α-Catenin levels determine direction of YAP/TAZ response to autophagy perturbation.
Adaptor Proteins, Signal Transducing
/ metabolism
Animals
Autophagy
/ physiology
Cells, Cultured
Epithelial Cells
Feedback, Physiological
Humans
Mice
Microtubule-Associated Proteins
/ metabolism
Mutation
Protein Binding
Protein Interaction Domains and Motifs
/ genetics
Signal Transduction
Trans-Activators
/ metabolism
Transcription Factors
/ metabolism
Transcriptional Coactivator with PDZ-Binding Motif Proteins
YAP-Signaling Proteins
alpha Catenin
/ chemistry
Journal
Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555
Informations de publication
Date de publication:
17 03 2021
17 03 2021
Historique:
received:
19
02
2020
accepted:
18
02
2021
entrez:
18
3
2021
pubmed:
19
3
2021
medline:
27
3
2021
Statut:
epublish
Résumé
The factors regulating cellular identity are critical for understanding the transition from health to disease and responses to therapies. Recent literature suggests that autophagy compromise may cause opposite effects in different contexts by either activating or inhibiting YAP/TAZ co-transcriptional regulators of the Hippo pathway via unrelated mechanisms. Here, we confirm that autophagy perturbation in different cell types can cause opposite responses in growth-promoting oncogenic YAP/TAZ transcriptional signalling. These apparently contradictory responses can be resolved by a feedback loop where autophagy negatively regulates the levels of α-catenins, LC3-interacting proteins that inhibit YAP/TAZ, which, in turn, positively regulate autophagy. High basal levels of α-catenins enable autophagy induction to positively regulate YAP/TAZ, while low α-catenins cause YAP/TAZ activation upon autophagy inhibition. These data reveal how feedback loops enable post-transcriptional determination of cell identity and how levels of a single intermediary protein can dictate the direction of response to external or internal perturbations.
Identifiants
pubmed: 33731717
doi: 10.1038/s41467-021-21882-1
pii: 10.1038/s41467-021-21882-1
pmc: PMC7969950
doi:
Substances chimiques
Adaptor Proteins, Signal Transducing
0
MAP1LC3A protein, human
0
Microtubule-Associated Proteins
0
Trans-Activators
0
Transcription Factors
0
Transcriptional Coactivator with PDZ-Binding Motif Proteins
0
WWTR1 protein, human
0
YAP-Signaling Proteins
0
YAP1 protein, human
0
alpha Catenin
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1703Subventions
Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Medical Research Council
ID : UKDRI-2002
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 095317/Z/11/Z
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 100140/Z/12/Z
Pays : United Kingdom
Commentaires et corrections
Type : CommentIn
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