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Thyroid hormone regulates proximodistal patterning in fin rays
Processes that regulate size and patterning along an axis must be highly integrated to generate robust shapes; relative changes in these processes underlie both congenital disease and evolutionary change. Fin length mutants in zebrafish have provided considerable insight into the pathways regulating...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10214145/ https://www.ncbi.nlm.nih.gov/pubmed/37186843 http://dx.doi.org/10.1073/pnas.2219770120 |
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author | Harper, Melody Hu, Yinan Donahue, Joan Acosta, Benjamin Dievenich Braes, Flora Nguyen, Stacy Zeng, Jenny Barbaro, Julianna Lee, Hyungwoo Bui, Hoa McMenamin, Sarah K. |
author_facet | Harper, Melody Hu, Yinan Donahue, Joan Acosta, Benjamin Dievenich Braes, Flora Nguyen, Stacy Zeng, Jenny Barbaro, Julianna Lee, Hyungwoo Bui, Hoa McMenamin, Sarah K. |
author_sort | Harper, Melody |
collection | PubMed |
description | Processes that regulate size and patterning along an axis must be highly integrated to generate robust shapes; relative changes in these processes underlie both congenital disease and evolutionary change. Fin length mutants in zebrafish have provided considerable insight into the pathways regulating fin size, yet signals underlying patterning have remained less clear. The bony rays of the fins possess distinct patterning along the proximodistal axis, reflected in the location of ray bifurcations and the lengths of ray segments, which show progressive shortening along the axis. Here, we show that thyroid hormone (TH) regulates aspects of proximodistal patterning of the caudal fin rays, regardless of fin size. TH promotes distal gene expression patterns, coordinating ray bifurcations and segment shortening with skeletal outgrowth along the proximodistal axis. This distalizing role for TH is conserved between development and regeneration, in all fins (paired and medial), and between Danio species as well as distantly related medaka. During regenerative outgrowth, TH acutely induces Shh-mediated skeletal bifurcation. Zebrafish have multiple nuclear TH receptors, and we found that unliganded Thrab—but not Thraa or Thrb—inhibits the formation of distal features. Broadly, these results demonstrate that proximodistal morphology is regulated independently from size-instructive signals. Modulating proximodistal patterning relative to size—either through changes to TH metabolism or other hormone-independent pathways—can shift skeletal patterning in ways that recapitulate aspects of fin ray diversity found in nature. |
format | Online Article Text |
id | pubmed-10214145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-102141452023-11-15 Thyroid hormone regulates proximodistal patterning in fin rays Harper, Melody Hu, Yinan Donahue, Joan Acosta, Benjamin Dievenich Braes, Flora Nguyen, Stacy Zeng, Jenny Barbaro, Julianna Lee, Hyungwoo Bui, Hoa McMenamin, Sarah K. Proc Natl Acad Sci U S A Biological Sciences Processes that regulate size and patterning along an axis must be highly integrated to generate robust shapes; relative changes in these processes underlie both congenital disease and evolutionary change. Fin length mutants in zebrafish have provided considerable insight into the pathways regulating fin size, yet signals underlying patterning have remained less clear. The bony rays of the fins possess distinct patterning along the proximodistal axis, reflected in the location of ray bifurcations and the lengths of ray segments, which show progressive shortening along the axis. Here, we show that thyroid hormone (TH) regulates aspects of proximodistal patterning of the caudal fin rays, regardless of fin size. TH promotes distal gene expression patterns, coordinating ray bifurcations and segment shortening with skeletal outgrowth along the proximodistal axis. This distalizing role for TH is conserved between development and regeneration, in all fins (paired and medial), and between Danio species as well as distantly related medaka. During regenerative outgrowth, TH acutely induces Shh-mediated skeletal bifurcation. Zebrafish have multiple nuclear TH receptors, and we found that unliganded Thrab—but not Thraa or Thrb—inhibits the formation of distal features. Broadly, these results demonstrate that proximodistal morphology is regulated independently from size-instructive signals. Modulating proximodistal patterning relative to size—either through changes to TH metabolism or other hormone-independent pathways—can shift skeletal patterning in ways that recapitulate aspects of fin ray diversity found in nature. National Academy of Sciences 2023-05-15 2023-05-23 /pmc/articles/PMC10214145/ /pubmed/37186843 http://dx.doi.org/10.1073/pnas.2219770120 Text en Copyright © 2023 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Harper, Melody Hu, Yinan Donahue, Joan Acosta, Benjamin Dievenich Braes, Flora Nguyen, Stacy Zeng, Jenny Barbaro, Julianna Lee, Hyungwoo Bui, Hoa McMenamin, Sarah K. Thyroid hormone regulates proximodistal patterning in fin rays |
title | Thyroid hormone regulates proximodistal patterning in fin rays |
title_full | Thyroid hormone regulates proximodistal patterning in fin rays |
title_fullStr | Thyroid hormone regulates proximodistal patterning in fin rays |
title_full_unstemmed | Thyroid hormone regulates proximodistal patterning in fin rays |
title_short | Thyroid hormone regulates proximodistal patterning in fin rays |
title_sort | thyroid hormone regulates proximodistal patterning in fin rays |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10214145/ https://www.ncbi.nlm.nih.gov/pubmed/37186843 http://dx.doi.org/10.1073/pnas.2219770120 |
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