Lysine-specific demethylase 3A is important for autophagic occurrence

Biochem Biophys Res Commun. 2020 May 21;526(1):176-183. doi: 10.1016/j.bbrc.2020.03.058. Epub 2020 Mar 20.

Abstract

Autophagy is an essential process to maintain cell survival and homeostasis under various stress conditions. Here, we report that lysine-specific demethylase 3A (KDM3A) plays an important role in starvation-induced autophagy. Using Kdm3a knockout mice, we demonstrate that KDM3A is crucial for proper hepatic autophagy in vivo. Hepatic mRNA expression analysis and ChIP assay in WT and Kdm3a knockout mouse livers reveal that KDM3A activates autophagy genes by reducing histone H3K9me2 levels upon fasting. Together, our finding represents previously unidentified function of KDM3A as a key regulator of autophagy, implicating potential therapeutic approaches for autophagy-related diseases.

Keywords: Autophagy; H3K9 demethylation; KDM3A.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autophagosomes / metabolism
  • Autophagy*
  • Fasting
  • Fibroblasts / metabolism
  • Gene Expression Regulation
  • Hep G2 Cells
  • Humans
  • Jumonji Domain-Containing Histone Demethylases / genetics
  • Jumonji Domain-Containing Histone Demethylases / metabolism*
  • Liver / cytology
  • Liver / metabolism
  • Lysosomes / metabolism
  • Male
  • Mice, Inbred C57BL
  • Mice, Knockout
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism

Substances

  • RNA, Messenger
  • Jumonji Domain-Containing Histone Demethylases
  • Kdm3a protein, mouse