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Cloning and expression of hepatic synaptotagmin 1 in mouse.
Sancho-Knapik, Sara; Guillén, Natalia; Osada, Jesús.
Afiliación
  • Sancho-Knapik S; Departamento Bioquímica y Biología Molecular y Celular, Facultad de Veterinaria, Instituto de Investigación Sanitaria de Aragón (IIS), Universidad de Zaragoza, Spain.
  • Guillén N; Departamento de Toxicología, Facultad de Veterinaria, Universidad de Zaragoza, Spain.
  • Osada J; Departamento Bioquímica y Biología Molecular y Celular, Facultad de Veterinaria, Instituto de Investigación Sanitaria de Aragón (IIS), Universidad de Zaragoza, Spain; CIBER de Fisiopatología de la Obesidad y Nutrición, Instituto de Salud Carlos III, Spain. Electronic address: Josada@unizar.es.
Gene ; 562(2): 236-43, 2015 May 15.
Article en En | MEDLINE | ID: mdl-25735570
ABSTRACT
Mouse hepatic synaptotagmin 1 (SYT1) cDNA was cloned, characterized and compared to the brain one. The hepatic transcript was 1807 bp in length, smaller than the brain, and only encoded by 9 of 11 gene exons. In this regard, 5'-and 3'-untranslated regions were 66 and 476 bp, respectively; the open reading frame of 1266 bp codified for a protein of 421 amino acids, identical to the brain, with a predicted molecular mass of 47.4 kDa and highly conserved across different species. Immunoblotting of protein showed two isoforms of higher molecular masses than the theoretical prediction based on amino acid sequence suggesting posttranslational modifications. Subcellular distribution of protein isoforms corresponded to plasma membrane, lysosomes and microsomes and was identical between the brain and liver. Nonetheless, the highest molecular weight isoform was smaller in the liver, irrespective of subcellular location. Quantitative mRNA tissue distribution showed that it was widely expressed and that the highest values corresponded to the brain, followed by the liver, spleen, abdominal fat, intestine and skeletal muscle. These findings indicate tissue-specific splicing of the gene and posttranslational modification and the variation in expression in the different tissues might suggest a different requirement of SYT1 for the specific function in each organ.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Expresión Génica / Sinaptotagmina I Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Gene Año: 2015 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Expresión Génica / Sinaptotagmina I Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Gene Año: 2015 Tipo del documento: Article País de afiliación: España