十三线地松鼠(Ictidomys tridecemlineatus)线粒体微RNA谱在冬眠期间发生变化。

IF 2.5 4区 生物学 Q3 CELL BIOLOGY Physiological genomics Pub Date : 2024-08-01 Epub Date: 2024-06-17 DOI:10.1152/physiolgenomics.00017.2024
Karyn Robichaud, Brynne Duffy, James F Staples, Paul M Craig
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引用次数: 0

摘要

十三线地松鼠(TLGS)是一种强制性冬眠动物,从秋末到春季,它们在冬眠(低代谢率和低体温)和 "胫间热病"(IBE;典型的热病体温和新陈代谢)之间循环。整个冬眠过程中会发生许多生理变化,包括在冬眠期间肝脏线粒体代谢减少,而在唤醒至 "interbout euthermia "期间这种变化会逆转。核编码的 microRNA(转录后调控小分子)在整个 TLGS 冬眠期间的丰度不同,在哺乳动物细胞培养中已被证明可以调控线粒体基因的表达(在哺乳动物细胞培养中被称为 mitomiRs)。本研究描述了从夏季、冬眠和 IBE 期间分离的 TLGS 肝线粒体中提取的 mitomiR 的差异,并预测了它们的线粒体靶标。利用小 RNA 测序,我们确定了冬眠状态之间不同的丰度的 mitomiR,并利用 qPCR 分析量化了预测的线粒体 mRNA 靶标的表达。mitomiR丰度的大部分差异是季节性的(即夏季和冬季之间),只有一个mitomiR在IBE和torpor之间丰度不同。多因素分析显示,根据冬眠状态划分的三个聚类主要由mitomiR丰度驱动。在这些丰度不同的mitomiRs中,有九个具有预测的线粒体RNA靶标,包括电子传递系统复合物I和IV的亚基、12S rRNA和两个tRNA。总体而言,据预测,mitomiRs 可抑制其线粒体靶标的表达,并可能在一定程度上参与调节线粒体中蛋白质的翻译。这项研究发现了TLGS在不同季节和冬眠状态下的mitomiR丰度差异,并提出了调节线粒体电子传递系统的潜在机制。
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Mitochondrial microRNA profiles are altered in thirteen-lined ground squirrels (Ictidomys tridecemlineatus) during hibernation.

Thirteen-lined ground squirrels (TLGSs) are obligate hibernators that cycle between torpor (low metabolic rate and body temperature) and interbout euthermia (IBE; typical euthermic body temperature and metabolism) from late autumn to spring. Many physiological changes occur throughout hibernation, including a reduction in liver mitochondrial metabolism during torpor, which is reversed during arousal to interbout euthermia. Nuclear-encoded microRNA (miRNA, small posttranscriptional regulator molecules) differ in abundance throughout TLGS hibernation and have been shown to regulate mitochondrial gene expression in mammalian cell culture (where they are referred to as mitomiRs). This study characterized differences in mitomiR profiles from TLGS liver mitochondria isolated during summer, torpor, and IBE, and predicted their mitochondrial targets. Using small RNA sequencing, differentially abundant mitomiRs were identified between hibernation states, and using quantitative PCR analysis, we quantified the expression of predicted mitochondrial mRNA targets. Most differences in mitomiR abundances were seasonal (i.e., between summer and winter) with only one mitomiR differentially abundant between IBE and torpor. Multiple factor analysis (MFA) revealed three clusters divided by hibernation states, where clustering was predominantly driven by mitomiR abundances. Nine of these differentially abundant mitomiRs had predicted mitochondrial RNA targets, including subunits of electron transfer system complexes I and IV, 12S rRNA, and two tRNAs. Overall, mitomiRs were predicted to suppress the expression of their mitochondrial targets and may have some involvement in regulating protein translation in mitochondria. This study found differences in mitomiR abundances between seasons and hibernation states of TLGS and suggests potential mechanisms for regulating the mitochondrial electron transfer system.NEW & NOTEWORTHY During the hibernation season, thirteen-lined ground squirrels periodically increase metabolism remarkably between torpor and interbout euthermia (IBE). This process involves rapid reactivation of mitochondrial respiration. We predicted that mitochondrial microRNA (mitomiRs) might be altered during this response. We found that the abundance of 38 liver mitomiRs differs based on hibernation state (summer, IBE, and torpor). Small RNA sequencing identified mitomiR profiles, including some mitomiRs that are predicted to bind to mitochondrial RNAs.

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来源期刊
Physiological genomics
Physiological genomics 生物-生理学
CiteScore
6.10
自引率
0.00%
发文量
46
审稿时长
4-8 weeks
期刊介绍: The Physiological Genomics publishes original papers, reviews and rapid reports in a wide area of research focused on uncovering the links between genes and physiology at all levels of biological organization. Articles on topics ranging from single genes to the whole genome and their links to the physiology of humans, any model organism, organ, tissue or cell are welcome. Areas of interest include complex polygenic traits preferably of importance to human health and gene-function relationships of disease processes. Specifically, the Journal has dedicated Sections focused on genome-wide association studies (GWAS) to function, cardiovascular, renal, metabolic and neurological systems, exercise physiology, pharmacogenomics, clinical, translational and genomics for precision medicine, comparative and statistical genomics and databases. For further details on research themes covered within these Sections, please refer to the descriptions given under each Section.
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