Weber-Hall S, McManus A, Anderson J, Nojima T, Abe S, Pritchard-Jones K, Shipley J
Section of Paediatrics, Institute of Cancer Research, Sutton, Surrey, United Kingdom.
Genes Chromosomes Cancer. 1996 Sep;17(1):7-13. doi: 10.1002/(SICI)1098-2264(199609)17:1<7::AID-GCC2>3.0.CO;2-0.
Alveolar rhabdomyosarcomas frequently exhibit specific translocations, resulting in the fusion of the FKHR gene at 13q14 with either the PAX3 or PAX7 gene at 2q35 and 1p36, respectively. Comparative genomic hybridization revealed amplification at 13q14 and 1p36, suggesting amplification of the PAX7-FKHR fusion gene in two cases of alveolar rhabdomyosarcoma. A PAX7-FKHR fusion transcript was demonstrated in both cases by reverse transcription-polymerase chain reaction followed by sequence analysis. In one case, amplification of the PAX7 gene and 3'-and 5'-FKHR gene sequences was demonstrated by using interphase fluorescence in situ hybridization on tumor imprints. The colocalization, variable copy number, and distribution of signals from the three cosmids was consistent with amplification of these sequences on double minutes, which were present cytogenetically. Chromatin release studies suggested that the amplified sequences correlated with amplification of the PAX7-FKHR fusion gene which resulted from the insertion of PAX7 sequences into the first intron of FKHR gene, in keeping with the absence of cytogenetic evidence for derivative chromosomes.
肺泡横纹肌肉瘤常出现特定的易位,导致位于13q14的FKHR基因分别与位于2q35和1p36的PAX3或PAX7基因融合。比较基因组杂交显示13q14和1p36存在扩增,提示两例肺泡横纹肌肉瘤中PAX7 - FKHR融合基因发生扩增。通过逆转录 - 聚合酶链反应及序列分析,在两例中均证实了PAX7 - FKHR融合转录本。在其中一例中,利用肿瘤印片进行间期荧光原位杂交,证实了PAX7基因以及3'端和5'端FKHR基因序列的扩增。三个黏粒的信号共定位、可变拷贝数及分布与双微体上这些序列的扩增一致,双微体在细胞遗传学上是存在的。染色质释放研究表明,扩增序列与PAX7 - FKHR融合基因的扩增相关,该融合基因是由于PAX7序列插入FKHR基因的第一个内含子所致,这与缺乏衍生染色体的细胞遗传学证据相符。