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Recurrence of OTT-MAL fusion in t(1;22) of infant AML-M7.
Genes Chromosomes Cancer ; 33(1): 22-8, 2002 Jan.
Article em En | MEDLINE | ID: mdl-11746984
ABSTRACT
Translocation t(1;22)(p13;q13) is associated with a peculiar subtype of acute megakaryocytic leukemia (M7) occurring in infants. We have recently characterized a fusion gene, OTT-MAL, resulting from this translocation. We now report three additional cases and show that this gene fusion is present in all five t(1;22) cases studied to date. Nucleotide sequence analysis of two translocation breakpoints suggests a nonhomologous end joining mechanism in the genesis of this translocation and reveals a noncanonical topoisomerase II-like consensus sequence within the OTT gene. FISH and PCR techniques described in this work are useful for identifying t(1;22) associated with M7.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Translocação Genética / Cromossomos Humanos Par 1 / Cromossomos Humanos Par 22 / Proteínas / Leucemia Megacarioblástica Aguda / Proteínas de Ligação a RNA Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Infant / Male / Newborn Idioma: En Ano de publicação: 2002 Tipo de documento: Article
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Translocação Genética / Cromossomos Humanos Par 1 / Cromossomos Humanos Par 22 / Proteínas / Leucemia Megacarioblástica Aguda / Proteínas de Ligação a RNA Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Infant / Male / Newborn Idioma: En Ano de publicação: 2002 Tipo de documento: Article