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Heterotrimeric G proteins regulate planarian regeneration and behavior
G protein-coupled receptors play broad roles in development and stem cell biology, but few roles for G protein-coupled receptor signaling in complex tissue regeneration have been uncovered. Planarian flatworms robustly regenerate all tissues and provide a model with which to explore potential functi...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10078920/ https://www.ncbi.nlm.nih.gov/pubmed/36763503 http://dx.doi.org/10.1093/genetics/iyad019 |
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author | Jenkins, Jennifer E Roberts-Galbraith, Rachel H |
author_facet | Jenkins, Jennifer E Roberts-Galbraith, Rachel H |
author_sort | Jenkins, Jennifer E |
collection | PubMed |
description | G protein-coupled receptors play broad roles in development and stem cell biology, but few roles for G protein-coupled receptor signaling in complex tissue regeneration have been uncovered. Planarian flatworms robustly regenerate all tissues and provide a model with which to explore potential functions for G protein-coupled receptor signaling in somatic regeneration and pluripotent stem cell biology. As a first step toward exploring G protein-coupled receptor function in planarians, we investigated downstream signal transducers that work with G protein-coupled receptors, called heterotrimeric G proteins. Here, we characterized the complete heterotrimeric G protein complement in Schmidtea mediterranea for the first time and found that 7 heterotrimeric G protein subunits promote regeneration. We further characterized 2 subunits critical for regeneration, Gαq1 and Gβ1-4a, finding that they promote the late phase of anterior polarity reestablishment, likely through anterior pole-produced Follistatin. Incidentally, we also found that 5 G protein subunits modulate planarian behavior. We further identified a putative serotonin receptor, gcr052, that we propose works with Gαs2 and Gβx2 in planarian locomotion, demonstrating the utility of our strategy for identifying relevant G protein-coupled receptors. Our work provides foundational insight into roles of heterotrimeric G proteins in planarian biology and serves as a useful springboard toward broadening our understanding of G protein-coupled receptor signaling in adult tissue regeneration. |
format | Online Article Text |
id | pubmed-10078920 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-100789202023-04-07 Heterotrimeric G proteins regulate planarian regeneration and behavior Jenkins, Jennifer E Roberts-Galbraith, Rachel H Genetics Investigation G protein-coupled receptors play broad roles in development and stem cell biology, but few roles for G protein-coupled receptor signaling in complex tissue regeneration have been uncovered. Planarian flatworms robustly regenerate all tissues and provide a model with which to explore potential functions for G protein-coupled receptor signaling in somatic regeneration and pluripotent stem cell biology. As a first step toward exploring G protein-coupled receptor function in planarians, we investigated downstream signal transducers that work with G protein-coupled receptors, called heterotrimeric G proteins. Here, we characterized the complete heterotrimeric G protein complement in Schmidtea mediterranea for the first time and found that 7 heterotrimeric G protein subunits promote regeneration. We further characterized 2 subunits critical for regeneration, Gαq1 and Gβ1-4a, finding that they promote the late phase of anterior polarity reestablishment, likely through anterior pole-produced Follistatin. Incidentally, we also found that 5 G protein subunits modulate planarian behavior. We further identified a putative serotonin receptor, gcr052, that we propose works with Gαs2 and Gβx2 in planarian locomotion, demonstrating the utility of our strategy for identifying relevant G protein-coupled receptors. Our work provides foundational insight into roles of heterotrimeric G proteins in planarian biology and serves as a useful springboard toward broadening our understanding of G protein-coupled receptor signaling in adult tissue regeneration. Oxford University Press 2023-02-10 /pmc/articles/PMC10078920/ /pubmed/36763503 http://dx.doi.org/10.1093/genetics/iyad019 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Genetics Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Investigation Jenkins, Jennifer E Roberts-Galbraith, Rachel H Heterotrimeric G proteins regulate planarian regeneration and behavior |
title | Heterotrimeric G proteins regulate planarian regeneration and behavior |
title_full | Heterotrimeric G proteins regulate planarian regeneration and behavior |
title_fullStr | Heterotrimeric G proteins regulate planarian regeneration and behavior |
title_full_unstemmed | Heterotrimeric G proteins regulate planarian regeneration and behavior |
title_short | Heterotrimeric G proteins regulate planarian regeneration and behavior |
title_sort | heterotrimeric g proteins regulate planarian regeneration and behavior |
topic | Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10078920/ https://www.ncbi.nlm.nih.gov/pubmed/36763503 http://dx.doi.org/10.1093/genetics/iyad019 |
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