Evidence map›Paper›PMID 32150788›Full record

ArticleThe FEBS journal2020

Autism-associated PTEN missense mutation leads to enhanced nuclear localization and neurite outgrowth in an induced pluripotent stem cell line.

Chi Wai Wong, Yubing Wang, Tian Liu, Lisha Li, Stanley Kwok Kuen Cheung, Penelope Mei-Yu Or, Alfred Sze-Lok Cheng, Kwong Wai Choy, Johannes Peter Henri Burbach, Bo Feng and 2 more

Abstract read
In one paragraph

Article in The FEBS journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. PTEN Subcellular Localization Dictates Function.bioRxiv : the preprint server for biology · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. mTOR-Dependent Spine Dynamics in Autism.Frontiers in molecular neuroscience · 2022
    Review
  8. Review
  9. 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

12 authors.

Chi Wai WongSchool of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China.
Yubing WangSchool of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China.
Tian LiuSchool of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China.
Lisha LiSchool of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China.
Stanley Kwok Kuen CheungSchool of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China.
Penelope Mei-Yu OrSchool of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China.
Alfred Sze-Lok ChengSchool of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China.
Kwong Wai ChoyDepartment of Obstetrics and Gynaecology, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong SAR, China.
Johannes Peter Henri BurbachDepartment of Translational Neuroscience, Brain Center Rudolf Magnus, University Medical Center Utrecht, The Netherlands.
Bo FengSchool of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China.
Raymond Chuen Chung ChangLaboratory of Neurodegenerative Diseases, School of Biomedical Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
Andrew M ChanSchool of Biomedical Sciences, The Chinese University of Hong Kong, Hong Kong SAR, China.ORCID 0000-0001-9923-5464

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Germline mutation in the PTEN gene is the genetic basis of PTEN hamartoma tumor syndrome with the affected individuals harboring features of autism spectrum disorders. Characterizing a panel of 14 autism-associated PTEN missense mutations revealed reduced protein stability, catalytic activity, and subcellular distribution. Nine out of 14 (64%) PTEN missense mutants had reduced protein expression with most mutations confined to the C2 domain. Selected mutants displayed enhanced polyubiquitination and shortened protein half-life, but that did not appear to involve the polyubiquitination sites at lysine residues at codon 13 or 289. Analyzing their intrinsic lipid phosphatase activities revealed that 78% (11 out of 14) of these mutants had twofold to 10-fold reduction in catalytic activity toward phosphatidylinositol phosphate substrates. Analyzing the subcellular localization of the PTEN missense mutants showed that 64% (nine out of 14) had altered nuclear-to-cytosol ratios with four mutants (G44D, H123Q, E157G, and D326N) showing greater nuclear localization. The E157G mutant was knocked-in to an induced pluripotent stem cell line and recapitulated a similar nuclear targeting preference. Furthermore, iPSCs expressing the E157G mutant were more proliferative at the neural progenitor cell stage but exhibited more extensive dendritic outgrowth. In summary, the combination of biological changes in PTEN is expected to contribute to the behavioral and cellular features of this neurodevelopmental disorder.

Indexed as

Mutation, MissenseAutism Spectrum DisorderBlotting, WesternCell Line, TumorCell NucleusHEK293 CellsHumansInduced Pluripotent Stem CellsNeuronal OutgrowthPC-3 CellsPhosphatidate PhosphatasePhosphorylationProtein StabilityPTEN Phosphohydrolaselipid phosphate phosphatasePhosphatidate PhosphatasePTEN PhosphohydrolasePTEN protein, humanautism spectrum disordersmacrocephalyneurodevelopmental disordersPTENPTEN hamartoma tumor syndrome

Identifiers

PMID32150788
PMCPMC7754348

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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.