Epigenetic Regulation Associated With Sirtuin 1 in Complications of Diabetes Mellitus

Front Endocrinol (Lausanne). 2021 Jan 18:11:598012. doi: 10.3389/fendo.2020.598012. eCollection 2020.

Abstract

Diabetes mellitus (DM) has been one of the largest health concerns of the 21st century due to the serious complications associated with the disease. Therefore, it is essential to investigate the pathogenesis of DM and develop novel strategies to reduce the burden of diabetic complications. Sirtuin 1 (SIRT1), a nicotinamide adenosine dinucleotide (NAD+)-dependent deacetylase, has been reported to not only deacetylate histones to modulate chromatin function but also deacetylate numerous transcription factors to regulate the expression of target genes, both positively and negatively. SIRT1 also plays a crucial role in regulating histone and DNA methylation through the recruitment of other nuclear enzymes to the chromatin. Furthermore, SIRT1 has been verified as a direct target of many microRNAs (miRNAs). Recently, numerous studies have explored the key roles of SIRT1 and other related epigenetic mechanisms in diabetic complications. Thus, this review aims to present a summary of the rapidly growing field of epigenetic regulatory mechanisms, as well as the epigenetic influence of SIRT1 on the development and progression of diabetic complications, including cardiomyopathy, nephropathy, and retinopathy.

Keywords: SIRT1; deacetylation; diabetes mellitus; diabetic complications; epigenetics.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • DNA Methylation*
  • Diabetes Complications / epidemiology
  • Diabetes Complications / genetics
  • Diabetes Complications / pathology*
  • Diabetes Mellitus / physiopathology*
  • Epigenesis, Genetic*
  • Gene Expression Regulation*
  • Humans
  • MicroRNAs / genetics*
  • Sirtuin 1 / genetics*

Substances

  • MicroRNAs
  • SIRT1 protein, human
  • Sirtuin 1