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ANKK1 is found in myogenic precursors and muscle fibers subtypes with glycolytic metabolism

Ankyrin repeat and kinase domain containing 1 (ANKK1) gene has been widely related to neuropsychiatry disorders. The localization of ANKK1 in neural progenitors and its correlation with the cell cycle has suggested its participation in development. However, ANKK1 functions still need to be identifie...

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Autores principales: Rubio-Solsona, Estrella, Martí, Salvador, Vílchez, Juan J., Palau, Francesc, Hoenicka, Janet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5951577/
https://www.ncbi.nlm.nih.gov/pubmed/29758057
http://dx.doi.org/10.1371/journal.pone.0197254
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author Rubio-Solsona, Estrella
Martí, Salvador
Vílchez, Juan J.
Palau, Francesc
Hoenicka, Janet
author_facet Rubio-Solsona, Estrella
Martí, Salvador
Vílchez, Juan J.
Palau, Francesc
Hoenicka, Janet
author_sort Rubio-Solsona, Estrella
collection PubMed
description Ankyrin repeat and kinase domain containing 1 (ANKK1) gene has been widely related to neuropsychiatry disorders. The localization of ANKK1 in neural progenitors and its correlation with the cell cycle has suggested its participation in development. However, ANKK1 functions still need to be identified. Here, we have further characterized the ANKK1 localization in vivo and in vitro, by using immunolabeling, quantitative real-time PCR and Western blot in the myogenic lineage. Histologic investigations in mice and humans revealed that ANKK1 is expressed in precursors of embryonic and adult muscles. In mice embryos, ANKK1 was found in migrating myotubes where it shows a polarized cytoplasmic distribution, while proliferative myoblasts and satellite cells show different isoforms in their nuclei and cytoplasm. In vitro studies of ANKK1 protein isoforms along the myogenic progression showed the decline of nuclear ANKK1-kinase until its total exclusion in myotubes. In adult mice, ANKK1 was expressed exclusively in the Fast-Twitch muscles fibers subtype. The induction of glycolytic metabolism in C2C12 cells with high glucose concentration or treatment with berberine caused a significant increase in the ANKK1 mRNA. Similarly, C2C12 cells under hypoxic conditions caused the increase of nuclear ANKK1. These results altogether show a relationship between ANKK1 gene regulation and the metabolism of muscles during development and in adulthood. Finally, we found ANKK1 expression in regenerative fibers of muscles from dystrophic patients. Future studies in ANKK1 biology and the pathological response of muscles will reveal whether this protein is a novel muscle disease biomarker.
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spelling pubmed-59515772018-05-25 ANKK1 is found in myogenic precursors and muscle fibers subtypes with glycolytic metabolism Rubio-Solsona, Estrella Martí, Salvador Vílchez, Juan J. Palau, Francesc Hoenicka, Janet PLoS One Research Article Ankyrin repeat and kinase domain containing 1 (ANKK1) gene has been widely related to neuropsychiatry disorders. The localization of ANKK1 in neural progenitors and its correlation with the cell cycle has suggested its participation in development. However, ANKK1 functions still need to be identified. Here, we have further characterized the ANKK1 localization in vivo and in vitro, by using immunolabeling, quantitative real-time PCR and Western blot in the myogenic lineage. Histologic investigations in mice and humans revealed that ANKK1 is expressed in precursors of embryonic and adult muscles. In mice embryos, ANKK1 was found in migrating myotubes where it shows a polarized cytoplasmic distribution, while proliferative myoblasts and satellite cells show different isoforms in their nuclei and cytoplasm. In vitro studies of ANKK1 protein isoforms along the myogenic progression showed the decline of nuclear ANKK1-kinase until its total exclusion in myotubes. In adult mice, ANKK1 was expressed exclusively in the Fast-Twitch muscles fibers subtype. The induction of glycolytic metabolism in C2C12 cells with high glucose concentration or treatment with berberine caused a significant increase in the ANKK1 mRNA. Similarly, C2C12 cells under hypoxic conditions caused the increase of nuclear ANKK1. These results altogether show a relationship between ANKK1 gene regulation and the metabolism of muscles during development and in adulthood. Finally, we found ANKK1 expression in regenerative fibers of muscles from dystrophic patients. Future studies in ANKK1 biology and the pathological response of muscles will reveal whether this protein is a novel muscle disease biomarker. Public Library of Science 2018-05-14 /pmc/articles/PMC5951577/ /pubmed/29758057 http://dx.doi.org/10.1371/journal.pone.0197254 Text en © 2018 Rubio-Solsona et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Rubio-Solsona, Estrella
Martí, Salvador
Vílchez, Juan J.
Palau, Francesc
Hoenicka, Janet
ANKK1 is found in myogenic precursors and muscle fibers subtypes with glycolytic metabolism
title ANKK1 is found in myogenic precursors and muscle fibers subtypes with glycolytic metabolism
title_full ANKK1 is found in myogenic precursors and muscle fibers subtypes with glycolytic metabolism
title_fullStr ANKK1 is found in myogenic precursors and muscle fibers subtypes with glycolytic metabolism
title_full_unstemmed ANKK1 is found in myogenic precursors and muscle fibers subtypes with glycolytic metabolism
title_short ANKK1 is found in myogenic precursors and muscle fibers subtypes with glycolytic metabolism
title_sort ankk1 is found in myogenic precursors and muscle fibers subtypes with glycolytic metabolism
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5951577/
https://www.ncbi.nlm.nih.gov/pubmed/29758057
http://dx.doi.org/10.1371/journal.pone.0197254
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