Fusion of splicing factor genes PSF and NonO (p54(nrb)) to the TFE3 gene in papillary renal cell carcinoma

被引:266
|
作者
Clark, J
Lu, YJ
Sidhar, SK
Parker, C
Gill, S
Smedley, D
Hamoudi, R
Linehan, WM
Shipley, J
Cooper, CS
机构
[1] INST CANC RES, HADDOW LABS, SECT CELL BIOL & EXPT PATHOL, SUTTON SM2 5NG, SURREY, ENGLAND
[2] INST CANC RES, HADDOW LABS, CANC GENE CLONING LAB, SUTTON SM2 5NG, SURREY, ENGLAND
[3] NCI, UROL ONCOL SECT, BETHESDA, MD 20892 USA
关键词
renal cell carcinoma; PSF splicing factor; NonO (p54(nrb)) splicing factor; chromosome translocations; TFE3 transcription factor;
D O I
10.1038/sj.onc.1201394
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We demonstrate that the cytogenetically defined translocation t(X;1)(p11.2;p34) observed in papillary renal cell carcinomas results in the fusion of the splicing factor gene PSF located at 1p34 to the TFE3 helix-loop-helix transcription factor gene at Xp11.2. In addition we define an X chromosome inversion inv(X)(p11.2;q12) that results in the fusion of the NonO (p54(nrb)) gene to TFE3. NonO (p54(nrb)), the human homologue of the Drosophila gene NonA(diss) which controls the male courtship song, is closely related to PSF and also believed to be involved in RNA splicing. In each case the rearrangement results in the fusion of almost the entire splicing factor protein to the TFE3 DIVA-binding domain. These observations suggest the possibility of intriguing links between the processes of RNA splicing, DNA transcription and oncogenesis.
引用
收藏
页码:2233 / 2239
页数:7
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