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Characterization of the MCT-1 pseudogene: identification and implication of its location in a highly amplified region of chromosome 20.
Nandi, Suvobroto; Shi, Bo; Perreault, Jonathan; Gartenhaus, Ronald B.
Afiliação
  • Nandi S; University of Maryland Greenebaum Cancer Center, Department of Medicine, 655 W Baltimore Street, Baltimore, MD 21201, USA. sunandi@som.umaryland.edu
Biochim Biophys Acta ; 1759(5): 234-9, 2006 May.
Article em En | MEDLINE | ID: mdl-16815567
The MCT-1 oncogene was initially identified as an amplified gene on chromosome Xq22-24 in a T-cell lymphoma. MCT-1 is over-expressed in a subset of diffuse large B-cell lymphoma (DLBCL), a common form of Non-Hodgkin's Lymphoma (NHL). We have identified a pseudogene for MCT-1 (PsiMCT-1) that is located on chromosome 20q11.2, a region within an amplicon containing several important genes frequently amplified in certain breast and ovarian cancers. Genomic analysis revealed that PsiMCT-1 is a processed pseudogene. Interestingly, both MCT-1 and its pseudogene are located on regions of the genome that are frequently amplified in several different human malignancies. MCT-1 is the oldest known oncogene and its insertion as a pseudogene occurred at a later time point in evolution. Existence of PsiMCT-1 should be considered when analyzing genomic amplification and or expression of MCT-1. Analysis of MCT-1 and PsiMCT-1 might provide clues to cancer genes and their evolution across species.
Assuntos
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Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 20 / Pseudogenes / Amplificação de Genes / Proteínas Oncogênicas / Proteínas de Ciclo Celular Tipo de estudo: Diagnostic_studies Limite: Female / Humans Idioma: En Revista: Biochim Biophys Acta Ano de publicação: 2006 Tipo de documento: Article País de afiliação: Estados Unidos
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Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 20 / Pseudogenes / Amplificação de Genes / Proteínas Oncogênicas / Proteínas de Ciclo Celular Tipo de estudo: Diagnostic_studies Limite: Female / Humans Idioma: En Revista: Biochim Biophys Acta Ano de publicação: 2006 Tipo de documento: Article País de afiliação: Estados Unidos