A KRAS-directed transcriptional silencing pathway that mediates the CpG island methylator phenotype

Elife. 2014 Mar 12:3:e02313. doi: 10.7554/eLife.02313.

Abstract

Approximately 70% of KRAS-positive colorectal cancers (CRCs) have a CpG island methylator phenotype (CIMP) characterized by aberrant DNA hypermethylation and transcriptional silencing of many genes. The factors involved in, and the mechanistic basis of, CIMP is not understood. Among the CIMP genes are the tumor suppressors p14(ARF), p15(INK4B), and p16(INK4A), encoded by the INK4-ARF locus. In this study, we perform an RNA interference screen and identify ZNF304, a zinc-finger DNA-binding protein, as the pivotal factor required for INK4-ARF silencing and CIMP in CRCs containing activated KRAS. In KRAS-positive human CRC cell lines and tumors, ZNF304 is bound at the promoters of INK4-ARF and other CIMP genes. Promoter-bound ZNF304 recruits a corepressor complex that includes the DNA methyltransferase DNMT1, resulting in DNA hypermethylation and transcriptional silencing. KRAS promotes silencing through upregulation of ZNF304, which drives DNA binding. Finally, we show that ZNF304 also directs transcriptional silencing of INK4-ARF in human embryonic stem cells. DOI: http://dx.doi.org/10.7554/eLife.02313.001.

Keywords: CpG island methylator phenotype; DNMT1; INK4-ARF; KRAS; ZNF304; colorectal cancer.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • CpG Islands*
  • Cyclin-Dependent Kinase Inhibitor Proteins / genetics
  • DNA Methylation*
  • Gene Silencing*
  • Genes, ras*
  • Humans
  • Molecular Sequence Data
  • Phenotype
  • RNA Interference
  • Sequence Homology, Amino Acid
  • Transcription Factors / metabolism
  • Transcription, Genetic*
  • Ubiquitin Thiolesterase / metabolism
  • Up-Regulation

Substances

  • Cyclin-Dependent Kinase Inhibitor Proteins
  • Transcription Factors
  • USP28 protein, human
  • ZNF304 protein, human
  • Ubiquitin Thiolesterase