Author/Authors :
Morimoto، نويسنده , , Yuki and Ouchida، نويسنده , , Mamoru and Ozaki، نويسنده , , Toshifumi and Kawai، نويسنده , , Akira and Ito، نويسنده , , Tatsuo and Yoshida، نويسنده , , Aki and Inoue، نويسنده , , Hajime and Shimizu، نويسنده , , Kenji، نويسنده ,
Abstract :
The human SYT–SSX gene has two splicing isoforms (type N and I), the latter of which contains an additional insertion of 93 bases. In the present study, we found increased transcriptional activity of the SYT–SSX type I protein in luciferase assay. When the SYT–SSX cDNAs were transfected to NIH3T3 cells, the type I transformant grew faster than the type N transformant. Furthermore, we evaluated the isoform ratio of the SYT or SYT–SSX transcripts in various tissues. Our results suggest that the SYT–SSX type I protein plays a critical role in the tumorigenesis of synovial sarcomas through increased transcriptional activity.
Keywords :
cell growth , transcriptional activity , Alternative splicing , SYT , Synovial sarcoma , SSX