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Physiological inputs regulate species-specific anatomy during embryogenesis and regeneration
A key problem in evolutionary developmental biology is identifying the sources of instructive information that determine species-specific anatomical pattern. Understanding the inputs to large-scale morphology is also crucial for efforts to manipulate pattern formation in regenerative medicine and sy...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4988443/ https://www.ncbi.nlm.nih.gov/pubmed/27574538 http://dx.doi.org/10.1080/19420889.2016.1192733 |
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author | Sullivan, Kelly G. Emmons-Bell, Maya Levin, Michael |
author_facet | Sullivan, Kelly G. Emmons-Bell, Maya Levin, Michael |
author_sort | Sullivan, Kelly G. |
collection | PubMed |
description | A key problem in evolutionary developmental biology is identifying the sources of instructive information that determine species-specific anatomical pattern. Understanding the inputs to large-scale morphology is also crucial for efforts to manipulate pattern formation in regenerative medicine and synthetic bioengineering. Recent studies have revealed a physiological system of communication among cells that regulates pattern during embryogenesis and regeneration in vertebrate and invertebrate models. Somatic tissues form networks using the same ion channels, electrical synapses, and neurotransmitter mechanisms exploited by the brain for information-processing. Experimental manipulation of these circuits was recently shown to override genome default patterning outcomes, resulting in head shapes resembling those of other species in planaria and Xenopus. The ability to drastically alter macroscopic anatomy to that of other extant species, despite a wild-type genomic sequence, suggests exciting new approaches to the understanding and control of patterning. Here, we review these results and discuss hypotheses regarding non-genomic systems of instructive information that determine biological growth and form. |
format | Online Article Text |
id | pubmed-4988443 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-49884432016-08-29 Physiological inputs regulate species-specific anatomy during embryogenesis and regeneration Sullivan, Kelly G. Emmons-Bell, Maya Levin, Michael Commun Integr Biol Article Addendum A key problem in evolutionary developmental biology is identifying the sources of instructive information that determine species-specific anatomical pattern. Understanding the inputs to large-scale morphology is also crucial for efforts to manipulate pattern formation in regenerative medicine and synthetic bioengineering. Recent studies have revealed a physiological system of communication among cells that regulates pattern during embryogenesis and regeneration in vertebrate and invertebrate models. Somatic tissues form networks using the same ion channels, electrical synapses, and neurotransmitter mechanisms exploited by the brain for information-processing. Experimental manipulation of these circuits was recently shown to override genome default patterning outcomes, resulting in head shapes resembling those of other species in planaria and Xenopus. The ability to drastically alter macroscopic anatomy to that of other extant species, despite a wild-type genomic sequence, suggests exciting new approaches to the understanding and control of patterning. Here, we review these results and discuss hypotheses regarding non-genomic systems of instructive information that determine biological growth and form. Taylor & Francis 2016-07-15 /pmc/articles/PMC4988443/ /pubmed/27574538 http://dx.doi.org/10.1080/19420889.2016.1192733 Text en © 2016 The Author(s). Published with license by Taylor & Francis. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted. |
spellingShingle | Article Addendum Sullivan, Kelly G. Emmons-Bell, Maya Levin, Michael Physiological inputs regulate species-specific anatomy during embryogenesis and regeneration |
title | Physiological inputs regulate species-specific anatomy during embryogenesis and regeneration |
title_full | Physiological inputs regulate species-specific anatomy during embryogenesis and regeneration |
title_fullStr | Physiological inputs regulate species-specific anatomy during embryogenesis and regeneration |
title_full_unstemmed | Physiological inputs regulate species-specific anatomy during embryogenesis and regeneration |
title_short | Physiological inputs regulate species-specific anatomy during embryogenesis and regeneration |
title_sort | physiological inputs regulate species-specific anatomy during embryogenesis and regeneration |
topic | Article Addendum |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4988443/ https://www.ncbi.nlm.nih.gov/pubmed/27574538 http://dx.doi.org/10.1080/19420889.2016.1192733 |
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