Regulation of Autophagy through TORC1 and mTORC1

Autophagy is an intracellular protein-degradation process that is conserved across eukaryotes including yeast and humans. Under nutrient starvation conditions, intracellular proteins are transported to lysosomes and vacuoles via membranous structures known as autophagosomes, and are degraded. The va...

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Main Author: Takeshi Noda
Format: Article
Language:English
Published: MDPI AG 2017-07-01
Series:Biomolecules
Subjects:
PAS
Online Access:https://www.mdpi.com/2218-273X/7/3/52
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spelling doaj-c10182f4e8f443449afa4579c61d99832020-11-24T23:43:17ZengMDPI AGBiomolecules2218-273X2017-07-01735210.3390/biom7030052biom7030052Regulation of Autophagy through TORC1 and mTORC1Takeshi Noda0Center for Frontier Oral Science, Graduate School of Dentistry, Osaka University, Suita, Osaka 565-0871, JapanAutophagy is an intracellular protein-degradation process that is conserved across eukaryotes including yeast and humans. Under nutrient starvation conditions, intracellular proteins are transported to lysosomes and vacuoles via membranous structures known as autophagosomes, and are degraded. The various steps of autophagy are regulated by the target of rapamycin complex 1 (TORC1/mTORC1). In this review, a history of this regulation and recent advances in such regulation both in yeast and mammals will be discussed. Recently, the mechanism of autophagy initiation in yeast has been deduced. The autophagy-related gene 13 (Atg13) and the unc-51 like autophagy activating kinase 1 (Ulk1) are the most crucial substrates of TORC1 in autophagy, and by its dephosphorylation, autophagosome formation is initiated. Phosphorylation/dephosphorylation of Atg13 is regulated spatially inside the cell. Another TORC1-dependent regulation lies in the expression of autophagy genes and vacuolar/lysosomal hydrolases. Several transcriptional and post-transcriptional regulations are controlled by TORC1, which affects autophagy activity in yeast and mammals.https://www.mdpi.com/2218-273X/7/3/52autophagyTORC1Atg13Atg1Atg9Atg8PASGln3TFEB
collection DOAJ
language English
format Article
sources DOAJ
author Takeshi Noda
spellingShingle Takeshi Noda
Regulation of Autophagy through TORC1 and mTORC1
Biomolecules
autophagy
TORC1
Atg13
Atg1
Atg9
Atg8
PAS
Gln3
TFEB
author_facet Takeshi Noda
author_sort Takeshi Noda
title Regulation of Autophagy through TORC1 and mTORC1
title_short Regulation of Autophagy through TORC1 and mTORC1
title_full Regulation of Autophagy through TORC1 and mTORC1
title_fullStr Regulation of Autophagy through TORC1 and mTORC1
title_full_unstemmed Regulation of Autophagy through TORC1 and mTORC1
title_sort regulation of autophagy through torc1 and mtorc1
publisher MDPI AG
series Biomolecules
issn 2218-273X
publishDate 2017-07-01
description Autophagy is an intracellular protein-degradation process that is conserved across eukaryotes including yeast and humans. Under nutrient starvation conditions, intracellular proteins are transported to lysosomes and vacuoles via membranous structures known as autophagosomes, and are degraded. The various steps of autophagy are regulated by the target of rapamycin complex 1 (TORC1/mTORC1). In this review, a history of this regulation and recent advances in such regulation both in yeast and mammals will be discussed. Recently, the mechanism of autophagy initiation in yeast has been deduced. The autophagy-related gene 13 (Atg13) and the unc-51 like autophagy activating kinase 1 (Ulk1) are the most crucial substrates of TORC1 in autophagy, and by its dephosphorylation, autophagosome formation is initiated. Phosphorylation/dephosphorylation of Atg13 is regulated spatially inside the cell. Another TORC1-dependent regulation lies in the expression of autophagy genes and vacuolar/lysosomal hydrolases. Several transcriptional and post-transcriptional regulations are controlled by TORC1, which affects autophagy activity in yeast and mammals.
topic autophagy
TORC1
Atg13
Atg1
Atg9
Atg8
PAS
Gln3
TFEB
url https://www.mdpi.com/2218-273X/7/3/52
work_keys_str_mv AT takeshinoda regulationofautophagythroughtorc1andmtorc1
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