4.6 Article

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

Journal

FRONTIERS IN PHYSIOLOGY
Volume 11, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fphys.2020.624677

Keywords

AU-rich element (ARE); ARE binding proteins; forebrain; hypothalamus; Ictidomys tridecemlineatus; medulla; pre-miRNA; RNA binding protein

Categories

Funding

  1. NIH [P30 CA046934, R01 HL089049, R21 NS088315, R35 GM119550]
  2. NSF [1642184]
  3. RNA Bioscience Initiative at the University of Colorado School of Medicine
  4. Division Of Integrative Organismal Systems
  5. Direct For Biological Sciences [1642184] Funding Source: National Science Foundation

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Hibernation is a phenotype that minimizes energy expenditure and challenges our understanding of mammalian homeostasis. The study enhances the genome integrity and annotation of a model hibernator, the 13-lined ground squirrel, and identifies hibernation-related genes using new genomic resources. The research provides insights into the regulatory network of RNA binding proteins and other mechanisms in hibernating animals.
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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