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Differential expression and localization of Ankrd2 isoforms in human skeletal and cardiac muscles.
Jasnic-Savovic, Jovana; Krause, Sabine; Savic, Slobodan; Kojic, Ana; Kovcic, Vlado; Boskovic, Srdjan; Nestorovic, Aleksandra; Rakicevic, Ljiljana; Schreiber-Katz, Olivia; Vogel, Johannes G; Schoser, Benedikt G; Walter, Maggie C; Valle, Giorgio; Radojkovic, Dragica; Faulkner, Georgine; Kojic, Snezana.
Afiliação
  • Jasnic-Savovic J; Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Vojvode Stepe 444a, PO Box 23, Belgrade, 11010, Serbia.
  • Krause S; Department of Neurology, Friedrich Baur Institute, Ludwig Maximilians University, Ziemssenstr. 1a, 80336, Munich, Germany.
  • Savic S; Institute of Forensic Medicine, School of Medicine, University of Belgrade, Deligradska 31a, Belgrade, 11000, Serbia.
  • Kojic A; Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Vojvode Stepe 444a, PO Box 23, Belgrade, 11010, Serbia.
  • Kovcic V; Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Vojvode Stepe 444a, PO Box 23, Belgrade, 11010, Serbia.
  • Boskovic S; Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Vojvode Stepe 444a, PO Box 23, Belgrade, 11010, Serbia.
  • Nestorovic A; Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Vojvode Stepe 444a, PO Box 23, Belgrade, 11010, Serbia.
  • Rakicevic L; Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Vojvode Stepe 444a, PO Box 23, Belgrade, 11010, Serbia.
  • Schreiber-Katz O; Department of Neurology, Friedrich Baur Institute, Ludwig Maximilians University, Ziemssenstr. 1a, 80336, Munich, Germany.
  • Vogel JG; Department of Neurology, Friedrich Baur Institute, Ludwig Maximilians University, Ziemssenstr. 1a, 80336, Munich, Germany.
  • Schoser BG; Department of Neurology, Friedrich Baur Institute, Ludwig Maximilians University, Ziemssenstr. 1a, 80336, Munich, Germany.
  • Walter MC; Department of Neurology, Friedrich Baur Institute, Ludwig Maximilians University, Ziemssenstr. 1a, 80336, Munich, Germany.
  • Valle G; CRIBI, University of Padova, Via Ugo Bassi 58b, 35121, Padua, Italy.
  • Radojkovic D; Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Vojvode Stepe 444a, PO Box 23, Belgrade, 11010, Serbia.
  • Faulkner G; CRIBI, University of Padova, Via Ugo Bassi 58b, 35121, Padua, Italy.
  • Kojic S; Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Vojvode Stepe 444a, PO Box 23, Belgrade, 11010, Serbia. snezanakojic@imgge.bg.ac.rs.
Histochem Cell Biol ; 146(5): 569-584, 2016 Nov.
Article em En | MEDLINE | ID: mdl-27393496
ABSTRACT
Four human Ankrd2 transcripts, reported in the Ensembl database, code for distinct protein isoforms (360, 333, 327 and 300 aa), and so far, their existence, specific expression and localization patterns have not been studied in detail. Ankrd2 is preferentially expressed in the slow fibers of skeletal muscle. It is found in both the nuclei and the cytoplasm of skeletal muscle cells, and its localization is prone to change during differentiation and upon stress. Ankrd2 has also been detected in the heart, in ventricular cardiomyocytes and in the intercalated disks (ICDs). The main objective of this study was to distinguish between the Ankrd2 isoforms and to determine the contribution of each one to the general profile of Ankrd2 expression in striated muscles. We demonstrated that the known expression and localization pattern of Ankrd2 in striated muscle can be attributed to the isoform of 333 aa which is dominant in both tissues, while the designated cardiac and canonical isoform of 360 aa was less expressed in both tissues. The 360 aa isoform has a distinct nuclear localization in human skeletal muscle, as well as in primary myoblasts and myotubes. In contrast to the isoform of 333 aa, it was not preferentially expressed in slow fibers and not localized to the ICDs of human cardiomyocytes. Regulation of the expression of both isoforms is achieved at the transcriptional level. Our results set the stage for investigation of the specific functions and interactions of the Ankrd2 isoforms in healthy and diseased human striated muscles.
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Base de dados: MEDLINE Assunto principal: Proteínas Repressoras / Proteínas Nucleares / Músculo Esquelético / Proteínas Musculares / Miocárdio Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article
Buscar no Google
Base de dados: MEDLINE Assunto principal: Proteínas Repressoras / Proteínas Nucleares / Músculo Esquelético / Proteínas Musculares / Miocárdio Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article