Cargando…
A transcriptional time-course analysis of oral vs. aboral whole-body regeneration in the Sea anemone Nematostella vectensis
BACKGROUND: The ability of regeneration is essential for the homeostasis of all animals as it allows the repair and renewal of tissues and body parts upon normal turnover or injury. The extent of this ability varies greatly in different animals with the sea anemone Nematostella vectensis, a basal cn...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5015328/ https://www.ncbi.nlm.nih.gov/pubmed/27605362 http://dx.doi.org/10.1186/s12864-016-3027-1 |
_version_ | 1782452418879946752 |
---|---|
author | Schaffer, Amos A. Bazarsky, Michael Levy, Karine Chalifa-Caspi, Vered Gat, Uri |
author_facet | Schaffer, Amos A. Bazarsky, Michael Levy, Karine Chalifa-Caspi, Vered Gat, Uri |
author_sort | Schaffer, Amos A. |
collection | PubMed |
description | BACKGROUND: The ability of regeneration is essential for the homeostasis of all animals as it allows the repair and renewal of tissues and body parts upon normal turnover or injury. The extent of this ability varies greatly in different animals with the sea anemone Nematostella vectensis, a basal cnidarian model animal, displaying remarkable whole-body regeneration competence. RESULTS: In order to study this process in Nematostella we performed an RNA-Seq screen wherein we analyzed and compared the transcriptional response to bisection in the wound-proximal body parts undergoing oral (head) or aboral (tail) regeneration at several time points up to the initial restoration of the basic body shape. The transcriptional profiles of regeneration responsive genes were analyzed so as to define the temporal pattern of differential gene expression associated with the tissue-specific oral and aboral regeneration. The identified genes were characterized according to their GO (gene ontology) assignations revealing groups that were enriched in the regeneration process with particular attention to their affiliation to the major developmental signaling pathways. While some of the genes and gene groups thus analyzed were previously known to be active in regeneration, we have also revealed novel and surprising candidate genes such as cilia-associated genes that likely participate in this important developmental program. CONCLUSIONS: This work highlighted the main groups of genes which showed polarization upon regeneration, notably the proteinases, multiple transcription factors and the Wnt pathway genes that were highly represented, all displaying an intricate temporal balance between the two sides. In addition, the evolutionary comparison performed between regeneration in different animal model systems may reveal the basic mechanisms playing a role in this fascinating process. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3027-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5015328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50153282016-09-09 A transcriptional time-course analysis of oral vs. aboral whole-body regeneration in the Sea anemone Nematostella vectensis Schaffer, Amos A. Bazarsky, Michael Levy, Karine Chalifa-Caspi, Vered Gat, Uri BMC Genomics Research Article BACKGROUND: The ability of regeneration is essential for the homeostasis of all animals as it allows the repair and renewal of tissues and body parts upon normal turnover or injury. The extent of this ability varies greatly in different animals with the sea anemone Nematostella vectensis, a basal cnidarian model animal, displaying remarkable whole-body regeneration competence. RESULTS: In order to study this process in Nematostella we performed an RNA-Seq screen wherein we analyzed and compared the transcriptional response to bisection in the wound-proximal body parts undergoing oral (head) or aboral (tail) regeneration at several time points up to the initial restoration of the basic body shape. The transcriptional profiles of regeneration responsive genes were analyzed so as to define the temporal pattern of differential gene expression associated with the tissue-specific oral and aboral regeneration. The identified genes were characterized according to their GO (gene ontology) assignations revealing groups that were enriched in the regeneration process with particular attention to their affiliation to the major developmental signaling pathways. While some of the genes and gene groups thus analyzed were previously known to be active in regeneration, we have also revealed novel and surprising candidate genes such as cilia-associated genes that likely participate in this important developmental program. CONCLUSIONS: This work highlighted the main groups of genes which showed polarization upon regeneration, notably the proteinases, multiple transcription factors and the Wnt pathway genes that were highly represented, all displaying an intricate temporal balance between the two sides. In addition, the evolutionary comparison performed between regeneration in different animal model systems may reveal the basic mechanisms playing a role in this fascinating process. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-3027-1) contains supplementary material, which is available to authorized users. BioMed Central 2016-09-07 /pmc/articles/PMC5015328/ /pubmed/27605362 http://dx.doi.org/10.1186/s12864-016-3027-1 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Schaffer, Amos A. Bazarsky, Michael Levy, Karine Chalifa-Caspi, Vered Gat, Uri A transcriptional time-course analysis of oral vs. aboral whole-body regeneration in the Sea anemone Nematostella vectensis |
title | A transcriptional time-course analysis of oral vs. aboral whole-body regeneration in the Sea anemone Nematostella vectensis |
title_full | A transcriptional time-course analysis of oral vs. aboral whole-body regeneration in the Sea anemone Nematostella vectensis |
title_fullStr | A transcriptional time-course analysis of oral vs. aboral whole-body regeneration in the Sea anemone Nematostella vectensis |
title_full_unstemmed | A transcriptional time-course analysis of oral vs. aboral whole-body regeneration in the Sea anemone Nematostella vectensis |
title_short | A transcriptional time-course analysis of oral vs. aboral whole-body regeneration in the Sea anemone Nematostella vectensis |
title_sort | transcriptional time-course analysis of oral vs. aboral whole-body regeneration in the sea anemone nematostella vectensis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5015328/ https://www.ncbi.nlm.nih.gov/pubmed/27605362 http://dx.doi.org/10.1186/s12864-016-3027-1 |
work_keys_str_mv | AT schafferamosa atranscriptionaltimecourseanalysisoforalvsaboralwholebodyregenerationintheseaanemonenematostellavectensis AT bazarskymichael atranscriptionaltimecourseanalysisoforalvsaboralwholebodyregenerationintheseaanemonenematostellavectensis AT levykarine atranscriptionaltimecourseanalysisoforalvsaboralwholebodyregenerationintheseaanemonenematostellavectensis AT chalifacaspivered atranscriptionaltimecourseanalysisoforalvsaboralwholebodyregenerationintheseaanemonenematostellavectensis AT gaturi atranscriptionaltimecourseanalysisoforalvsaboralwholebodyregenerationintheseaanemonenematostellavectensis AT schafferamosa transcriptionaltimecourseanalysisoforalvsaboralwholebodyregenerationintheseaanemonenematostellavectensis AT bazarskymichael transcriptionaltimecourseanalysisoforalvsaboralwholebodyregenerationintheseaanemonenematostellavectensis AT levykarine transcriptionaltimecourseanalysisoforalvsaboralwholebodyregenerationintheseaanemonenematostellavectensis AT chalifacaspivered transcriptionaltimecourseanalysisoforalvsaboralwholebodyregenerationintheseaanemonenematostellavectensis AT gaturi transcriptionaltimecourseanalysisoforalvsaboralwholebodyregenerationintheseaanemonenematostellavectensis |