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环状锌指蛋白609的下调通过调节RNA N-甲基腺苷修饰的表达促进心脏修复。

Downregulation of circ-ZNF609 Promotes Heart Repair by Modulating RNA N-Methyladenosine-Modified Expression.

作者信息

Wang Lijun, Yu Pujiao, Wang Jiaqi, Xu Guie, Wang Tianhui, Feng Jingyi, Bei Yihua, Xu Jiahong, Wang Hongbao, Das Saumya, Xiao Junjie

机构信息

Cardiac Regeneration and Ageing Lab, Institute of Geriatrics (Shanghai University), Affiliated Nantong Hospital of Shanghai University (The Sixth People's Hospital of Nantong), School of Medicine, Shanghai University, Nantong 226011, China.

Shanghai Engineering Research Center of Organ Repair, School of Life Science, Shanghai University, Shanghai 200444, China.

出版信息

Research (Wash D C). 2022 Apr 7;2022:9825916. doi: 10.34133/2022/9825916. eCollection 2022.

Abstract

Circular RNAs take crucial roles in several pathophysiological processes. The regulatory role and its underlying mechanisms of circ-ZNF609 in the heart remains largely unknown. Here, we report that circ-ZNF609 is upregulated during myocardial ischemia/reperfusion (I/R) remodeling. Knockdown of circ-ZNF609 protects against acute I/R injury and attenuates left ventricle dysfunction after I/R remodeling . , circ-ZNF609 regulates cardiomyocyte survival and proliferation via modulating the crosstalk between Hippo-YAP and Akt signaling. Mechanically, N-methyladenosine-modification is involved in the regulatory role of circ-ZNF609 on YAP. An in-depth study indicates that knockdown of circ-ZNF609 decreases the expression of YTHDF3 and further fine-tuned the accessibility of mRNA to YTHDF1 and YTHDF2 to regulate YAP expression. circ-ZNF609 knockdown represents a promising therapeutic strategy to combat the pathological process of myocardial I/R injury.

摘要

环状RNA在多个病理生理过程中发挥关键作用。circ-ZNF609在心脏中的调节作用及其潜在机制在很大程度上仍不清楚。在此,我们报道circ-ZNF609在心肌缺血/再灌注(I/R)重塑过程中上调。敲低circ-ZNF609可预防急性I/R损伤,并减轻I/R重塑后的左心室功能障碍。circ-ZNF609通过调节Hippo-YAP和Akt信号通路之间的相互作用来调节心肌细胞的存活和增殖。机制上,N-甲基腺苷修饰参与了circ-ZNF609对YAP的调节作用。深入研究表明,敲低circ-ZNF609可降低YTHDF3的表达,并进一步微调mRNA对YTHDF1和YTHDF2的可及性以调节YAP表达。敲低circ-ZNF609代表了一种对抗心肌I/R损伤病理过程的有前景的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10d0/9012977/adbba1859e88/RESEARCH2022-9825916.001.jpg

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