A novel isoform ratio switch of the polypyrimidine tract binding protein

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

In this report we present evidence for a novel switch in the ratio of the two major iso-forms of the polypyrimidine tract binding protein (PTB) in two related prostate cancer cell lines. The existence of different isoforms of PTB is thought to be the result of alternative splicing. We used UV cross-linking to identify a PTB doublet in the DT3 cell line, which is a rat prostate epithelial cancer line that is androgen-dependent and nonmetastatic. The AT3 cell line, a metastatic, androgen-independent cell line derived from the same tumor as the DT3 cells, was noted here to have a different isoform ratio of PTB. The two most prevalent isoforms of PTB were found to bind to an RNA probe containing a pyrimidine stretch. Western blot analysis demonstrated that these isoforms are indeed expressed differently in the two cell lines and that the observed binding is the result of this differential expression. These two cell lines are derived from the original Dunning prostate tumor, which is a model for studying tumor progression in the prostate. This ratio switch may be an important event in tumor progression in this model system of prostate cancer.

Original languageEnglish (US)
Title of host publicationFrom Genome to Proteome: Advances in the Practice & Application of Proteomics
PublisherWiley Blackwell
Pages502-506
Number of pages5
ISBN (Print)9783527613489, 9783527301546
DOIs
StatePublished - Dec 26 2007
Externally publishedYes

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Keywords

  • Alternative splicing
  • Isoforms
  • Polypyrimidine tract binding protein
  • Prostate cancer

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)

Cite this

Wagner, E., Carstens, R. P., & Garcia-Blanco, M. (2007). A novel isoform ratio switch of the polypyrimidine tract binding protein. In From Genome to Proteome: Advances in the Practice & Application of Proteomics (pp. 502-506). Wiley Blackwell. https://doi.org/10.1002/9783527613489.ch65