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Dynamic RNA Regulation in the Brain Underlies Physiological Plasticity in a Hibernating Mammal

Hibernation is a physiological and behavioral phenotype that minimizes energy expenditure. Hibernators cycle between profound depression and rapid hyperactivation of multiple physiological processes, challenging our concept of mammalian homeostasis. How the hibernator orchestrates and survives these...

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Autores principales: Fu, Rui, Gillen, Austin E., Grabek, Katharine R., Riemondy, Kent A., Epperson, L. Elaine, Bustamante, Carlos D., Hesselberth, Jay R., Martin, Sandra L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7848201/
https://www.ncbi.nlm.nih.gov/pubmed/33536943
http://dx.doi.org/10.3389/fphys.2020.624677
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author Fu, Rui
Gillen, Austin E.
Grabek, Katharine R.
Riemondy, Kent A.
Epperson, L. Elaine
Bustamante, Carlos D.
Hesselberth, Jay R.
Martin, Sandra L.
author_facet Fu, Rui
Gillen, Austin E.
Grabek, Katharine R.
Riemondy, Kent A.
Epperson, L. Elaine
Bustamante, Carlos D.
Hesselberth, Jay R.
Martin, Sandra L.
author_sort Fu, Rui
collection PubMed
description Hibernation is a physiological and behavioral phenotype that minimizes energy expenditure. Hibernators cycle between profound depression and rapid hyperactivation of multiple physiological processes, challenging our concept of mammalian homeostasis. How the hibernator orchestrates and survives these extremes while maintaining cell to organismal viability is unknown. Here, we enhance the genome integrity and annotation of a model hibernator, the 13-lined ground squirrel. Our new assembly brings this genome to near chromosome-level contiguity and adds thousands of previously unannotated genes. These new genomic resources were used to identify 6,505 hibernation-related, differentially-expressed and processed transcripts using RNA-seq data from three brain regions in animals whose physiological status was precisely defined using body temperature telemetry. A software tool, squirrelBox, was developed to foster further data analyses and visualization. SquirrelBox includes a comprehensive toolset for rapid visualization of gene level and cluster group dynamics, sequence scanning of k-mer and domains, and interactive exploration of gene lists. Using these new tools and data, we deconvolute seasonal from temperature-dependent effects on the brain transcriptome during hibernation for the first time, highlighting the importance of carefully timed samples for studies of differential gene expression in hibernation. The identified genes include a regulatory network of RNA binding proteins that are dynamic in hibernation along with the composition of the RNA pool. In addition to passive effects of temperature, we provide evidence for regulated transcription and RNA turnover during hibernation. Significant alternative splicing, largely temperature dependent, also occurs during hibernation. These findings form a crucial first step and provide a roadmap for future work toward defining novel mechanisms of tissue protection and metabolic depression that may 1 day be applied toward improving human health.
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spelling pubmed-78482012021-02-02 Dynamic RNA Regulation in the Brain Underlies Physiological Plasticity in a Hibernating Mammal Fu, Rui Gillen, Austin E. Grabek, Katharine R. Riemondy, Kent A. Epperson, L. Elaine Bustamante, Carlos D. Hesselberth, Jay R. Martin, Sandra L. Front Physiol Physiology Hibernation is a physiological and behavioral phenotype that minimizes energy expenditure. Hibernators cycle between profound depression and rapid hyperactivation of multiple physiological processes, challenging our concept of mammalian homeostasis. How the hibernator orchestrates and survives these extremes while maintaining cell to organismal viability is unknown. Here, we enhance the genome integrity and annotation of a model hibernator, the 13-lined ground squirrel. Our new assembly brings this genome to near chromosome-level contiguity and adds thousands of previously unannotated genes. These new genomic resources were used to identify 6,505 hibernation-related, differentially-expressed and processed transcripts using RNA-seq data from three brain regions in animals whose physiological status was precisely defined using body temperature telemetry. A software tool, squirrelBox, was developed to foster further data analyses and visualization. SquirrelBox includes a comprehensive toolset for rapid visualization of gene level and cluster group dynamics, sequence scanning of k-mer and domains, and interactive exploration of gene lists. Using these new tools and data, we deconvolute seasonal from temperature-dependent effects on the brain transcriptome during hibernation for the first time, highlighting the importance of carefully timed samples for studies of differential gene expression in hibernation. The identified genes include a regulatory network of RNA binding proteins that are dynamic in hibernation along with the composition of the RNA pool. In addition to passive effects of temperature, we provide evidence for regulated transcription and RNA turnover during hibernation. Significant alternative splicing, largely temperature dependent, also occurs during hibernation. These findings form a crucial first step and provide a roadmap for future work toward defining novel mechanisms of tissue protection and metabolic depression that may 1 day be applied toward improving human health. Frontiers Media S.A. 2021-01-18 /pmc/articles/PMC7848201/ /pubmed/33536943 http://dx.doi.org/10.3389/fphys.2020.624677 Text en Copyright © 2021 Fu, Gillen, Grabek, Riemondy, Epperson, Bustamante, Hesselberth and Martin. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Fu, Rui
Gillen, Austin E.
Grabek, Katharine R.
Riemondy, Kent A.
Epperson, L. Elaine
Bustamante, Carlos D.
Hesselberth, Jay R.
Martin, Sandra L.
Dynamic RNA Regulation in the Brain Underlies Physiological Plasticity in a Hibernating Mammal
title Dynamic RNA Regulation in the Brain Underlies Physiological Plasticity in a Hibernating Mammal
title_full Dynamic RNA Regulation in the Brain Underlies Physiological Plasticity in a Hibernating Mammal
title_fullStr Dynamic RNA Regulation in the Brain Underlies Physiological Plasticity in a Hibernating Mammal
title_full_unstemmed Dynamic RNA Regulation in the Brain Underlies Physiological Plasticity in a Hibernating Mammal
title_short Dynamic RNA Regulation in the Brain Underlies Physiological Plasticity in a Hibernating Mammal
title_sort dynamic rna regulation in the brain underlies physiological plasticity in a hibernating mammal
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7848201/
https://www.ncbi.nlm.nih.gov/pubmed/33536943
http://dx.doi.org/10.3389/fphys.2020.624677
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