Study of Telomere Dysfunction in TP53 Mutant LoVo Cell Lines as a Model for Genomic Instability

Methods Mol Biol. 2018:1769:209-230. doi: 10.1007/978-1-4939-7780-2_14.

Abstract

Telomere restriction fragment, 3D quantitative FISH on nuclei, and quantitative FISH on metaphases are complementary approaches that explore telomere dysfunction genomically, cellularly, and chromosomally, respectively. We used these approaches to study association between telomere dysfunction and degree of genomic instability related to TP53 mutations in LoVo isogenic cell lines. We found a strong correlation between degree of genomic instability, telomere dysfunction, and specific mutations of TP53. The use of complementary approaches to study telomere biology is essential to have a comprehensive understanding of telomere involvement in genomic instability.

Keywords: 3D telomere quantitative FISH; Genomic instability; MFISH; Telomere; Telomere aggregates; Telomere length; Telomere restriction fragment.

MeSH terms

  • Cell Cycle
  • Cell Line
  • Genomic Instability*
  • In Situ Hybridization, Fluorescence
  • Models, Genetic*
  • Mutation*
  • Telomere / genetics*
  • Telomere / metabolism
  • Telomere Homeostasis
  • Tumor Suppressor Protein p53 / genetics*

Substances

  • Tumor Suppressor Protein p53