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The acute transcriptome response of the midbrain/diencephalon to injury in the adult mummichog (Fundulus heteroclitus)

Adult fish produce new cells throughout their central nervous system during the course of their lives and maintain a tremendous capacity to repair damaged neural tissue. Much of the focus on understanding brain repair and regeneration in adult fish has been directed at regions of the brainstem and f...

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Autores principales: Bisese, Eleanor C., Ciuba, Chandler M., Davidson, Amelia L., Kaushik, Akanksha, Mullen, Sabrina M., Barth, Jeremy L., Hazard, E. Starr, Wilson, Robert C., Hardiman, Gary, Hollis, David M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6937918/
https://www.ncbi.nlm.nih.gov/pubmed/31888716
http://dx.doi.org/10.1186/s13041-019-0542-4
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author Bisese, Eleanor C.
Ciuba, Chandler M.
Davidson, Amelia L.
Kaushik, Akanksha
Mullen, Sabrina M.
Barth, Jeremy L.
Hazard, E. Starr
Wilson, Robert C.
Hardiman, Gary
Hollis, David M.
author_facet Bisese, Eleanor C.
Ciuba, Chandler M.
Davidson, Amelia L.
Kaushik, Akanksha
Mullen, Sabrina M.
Barth, Jeremy L.
Hazard, E. Starr
Wilson, Robert C.
Hardiman, Gary
Hollis, David M.
author_sort Bisese, Eleanor C.
collection PubMed
description Adult fish produce new cells throughout their central nervous system during the course of their lives and maintain a tremendous capacity to repair damaged neural tissue. Much of the focus on understanding brain repair and regeneration in adult fish has been directed at regions of the brainstem and forebrain; however, the mesencephalon (midbrain) and diencephalon have received little attention. We sought to examine differential gene expression in the midbrain/diencephalon in response to injury in the adult fish using RNA-seq. Using the mummichog (Fundulus heteroclitus), we administered a mechanical lesion to the midbrain/diencephalon and examined differentially expressed genes (DEGs) at an acute recovery time of 1 h post-injury. Comparisons of whole transcriptomes derived from isolated RNA of intact and injured midbrain/diencephalic tissue identified 404 DEGs with the vast majority being upregulated. Using qPCR, we validated the upregulation of DEGs pim-2-like, syndecan-4-like, and cd83. Based on genes both familiar and novel regarding the adult brain response to injury, these data provide an extensive molecular profile giving insight into a range of cellular processes involved in the injury response of a brain regenerative-capable vertebrate.
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spelling pubmed-69379182019-12-31 The acute transcriptome response of the midbrain/diencephalon to injury in the adult mummichog (Fundulus heteroclitus) Bisese, Eleanor C. Ciuba, Chandler M. Davidson, Amelia L. Kaushik, Akanksha Mullen, Sabrina M. Barth, Jeremy L. Hazard, E. Starr Wilson, Robert C. Hardiman, Gary Hollis, David M. Mol Brain Micro Report Adult fish produce new cells throughout their central nervous system during the course of their lives and maintain a tremendous capacity to repair damaged neural tissue. Much of the focus on understanding brain repair and regeneration in adult fish has been directed at regions of the brainstem and forebrain; however, the mesencephalon (midbrain) and diencephalon have received little attention. We sought to examine differential gene expression in the midbrain/diencephalon in response to injury in the adult fish using RNA-seq. Using the mummichog (Fundulus heteroclitus), we administered a mechanical lesion to the midbrain/diencephalon and examined differentially expressed genes (DEGs) at an acute recovery time of 1 h post-injury. Comparisons of whole transcriptomes derived from isolated RNA of intact and injured midbrain/diencephalic tissue identified 404 DEGs with the vast majority being upregulated. Using qPCR, we validated the upregulation of DEGs pim-2-like, syndecan-4-like, and cd83. Based on genes both familiar and novel regarding the adult brain response to injury, these data provide an extensive molecular profile giving insight into a range of cellular processes involved in the injury response of a brain regenerative-capable vertebrate. BioMed Central 2019-12-30 /pmc/articles/PMC6937918/ /pubmed/31888716 http://dx.doi.org/10.1186/s13041-019-0542-4 Text en © The Author(s). 2019 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 Micro Report
Bisese, Eleanor C.
Ciuba, Chandler M.
Davidson, Amelia L.
Kaushik, Akanksha
Mullen, Sabrina M.
Barth, Jeremy L.
Hazard, E. Starr
Wilson, Robert C.
Hardiman, Gary
Hollis, David M.
The acute transcriptome response of the midbrain/diencephalon to injury in the adult mummichog (Fundulus heteroclitus)
title The acute transcriptome response of the midbrain/diencephalon to injury in the adult mummichog (Fundulus heteroclitus)
title_full The acute transcriptome response of the midbrain/diencephalon to injury in the adult mummichog (Fundulus heteroclitus)
title_fullStr The acute transcriptome response of the midbrain/diencephalon to injury in the adult mummichog (Fundulus heteroclitus)
title_full_unstemmed The acute transcriptome response of the midbrain/diencephalon to injury in the adult mummichog (Fundulus heteroclitus)
title_short The acute transcriptome response of the midbrain/diencephalon to injury in the adult mummichog (Fundulus heteroclitus)
title_sort acute transcriptome response of the midbrain/diencephalon to injury in the adult mummichog (fundulus heteroclitus)
topic Micro Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6937918/
https://www.ncbi.nlm.nih.gov/pubmed/31888716
http://dx.doi.org/10.1186/s13041-019-0542-4
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