TFEB; Beyond Its Role as an Autophagy and Lysosomes Regulator

Cells. 2022 Oct 7;11(19):3153. doi: 10.3390/cells11193153.

Abstract

Transcription factor EB (TFEB) is considered the master transcriptional regulator of autophagy and lysosomal biogenesis, which regulates target gene expression through binding to CLEAR motifs. TFEB dysregulation has been linked to the development of numerous pathological conditions; however, several other lines of evidence show that TFEB might be a point of convergence of diverse signaling pathways and might therefore modulate other important biological processes such as cellular senescence, DNA repair, ER stress, carbohydrates, and lipid metabolism and WNT signaling-related processes. The regulation of TFEB occurs predominantly at the post-translational level, including phosphorylation, acetylation, SUMOylating, PARsylation, and glycosylation. It is noteworthy that TFEB activation is context-dependent; therefore, its regulation is subjected to coordinated mechanisms that respond not only to nutrient fluctuations but also to stress cell programs to ensure proper cell homeostasis and organismal health. In this review, we provide updated insights into novel post-translational modifications that regulate TFEB activity and give an overview of TFEB beyond its widely known role in autophagy and the lysosomal pathway, thus opening the possibility of considering TFEB as a potential therapeutic target.

Keywords: DNA damage repair and cell cycle; WNT signaling; carbohydrate; cellular senescence; endoplasmic reticulum stress; lipids; metabolism; transcriptional factor EB (TFEB).

Publication types

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

MeSH terms

  • Autophagy* / genetics
  • Carbohydrates
  • Gene Expression Regulation
  • Lysosomes* / metabolism
  • Phosphorylation

Substances

  • Carbohydrates

Grants and funding

We appreciate the support of the E022 Program, National Institute of Pediatrics, Mexico City, Mexico (Recursos Fiscales para la Investigación). D.O.-C was supported by 033/2022. S.G.-M was supported by 034/2022. CONACyT doctoral fellowship was awarded to B.F-J (857097).