Davis R J, D'Cruz C M, Lovell M A, Biegel J A, Barr F G
Department of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, Philadelphia 19104.
Cancer Res. 1994 Jun 1;54(11):2869-72.
Although the t(2;13)(q35;q14) translocation has been found in most cases of the pediatric cancer alveolar rhabdomyosarcoma, several cases have been reported with a variant t(1;13)(p36;q14) translocation. Our findings indicate that this t(1;13) rearranges PAX7 on chromosome 1 and fuses it to FKHR on chromosome 13. This fusion results in a chimeric transcript consisting of 5' PAX7 and 3' FKHR regions, which is similar to the 5' PAX3-3' FKHR transcript formed by the t(2;13). The 5' PAX3 and PAX7 regions encode related DNA binding domains, and therefore we postulate that these translocations create similar chimeric transcription factors that alter expression of a common group of target genes.
尽管在大多数小儿癌症肺泡横纹肌肉瘤病例中都发现了t(2;13)(q35;q14)易位,但也有几例报告显示存在变异的t(1;13)(p36;q14)易位。我们的研究结果表明,这种t(1;13)易位会重排1号染色体上的PAX7,并将其与13号染色体上的FKHR融合。这种融合产生了一个由5' PAX7和3' FKHR区域组成的嵌合转录本,这与由t(2;13)形成的5' PAX3-3' FKHR转录本相似。5' PAX3和PAX7区域编码相关的DNA结合结构域,因此我们推测这些易位会产生相似的嵌合转录因子,从而改变一组共同靶基因的表达。