Evidence map›Paper›PMID 32133736›Full record

ArticleEMBO reports2020

USP1 deubiquitinates Akt to inhibit PI3K-Akt-FoxO signaling in muscle during prolonged starvation.

Dana Goldbraikh, Danielle Neufeld, Yara Eid-Mutlak, Inbal Lasry, Jennifer E Gilda, Anna Parnis, Shenhav Cohen

Open access · bronzeAbstract read
In one paragraph

Article in EMBO reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
5.4field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

70 citing papers in PubMed, 116 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. PHLPP is neither a Phosphatase nor a Tumor Suppressor.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Obesity Affects IVF Outcomes and Mevalonic Acid Rescues the Side Effects of Statins on Follicle Growth.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  19. AKT and DUBs: a bidirectional relationship.Cellular & molecular biology letters · 2025
    Review
  20. Review

10 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Dana Goldbraikh *Faculty of Biology, Technion Institute of Technology, Haifa, Israel.
Danielle Neufeld *Faculty of Biology, Technion Institute of Technology, Haifa, Israel.
Yara Eid-MutlakFaculty of Biology, Technion Institute of Technology, Haifa, Israel.
Inbal LasryFaculty of Biology, Technion Institute of Technology, Haifa, Israel.
Jennifer E GildaFaculty of Biology, Technion Institute of Technology, Haifa, Israel.
Anna ParnisFaculty of Biology, Technion Institute of Technology, Haifa, Israel.
Shenhav CohenFaculty of Biology, Technion Institute of Technology, Haifa, Israel.ORCID 0000-0001-8307-466X
Technion – Israel Institute of Technology · IL

Funding

Israel Ministry of Science, Technology and Space 2015-3-74Israel Science Foundation 623/15Niedersachsen-Deutsche ZN3008Zuckerman STEM Postdoctoral Fellowship to J.E. Gilda
6 · The paper itself

Abstract

PI3K-Akt-FoxO-mTOR signaling is the central pathway controlling growth and metabolism in all cells. Ubiquitination of the protein kinase Akt prior to its phosphorylation is required for PI3K-Akt activity. Here, we found that the deubiquitinating (DUB) enzyme USP1 removes K63-linked polyubiquitin chains on Akt to restrict PI3K-Akt-FoxO signaling in mouse muscle during prolonged starvation. DUB screening platform identified USP1 as a direct DUB for Akt, and USP1 depletion in mouse muscle increased Akt ubiquitination, PI3K-Akt-FoxO signaling, and glucose uptake during fasting. Co-immunoprecipitation and mass spectrometry identified disabled homolog-2 (Dab2), the tuberous sclerosis complex TSC1/TSC2, and PHLPP1 as USP1 bound proteins. During starvation, Dab2 is essential for Akt recruitment to USP1-TSC1-PHLPP1 complex, and for PI3K-Akt-FoxO inhibition. Surprisingly, USP1 limits TSC1 levels to sustain mTOR-mediated basal protein synthesis rates and maintain its own protein levels. We propose that Dab2 recruits Akt to USP1-TSC1-PHLPP1 complex to efficiently terminate the transmission of growth signals when cellular energy level is low.

Indexed as

Forkhead Box Protein O1Phosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktStarvationAnimalsMiceMusclesPhosphorylationSignal TransductionUbiquitinationUbiquitin-Specific ProteasesForkhead Box Protein O1Foxo1 protein, mousePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktUbiquitin-Specific ProteasesUsp1 protein, mouseDab2fastingmuscle atrophyPI3K-Akt signalingUSP1

Identifiers

PMID32133736
PMCPMC7132338
OpenAlexW3010539078

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.