肌萎缩
转录组
基因敲除
C2C12型
骨骼肌
生物
糖尿病
肌球蛋白
长非编码RNA
功能(生物学)
2型糖尿病
细胞生物学
生物信息学
内分泌学
肌发生
核糖核酸
基因表达
基因
遗传学
作者
Jing Yu,Kim Loh,He-qin Yang,Meng-ran Du,Yongxin Wu,Zhiyin Liao,Ai Guo,Yunfei Yang,Bo Chen,Yuxing Zhao,Jinliang Chen,Jing Zhou,Yue Sun,Qian Xiao
标识
DOI:10.1038/s42003-022-03728-8
摘要
Abstract While the exact mechanism remains unclear, type 2 diabetes mellitus increases the risk of sarcopenia which is characterized by decreased muscle mass, strength, and function. Whole-transcriptome RNA sequencing and informatics were performed on the diabetes-induced sarcopenia model of db/db mice. To determine the specific function of lncRNA Gm20743 , the detection of Mito-Sox, reactive oxygen species, Ethynyl-2′-deoxyuridine, and myosin heavy chain was performed in overexpressed and knockdown- Gm20743 C2C12 cells. RNA-seq data and informatics revealed the key lncRNA-mRNA interactions and indicated a potential regulatory role of lncRNAs. We characterized three core candidate lncRNAs Gm20743, Gm35438, 1700047G03Rik , and their potential function. Furthermore, the results suggested lncRNA Gm20743 may be involved in regulating mitochondrial function, oxidative stress, cell proliferation, and myotube differentiation in skeletal muscle cells. These findings significantly improve our understanding of lncRNAs that may mediate muscle mass, strength, and function in diabetes and represent potential therapeutic targets for diabetes-induced sarcopenia.
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