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TTF-2 stimulates expression of 17 genes, including one novel thyroid-specific gene which might be involved in thyroid development.
Hishinuma, Akira; Ohmika, Narumi; Namatame, Takashi; Ieiri, Tamio.
Afiliación
  • Hishinuma A; Department of Clinical Laboratory Medicine, Dokkyo University School of Medicine, Kitakobayashi 880, Mibu, Tochigi 321-0293, Japan. a-hishi@dokkyomed.ac.jp
Mol Cell Endocrinol ; 221(1-2): 33-46, 2004 Jun 30.
Article en En | MEDLINE | ID: mdl-15223130
Thyroid dysgenesis is the most frequent cause of congenital hypothyroidism, but its molecular pathophysiology is largely unknown. Our hypothesis that some genes downstream to thyroid transcription factor-2 (TTF-2) might be responsible for development of the thyroid prompted us to identify genes whose expression is stimulated by TTF-2. PCR products of cDNA clones obtained by a subtraction PCR method in TTF-2 expressing cell lines were screened with labeled cDNA by microarray analysis. We isolated 17 genes up-regulated by TTF-2, which were subsequently confirmed by quantitative reverse transcription-polymerase chain reaction (RT-PCR). One of them is a novel gene designated T1560 that showed a highly thyroid-specific expression pattern. Luciferase reporter assays showed that expression of all of the 14 genes tested was stimulated by both TTF-2 and TTF-1, another thyroid-specific transcription factor. Our results have important implications for understanding normal thyroid development as well as the molecular defects underlying thyroid dysgenesis.
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Bases de datos: MEDLINE Asunto principal: Proteínas Represoras / Glándula Tiroides / Activación Transcripcional / Proteínas de Unión al ADN / Proteínas de la Membrana Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Mol Cell Endocrinol Año: 2004 Tipo del documento: Article País de afiliación: Japón
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Bases de datos: MEDLINE Asunto principal: Proteínas Represoras / Glándula Tiroides / Activación Transcripcional / Proteínas de Unión al ADN / Proteínas de la Membrana Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Mol Cell Endocrinol Año: 2004 Tipo del documento: Article País de afiliación: Japón