Literature DB >> 24600040

DNA repair pathways in trypanosomatids: from DNA repair to drug resistance.

Marie-Michelle Genois1, Eric R Paquet, Marie-Claude N Laffitte, Ranjan Maity, Amélie Rodrigue, Marc Ouellette, Jean-Yves Masson.   

Abstract

All living organisms are continuously faced with endogenous or exogenous stress conditions affecting genome stability. DNA repair pathways act as a defense mechanism, which is essential to maintain DNA integrity. There is much to learn about the regulation and functions of these mechanisms, not only in human cells but also equally in divergent organisms. In trypanosomatids, DNA repair pathways protect the genome against mutations but also act as an adaptive mechanism to promote drug resistance. In this review, we scrutinize the molecular mechanisms and DNA repair pathways which are conserved in trypanosomatids. The recent advances made by the genome consortiums reveal the complete genomic sequences of several pathogens. Therefore, using bioinformatics and genomic sequences, we analyze the conservation of DNA repair proteins and their key protein motifs in trypanosomatids. We thus present a comprehensive view of DNA repair processes in trypanosomatids at the crossroads of DNA repair and drug resistance.

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Year:  2014        PMID: 24600040      PMCID: PMC3957735          DOI: 10.1128/MMBR.00045-13

Source DB:  PubMed          Journal:  Microbiol Mol Biol Rev        ISSN: 1092-2172            Impact factor:   11.056


  290 in total

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5.  XRCC2 is a nuclear RAD51-like protein required for damage-dependent RAD51 focus formation without the need for ATP binding.

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6.  Rad54, a Swi2/Snf2-like recombinational repair protein, disassembles Rad51:dsDNA filaments.

Authors:  Jachen A Solinger; Konstantin Kiianitsa; Wolf-Dietrich Heyer
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7.  Identification of the meiotic life cycle stage of Trypanosoma brucei in the tsetse fly.

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10.  Trypanosoma brucei has two distinct mitochondrial DNA polymerase beta enzymes.

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Review 7.  Read, Write, Adapt: Challenges and Opportunities during Kinetoplastid Genome Replication.

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8.  Distinct Phenotypes Caused by Mutation of MSH2 in Trypanosome Insect and Mammalian Life Cycle Forms Are Associated with Parasite Adaptation to Oxidative Stress.

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