Defining the Consequence of CHD1 Loss on Transcriptional Regulation and Therapeutic Response

Abstract

Genome wide studies have identified a high prevalence of inactivating genomic alterations associated with nucleosome remodeling and modifying enzymes, suggesting that deregulation of chromatin architecture is critical in tumor initiation/progression. CHD1 is a founding member of the chromatin remodeling family, characterized by tandem Chromo-domains, a DNA Helicase domain, and DNA binding domain (CHD1). A multitude of studies have demonstrated that CHD1 is recruited to the promoters of highly transcribed genes by the epigenetic mark H3K4me3, where it redistributes local nucleosomes ahead of RNA polymerase to facilitate efficient transcriptional initiation and RNA processing. While a majority of cell types appear to be dependent upon the function of CHD1, a subclass of primary PCa is characterized by the genomic loss of this chromatin remodeler. Given that PCa is a disease driven by aberrant transcriptional regulation mediated by oncogenic transcriptional factors (e.g. AR and MYC), it is imperative to understand the molecular underpinnings of CHD1 loss in driving these oncogenic programs. For the first time, our preliminary data demonstrate that in a prostate-specific background, CHD1 localizes to enhancer-like regions of the genome specifically occupied by AR and its associated transcriptional regulators (FOXA1 and HOXB13). This CHD1 binding signature is highly consistent with epigenetic marks identifying these enhancer sites, suggesting that CHD1 remodels enhancer-like chromatin to define a unique AR cistrome. Furthermore, CHD1 was found to be dispensable for global transcriptional output in prostate derived models, but was essential for efficient transcriptional processing. Thus, loss of CHD1 may have a global impact on the AR transcriptional network, deregulating both genomic binding and resultant transcriptional output, via distinct molecular mechanisms.

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Document Details

Document Type
Technical Report
Publication Date
Sep 01, 2019
Accession Number
AD1093439

Entities

People

  • Michael A. Augello

Organizations

  • Weill Cornell Medicine

Tags

DTIC Thesaurus Topics

  • Androgen Receptors
  • Biomedical Research
  • Cancer
  • Cell Line
  • Cells
  • Chemistry
  • Databases
  • Department Of Defense
  • Gene Expression
  • Genetics
  • Indicator Dyes
  • Mass Spectrometry
  • Medical Personnel
  • Neoplasms
  • New York
  • Prostate Cancer
  • Stem Cells

Fields of Study

  • Biology

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