Phosphorylation of ULK1 (hATG1) by AMP-Activated Protein Kinase Connects Energy Sensing to Mitophagy
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A protein kinase links energy stores to control of autophagy.
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AMPK regulates autophagic turnover of dysfunctional mitochondria by initiating mitophagy through phosphorylation and activation of ULK1.
“AMPK is believed to regulate the autophagic turnover of dysfunctional mitochondria through initiation of mitophagy by phosphorylation and activation of the pro-mitophagic factor UNC51-like kinase 1 (ULK1)42.”
From Mitochondrial and metabolic dysfunction in ageing and age-related diseases (2022) · cites this paper as [42]
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- Authors
- Egan, D. F., Shackelford, D. B., Mihaylova, M. M., Gelino, S., Kohnz, R. A., Mair, W., Vasquez, D. S., Joshi, A., Gwinn, D. M., Taylor, R., Asara, J. M., Fitzpatrick, J., Dillin, A., Viollet, B., Kundu, M., Hansen, M., & Shaw, R. J.
- Affiliations
- Salk Institute for Biological Studies (US)
- Sanford Burnham Prebys Medical Discovery Institute (US)
- St. Jude Children's Research Hospital (US)
- Beth Israel Deaconess Medical Center (US)
- Inserm, U1016, Institut Cochin, Université Paris Descartes, CNRS (UMR 8104), Paris, France.
- Corresponding author
- Shaw, Reuben J.
- ORCID
- Venue
- Science
- Published
- 2011-01-28
- Volume
- 331
- Issue
- 6016
- Pages
- 456-461
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC3030664
- OpenAlex
- W2103659405
- Cited by
- 2,600
- References
- 39
- Citations by year
- 2026: 143 · 2025: 137 · 2024: 172 · 2023: 125 · 2022: 161 · 2021: 208 · 2020: 193 · 2019: 169 · 2018: 201 · 2017: 184 · 2016: 182 · 2015: 176 · 2014: 152 · 2013: 154 · 2012: 145
- FWCI
- 91.93
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- UEA Digital Repository (University of East Anglia) (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- National Cancer Institute (1P01CA120964-01A, P01CA120964, T32CA009370, P30CA014195, P30CA006516)
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK080425)
- Topics
- Health Sciences › Medicine › Epidemiology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Keywords
- AMPK, ULK1, ULK2, Atg1, autophagy, mitophagy, phosphorylation, energy sensing, p62, mitochondrial homeostasis, starvation, nutrient availability, Caenorhabditis elegans, liver
- MeSH terms
- Autophagy-Related Protein-1 Homolog, Sequestosome-1 Protein, Animals, Autophagy, Cell Line, Cell Survival, Energy Metabolism, Humans, Insulin, Liver, Metformin, Mitochondria, Liver, Phenformin, Phosphorylation, Transcription Factors, Signal Transduction, Caenorhabditis elegans, Protein Serine-Threonine Kinases, Hepatocytes, Caenorhabditis elegans Proteins, Cell Line, Tumor, Intracellular Signaling Peptides and Proteins, Adaptor Proteins, Signal Transducing, Mice, Transcription Factor TFIIH, AMP-Activated Protein Kinases
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