Nakashima Moeka, Suga Naoko, Ikeda Yuka, Yoshikawa Sayuri, Matsuda Satoru
Department of Food Science and Nutrition, Nara Women's University, Kita-Uoya Nishimachi, Nara 630-8506, Japan.
Noncoding RNA. 2024 Feb 5;10(1):11. doi: 10.3390/ncrna10010011.
Noncoding RNAs (ncRNAs), including circular RNAs (circRNAs) and N6-methyladenosine (m6A), have been shown to play a critical role in the development of various diseases including obesity and metabolic disorder-associated fatty liver disease (MAFLD). Obesity is a chronic disease caused by excessive fat accumulation in the body, which has recently become more prevalent and is the foremost risk factor for MAFLD. Causes of obesity may involve the interaction of genetic, behavioral, and social factors. m6A RNA methylation might add a novel inspiration for understanding the development of obesity and MAFLD with post-transcriptional regulation of gene expression. In particular, circRNAs, microRNAs (miRNAs), and m6A might be implicated in the progression of MAFLD. Interestingly, m6A modification can modulate the translation, degradation, and other functions of ncRNAs. miRNAs/circRNAs can also modulate m6A modifications by affecting writers, erasers, and readers. In turn, ncRNAs could modulate the expression of m6A regulators in different ways. However, there is limited evidence on how these ncRNAs and m6A interact to affect the promotion of liver diseases. It seems that m6A can occur in DNA, RNA, and proteins that may be associated with several biological properties. This study provides a mechanistic understanding of the association of m6A modification and ncRNAs with liver diseases, especially for MAFLD. Comprehension of the association between m6A modification and ncRNAs may contribute to the development of treatment tactics for MAFLD.
非编码RNA(ncRNAs),包括环状RNA(circRNAs)和N6-甲基腺苷(m6A),已被证明在包括肥胖症和代谢紊乱相关脂肪性肝病(MAFLD)在内的各种疾病的发展中起关键作用。肥胖症是一种由体内脂肪过度积累引起的慢性疾病,最近变得更加普遍,并且是MAFLD的首要危险因素。肥胖症的病因可能涉及遗传、行为和社会因素的相互作用。m6A RNA甲基化可能为通过基因表达的转录后调控来理解肥胖症和MAFLD的发展提供新的思路。特别是,circRNAs、微小RNA(miRNAs)和m6A可能与MAFLD的进展有关。有趣的是,m6A修饰可以调节ncRNAs的翻译、降解及其他功能。miRNAs/circRNAs也可以通过影响甲基化酶、去甲基化酶和甲基化阅读蛋白来调节m6A修饰。反过来,ncRNAs可以以不同方式调节m6A调节因子的表达。然而,关于这些ncRNAs和m6A如何相互作用以影响肝脏疾病的进展,证据有限。似乎m6A可以出现在可能与多种生物学特性相关的DNA、RNA和蛋白质中。本研究提供了对m6A修饰和ncRNAs与肝脏疾病,特别是MAFLD之间关联的机制理解。理解m6A修饰和ncRNAs之间的关联可能有助于MAFLD治疗策略的发展。