EWS AND ATF-1 GENE FUSION INDUCED BY T(12-22) TRANSLOCATION IN MALIGNANT-MELANOMA OF SOFT PARTS

被引:428
作者
ZUCMAN, J
DELATTRE, O
DESMAZE, C
EPSTEIN, AL
STENMAN, G
SPELEMAN, F
FLETCHERS, CDM
AURIAS, A
THOMAS, G
机构
[1] INST CURIE, INSERM, TUMOUR GENET LAB, CJF 9201, 26 RUE ULM, F-75231 PARIS 05, FRANCE
[2] UNIV SO CALIF, MED CTR, DEPT PATHOL, LOS ANGELES, CA 90033 USA
[3] GOTHENBURG UNIV, DEPT ODONTOL, S-400330 GOTEBOTG, SWEDEN
[4] STATE UNIV GHENT HOSP, DEPT MED GENET, B-9000 GHENT, BELGIUM
[5] ST THOMAS HOSP, DEPT HISTOPATHOL, LONDON SE1 7EH, ENGLAND
关键词
D O I
10.1038/ng0893-341
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The genes involved in the t(12;22)(q13;q12) translocation found recurrently in malignant melanoma of soft parts have been characterized and shown to form, in four cases studied, hybrid transcripts. The deduced chimaeric protein encoded by the der(22) chromosome consists of the N-terminal domain of EWS linked to the bZIP domain of ATF-1, a transcription factor which may normally be regulated by cAMP. ATF-1 has not previously been implicated in oncogenesis. EWS was first identified as forming a hybrid transcript in Ewing's sarcoma, which links its N-terminal domain to the DNA binding domain of the FLI-1 gene. Thus the oncogenic conversion of EWS follows a common scheme of activation, exchanging its putative RNA binding domain with different DNA binding domains that appear to be tumour-specific.
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收藏
页码:341 / 345
页数:5
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