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PRCC, the commonest TFE3 fusion partner in papillary renal carcinoma is associated with pre-mRNA splicing factors.

Abstract
In papillary renal cell carcinomas the TFE3 transcription factor becomes fused to the PSF and NonO pre-mRNA splicing factors and most commonly to a protein of unknown function designated PRCC. In this study we have examined the ability of the resulting PRCC-TFE3 and NonO-TFE3 fusions to activate transcription from the plasminogen activator inhibitor-1 (PAI-1) promoter. The results show that only fusion to PRCC enhanced transcriptional activation, indicating that the ability to enhance the level of transcription from endogenous TFE3 promoters is not a consistent feature of TFE3 fusions. In investigations of the normal function of PRCC we observed that PRCC expressed as a green fluorescent fusion protein colocalizes within the nucleus with Sm pre-mRNA splicing factors. It was also found that endogenous PRCC is coimmunoprecipitated by antibodies that recognize a variety of pre-mRNA splicing factors including SC35, PRL1 and CDC5. Association with the cellular splicing machinery is therefore, a common feature of the proteins that become fused to TFE3 in papillary renal cell carcinomas.
AuthorsY M Skalsky, P M Ajuh, C Parker, A I Lamond, G Goodwin, C S Cooper
JournalOncogene (Oncogene) Vol. 20 Issue 2 Pg. 178-87 (Jan 11 2001) ISSN: 0950-9232 [Print] England
PMID11313942 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Amanitins
  • Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
  • Cell Cycle Proteins
  • DNA-Binding Proteins
  • Enzyme Inhibitors
  • Luminescent Proteins
  • Neoplasm Proteins
  • Nuclear Proteins
  • PRCC protein, human
  • Proteins
  • RNA Precursors
  • RNA, Messenger
  • Recombinant Fusion Proteins
  • Ribonucleoproteins
  • Ribonucleoproteins, Small Nuclear
  • Saccharomyces cerevisiae Proteins
  • TFE3 protein, human
  • Transcription Factors
  • SRSF2 protein, human
  • Green Fluorescent Proteins
  • Serine-Arginine Splicing Factors
  • Protein Kinases
  • Protein Serine-Threonine Kinases
  • CDC5 protein, S cerevisiae
Topics
  • Adult
  • Amanitins (pharmacology)
  • Animals
  • Artificial Gene Fusion
  • Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
  • Carcinoma, Papillary (drug therapy, genetics, metabolism)
  • Carcinoma, Renal Cell (drug therapy, genetics, metabolism)
  • Cell Cycle Proteins
  • DNA-Binding Proteins (genetics, metabolism)
  • Enzyme Inhibitors (pharmacology)
  • Female
  • Green Fluorescent Proteins
  • Humans
  • Kidney Neoplasms (drug therapy, genetics, metabolism)
  • Luminescent Proteins (genetics, metabolism)
  • Male
  • Neoplasm Proteins
  • Nuclear Proteins (metabolism)
  • Protein Kinases (metabolism)
  • Protein Serine-Threonine Kinases
  • Proteins (genetics, metabolism)
  • RNA Precursors (genetics)
  • RNA Splicing
  • RNA, Messenger (genetics)
  • Recombinant Fusion Proteins (genetics, metabolism)
  • Ribonucleoproteins
  • Ribonucleoproteins, Small Nuclear (metabolism)
  • Saccharomyces cerevisiae Proteins
  • Serine-Arginine Splicing Factors
  • Transcription Factors (genetics, metabolism)
  • Transcription, Genetic
  • Tumor Cells, Cultured

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