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Transcriptomic Analysis of Tail Regeneration in the Lizard Anolis carolinensis Reveals Activation of Conserved Vertebrate Developmental and Repair Mechanisms

Lizards, which are amniote vertebrates like humans, are able to lose and regenerate a functional tail. Understanding the molecular basis of this process would advance regenerative approaches in amniotes, including humans. We have carried out the first transcriptomic analysis of tail regeneration in...

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Autores principales: Hutchins, Elizabeth D., Markov, Glenn J., Eckalbar, Walter L., George, Rajani M., King, Jesse M., Tokuyama, Minami A., Geiger, Lauren A., Emmert, Nataliya, Ammar, Michael J., Allen, April N., Siniard, Ashley L., Corneveaux, Jason J., Fisher, Rebecca E., Wade, Juli, DeNardo, Dale F., Rawls, J. Alan, Huentelman, Matthew J., Wilson-Rawls, Jeanne, Kusumi, Kenro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4139331/
https://www.ncbi.nlm.nih.gov/pubmed/25140675
http://dx.doi.org/10.1371/journal.pone.0105004
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author Hutchins, Elizabeth D.
Markov, Glenn J.
Eckalbar, Walter L.
George, Rajani M.
King, Jesse M.
Tokuyama, Minami A.
Geiger, Lauren A.
Emmert, Nataliya
Ammar, Michael J.
Allen, April N.
Siniard, Ashley L.
Corneveaux, Jason J.
Fisher, Rebecca E.
Wade, Juli
DeNardo, Dale F.
Rawls, J. Alan
Huentelman, Matthew J.
Wilson-Rawls, Jeanne
Kusumi, Kenro
author_facet Hutchins, Elizabeth D.
Markov, Glenn J.
Eckalbar, Walter L.
George, Rajani M.
King, Jesse M.
Tokuyama, Minami A.
Geiger, Lauren A.
Emmert, Nataliya
Ammar, Michael J.
Allen, April N.
Siniard, Ashley L.
Corneveaux, Jason J.
Fisher, Rebecca E.
Wade, Juli
DeNardo, Dale F.
Rawls, J. Alan
Huentelman, Matthew J.
Wilson-Rawls, Jeanne
Kusumi, Kenro
author_sort Hutchins, Elizabeth D.
collection PubMed
description Lizards, which are amniote vertebrates like humans, are able to lose and regenerate a functional tail. Understanding the molecular basis of this process would advance regenerative approaches in amniotes, including humans. We have carried out the first transcriptomic analysis of tail regeneration in a lizard, the green anole Anolis carolinensis, which revealed 326 differentially expressed genes activating multiple developmental and repair mechanisms. Specifically, genes involved in wound response, hormonal regulation, musculoskeletal development, and the Wnt and MAPK/FGF pathways were differentially expressed along the regenerating tail axis. Furthermore, we identified 2 microRNA precursor families, 22 unclassified non-coding RNAs, and 3 novel protein-coding genes significantly enriched in the regenerating tail. However, high levels of progenitor/stem cell markers were not observed in any region of the regenerating tail. Furthermore, we observed multiple tissue-type specific clusters of proliferating cells along the regenerating tail, not localized to the tail tip. These findings predict a different mechanism of regeneration in the lizard than the blastema model described in the salamander and the zebrafish, which are anamniote vertebrates. Thus, lizard tail regrowth involves the activation of conserved developmental and wound response pathways, which are potential targets for regenerative medical therapies.
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spelling pubmed-41393312014-08-25 Transcriptomic Analysis of Tail Regeneration in the Lizard Anolis carolinensis Reveals Activation of Conserved Vertebrate Developmental and Repair Mechanisms Hutchins, Elizabeth D. Markov, Glenn J. Eckalbar, Walter L. George, Rajani M. King, Jesse M. Tokuyama, Minami A. Geiger, Lauren A. Emmert, Nataliya Ammar, Michael J. Allen, April N. Siniard, Ashley L. Corneveaux, Jason J. Fisher, Rebecca E. Wade, Juli DeNardo, Dale F. Rawls, J. Alan Huentelman, Matthew J. Wilson-Rawls, Jeanne Kusumi, Kenro PLoS One Research Article Lizards, which are amniote vertebrates like humans, are able to lose and regenerate a functional tail. Understanding the molecular basis of this process would advance regenerative approaches in amniotes, including humans. We have carried out the first transcriptomic analysis of tail regeneration in a lizard, the green anole Anolis carolinensis, which revealed 326 differentially expressed genes activating multiple developmental and repair mechanisms. Specifically, genes involved in wound response, hormonal regulation, musculoskeletal development, and the Wnt and MAPK/FGF pathways were differentially expressed along the regenerating tail axis. Furthermore, we identified 2 microRNA precursor families, 22 unclassified non-coding RNAs, and 3 novel protein-coding genes significantly enriched in the regenerating tail. However, high levels of progenitor/stem cell markers were not observed in any region of the regenerating tail. Furthermore, we observed multiple tissue-type specific clusters of proliferating cells along the regenerating tail, not localized to the tail tip. These findings predict a different mechanism of regeneration in the lizard than the blastema model described in the salamander and the zebrafish, which are anamniote vertebrates. Thus, lizard tail regrowth involves the activation of conserved developmental and wound response pathways, which are potential targets for regenerative medical therapies. Public Library of Science 2014-08-20 /pmc/articles/PMC4139331/ /pubmed/25140675 http://dx.doi.org/10.1371/journal.pone.0105004 Text en © 2014 Hutchins et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Hutchins, Elizabeth D.
Markov, Glenn J.
Eckalbar, Walter L.
George, Rajani M.
King, Jesse M.
Tokuyama, Minami A.
Geiger, Lauren A.
Emmert, Nataliya
Ammar, Michael J.
Allen, April N.
Siniard, Ashley L.
Corneveaux, Jason J.
Fisher, Rebecca E.
Wade, Juli
DeNardo, Dale F.
Rawls, J. Alan
Huentelman, Matthew J.
Wilson-Rawls, Jeanne
Kusumi, Kenro
Transcriptomic Analysis of Tail Regeneration in the Lizard Anolis carolinensis Reveals Activation of Conserved Vertebrate Developmental and Repair Mechanisms
title Transcriptomic Analysis of Tail Regeneration in the Lizard Anolis carolinensis Reveals Activation of Conserved Vertebrate Developmental and Repair Mechanisms
title_full Transcriptomic Analysis of Tail Regeneration in the Lizard Anolis carolinensis Reveals Activation of Conserved Vertebrate Developmental and Repair Mechanisms
title_fullStr Transcriptomic Analysis of Tail Regeneration in the Lizard Anolis carolinensis Reveals Activation of Conserved Vertebrate Developmental and Repair Mechanisms
title_full_unstemmed Transcriptomic Analysis of Tail Regeneration in the Lizard Anolis carolinensis Reveals Activation of Conserved Vertebrate Developmental and Repair Mechanisms
title_short Transcriptomic Analysis of Tail Regeneration in the Lizard Anolis carolinensis Reveals Activation of Conserved Vertebrate Developmental and Repair Mechanisms
title_sort transcriptomic analysis of tail regeneration in the lizard anolis carolinensis reveals activation of conserved vertebrate developmental and repair mechanisms
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4139331/
https://www.ncbi.nlm.nih.gov/pubmed/25140675
http://dx.doi.org/10.1371/journal.pone.0105004
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