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

Authors :
Fu R
Gillen AE
Grabek KR
Riemondy KA
Epperson LE
Bustamante CD
Hesselberth JR
Martin SL
Source :
Frontiers in physiology [Front Physiol] 2021 Jan 18; Vol. 11, pp. 624677. Date of Electronic Publication: 2021 Jan 18 (Print Publication: 2020).
Publication Year :
2021

Abstract

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.<br />Competing Interests: KG is CSO for Fauna Bio and SM and CB serve on its SAB. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2021 Fu, Gillen, Grabek, Riemondy, Epperson, Bustamante, Hesselberth and Martin.)

Details

Language :
English
ISSN :
1664-042X
Volume :
11
Database :
MEDLINE
Journal :
Frontiers in physiology
Publication Type :
Academic Journal
Accession number :
33536943
Full Text :
https://doi.org/10.3389/fphys.2020.624677