Scheidler S, Fredericks W J, Rauscher F J, Barr F G, Vogt P K
Scripps Research Institute, La Jolla, CA 92037, USA.
Proc Natl Acad Sci U S A. 1996 Sep 3;93(18):9805-9. doi: 10.1073/pnas.93.18.9805.
Pediatric alveolar rhabdomyosarcoma is characterized by a chromosomal translocation that fuses parts of the PAX3 and FKHR genes. PAX3 codes for a transcriptional regulator that controls developmental programs, and FKHR codes for a forkhead-winged helix protein, also a likely transcription factor. The PAX3-FKHR fusion product retains the DNA binding domains of the PAX3 protein and the putative activator domain of the FKHR protein. The PAX3-FKHR protein has been shown to function as a transcriptional activator. Using the RCAS retroviral vector, we have introduced the PAX3-FKHR gene into chicken embryo fibroblasts. Expression of the PAX3-FKHR protein in these cells leads to transformation: the cells become enlarged, grow tightly packed and in multiple layers, and acquire the ability for anchorage-independent growth. This cellular transformation in vitro will facilitate studies on the mechanism of PAX3-FKHR-induced oncogenesis.
小儿肺泡横纹肌肉瘤的特征是一种染色体易位,该易位使PAX3基因和FKHR基因的部分片段融合。PAX3编码一种控制发育程序的转录调节因子,FKHR编码一种叉头翼状螺旋蛋白,它也可能是一种转录因子。PAX3-FKHR融合产物保留了PAX3蛋白的DNA结合结构域和FKHR蛋白的假定激活结构域。PAX3-FKHR蛋白已被证明可作为转录激活因子发挥作用。利用RCAS逆转录病毒载体,我们已将PAX3-FKHR基因导入鸡胚成纤维细胞。PAX3-FKHR蛋白在这些细胞中的表达导致细胞转化:细胞变大,紧密堆积并形成多层生长,并获得非锚定依赖性生长的能力。这种体外细胞转化将有助于研究PAX3-FKHR诱导肿瘤发生的机制。