RRC ID 57231
Author An PNT, Shimaji K, Tanaka R, Yoshida H, Kimura H, Fukusaki E, Yamaguchi M.
Title Epigenetic regulation of starvation-induced autophagy in Drosophila by histone methyltransferase G9a.
Journal Sci Rep
Abstract Epigenetics is now emerging as a key regulation in response to various stresses. We herein identified the Drosophila histone methyltransferase G9a (dG9a) as a key factor to acquire tolerance to starvation stress. The depletion of dG9a led to high sensitivity to starvation stress in adult flies, while its overexpression induced starvation stress resistance. The catalytic domain of dG9a was not required for starvation stress resistance. dG9a plays no apparent role in tolerance to other stresses including heat and oxidative stresses. Metabolomic approaches were applied to investigate global changes in the metabolome due to the loss of dG9a during starvation stress. The results obtained indicated that dG9a plays an important role in maintaining energy reservoirs including amino acid, trehalose, glycogen, and triacylglycerol levels during starvation. Further investigations on the underlying mechanisms showed that the depletion of dG9a repressed starvation-induced autophagy by controlling the expression level of Atg8a, a critical gene for the progression of autophagy, in a different manner to that in cancer cells. These results indicate a positive role for dG9a in starvation-induced autophagy.
Volume 7(1)
Pages 7343
Published 2017-8-4
DOI 10.1038/s41598-017-07566-1
PII 10.1038/s41598-017-07566-1
PMID 28779125
PMC PMC5544687
MeSH Amino Acids / metabolism Animals Autophagy* Chromatography, Liquid Drosophila / genetics* Drosophila / metabolism* Epigenesis, Genetic* Female Gas Chromatography-Mass Spectrometry Histone-Lysine N-Methyltransferase / genetics Histone-Lysine N-Methyltransferase / metabolism* Male Metabolome Metabolomics / methods Mutation Oxidative Stress Starvation*
IF 4.011
Times Cited 17
Resource
Drosophila