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可变聚腺苷酸化及其差异调控:对跨物种棕色脂肪组织产热的影响

Alternative Polyadenylation and Differential Regulation of : Implications for Brown Adipose Tissue Thermogenesis Across Species.

作者信息

Lu Wen-Hsin, Chang Yao-Ming, Huang Yi-Shuian

机构信息

Institute of Biomedical Sciences, Academia Sinica, Taipei, Taiwan.

出版信息

Front Pediatr. 2021 Feb 9;8:612279. doi: 10.3389/fped.2020.612279. eCollection 2020.

Abstract

Brown adipose tissue (BAT) is a thermogenic organ owing to its unique expression of uncoupling protein 1 (UCP1), which is a proton channel in the inner mitochondrial membrane used to dissipate the proton gradient and uncouple the electron transport chain to generate heat instead of adenosine triphosphate. The discovery of metabolically active BAT in human adults, especially in lean people after cold exposure, has provoked the "thermogenic anti-obesity" idea to battle weight gain. Because BAT can expend energy through UCP1-mediated thermogenesis, the molecular mechanisms regulating UCP1 expression have been extensively investigated at both transcriptional and posttranscriptional levels. Of note, the 3'-untranslated region (3'-UTR) of mRNA is differentially processed between mice and humans that quantitatively affects UCP1 synthesis and thermogenesis. Here, we summarize the regulatory mechanisms underlying UCP1 expression, report the number of poly(A) signals identified or predicted in genes across species, and discuss the potential and caution in targeting UCP1 for enhancing thermogenesis and metabolic fitness.

摘要

棕色脂肪组织(BAT)是一种产热器官,这归因于其独特表达的解偶联蛋白1(UCP1),UCP1是线粒体内膜中的一种质子通道,用于耗散质子梯度并使电子传递链解偶联,从而产生热量而非三磷酸腺苷。在成年人体内发现具有代谢活性的BAT,尤其是在冷暴露后的瘦人中发现,引发了对抗体重增加的“产热抗肥胖”理念。由于BAT可通过UCP1介导的产热消耗能量,因此在转录和转录后水平上对调节UCP1表达的分子机制进行了广泛研究。值得注意的是,mRNA的3'非翻译区(3'-UTR)在小鼠和人类之间的加工方式不同,这在数量上影响了UCP1的合成和产热。在此,我们总结了UCP1表达的调控机制,报告了跨物种在基因中鉴定或预测的多聚腺苷酸化信号的数量,并讨论了以UCP1为靶点增强产热和代谢适应性的潜力与注意事项。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac34/7899972/311a279fbbeb/fped-08-612279-g0001.jpg

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