Literature DB >> 17242181

Inverted DNA repeats channel repair of distant double-strand breaks into chromatid fusions and chromosomal rearrangements.

Kelly VanHulle1, Francene J Lemoine, Vidhya Narayanan, Brandon Downing, Krista Hull, Christy McCullough, Melissa Bellinger, Kirill Lobachev, Thomas D Petes, Anna Malkova.   

Abstract

Inverted DNA repeats are known to cause genomic instabilities. Here we demonstrate that double-strand DNA breaks (DSBs) introduced a large distance from inverted repeats in the yeast (Saccharomyces cerevisiae) chromosome lead to a burst of genomic instability. Inverted repeats located as far as 21 kb from each other caused chromosome rearrangements in response to a single DSB. We demonstrate that the DSB initiates a pairing interaction between inverted repeats, resulting in the formation of large dicentric inverted dimers. Furthermore, we observed that propagation of cells containing inverted dimers led to gross chromosomal rearrangements, including translocations, truncations, and amplifications. Finally, our data suggest that break-induced replication is responsible for the formation of translocations resulting from anaphase breakage of inverted dimers. We propose a model explaining the formation of inverted dicentric dimers by intermolecular single-strand annealing (SSA) between inverted DNA repeats. According to this model, anaphase breakage of inverted dicentric dimers leads to gross chromosomal rearrangements (GCR). This "SSA-GCR" pathway is likely to be important in the repair of isochromatid breaks resulting from collapsed replication forks, certain types of radiation, or telomere aberrations that mimic isochromatid breaks.

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Year:  2007        PMID: 17242181      PMCID: PMC1899885          DOI: 10.1128/MCB.01740-06

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  51 in total

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3.  Genetic requirements for RAD51- and RAD54-independent break-induced replication repair of a chromosomal double-strand break.

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Review 4.  Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiae.

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5.  High-linear energy transfer (LET) alpha versus low-LET beta emitters in radioimmunotherapy of solid tumors: therapeutic efficacy and dose-limiting toxicity of 213Bi- versus 90Y-labeled CO17-1A Fab' fragments in a human colonic cancer model.

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Review 7.  Chromosomal alterations in squamous cell carcinomas of the head and neck: window to the biology of disease.

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8.  Rad52-independent mitotic gene conversion in Saccharomyces cerevisiae frequently results in chromosomal loss.

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9.  Homothallic mating type switching generates lethal chromosome breaks in rad52 strains of Saccharomyces cerevisiae.

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10.  DNA end resection, homologous recombination and DNA damage checkpoint activation require CDK1.

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  64 in total

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2.  Assessment of palindromes as platforms for DNA amplification in breast cancer.

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3.  A recombination execution checkpoint regulates the choice of homologous recombination pathway during DNA double-strand break repair.

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4.  Double-strand breaks associated with repetitive DNA can reshape the genome.

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5.  Sgs1 helicase and two nucleases Dna2 and Exo1 resect DNA double-strand break ends.

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Review 6.  Non-B DNA structure-induced genetic instability and evolution.

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7.  Failed gene conversion leads to extensive end processing and chromosomal rearrangements in fission yeast.

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Review 10.  Palindromic gene amplification--an evolutionarily conserved role for DNA inverted repeats in the genome.

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