Evidence map›Paper›PMID 41042873›Full record

ArticleScience advances2025

The PP2A-B55α phosphatase is a master regulator of mitochondrial degradation and biogenesis.

Valentina Cianfanelli, Monica Nanni, Samantha Corrà, Sofia Mauri, David Sumpton, Sergio Lilla, Rossella De Cegli, Matteo Bordi, Giacomo Milletti, Caterina Ferraina and 18 more

Abstract read
In one paragraph

Article in Science advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
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

28 authors.

Valentina CianfanelliDepartment of Science, University "Roma TRE", Rome, Italy.ORCID 0000-0002-3857-9463
Monica NanniDepartment of Clinical and Molecular Medicine, Sapienza University of Rome, Rome, Italy.ORCID 0000-0001-5706-0053
Samantha CorràDepartment of Biology, University of Padua, Padua, Italy.ORCID 0000-0003-1985-6194
Sofia MauriDepartment of Biology, University of Padua, Padua, Italy.ORCID 0000-0003-3931-1490
David SumptonCancer Research UK Scotland Institute, Glasgow, UK.ORCID 0000-0002-9004-4079
Sergio LillaCancer Research UK Scotland Institute, Glasgow, UK.ORCID 0000-0003-3142-7640
Rossella De CegliTelethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, Italy.ORCID 0000-0002-8526-8692
Matteo BordiDipartimento di Scienze Biotecnologiche di Base, Cliniche Intensivologiche e Perioperatorie, Università Cattolica del Sacro Cuore, Rome, Italy.ORCID 0000-0001-8207-8546
Giacomo MillettiDNA Replication and Cancer Group, Danish Cancer Institute, Copenhagen, Denmark.ORCID 0000-0003-2391-342X
Caterina FerrainaGynecologic Oncology Unit, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.ORCID 0000-0002-3770-4437
Arnaldur HallGenome Integrity Group, Danish Cancer Institute, Copenhagen, Denmark.ORCID 0000-0001-6847-4438
Michele PetraroiaDepartment of Science, University "Roma TRE", Rome, Italy.ORCID 0009-0000-0329-1155
Valentina ClausiDepartment of Science, University "Roma TRE", Rome, Italy.ORCID 0009-0008-2662-4774
Ezio GiordaResearch Laboratories, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.ORCID 0000-0002-5875-832X
Marco ScarsellaResearch Laboratories, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.ORCID 0000-0002-3386-9664
Alessandra BarbieraGynecologic Oncology Unit, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.ORCID 0000-0002-2051-2359
Giulia CadedduPhD Program in Cellular and Molecular Biology, Department of Biology, University of Rome "Tor Vergata," Rome, Italy.ORCID 0000-0003-1841-8395
Marco ColasantiDepartment of Science, University "Roma TRE", Rome, Italy.ORCID 0000-0002-5752-4943
Tiziana PersichiniDepartment of Science, University "Roma TRE", Rome, Italy.ORCID 0000-0001-8291-6706
Kenji MaedaCell Death and Metabolism, Center for Autophagy, Recycling and Disease (CARD), Danish Cancer Institute, Copenhagen, Denmark.ORCID 0000-0002-9080-5691
Apolinar Maya-MendozaDNA Replication and Cancer Group, Danish Cancer Institute, Copenhagen, Denmark.ORCID 0000-0001-7452-9896
Jiri BartekGenome Integrity Group, Danish Cancer Institute, Copenhagen, Denmark.ORCID 0000-0003-2013-7525
Chiara Di MaltaTelethon Institute of Genetics and Medicine (TIGEM), Pozzuoli, Italy.ORCID 0000-0001-6524-4354
Franco LocatelliDepartment of Onco-Haematology and Cell and Gene Therapy, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.ORCID 0000-0002-7976-3654
Sara ZanivanCancer Research UK Scotland Institute, Glasgow, UK.
Shehab IsmailBiochemistry, Molecular and Structural Biology, Department of Chemistry, KU Leuven, Leuven, Belgium.ORCID 0000-0002-4150-1077
Elena ZivianiDepartment of Biology, University of Padua, Padua, Italy.
Francesco CecconiDipartimento di Scienze Biotecnologiche di Base, Cliniche Intensivologiche e Perioperatorie, Università Cattolica del Sacro Cuore, Rome, Italy.ORCID 0000-0002-5614-4359

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondrial homeostasis relies on a tight balance between mitochondrial biogenesis and degradation. Although mitophagy is one of the main pathways involved in the clearance of damaged or old mitochondria, its coordination with mitochondrial biogenesis is poorly characterized. Here, by unbiased approaches including last-generation liquid chromatography coupled to mass spectrometry and transcriptomics, we identify the protein phosphatase PP2A-B55α/PPP2R2A as a Parkin-dependent regulator of mitochondrial number. Upon mitochondrial damage, PP2A-B55α determines the amplitude of mitophagy induction and execution by regulating both early and late mitophagy events. A few minutes after the insult, ULK1 is released from the inhibitory regulation of PP2A-B55α, whereas 2 to 4 hours later, PP2A-B55α promotes the nuclear translocation of TFEB, the master regulator of autophagy and lysosome genes, to support mitophagy execution. Moreover, PP2A-B55α controls a transcriptional program of mitochondrial biogenesis by stabilizing the Parkin substrate and PGC-1α inhibitor PARIS. PP2A-B55α targeting rescues neurodegenerative phenotypes in a fly model of Parkinson's disease, thus suggesting potential therapeutic application.

Indexed as

MitochondriaMitophagyOrganelle BiogenesisProtein Phosphatase 2AnimalsAutophagyHumansParkinson DiseaseUbiquitin-Protein Ligasesparkin proteinProtein Phosphatase 2Ubiquitin-Protein Ligases

Identifiers

PMID41042873
PMCPMC12494018

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Registered trials

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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.