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.
Original language | English |
---|---|
Pages (from-to) | 178-187 |
Number of pages | 10 |
Journal | Oncogene |
Volume | 20 |
Issue number | 2 |
DOIs | |
Publication status | Published - 25 Dec 2000 |
Keywords
- PRCC
- Pre-mRNA splicing
- TFE3
- Transcription activation
ASJC Scopus subject areas
- Molecular Biology
- Genetics
- Cancer Research