Nutrient-sensitive transcription factors TFEB and TFE3 couple autophagy and metabolism to the peripheral clock

EMBO J. 2019 Jun 17;38(12):e101347. doi: 10.15252/embj.2018101347. Epub 2019 May 24.

Abstract

Autophagy and energy metabolism are known to follow a circadian pattern. However, it is unclear whether autophagy and the circadian clock are coordinated by common control mechanisms. Here, we show that the oscillation of autophagy genes is dependent on the nutrient-sensitive activation of TFEB and TFE3, key regulators of autophagy, lysosomal biogenesis, and cell homeostasis. TFEB and TFE3 display a circadian activation over the 24-h cycle and are responsible for the rhythmic induction of genes involved in autophagy during the light phase. Genetic ablation of TFEB and TFE3 in mice results in deregulated autophagy over the diurnal cycle and altered gene expression causing abnormal circadian wheel-running behavior. In addition, TFEB and TFE3 directly regulate the expression of Rev-erbα (Nr1d1), a transcriptional repressor component of the core clock machinery also involved in the regulation of whole-body metabolism and autophagy. Comparative analysis of the cistromes of TFEB/TFE3 and REV-ERBα showed an extensive overlap of their binding sites, particularly in genes involved in autophagy and metabolic functions. These data reveal a direct link between nutrient and clock-dependent regulation of gene expression shedding a new light on the crosstalk between autophagy, metabolism, and circadian cycles.

Keywords: MiT‐TFE; REV‐ERBα; circadian rhythm; gene oscillation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autophagy* / drug effects
  • Autophagy* / genetics
  • Basic Helix-Loop-Helix Leucine Zipper Transcription Factors / drug effects
  • Basic Helix-Loop-Helix Leucine Zipper Transcription Factors / genetics
  • Basic Helix-Loop-Helix Leucine Zipper Transcription Factors / physiology*
  • Binding Sites
  • Cells, Cultured
  • Circadian Clocks* / drug effects
  • Circadian Clocks* / genetics
  • Circadian Rhythm / drug effects
  • Circadian Rhythm / physiology
  • Energy Metabolism* / drug effects
  • Energy Metabolism* / genetics
  • Gene Expression Regulation
  • HEK293 Cells
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Nuclear Receptor Subfamily 1, Group D, Member 1 / genetics
  • Nuclear Receptor Subfamily 1, Group D, Member 1 / physiology
  • Nutrients / pharmacology
  • Nutrients / physiology*
  • Transcription Factors / drug effects
  • Transcription Factors / genetics
  • Transcription Factors / physiology

Substances

  • Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
  • Nr1d1 protein, mouse
  • Nuclear Receptor Subfamily 1, Group D, Member 1
  • Tcfeb protein, mouse
  • Transcription Factors
  • Tcfe3 protein, mouse