Feeding during hibernation shifts gene expression toward active season levels in brown bears (Ursus arctos).

IF 2.5 4区 生物学 Q3 CELL BIOLOGY Physiological genomics Pub Date : 2023-09-01 Epub Date: 2023-07-24 DOI:10.1152/physiolgenomics.00030.2023
Blair W Perry, Anna L McDonald, Shawn Trojahn, Michael W Saxton, Ellery P Vincent, Courtney Lowry, Brandon D Evans Hutzenbiler, Omar E Cornejo, Charles T Robbins, Heiko T Jansen, Joanna L Kelley
{"title":"Feeding during hibernation shifts gene expression toward active season levels in brown bears (<i>Ursus arctos</i>).","authors":"Blair W Perry, Anna L McDonald, Shawn Trojahn, Michael W Saxton, Ellery P Vincent, Courtney Lowry, Brandon D Evans Hutzenbiler, Omar E Cornejo, Charles T Robbins, Heiko T Jansen, Joanna L Kelley","doi":"10.1152/physiolgenomics.00030.2023","DOIUrl":null,"url":null,"abstract":"<p><p>Hibernation in bears involves a suite of metabolical and physiological changes, including the onset of insulin resistance, that are driven in part by sweeping changes in gene expression in multiple tissues. Feeding bears glucose during hibernation partially restores active season physiological phenotypes, including partial resensitization to insulin, but the molecular mechanisms underlying this transition remain poorly understood. Here, we analyze tissue-level gene expression in adipose, liver, and muscle to identify genes that respond to midhibernation glucose feeding and thus potentially drive postfeeding metabolical and physiological shifts. We show that midhibernation feeding stimulates differential expression in all analyzed tissues of hibernating bears and that a subset of these genes responds specifically by shifting expression toward levels typical of the active season. Inferences of upstream regulatory molecules potentially driving these postfeeding responses implicate peroxisome proliferator-activated receptor gamma (PPARG) and other known regulators of insulin sensitivity, providing new insight into high-level regulatory mechanisms involved in shifting metabolic phenotypes between hibernation and active states.</p>","PeriodicalId":20129,"journal":{"name":"Physiological genomics","volume":null,"pages":null},"PeriodicalIF":2.5000,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10642923/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physiological genomics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1152/physiolgenomics.00030.2023","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/7/24 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Hibernation in bears involves a suite of metabolical and physiological changes, including the onset of insulin resistance, that are driven in part by sweeping changes in gene expression in multiple tissues. Feeding bears glucose during hibernation partially restores active season physiological phenotypes, including partial resensitization to insulin, but the molecular mechanisms underlying this transition remain poorly understood. Here, we analyze tissue-level gene expression in adipose, liver, and muscle to identify genes that respond to midhibernation glucose feeding and thus potentially drive postfeeding metabolical and physiological shifts. We show that midhibernation feeding stimulates differential expression in all analyzed tissues of hibernating bears and that a subset of these genes responds specifically by shifting expression toward levels typical of the active season. Inferences of upstream regulatory molecules potentially driving these postfeeding responses implicate peroxisome proliferator-activated receptor gamma (PPARG) and other known regulators of insulin sensitivity, providing new insight into high-level regulatory mechanisms involved in shifting metabolic phenotypes between hibernation and active states.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
冬眠期间的喂养使棕熊的基因表达向活跃季节水平转变。
熊的冬眠涉及一系列代谢和生理变化,包括胰岛素抵抗的发作,这在一定程度上是由多个组织中基因表达的全面变化驱动的。在冬眠期间喂养熊的葡萄糖部分恢复了活跃季节的生理表型,包括对胰岛素的部分再敏感,但这种转变的分子机制仍知之甚少。在这里,我们分析了脂肪、肝脏和肌肉中组织水平的基因表达,以确定对冬眠中期葡萄糖喂养有反应的基因,从而可能驱动喂养后的代谢和生理变化。我们发现,冬眠中期的喂养刺激了冬眠熊所有分析组织中的差异表达,这些基因的一个子集通过将表达转移到活跃季节的典型水平来做出特异性反应。对可能驱动这些进食后反应的上游调节分子的推断涉及过氧化物酶体增殖物激活受体γ(PPARG)和其他已知的胰岛素敏感性调节因子,为了解冬眠和活动状态之间代谢表型变化的高水平调节机制提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
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.
期刊最新文献
Exercise and tumor proteome: insights from a neuroblastoma model. A long-term high-fat diet induces differential gene expression changes in spatially distinct adipose tissue of male mice. Three decades of rat genomics: approaching the finish(ed) line. Differences in gut microbiota and metabolites between wrestlers with varying precompetition weight control effect. Ameliorating Immune-dependent Inflammation and Apoptosis by Targeting TLR4/MYD88/NF-ᵰ5B Pathway by Celastrol Mitigates the Diabetic Reproductive Dysfunction.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1