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Temporal Dysynchrony in brain connectivity gene expression following hypoxia

BACKGROUND: Despite the fundamental biological importance and clinical relevance of characterizing the effects of chronic hypoxia exposure on central nervous system (CNS) development, the changes in gene expression from hypoxia are unknown. It is not known if there are unifying principles, propertie...

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Autores principales: Milash, Brett, Gao, Jingxia, Stevenson, Tamara J., Son, Jong-Hyun, Dahl, Tiffanie, Bonkowsky, Joshua L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857255/
https://www.ncbi.nlm.nih.gov/pubmed/27146468
http://dx.doi.org/10.1186/s12864-016-2638-x
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author Milash, Brett
Gao, Jingxia
Stevenson, Tamara J.
Son, Jong-Hyun
Dahl, Tiffanie
Bonkowsky, Joshua L.
author_facet Milash, Brett
Gao, Jingxia
Stevenson, Tamara J.
Son, Jong-Hyun
Dahl, Tiffanie
Bonkowsky, Joshua L.
author_sort Milash, Brett
collection PubMed
description BACKGROUND: Despite the fundamental biological importance and clinical relevance of characterizing the effects of chronic hypoxia exposure on central nervous system (CNS) development, the changes in gene expression from hypoxia are unknown. It is not known if there are unifying principles, properties, or logic in the response of the developing CNS to hypoxic exposure. Here, we use the small vertebrate zebrafish (Danio rerio) to study the effects of hypoxia on connectivity gene expression across development. We perform transcriptional profiling at high temporal resolution to systematically determine and then experimentally validate the response of CNS connectivity genes to hypoxia exposure. RESULTS: We characterized mRNA changes during development, comparing the effects of chronic hypoxia exposure at different time-points. We focused on changes in expression levels of a subset of 1270 genes selected for their roles in development of CNS connectivity, including axon pathfinding and synapse formation. We found that the majority of CNS connectivity genes were unaffected by hypoxia. However, for a small subset of genes hypoxia significantly affected their gene expression profiles. In particular, hypoxia appeared to affect both the timing and levels of expression, including altering expression of interacting gene pairs in a fashion that would potentially disrupt normal function. CONCLUSIONS: Overall, our study identifies the response of CNS connectivity genes to hypoxia exposure during development. While for most genes hypoxia did not significantly affect expression, for a subset of genes hypoxia changed both levels and timing of expression. Importantly, we identified that some genes with interacting proteins, for example receptor/ligand pairs, had dissimilar responses to hypoxia that would be expected to interfere with their function. The observed dysynchrony of gene expression could impair the development of normal CNS connectivity maps. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2638-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-48572552016-05-06 Temporal Dysynchrony in brain connectivity gene expression following hypoxia Milash, Brett Gao, Jingxia Stevenson, Tamara J. Son, Jong-Hyun Dahl, Tiffanie Bonkowsky, Joshua L. BMC Genomics Research Article BACKGROUND: Despite the fundamental biological importance and clinical relevance of characterizing the effects of chronic hypoxia exposure on central nervous system (CNS) development, the changes in gene expression from hypoxia are unknown. It is not known if there are unifying principles, properties, or logic in the response of the developing CNS to hypoxic exposure. Here, we use the small vertebrate zebrafish (Danio rerio) to study the effects of hypoxia on connectivity gene expression across development. We perform transcriptional profiling at high temporal resolution to systematically determine and then experimentally validate the response of CNS connectivity genes to hypoxia exposure. RESULTS: We characterized mRNA changes during development, comparing the effects of chronic hypoxia exposure at different time-points. We focused on changes in expression levels of a subset of 1270 genes selected for their roles in development of CNS connectivity, including axon pathfinding and synapse formation. We found that the majority of CNS connectivity genes were unaffected by hypoxia. However, for a small subset of genes hypoxia significantly affected their gene expression profiles. In particular, hypoxia appeared to affect both the timing and levels of expression, including altering expression of interacting gene pairs in a fashion that would potentially disrupt normal function. CONCLUSIONS: Overall, our study identifies the response of CNS connectivity genes to hypoxia exposure during development. While for most genes hypoxia did not significantly affect expression, for a subset of genes hypoxia changed both levels and timing of expression. Importantly, we identified that some genes with interacting proteins, for example receptor/ligand pairs, had dissimilar responses to hypoxia that would be expected to interfere with their function. The observed dysynchrony of gene expression could impair the development of normal CNS connectivity maps. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-016-2638-x) contains supplementary material, which is available to authorized users. BioMed Central 2016-05-04 /pmc/articles/PMC4857255/ /pubmed/27146468 http://dx.doi.org/10.1186/s12864-016-2638-x Text en © Milash et al. 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
Milash, Brett
Gao, Jingxia
Stevenson, Tamara J.
Son, Jong-Hyun
Dahl, Tiffanie
Bonkowsky, Joshua L.
Temporal Dysynchrony in brain connectivity gene expression following hypoxia
title Temporal Dysynchrony in brain connectivity gene expression following hypoxia
title_full Temporal Dysynchrony in brain connectivity gene expression following hypoxia
title_fullStr Temporal Dysynchrony in brain connectivity gene expression following hypoxia
title_full_unstemmed Temporal Dysynchrony in brain connectivity gene expression following hypoxia
title_short Temporal Dysynchrony in brain connectivity gene expression following hypoxia
title_sort temporal dysynchrony in brain connectivity gene expression following hypoxia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4857255/
https://www.ncbi.nlm.nih.gov/pubmed/27146468
http://dx.doi.org/10.1186/s12864-016-2638-x
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