The LIM domain protein nTRIP6 modulates the dynamics of myogenic differentiation

Abstract The process of myogenesis which operates during skeletal muscle regeneration involves the activation of muscle stem cells, the so-called satellite cells. These then give rise to proliferating progenitors, the myoblasts which subsequently exit the cell cycle and differentiate into committed...

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Autores principales: Tannaz Norizadeh Abbariki, Zita Gonda, Denise Kemler, Pavel Urbanek, Tabea Wagner, Margarethe Litfin, Zhao-Qi Wang, Peter Herrlich, Olivier Kassel
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/963e02f1d9ae4bd6815ed8cea91f78f5
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spelling oai:doaj.org-article:963e02f1d9ae4bd6815ed8cea91f78f52021-12-02T17:41:26ZThe LIM domain protein nTRIP6 modulates the dynamics of myogenic differentiation10.1038/s41598-021-92331-82045-2322https://doaj.org/article/963e02f1d9ae4bd6815ed8cea91f78f52021-06-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-92331-8https://doaj.org/toc/2045-2322Abstract The process of myogenesis which operates during skeletal muscle regeneration involves the activation of muscle stem cells, the so-called satellite cells. These then give rise to proliferating progenitors, the myoblasts which subsequently exit the cell cycle and differentiate into committed precursors, the myocytes. Ultimately, the fusion of myocytes leads to myofiber formation. Here we reveal a role for the transcriptional co-regulator nTRIP6, the nuclear isoform of the LIM-domain protein TRIP6, in the temporal control of myogenesis. In an in vitro model of myogenesis, the expression of nTRIP6 is transiently up-regulated at the transition between proliferation and differentiation, whereas that of the cytosolic isoform TRIP6 is not altered. Selectively blocking nTRIP6 function results in accelerated early differentiation followed by deregulated late differentiation and fusion. Thus, the transient increase in nTRIP6 expression appears to prevent premature differentiation. Accordingly, knocking out the Trip6 gene in satellite cells leads to deregulated skeletal muscle regeneration dynamics in the mouse. Thus, dynamic changes in nTRIP6 expression contributes to the temporal control of myogenesis.Tannaz Norizadeh AbbarikiZita GondaDenise KemlerPavel UrbanekTabea WagnerMargarethe LitfinZhao-Qi WangPeter HerrlichOlivier KasselNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Tannaz Norizadeh Abbariki
Zita Gonda
Denise Kemler
Pavel Urbanek
Tabea Wagner
Margarethe Litfin
Zhao-Qi Wang
Peter Herrlich
Olivier Kassel
The LIM domain protein nTRIP6 modulates the dynamics of myogenic differentiation
description Abstract The process of myogenesis which operates during skeletal muscle regeneration involves the activation of muscle stem cells, the so-called satellite cells. These then give rise to proliferating progenitors, the myoblasts which subsequently exit the cell cycle and differentiate into committed precursors, the myocytes. Ultimately, the fusion of myocytes leads to myofiber formation. Here we reveal a role for the transcriptional co-regulator nTRIP6, the nuclear isoform of the LIM-domain protein TRIP6, in the temporal control of myogenesis. In an in vitro model of myogenesis, the expression of nTRIP6 is transiently up-regulated at the transition between proliferation and differentiation, whereas that of the cytosolic isoform TRIP6 is not altered. Selectively blocking nTRIP6 function results in accelerated early differentiation followed by deregulated late differentiation and fusion. Thus, the transient increase in nTRIP6 expression appears to prevent premature differentiation. Accordingly, knocking out the Trip6 gene in satellite cells leads to deregulated skeletal muscle regeneration dynamics in the mouse. Thus, dynamic changes in nTRIP6 expression contributes to the temporal control of myogenesis.
format article
author Tannaz Norizadeh Abbariki
Zita Gonda
Denise Kemler
Pavel Urbanek
Tabea Wagner
Margarethe Litfin
Zhao-Qi Wang
Peter Herrlich
Olivier Kassel
author_facet Tannaz Norizadeh Abbariki
Zita Gonda
Denise Kemler
Pavel Urbanek
Tabea Wagner
Margarethe Litfin
Zhao-Qi Wang
Peter Herrlich
Olivier Kassel
author_sort Tannaz Norizadeh Abbariki
title The LIM domain protein nTRIP6 modulates the dynamics of myogenic differentiation
title_short The LIM domain protein nTRIP6 modulates the dynamics of myogenic differentiation
title_full The LIM domain protein nTRIP6 modulates the dynamics of myogenic differentiation
title_fullStr The LIM domain protein nTRIP6 modulates the dynamics of myogenic differentiation
title_full_unstemmed The LIM domain protein nTRIP6 modulates the dynamics of myogenic differentiation
title_sort lim domain protein ntrip6 modulates the dynamics of myogenic differentiation
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/963e02f1d9ae4bd6815ed8cea91f78f5
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