Increased alternative lengthening of telomere phenotypes of telomerase-negative immortal cells upon trichostatin - A treatment

A. Ra Jung, Jeong Eun Yoo, Yhong Hee Shim, Ye Na Choi, Hei Cheul Jeung, Hyun Cheol Chung, Sun Young Rha, Bong Kyeong Oh

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

Human immortal cells maintain their telomeres either by telomerase or by alternative lengthening of telomeres (ALT) that is based on homologous telomeric recombination. Previous studies showed that the ALT mechanism is activated in non-ALT cells when heterochromatic features are reduced. In this study, we examined the ALT phenotypes of ALT cells after treatment with trichostatin-A (TSA), which is an inhibitor of histone deacetylases and causes global chromatin decondensation. The ALT cells remained telomerase-negative after TSA treatment. ALT-associated promyelocytic leukemia (PML) nuclear bodies and telomere sister chromatid exchanges, typical ALT phenotypes, markedly increased in the TSAtreated cells, while the telomere length remained unchanged. In addition, telomerase expression in the ALT cells suppressed TSA-mediated ALT phenotype enhancement. Our results show that certain ALT phenotypes become more pronounced when chromatin is decondensed, and also suggest that the ALT mechanism may compete with telomerase for telomere maintenance in cells that lack heterochromatin.

Original languageEnglish
Pages (from-to)821-830
Number of pages10
JournalAnticancer research
Volume33
Issue number3
Publication statusPublished - 2013 Mar

All Science Journal Classification (ASJC) codes

  • Oncology
  • Cancer Research

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