DNA Damage and Genomic Instability Induced by Inappropriate DNA Re-replication

Abstract

Chromosomal rearrangements and changes in copy number at various genomic loci are hallmarks of cancer cells and may be very early steps in tumorigenesis. The origins of genomic insults are poorly understood and this proposal aims to characterize one potential source of genomic instability, inappropriate DNA re-replication. In a normal eukaryotic cell cycle, the chromosomal DNA of a cell is replicated once, and only once, during S phase to ensure that each daughter cell receives exactly one complement of genomic material. By perturbing the regulation of several proteins involved in replication initiation, our laboratory has been able to conditionally induce varying amounts of re-replication in yeast cells. In the prior reporting period we demonstrated that re-replication induces a rapid and significant decrease in cell viability and a cellular DNA damage response. Strikingly, we have observed DNA damage in the absence of a classical replication stress response. In this reporting period we have demonstrated that re-replication leads to genome instability, in particular gene duplication. This is the first experimental evidence that re-replication might contribute to gene amplification and thus tumorigenesis.

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Document Details

Document Type
Technical Report
Publication Date
Apr 01, 2006
Accession Number
ADA483291

Entities

People

  • Brian Green

Organizations

  • University of California, San Francisco

Tags

DTIC Thesaurus Topics

  • Biological Sciences
  • Cell Physiological Processes
  • Cells
  • Chemistry
  • Chromosome Structures
  • Chromosomes
  • Electron Microscopy
  • Eukaryotes
  • Fungi
  • Gel Electrophoresis
  • Genetics
  • Genomic Instability
  • Materials
  • Molecular Biology
  • Reliability
  • Two Dimensional

Fields of Study

  • Biology

Readers

  • Molecular Biology and Genetics