A hypothesis: MiRNA‐124 mediated regulation of sirtuin 1 and vitamin D receptor gene expression accelerates aging

Abstract

Abstract Objectives Specific miRNAs are evident to be overexpressed with age, lifestyle, and environmental changes. Previous studies reported miR‐124 overexpression in different scenarios in aged skin, age‐related cognitive impairment, ischemic heart disease, muscle atrophy, and fractures. Thus miR‐124 was considered to be a reliable miRNA target to establish a hypothesis on aging epigenome. Parallelly the hypothesis focuses on the expression of SIRT1 and VDR genes as a target for this specific miRNA expression as these genes were believed to be related to aging. This study aims to derive facts and evidence from past studies on aging. The objective was to establish a hypothetical linkage between miR‐124 with age‐related genes like SIRT1 and VDR. Methods An in silico search was performed in the TargetScan and miRbase databases to analyze the aging‐associated miRNAs and their gene targets, the Python seaborn library was used, and the results were represented in terms of a bar plot. Results Based on an in silico analysis and studies available in the literature, we identified that miR‐124‐3p.1 and miR‐124‐3p.2 targets 3′ UTR of VDR and SIRT1 genes, and hence thereby indicates that the miR‐124 can regulate the expression of these genes. Further, few in vitro research studies have observed that miR‐124 overexpression leads to the downregulation of VDR and SIRT1 gene expression. These results indicate that the suppression of these target genes accelerates early aging and age‐related disorders. Conclusions Overall, this study hypothesizes that the overexpression of miR‐124 diminishes the expression of VDR and SIRT1 genes, and thereby advances the process of aging, resulting in the development of age‐associated complications.

Keywords

• aging
• epigenetics
• microRNA
• SIRT1
• VDR