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Reciprocal inhibition between Pax7 and muscle regulatory factors modulates myogenic cell fate determination
Postnatal growth and regeneration of skeletal muscle requires a population of resident myogenic precursors named satellite cells. The transcription factor Pax7 is critical for satellite cell biogenesis and survival and has been also implicated in satellite cell self-renewal; however, the underlying...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2064278/ https://www.ncbi.nlm.nih.gov/pubmed/17548510 http://dx.doi.org/10.1083/jcb.200608122 |
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author | Olguin, Hugo C. Yang, Zhihong Tapscott, Stephen J. Olwin, Bradley B. |
author_facet | Olguin, Hugo C. Yang, Zhihong Tapscott, Stephen J. Olwin, Bradley B. |
author_sort | Olguin, Hugo C. |
collection | PubMed |
description | Postnatal growth and regeneration of skeletal muscle requires a population of resident myogenic precursors named satellite cells. The transcription factor Pax7 is critical for satellite cell biogenesis and survival and has been also implicated in satellite cell self-renewal; however, the underlying molecular mechanisms remain unclear. Previously, we showed that Pax7 overexpression in adult primary myoblasts down-regulates MyoD and prevents myogenin induction, inhibiting myogenesis. We show that Pax7 prevents muscle differentiation independently of its transcriptional activity, affecting MyoD function. Conversely, myogenin directly affects Pax7 expression and may be critical for Pax7 down-regulation in differentiating cells. Our results provide evidence for a cross-inhibitory interaction between Pax7 and members of the muscle regulatory factor family. This could represent an additional mechanism for the control of satellite cell fate decisions resulting in proliferation, differentiation, and self-renewal, necessary for skeletal muscle maintenance and repair. |
format | Text |
id | pubmed-2064278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-20642782007-12-04 Reciprocal inhibition between Pax7 and muscle regulatory factors modulates myogenic cell fate determination Olguin, Hugo C. Yang, Zhihong Tapscott, Stephen J. Olwin, Bradley B. J Cell Biol Research Articles Postnatal growth and regeneration of skeletal muscle requires a population of resident myogenic precursors named satellite cells. The transcription factor Pax7 is critical for satellite cell biogenesis and survival and has been also implicated in satellite cell self-renewal; however, the underlying molecular mechanisms remain unclear. Previously, we showed that Pax7 overexpression in adult primary myoblasts down-regulates MyoD and prevents myogenin induction, inhibiting myogenesis. We show that Pax7 prevents muscle differentiation independently of its transcriptional activity, affecting MyoD function. Conversely, myogenin directly affects Pax7 expression and may be critical for Pax7 down-regulation in differentiating cells. Our results provide evidence for a cross-inhibitory interaction between Pax7 and members of the muscle regulatory factor family. This could represent an additional mechanism for the control of satellite cell fate decisions resulting in proliferation, differentiation, and self-renewal, necessary for skeletal muscle maintenance and repair. The Rockefeller University Press 2007-06-04 /pmc/articles/PMC2064278/ /pubmed/17548510 http://dx.doi.org/10.1083/jcb.200608122 Text en Copyright © 2007, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Research Articles Olguin, Hugo C. Yang, Zhihong Tapscott, Stephen J. Olwin, Bradley B. Reciprocal inhibition between Pax7 and muscle regulatory factors modulates myogenic cell fate determination |
title | Reciprocal inhibition between Pax7 and muscle regulatory factors modulates myogenic cell fate determination |
title_full | Reciprocal inhibition between Pax7 and muscle regulatory factors modulates myogenic cell fate determination |
title_fullStr | Reciprocal inhibition between Pax7 and muscle regulatory factors modulates myogenic cell fate determination |
title_full_unstemmed | Reciprocal inhibition between Pax7 and muscle regulatory factors modulates myogenic cell fate determination |
title_short | Reciprocal inhibition between Pax7 and muscle regulatory factors modulates myogenic cell fate determination |
title_sort | reciprocal inhibition between pax7 and muscle regulatory factors modulates myogenic cell fate determination |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2064278/ https://www.ncbi.nlm.nih.gov/pubmed/17548510 http://dx.doi.org/10.1083/jcb.200608122 |
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