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睡眠剥夺和饮食会影响转基因小鼠体内的人类生长激素(GH)基因表达。

Sleep deprivation and diet affect human GH gene expression in transgenic mice in vivo.

作者信息

Jarmasz Jessica S, Jin Yan, Vakili Hana, Cattini Peter A

机构信息

Department of Physiology & Pathophysiology, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.

Department of Pathology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.

出版信息

Endocr Connect. 2020 Dec;9(12):1135-1147. doi: 10.1530/EC-20-0354.

Abstract

Human (h) growth hormone (GH) production studies are largely limited to effects on secretion. How pituitary hGH gene (hGH-N/GH1) expression is regulated is important in our understanding of the role hGH plays in physiology and disease. Here we assess for the first time the effect of sleep deprivation (SD) and high-fat diet (HFD) on hGH-N expression in vivo using partially humanized 171hGH/CS transgenic (TG) mice, and attempted to elucidate a role for DNA methylation. Activation of hGH-N expression requires interactions between promoter and upstream locus control region (LCR) sequences including pituitary-specific hypersensitive site (HS) I/II. Both SD and diet affect hGH secretion, but the effect of SD on hGH-N expression is unknown. Mice fed a HFD or regular chow diet for 3 days underwent SD (or no SD) for 6 h at Zeitgeber time (ZT) 3. Serum and pituitaries were assessed over 24 h at 6-h intervals beginning at ZT 14. SD and HFD caused significant changes in serum corticosterone and insulin, as well as hGH and circadian clock-related gene RNA levels. No clear association between DNA methylation and the negative effects of SD or diet on hGH RNA levels was observed. However, a correlation with increased methylation at a CpG (cytosine paired with a guanine) in a putative E-box within the hGH LCR HS II was suggested in situ. Methylation at this site also increased BMAL1/CLOCK-related nuclear protein binding in vitro. These observations support an effect of SD on hGH synthesis at the level of gene expression.

摘要

人类(h)生长激素(GH)产生的研究在很大程度上局限于对其分泌的影响。垂体hGH基因(hGH-N/GH1)的表达调控机制对于我们理解hGH在生理和疾病中的作用至关重要。在此,我们首次使用部分人源化的171hGH/CS转基因(TG)小鼠评估睡眠剥夺(SD)和高脂饮食(HFD)对体内hGH-N表达的影响,并试图阐明DNA甲基化的作用。hGH-N表达的激活需要启动子与上游基因座控制区(LCR)序列之间的相互作用,其中包括垂体特异性超敏位点(HS)I/II。SD和饮食都会影响hGH的分泌,但SD对hGH-N表达的影响尚不清楚。给小鼠喂食HFD或常规饲料3天,在时间点(ZT)3进行为期6小时的SD(或不进行SD)。从ZT 14开始,每隔6小时对血清和垂体进行24小时的评估。SD和HFD导致血清皮质酮、胰岛素以及hGH和昼夜节律相关基因RNA水平发生显著变化。未观察到DNA甲基化与SD或饮食对hGH RNA水平的负面影响之间存在明显关联。然而,原位研究提示hGH LCR HS II内一个假定的E盒中的CpG(胞嘧啶与鸟嘌呤配对)甲基化增加与之相关。该位点的甲基化在体外也增加了BMAL1/CLOCK相关核蛋白的结合。这些观察结果支持SD在基因表达水平上对hGH合成有影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8be6/7774756/d4e1718b967b/EC-20-0354fig1.jpg

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