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THOC4 regulates energy homeostasis by stabilizing TFEB mRNA during prolonged starvation
Author(s) -
Toshiharu Fujita,
Sayaka Kubo,
Tatsuya Shioda,
Ayaka Tokumura,
Satoshi Minami,
Megumi Tsuchiya,
Yoshitaka Isaka,
Hidesato Ogawa,
Maho Hamasaki,
Li Yu,
Tamotsu Yoshimori,
Shuhei Nakamura
Publication year - 2021
Publication title -
journal of cell science
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.248203
Subject(s) - tfeb , biology , autophagy , transcription factor , microbiology and biotechnology , basic helix loop helix leucine zipper transcription factors , basic helix loop helix , messenger rna , regulator , transcription (linguistics) , lysosome , gene knockdown , biochemistry , dna binding protein , gene , apoptosis , linguistics , philosophy , enzyme
TFEB, a basic helix-loop-helix transcription factor, is a master regulator of autophagy, lysosome biogenesis and lipid catabolism. Compared to posttranslational regulation of TFEB, the regulation of TFEB mRNA stability remains relatively uncharacterized. In this study, we identified the mRNA-binding protein THOC4 as a novel regulator of TFEB. In mammalian cells, siRNA-mediated knockdown of THOC4 decreased the level of TFEB protein to a greater extent than other bHLH transcription factors. THOC4 bound to TFEB mRNA and stabilized it after transcription by maintaining poly(A) tail length. We further found that this mode of regulation was conserved in Caenorhabditis elegans and was essential for TFEB-mediated lipid breakdown, which becomes over-represented during prolonged starvation. Taken together, our findings reveal the presence of an additional layer of TFEB regulation by THOC4 and provide novel insights into the function of TFEB in mediating autophagy and lipid metabolism.

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