生物
休眠(计算)
表型
熊
基因表达
PPARGC1A型
基因
胰岛素抵抗
胰岛素受体
过氧化物酶体增殖物激活受体
基因表达调控
过氧化物酶体增殖物激活受体γ
胰岛素
内分泌学
内科学
遗传学
转录因子
辅活化剂
医学
国家(计算机科学)
人口
人口学
算法
社会学
计算机科学
作者
Blair W. Perry,Anna McDonald,Shawn Trojahn,Michael W. Saxton,Emma E. Vincent,Charles V. Lowry,Brandon D. Evans Hutzenbiler,Omar E. Cornejo,Charles T. Robbins,Heiko T. Jansen,Joanna L. Kelley
出处
期刊:Physiological Genomics
[American Physiological Society]
日期:2023-09-01
卷期号:55 (9): 368-380
标识
DOI:10.1152/physiolgenomics.00030.2023
摘要
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.
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