4.6 Review

TFEB; Beyond Its Role as an Autophagy and Lysosomes Regulator

Journal

CELLS
Volume 11, Issue 19, Pages -

Publisher

MDPI
DOI: 10.3390/cells11193153

Keywords

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

Categories

Funding

  1. E022 Program, National Institute of Pediatrics, Mexico City, Mexico (Recursos Fiscales para la Investigacion)
  2. CONACyT doctoral fellowship [857097]
  3. [033/2022]
  4. [034/2022]

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TFEB is a key transcription factor involved in autophagy and lysosomal biogenesis, and it may also regulate other important biological processes. The regulation of TFEB occurs at the post-translational level and is influenced by various signaling pathways. Understanding the mechanisms of TFEB regulation can help in the development of potential therapeutic strategies.
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.

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