Chen Jianning, Zou Qin, Lv Daojun, Wei Yingying, Raza Muhammad Ali, Chen Yan, Li Peilin, Xi Xiaoyu, Xu Huaming, Wen Anxiang, Zhu Li, Tang Guoqing, Li Mingzhou, Jiang Anan, Liu Yihui, Fu Yuhua, Jiang Yanzhi, Li Xuewei
Department of Zoology, College of Life Science, Sichuan Agricultural University, Ya'an, Sichuan 625014, China.
Sichuan Weimu Modern Agricultural Science and Technology Co., Ltd., Chengdu, Sichuan 611130, China.
Oncotarget. 2017 Dec 15;9(2):1524-1541. doi: 10.18632/oncotarget.23290. eCollection 2018 Jan 5.
Aging significantly affects the cardiac muscle (CM) and skeletal muscles (SM). Since the aging process of CM and SM may be different, high throughput RNA sequencing was performed using CM and SM in different age conditions to evaluate the expression profiles of messenger RNA (mRNA), long non-coding RNA (lncRNA), micro RNA (miRNA), and circular (circRNA). Several mRNAs, lncRNAs, and miRNAs were highly expressed and consistently appeared in both ages in one of the two muscle tissues. Gene ontology (GO) annotation described that these genes were required for maintaining normal biological functions of CM and SM tissues. Furthermore, 26 mRNAs, 4 lncRNAs, 22 miRNAs, and 26 circRNAs were differentially expressed during cardiac muscle aging. Moreover, 81 mRNAs, 5 lncRNAs, 79 miRNAs, and 62 circRNAs were differentially expressed during aging of skeletal muscle. When comparing the expression profiles of CM and SM during aging, the senescence process in CM and SM was found to be fundamentally different. In addition, we assessed multi-group cooperative control relationships and constructed circRNA-miRNA-mRNA co-expression networks in muscular aging. In conclusion, our findings will contribute to the understanding of muscular aging and provide a foundation for future studies on the molecular mechanisms underlying muscular aging.
衰老对心肌(CM)和骨骼肌(SM)有显著影响。由于CM和SM的衰老过程可能不同,因此利用不同年龄条件下的CM和SM进行了高通量RNA测序,以评估信使RNA(mRNA)、长链非编码RNA(lncRNA)、微小RNA(miRNA)和环状RNA(circRNA)的表达谱。在两种肌肉组织之一中,有几种mRNA、lncRNA和miRNA在两个年龄段均高表达且持续出现。基因本体论(GO)注释表明,这些基因是维持CM和SM组织正常生物学功能所必需的。此外,在心肌衰老过程中有26种mRNA、4种lncRNA、22种miRNA和26种circRNA差异表达。而且,在骨骼肌衰老过程中有81种mRNA、5种lncRNA、79种miRNA和62种circRNA差异表达。在比较衰老过程中CM和SM的表达谱时,发现CM和SM的衰老过程存在根本差异。此外,我们评估了多组协同控制关系,并构建了肌肉衰老中的circRNA-miRNA-mRNA共表达网络。总之,我们的研究结果将有助于理解肌肉衰老,并为未来关于肌肉衰老分子机制的研究提供基础。