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Acoel regeneration mechanisms indicate an ancient role for muscle in regenerative patterning
Positional information is required for animal regeneration, yet how it is harbored in adult tissues is poorly understood. In planarians, positional control genes (PCGs) control regeneration outcomes and are regionally expressed predominately in the musculature. Acoels are early diverging bilaterally...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662612/ https://www.ncbi.nlm.nih.gov/pubmed/29084955 http://dx.doi.org/10.1038/s41467-017-01148-5 |
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author | Raz, Amelie A. Srivastava, Mansi Salvamoser, Ranja Reddien, Peter W. |
author_facet | Raz, Amelie A. Srivastava, Mansi Salvamoser, Ranja Reddien, Peter W. |
author_sort | Raz, Amelie A. |
collection | PubMed |
description | Positional information is required for animal regeneration, yet how it is harbored in adult tissues is poorly understood. In planarians, positional control genes (PCGs) control regeneration outcomes and are regionally expressed predominately in the musculature. Acoels are early diverging bilaterally symmetric animals, having separated from other bilaterians > 550 million years ago. Here, we find that PCGs in the acoel Hofstenia miamia are expressed together and specifically in a primary differentiated cell type: muscle. The vast majority of Hofstenia muscle cells in regions tested express PCGs, suggesting positional information is a major feature of muscle. PCG expression domains are dynamic in muscle after injury, consistent with known PCG roles in guiding regeneration. These data demonstrate an instructive positional role for Hofstenia muscle and this similarity with planarians suggests mesodermal muscle originated at the base of the Bilateria not only for contraction, but also as the source of positional information guiding regeneration. |
format | Online Article Text |
id | pubmed-5662612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56626122017-11-01 Acoel regeneration mechanisms indicate an ancient role for muscle in regenerative patterning Raz, Amelie A. Srivastava, Mansi Salvamoser, Ranja Reddien, Peter W. Nat Commun Article Positional information is required for animal regeneration, yet how it is harbored in adult tissues is poorly understood. In planarians, positional control genes (PCGs) control regeneration outcomes and are regionally expressed predominately in the musculature. Acoels are early diverging bilaterally symmetric animals, having separated from other bilaterians > 550 million years ago. Here, we find that PCGs in the acoel Hofstenia miamia are expressed together and specifically in a primary differentiated cell type: muscle. The vast majority of Hofstenia muscle cells in regions tested express PCGs, suggesting positional information is a major feature of muscle. PCG expression domains are dynamic in muscle after injury, consistent with known PCG roles in guiding regeneration. These data demonstrate an instructive positional role for Hofstenia muscle and this similarity with planarians suggests mesodermal muscle originated at the base of the Bilateria not only for contraction, but also as the source of positional information guiding regeneration. Nature Publishing Group UK 2017-10-30 /pmc/articles/PMC5662612/ /pubmed/29084955 http://dx.doi.org/10.1038/s41467-017-01148-5 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Raz, Amelie A. Srivastava, Mansi Salvamoser, Ranja Reddien, Peter W. Acoel regeneration mechanisms indicate an ancient role for muscle in regenerative patterning |
title | Acoel regeneration mechanisms indicate an ancient role for muscle in regenerative patterning |
title_full | Acoel regeneration mechanisms indicate an ancient role for muscle in regenerative patterning |
title_fullStr | Acoel regeneration mechanisms indicate an ancient role for muscle in regenerative patterning |
title_full_unstemmed | Acoel regeneration mechanisms indicate an ancient role for muscle in regenerative patterning |
title_short | Acoel regeneration mechanisms indicate an ancient role for muscle in regenerative patterning |
title_sort | acoel regeneration mechanisms indicate an ancient role for muscle in regenerative patterning |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662612/ https://www.ncbi.nlm.nih.gov/pubmed/29084955 http://dx.doi.org/10.1038/s41467-017-01148-5 |
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