while the resistance to far-UV and hydrogen peroxide remained unaffected. The overexpression of E. coli exonuclease I in Deinococcus inhibited DNA double-strand break repair. Such cells exhibited normal post-irradiation expression kinetics of RecA, PprA and single-stranded DNA-binding proteins but lacked the divalent cation manganese [(Mn(II)]-dependent protection from gamma radiation. The results strongly suggest that 3' (rho) 5' single-stranded DNA ends constitute an important component in recombination pathway involved in DNA double-strand break repair and that absence of sbcB from deinococcal genome may significantly aid its extreme radioresistance phenotype.
Document Type: Article
Language: English
Reprint Address: Misra, HS (reprint author), Bhabha Atom Res Ctr, Div Mol Biol, Bombay 400085, Maharashtra India
Addresses:
1. Bhabha Atom Res Ctr, Div Mol Biol, Bombay 400085, Maharashtra India
Publisher: BLACKWELL PUBLISHING, 9600 GARSINGTON RD, OXFORD OX4 2DQ, OXON, ENGLAND
Subject Category: Biochemistry & Molecular Biology; Microbiology
IDS Number: 005CQ
ISSN: 0950-382X
DOI: 10.1111/j.1365-2958.2005.05005.x
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