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Zebrafish as a model for monocarboxyl transporter 8-deficiency.
Vatine, Gad David; Zada, David; Lerer-Goldshtein, Tali; Tovin, Adi; Malkinson, Guy; Yaniv, Karina; Appelbaum, Lior.
Afiliação
  • Vatine GD; Mina & Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan 52900, Israel.
J Biol Chem ; 288(1): 169-80, 2013 Jan 04.
Article em En | MEDLINE | ID: mdl-23161551
Allan-Herndon-Dudley syndrome (AHDS) is a severe psychomotor retardation characterized by neurological impairment and abnormal thyroid hormone (TH) levels. Mutations in the TH transporter, monocarboxylate transporter 8 (MCT8), are associated with AHDS. MCT8 knock-out mice exhibit impaired TH levels; however, they lack neurological defects. Here, the zebrafish mct8 gene and promoter were isolated, and mct8 promoter-driven transgenic lines were used to show that, similar to humans, mct8 is primarily expressed in the nervous and vascular systems. Morpholino-based knockdown and rescue experiments revealed that MCT8 is strictly required for neural development in the brain and spinal cord. This study shows that MCT8 is a crucial regulator during embryonic development and establishes the first vertebrate model for MCT8 deficiency that exhibits a neurological phenotype.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Atrofia Muscular / Regulação da Expressão Gênica no Desenvolvimento / Deficiência Intelectual Ligada ao Cromossomo X / Hipotonia Muscular / Mutação Limite: Animals / Humans Idioma: En Ano de publicação: 2013 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Atrofia Muscular / Regulação da Expressão Gênica no Desenvolvimento / Deficiência Intelectual Ligada ao Cromossomo X / Hipotonia Muscular / Mutação Limite: Animals / Humans Idioma: En Ano de publicação: 2013 Tipo de documento: Article