Peer-reviewedCC BYMicroPublication biology
TBC-2, a Rab GTPase activating protein, regulates the localization of the HLH-30/TFEB and PQM-1 transcription factors in the C. elegans intestine.
- 1Department of Anatomy and Cell Biology, McGill University, Montreal, QC, Canada.
- 2Division of Endocrinology and Metabolism, Department of Medicine, McGill University, Montreal, QC, Canada.
- 3Metabolic Disorders and Complications Program, RI-MUHC, Montreal, QC, CA.
Abstract
Insulin/IGF signaling (IIS) inhibits the nuclear localization of the DAF-16 /FOXO transcription factor to regulate longevity and stress resistance in C. elegans . In the intestine, IIS promotes DAF-16 localization to endosomes and loss of TBC-2 , a RAB-5 GAP, results in increased endomembrane localization of DAF-16 at the expense of nuclear localization, decreased DAF-16 target gene expression, longevity and stress resistance. Here we found that TBC-2 differentially regulates the localization of the IIS-regulated transcription factors PQM-1 and HLH-30 /TFEB. Our results suggest a broader role for TBC-2 in regulating IIS and that TBC-2 likely functions at an upstream point in the IIS pathway.
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BibTeX
@article{saha2026tbc2,
title = {{TBC-2, a Rab GTPase activating protein, regulates the localization of the HLH-30/TFEB and PQM-1 transcription factors in the C. elegans intestine.}},
author = {Soumyendu Saha and Icten Meras and Christian E Rocheleau},
journal = {MicroPublication biology},
year = {2026},
month = oct,
doi = {10.17912/micropub.biology.002470},
url = {https://europepmc.org/article/MED/42953546},
note = {CC BY},
}
RIS
TY - JOUR
TI - TBC-2, a Rab GTPase activating protein, regulates the localization of the HLH-30/TFEB and PQM-1 transcription factors in the C. elegans intestine.
AU - Soumyendu Saha
AU - Icten Meras
AU - Christian E Rocheleau
PY - 2026
DA - 2026/10/13
JO - MicroPublication biology
DO - 10.17912/micropub.biology.002470
UR - https://europepmc.org/article/MED/42953546
AB - Insulin/IGF signaling (IIS) inhibits the nuclear localization of the DAF-16 /FOXO transcription factor to regulate longevity and stress resistance in C. elegans . In the intestine, IIS promotes DAF-16 localization to endosomes and loss of TBC-2 , a RAB-5 GAP, results in increased endomembrane localization of DAF-16 at the expense of nuclear localization, decreased DAF-16 target gene expression, longevity and stress resistance. Here we found that TBC-2 differentially regulates the localization of the IIS-regulated transcription factors PQM-1 and HLH-30 /TFEB. Our results suggest a broader role for TBC-2 in regulating IIS and that TBC-2 likely functions at an upstream point in the IIS pathway.
SN - 2578-9430
ER -