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软组织恶性黑色素瘤中由t(12;22)易位诱导的EWS和ATF-1基因融合。

EWS and ATF-1 gene fusion induced by t(12;22) translocation in malignant melanoma of soft parts.

作者信息

Zucman J, Delattre O, Desmaze C, Epstein A L, Stenman G, Speleman F, Fletchers C D, Aurias A, Thomas G

机构信息

Laboratory de Tumour Genetics, INSERM CJF 9201, Institut Curie, Paris, France.

出版信息

Nat Genet. 1993 Aug;4(4):341-5. doi: 10.1038/ng0893-341.

Abstract

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.

摘要

在软组织恶性黑色素瘤中反复发现的涉及t(12;22)(q13;q12)易位的基因已被鉴定,并在4例研究病例中显示形成了杂交转录本。由der(22)染色体编码的推导嵌合蛋白由EWS的N端结构域与ATF-1的bZIP结构域相连组成,ATF-1是一种转录因子,通常可能受cAMP调节。ATF-1以前未被认为与肿瘤发生有关。EWS最初被鉴定为在尤因肉瘤中形成杂交转录本,它将其N端结构域与FLI-1基因的DNA结合结构域相连。因此,EWS的致癌转化遵循一种常见的激活模式,将其假定的RNA结合结构域与不同的似乎是肿瘤特异性的DNA结合结构域进行交换。

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