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Increasing melanoma incidence: putatively explainable by retrotransposons. Experimental contributions of the xiphophorine Gordon-Kosswig melanoma system.
Anders, A; Petry, H; Fleming, C; Petry, K; Brix, P; Lüke, W; Gröger, H; Schneider, E; Kiefer, J; Anders, F.
Afiliação
  • Anders A; Genetisches Institut, Justus Liebig-Universität, Giessen, Germany.
Pigment Cell Res ; 7(6): 433-50, 1994 Dec.
Article em En | MEDLINE | ID: mdl-7761352
ABSTRACT
The worldwide accelerating increase of neoplasia in humans is difficult to explain. We use the Xiphophorus tumor model to approach this problem by melanoma provocation with X-rays. Melanoma develops following inappropriate expression of x-erb B-conducted developmental genes and their controllers. These oncodeterminants are inherited according to Mendelian rules. We detected a new type of oncodeterminants that, following a single treatment of embryos with X-rays, generates a self-generating non-Mendelian melanoma transmission and accelerating increase of its incidence in succeeding generations (e.g., 0-->18-->33-->52%). To localize these oncodeterminants, we crossed nonirradiated fish having half of their chromosomes irradiated with nonirradiated fish having none of, half of, or all of their chromosomes irradiated. Because tumor rate and expression in the following generations correspond to the rates of treated chromosomes, we conclude that the new oncodeterminants are distributed over the chromosomes of the fish, where they may increase in the changing generations. By means of xiphophorine-specific retroviral DNA, we isolated two retrotransposons that behave hereditarily like the new transgenerational oncodeterminants. Sequence analysis revealed three ORFs flanked by LTRs containing motives of regulatory sequences typical for known retroviral and retrotransposal LTRs. Pol- and env-resembling sequences are lacking. Southern and in situ hybridization showed their multiple and repetitive nature distributed throughout the chromosomes and indications for their capability to increase in number without further treatment. Their transcripts are expressed in concert with those of most of the other known xiphophorine tumor determinants. Their expression is extremely high in cell cultures from tumorous embryos derived from ancestors treated as embryos with X-rays.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oncogenes / Ciprinodontiformes / Elementos de DNA Transponíveis / Regulação Neoplásica da Expressão Gênica / Doenças dos Peixes / Melanoma / Modelos Biológicos / Neoplasias Induzidas por Radiação Tipo de estudo: Etiology_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies Limite: Animals / Female / Humans / Pregnancy Idioma: En Revista: Pigment Cell Res Ano de publicação: 1994 Tipo de documento: Article País de afiliação: Alemanha
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oncogenes / Ciprinodontiformes / Elementos de DNA Transponíveis / Regulação Neoplásica da Expressão Gênica / Doenças dos Peixes / Melanoma / Modelos Biológicos / Neoplasias Induzidas por Radiação Tipo de estudo: Etiology_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies Limite: Animals / Female / Humans / Pregnancy Idioma: En Revista: Pigment Cell Res Ano de publicação: 1994 Tipo de documento: Article País de afiliação: Alemanha
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