Cloning and Characterization of Active Egr-1 Target Genes by In Vivo Crosslinking

Abstract

The purpose of this project is to identify the profile of Egr-l target genes in breast cells. Normal breast cells are shown to express Egr-l, while breast cancer cells do not. It is, therefore, important to identify the nature of those target genes regulated by Egr- 1 which are absent in breast cancer cells. I have approached this goal by performing in vivo crosslinking of Egr-l to its target sites in breast cells, followed by immunocapture of Egr-l together with its targets. In this report I have proceeded with the identification, by multiplex PCR amplification, of Egr-l target genes. Specifically, I have successfully cloned a novel full length cDNA and describe anew Egr-l target gene called TEXl. Expression of TEXl has the biological activity of growth inhibition in a cell cycle dependent manner. I am proceeding to further characterize this new gene as well as identifying additional Egr-l target genes expressed in both normal and breast cancer cells.

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Document Details

Document Type
Technical Report
Publication Date
May 01, 2001
Accession Number
ADA393084

Entities

People

  • Ian De Belle

Organizations

  • Sanford Burnham Prebys Medical Discovery Institute

Tags

DTIC Thesaurus Topics

  • Abstracts
  • Amplification
  • Animals
  • Biomedical Research
  • Breast Cancer
  • Cancer
  • Cell Physiological Processes
  • Cells
  • Chromosomes
  • Deoxyribonucleic Acids
  • Dna Microarrays
  • Identification
  • Laboratory Animals
  • Materials
  • Neoplasms
  • Recombinant Dna
  • Transcription Factors

Fields of Study

  • Biology

Readers

  • Molecular Genetics
  • Oncology (Cancer Research).