Transcription factor NFE2L2/NRF2 is a regulator of macroautophagy genes

Autophagy. 2016 Oct 2;12(10):1902-1916. doi: 10.1080/15548627.2016.1208889. Epub 2016 Jul 18.

Abstract

Autophagy is a highly coordinated process that is controlled at several levels including transcriptional regulation. Here, we identify the transcription factor NFE2L2/NRF2 (nuclear factor, erythroid 2 like 2) as a regulator of autophagy gene expression and its relevance in a mouse model of Alzheimer disease (AD) that reproduces impaired APP (amyloid β precursor protein) and human (Hs)MAPT/TAU processing, clearance and aggregation. We screened the chromatin immunoprecipitation database ENCODE for 2 proteins, MAFK and BACH1, that bind the NFE2L2-regulated enhancer antioxidant response element (ARE). Using a script generated from the JASPAR's consensus ARE sequence, we identified 27 putative AREs in 16 autophagy-related genes. Twelve of these sequences were validated as NFE2L2 regulated AREs in 9 autophagy genes by additional ChIP assays and quantitative RT-PCR on human and mouse cells after NFE2L2 activation with sulforaphane. Mouse embryo fibroblasts of nfe2l2-knockout mice exhibited reduced expression of autophagy genes, which was rescued by an NFE2L2 expressing lentivirus, and impaired autophagy flux when exposed to hydrogen peroxide. NFE2L2-deficient mice co-expressing HsAPPV717I and HsMAPTP301L, exhibited more intracellular aggregates of these proteins and reduced neuronal levels of SQSTM1/p62, CALCOCO2/NDP52, ULK1, ATG5 and GABARAPL1. Also, colocalization of HsAPPV717I and HsMAPTP301L with the NFE2L2-regulated autophagy marker SQSTM1/p62 was reduced in the absence of NFE2L2. In AD patients, neurons expressing high levels of APP or MAPT also expressed SQSTM1/p62 and nuclear NFE2L2, suggesting their attempt to degrade intraneuronal aggregates through autophagy. This study shows that NFE2L2 modulates autophagy gene expression and suggests a new strategy to combat proteinopathies.

Keywords: Alzheimer disease; Tau; amyloid precursor protein; neurodegenerative diseases; neuroprotection; oxidative stress; proteostasis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / pathology
  • Amyloid beta-Peptides / metabolism
  • Animals
  • Antioxidant Response Elements / genetics
  • Autophagy / genetics*
  • Disease Models, Animal
  • Gene Expression Regulation*
  • HEK293 Cells
  • Humans
  • Mice, Transgenic
  • Microtubule-Associated Proteins / metabolism
  • Middle Aged
  • NF-E2-Related Factor 2 / deficiency
  • NF-E2-Related Factor 2 / metabolism*
  • Neurons / metabolism
  • Neurons / pathology
  • Promoter Regions, Genetic / genetics

Substances

  • Amyloid beta-Peptides
  • Microtubule-Associated Proteins
  • NF-E2-Related Factor 2