Evidence map›Paper›PMID 27807026›Full record

SynthesisBrain : a journal of neurology2017

Heterozygous PINK1 p.G411S increases risk of Parkinson's disease via a dominant-negative mechanism.

Andreas Puschmann, Fabienne C Fiesel, Thomas R Caulfield, Roman Hudec, Maya Ando, Dominika Truban, Xu Hou, Kotaro Ogaki, Michael G Heckman, Elle D James and 23 more

Erratum issuedAbstract readMeta-Analysis
In one paragraph

Synthesis in Brain : a journal of neurology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 84 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed, 1 pooled it
–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

84 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Rethinking 'rare'Journal of Parkinson's disease · 2025
    Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Genetic Sketch of Parkinson's Disease in India.Annals of Indian Academy of Neurology · 2025
    Article
  8. Article
  9. Genetic mutations in Parkinson's disease: screening of a selected population from North-Eastern Italy.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2025
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Review
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

33 authors.

Andreas Puschmann1 Lund University, Department of Clinical Sciences Lund, Neurology, Sweden Springer.Wolfdieter@mayo.edu Andreas.Puschmann@med.lu.se.
Fabienne C Fiesel3 Department of Neuroscience, Mayo Clinic, Jacksonville, FL 32224, USA.
Thomas R Caulfield3 Department of Neuroscience, Mayo Clinic, Jacksonville, FL 32224, USA.
Roman Hudec3 Department of Neuroscience, Mayo Clinic, Jacksonville, FL 32224, USA.
Maya Ando3 Department of Neuroscience, Mayo Clinic, Jacksonville, FL 32224, USA.
Dominika Truban3 Department of Neuroscience, Mayo Clinic, Jacksonville, FL 32224, USA.
Xu Hou3 Department of Neuroscience, Mayo Clinic, Jacksonville, FL 32224, USA.
Kotaro Ogaki3 Department of Neuroscience, Mayo Clinic, Jacksonville, FL 32224, USA.
Michael G Heckman4 Division of Biomedical Statistics and Informatics, Mayo Clinic, Jacksonville, FL 32224, USA.
Elle D James3 Department of Neuroscience, Mayo Clinic, Jacksonville, FL 32224, USA.
Maria Swanberg5 Lund University, Department of Experimental Medical Science, Lund, Sweden.
Itzia Jimenez-Ferrer5 Lund University, Department of Experimental Medical Science, Lund, Sweden.
Oskar Hansson6 Clinical Memory Research Unit, Department of Clinical Sciences Malmö, Lund University, Sweden.
Grzegorz Opala8 Department of Neurology, School of Medicine in Katowice, Medical University of Silesia, Katowice, Poland.
Joanna Siuda8 Department of Neurology, School of Medicine in Katowice, Medical University of Silesia, Katowice, Poland.
Magdalena Boczarska-Jedynak8 Department of Neurology, School of Medicine in Katowice, Medical University of Silesia, Katowice, Poland.
Andrzej Friedman9 Department of Neurology, Medical University of Warsaw, Poland.
Dariusz Koziorowski9 Department of Neurology, Medical University of Warsaw, Poland.
Monika Rudzińska-Bar
Jan O Aasly10 Department of Neurology, St. Olav's Hospital, and Department of Neuroscience, Norwegian University of Science and Technology, Trondheim, Norway.
Timothy Lynch11 Dublin Neurological Institute at the Mater Misericordiae University Hospital, Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Dublin, Ireland.
George D Mellick12 Eskitis Institute for Drug Discovery, Griffith University, Nathan, Queensland, Australia.
Megha Mohan12 Eskitis Institute for Drug Discovery, Griffith University, Nathan, Queensland, Australia.
Peter A Silburn12 Eskitis Institute for Drug Discovery, Griffith University, Nathan, Queensland, Australia.
Yanosh Sanotsky14 Lviv Regional Clinical Hospital, Lviv, Ukraine.
Carles Vilariño-Güell3 Department of Neuroscience, Mayo Clinic, Jacksonville, FL 32224, USA.
Matthew J Farrer3 Department of Neuroscience, Mayo Clinic, Jacksonville, FL 32224, USA.
Li Chen16 Neuroregeneration and Stem Cell Programs, Institute for Cell Engineering, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Valina L Dawson16 Neuroregeneration and Stem Cell Programs, Institute for Cell Engineering, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Ted M Dawson16 Neuroregeneration and Stem Cell Programs, Institute for Cell Engineering, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Zbigniew K Wszolek22 Department of Neurology, Mayo Clinic, Jacksonville, FL 32224, USA.
Owen A Ross3 Department of Neuroscience, Mayo Clinic, Jacksonville, FL 32224, USA.
Wolfdieter Springer3 Department of Neuroscience, Mayo Clinic, Jacksonville, FL 32224, USA Springer.Wolfdieter@mayo.edu Andreas.Puschmann@med.lu.se.

Funding

Understanding Mechanisms of a-synuclein pathologyP50NS038377 · NINDS · JOHNS HOPKINS UNIVERSITY · PI KO, HANSEOK · 1998 to 2019
$38.8M
Neuropathology CoreP50NS072187 · NINDS · MAYO CLINIC JACKSONVILLE · PI DICKSON, DENNIS WILLIAM · 2010 to 2017
$8.7M
Parthanatos, AIF and PAAN-1 in Neuronal InjuryR37NS067525 · NINDS · JOHNS HOPKINS UNIVERSITY · PI DAWSON, TED M., DAWSON, VALINA L. · 2015 to 2021
$5.3M
Molecular mechanisms of PINK1-PRKN directed mitochondrial quality controlRF1NS085070 · NINDS · MAYO CLINIC JACKSONVILLE · PI SPRINGER, WOLFDIETER · 2019 to 2019
$2.8M
Molecular mechanisms of Parkin-directed mitochondrial quality controlR01NS085070 · NINDS · MAYO CLINIC JACKSONVILLE · PI SPRINGER, WOLFDIETER · 2014 to 2018
$1.7M
Understanding the role of MAPT in Parkinsonian disordersR01NS078086 · NINDS · MAYO CLINIC JACKSONVILLE · PI ROSS, OWEN A · 2012 to 2016
$1.7M
NINDS NIH HHS P50 NS038377NINDS NIH HHS P50 NS072187NINDS NIH HHS R01 NS078086NINDS NIH HHS R01 NS085070NINDS NIH HHS R37 NS067525NINDS NIH HHS RF1 NS085070
6 · The paper itself

Abstract

SEE GANDHI AND PLUN-FAVREAU DOI101093/AWW320 FOR A SCIENTIFIC COMMENTARY ON THIS ARTICLE: It has been postulated that heterozygous mutations in recessive Parkinson's genes may increase the risk of developing the disease. In particular, the PTEN-induced putative kinase 1 (PINK1) p.G411S (c.1231G>A, rs45478900) mutation has been reported in families with dominant inheritance patterns of Parkinson's disease, suggesting that it might confer a sizeable disease risk when present on only one allele. We examined families with PINK1 p.G411S and conducted a genetic association study with 2560 patients with Parkinson's disease and 2145 control subjects. Heterozygous PINK1 p.G411S mutations markedly increased Parkinson's disease risk (odds ratio = 2.92, P = 0.032); significance remained when supplementing with results from previous studies on 4437 additional subjects (odds ratio = 2.89, P = 0.027). We analysed primary human skin fibroblasts and induced neurons from heterozygous PINK1 p.G411S carriers compared to PINK1 p.Q456X heterozygotes and PINK1 wild-type controls under endogenous conditions. While cells from PINK1 p.Q456X heterozygotes showed reduced levels of PINK1 protein and decreased initial kinase activity upon mitochondrial damage, stress-response was largely unaffected over time, as expected for a recessive loss-of-function mutation. By contrast, PINK1 p.G411S heterozygotes showed no decrease of PINK1 protein levels but a sustained, significant reduction in kinase activity. Molecular modelling and dynamics simulations as well as multiple functional assays revealed that the p.G411S mutation interferes with ubiquitin phosphorylation by wild-type PINK1 in a heterodimeric complex. This impairs the protective functions of the PINK1/parkin-mediated mitochondrial quality control. Based on genetic and clinical evaluation as well as functional and structural characterization, we established p.G411S as a rare genetic risk factor with a relatively large effect size conferred by a partial dominant-negative function phenotype.

Indexed as

Genetic Association StudiesModels, MolecularAdolescentAdultAgedAged, 80 and overCase-Control StudiesFemaleFibroblastsGenetic Predisposition to DiseaseHeterozygoteHumansMaleMiddle AgedParkinson DiseasePedigreeProtein KinasesPTEN-Induced Putative Kinaseheterozygous mutationmitophagyParkinson’s diseasePINK1ubiquitin

Identifiers

PMID27807026
PMCPMC5379862

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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.