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Transcriptional Profiling of Caudal Fin Regeneration in Zebrafish
Regeneration of severed limbs in adult animals is restricted to urodele amphibians. Mammals, including humans, have very limited regenerative capabilities and even with proper treatment, only the tips of our digits can grow back. Teleost fish can regenerate amputated fins, the evolutionary ancestors...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
TheScientificWorldJOURNAL
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917411/ https://www.ncbi.nlm.nih.gov/pubmed/17205186 http://dx.doi.org/10.1100/tsw.2006.326 |
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author | Schebesta, Michael Lien, Ching-Ling Engel, Felix B. Keating, Mark T. |
author_facet | Schebesta, Michael Lien, Ching-Ling Engel, Felix B. Keating, Mark T. |
author_sort | Schebesta, Michael |
collection | PubMed |
description | Regeneration of severed limbs in adult animals is restricted to urodele amphibians. Mammals, including humans, have very limited regenerative capabilities and even with proper treatment, only the tips of our digits can grow back. Teleost fish can regenerate amputated fins, the evolutionary ancestors of limbs. To elucidate the principles of limb-fin regeneration, we performed an Affymetrix microarray screen on regenerating caudal fins 12, 24, 48, and 72 h post amputation. Approximately 15,000 zebrafish transcripts were analyzed, identifying 829 transcripts as differentially expressed during regeneration. Of those, 563 were up-regulated and 266 were down-regulated. We constructed a comprehensive database containing expression data, functional assignment, and background information from the literature for each differentially expressed transcript. In order to validate our findings, we employed three approaches: (1) microarray expression analysis of genes previously implicated in fin regeneration, (2) RT-PCR analysis of genes newly identified as differentially expressed during regeneration, and (3) in situ hybridization of the up-regulated genes bambi, dlx5A, and her6. Moreover, we show that Smad 1/5/8 proteins, effector molecules of Bmp signaling, are phosphorylated during fin regeneration. Taken together, we provide a comprehensive database of fin regeneration that will serve as an important tool for understanding the molecular mechanisms of regeneration. |
format | Online Article Text |
id | pubmed-5917411 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | TheScientificWorldJOURNAL |
record_format | MEDLINE/PubMed |
spelling | pubmed-59174112018-06-03 Transcriptional Profiling of Caudal Fin Regeneration in Zebrafish Schebesta, Michael Lien, Ching-Ling Engel, Felix B. Keating, Mark T. ScientificWorldJournal Research Article Regeneration of severed limbs in adult animals is restricted to urodele amphibians. Mammals, including humans, have very limited regenerative capabilities and even with proper treatment, only the tips of our digits can grow back. Teleost fish can regenerate amputated fins, the evolutionary ancestors of limbs. To elucidate the principles of limb-fin regeneration, we performed an Affymetrix microarray screen on regenerating caudal fins 12, 24, 48, and 72 h post amputation. Approximately 15,000 zebrafish transcripts were analyzed, identifying 829 transcripts as differentially expressed during regeneration. Of those, 563 were up-regulated and 266 were down-regulated. We constructed a comprehensive database containing expression data, functional assignment, and background information from the literature for each differentially expressed transcript. In order to validate our findings, we employed three approaches: (1) microarray expression analysis of genes previously implicated in fin regeneration, (2) RT-PCR analysis of genes newly identified as differentially expressed during regeneration, and (3) in situ hybridization of the up-regulated genes bambi, dlx5A, and her6. Moreover, we show that Smad 1/5/8 proteins, effector molecules of Bmp signaling, are phosphorylated during fin regeneration. Taken together, we provide a comprehensive database of fin regeneration that will serve as an important tool for understanding the molecular mechanisms of regeneration. TheScientificWorldJOURNAL 2006-06-02 /pmc/articles/PMC5917411/ /pubmed/17205186 http://dx.doi.org/10.1100/tsw.2006.326 Text en Copyright © 2006 Michael Schebesta et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Schebesta, Michael Lien, Ching-Ling Engel, Felix B. Keating, Mark T. Transcriptional Profiling of Caudal Fin Regeneration in Zebrafish |
title | Transcriptional Profiling of Caudal Fin Regeneration in Zebrafish |
title_full | Transcriptional Profiling of Caudal Fin Regeneration in Zebrafish |
title_fullStr | Transcriptional Profiling of Caudal Fin Regeneration in Zebrafish |
title_full_unstemmed | Transcriptional Profiling of Caudal Fin Regeneration in Zebrafish |
title_short | Transcriptional Profiling of Caudal Fin Regeneration in Zebrafish |
title_sort | transcriptional profiling of caudal fin regeneration in zebrafish |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917411/ https://www.ncbi.nlm.nih.gov/pubmed/17205186 http://dx.doi.org/10.1100/tsw.2006.326 |
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