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Comparative Transcriptomics Identifies Neuronal and Metabolic Adaptations to Hypergravity and Microgravity in Caenorhabditis elegans
Deep space exploration is firmly within reach, but health decline during extended spaceflight remains a key challenge. In this study, we performed comparative transcriptomic analysis of Caenorhabditis elegans responses to varying degrees of hypergravity and to two spaceflight experiments (ICE-FIRST...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756135/ https://www.ncbi.nlm.nih.gov/pubmed/33376968 http://dx.doi.org/10.1016/j.isci.2020.101734 |
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author | Willis, Craig R.G. Szewczyk, Nathaniel J. Costes, Sylvain V. Udranszky, Ingrid A. Reinsch, Sigrid S. Etheridge, Timothy Conley, Catharine A. |
author_facet | Willis, Craig R.G. Szewczyk, Nathaniel J. Costes, Sylvain V. Udranszky, Ingrid A. Reinsch, Sigrid S. Etheridge, Timothy Conley, Catharine A. |
author_sort | Willis, Craig R.G. |
collection | PubMed |
description | Deep space exploration is firmly within reach, but health decline during extended spaceflight remains a key challenge. In this study, we performed comparative transcriptomic analysis of Caenorhabditis elegans responses to varying degrees of hypergravity and to two spaceflight experiments (ICE-FIRST and CERISE). We found that progressive hypergravitational load concomitantly increases the extent of differential gene regulation and that subtle changes in ∼1,000 genes are reproducibly observed during spaceflight-induced microgravity. Consequently, we deduce those genes that are concordantly regulated by altered gravity per se or that display inverted expression profiles during hypergravity versus microgravity. Through doing so, we identify several candidate targets with terrestrial roles in neuronal function and/or cellular metabolism, which are linked to regulation by daf-16/FOXO signaling. These data offer a strong foundation from which to expedite mechanistic understanding of spaceflight-induced maladaptation in higher organisms and, ultimately, promote future targeted therapeutic development. |
format | Online Article Text |
id | pubmed-7756135 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-77561352020-12-28 Comparative Transcriptomics Identifies Neuronal and Metabolic Adaptations to Hypergravity and Microgravity in Caenorhabditis elegans Willis, Craig R.G. Szewczyk, Nathaniel J. Costes, Sylvain V. Udranszky, Ingrid A. Reinsch, Sigrid S. Etheridge, Timothy Conley, Catharine A. iScience Article Deep space exploration is firmly within reach, but health decline during extended spaceflight remains a key challenge. In this study, we performed comparative transcriptomic analysis of Caenorhabditis elegans responses to varying degrees of hypergravity and to two spaceflight experiments (ICE-FIRST and CERISE). We found that progressive hypergravitational load concomitantly increases the extent of differential gene regulation and that subtle changes in ∼1,000 genes are reproducibly observed during spaceflight-induced microgravity. Consequently, we deduce those genes that are concordantly regulated by altered gravity per se or that display inverted expression profiles during hypergravity versus microgravity. Through doing so, we identify several candidate targets with terrestrial roles in neuronal function and/or cellular metabolism, which are linked to regulation by daf-16/FOXO signaling. These data offer a strong foundation from which to expedite mechanistic understanding of spaceflight-induced maladaptation in higher organisms and, ultimately, promote future targeted therapeutic development. Elsevier 2020-11-25 /pmc/articles/PMC7756135/ /pubmed/33376968 http://dx.doi.org/10.1016/j.isci.2020.101734 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Willis, Craig R.G. Szewczyk, Nathaniel J. Costes, Sylvain V. Udranszky, Ingrid A. Reinsch, Sigrid S. Etheridge, Timothy Conley, Catharine A. Comparative Transcriptomics Identifies Neuronal and Metabolic Adaptations to Hypergravity and Microgravity in Caenorhabditis elegans |
title | Comparative Transcriptomics Identifies Neuronal and Metabolic Adaptations to Hypergravity and Microgravity in Caenorhabditis elegans |
title_full | Comparative Transcriptomics Identifies Neuronal and Metabolic Adaptations to Hypergravity and Microgravity in Caenorhabditis elegans |
title_fullStr | Comparative Transcriptomics Identifies Neuronal and Metabolic Adaptations to Hypergravity and Microgravity in Caenorhabditis elegans |
title_full_unstemmed | Comparative Transcriptomics Identifies Neuronal and Metabolic Adaptations to Hypergravity and Microgravity in Caenorhabditis elegans |
title_short | Comparative Transcriptomics Identifies Neuronal and Metabolic Adaptations to Hypergravity and Microgravity in Caenorhabditis elegans |
title_sort | comparative transcriptomics identifies neuronal and metabolic adaptations to hypergravity and microgravity in caenorhabditis elegans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756135/ https://www.ncbi.nlm.nih.gov/pubmed/33376968 http://dx.doi.org/10.1016/j.isci.2020.101734 |
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