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EWS and ATF-1 gene fusion induced by t(12;22) translocation in malignant melanoma of soft parts.
Zucman, J; Delattre, O; Desmaze, C; Epstein, A L; Stenman, G; Speleman, F; Fletchers, C D; Aurias, A; Thomas, G.
Afiliación
  • Zucman J; Laboratory de Tumour Genetics, INSERM CJF 9201, Institut Curie, Paris, France.
Nat Genet ; 4(4): 341-5, 1993 Aug.
Article en En | MEDLINE | ID: mdl-8401579
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.
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Banco de datos: MEDLINE Asunto principal: Oncogenes / Neoplasias de los Tejidos Blandos / Factores de Transcripción / Translocación Genética / Cromosomas Humanos Par 12 / Cromosomas Humanos Par 22 / Proteínas de Fusión Oncogénica / Clonación Molecular / Proteínas de Unión al ADN / Melanoma Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Año: 1993 Tipo del documento: Article
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Banco de datos: MEDLINE Asunto principal: Oncogenes / Neoplasias de los Tejidos Blandos / Factores de Transcripción / Translocación Genética / Cromosomas Humanos Par 12 / Cromosomas Humanos Par 22 / Proteínas de Fusión Oncogénica / Clonación Molecular / Proteínas de Unión al ADN / Melanoma Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Año: 1993 Tipo del documento: Article