Evidence map›Paper›PMID 38454084›Full record

ArticleMolecular psychiatry2024

Proteomic analysis of the developing mammalian brain links PCDH19 to the Wnt/β-catenin signalling pathway.

Rebekah de Nys, Alison Gardner, Clare van Eyk, Stefka Mincheva-Tasheva, Paul Thomas, Rudrarup Bhattacharjee, Lachlan Jolly, Isabel Martinez-Garay, Ian W J Fox, Karthik Shantharam Kamath and 2 more

Abstract read
In one paragraph

Article in Molecular psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. β-Catenin localization in the ctenophore Mnemiopsis leidyi suggests an ancestral role in cell adhesion and nuclear function.Developmental dynamics : an official publication of the American Association of Anatomists · 2025
    Article
  3. Article
  4. 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.

Rebekah de NysAdelaide Medical School, The University of Adelaide, Adelaide, SA, Australia.
Alison GardnerAdelaide Medical School, The University of Adelaide, Adelaide, SA, Australia.
Clare van EykAdelaide Medical School, The University of Adelaide, Adelaide, SA, Australia.ORCID 0000-0003-0345-9944
Stefka Mincheva-TashevaAdelaide Medical School, The University of Adelaide, Adelaide, SA, Australia.
Paul ThomasAdelaide Medical School, The University of Adelaide, Adelaide, SA, Australia.
Rudrarup BhattacharjeeAdelaide Medical School, The University of Adelaide, Adelaide, SA, Australia.ORCID 0000-0003-2740-6986
Lachlan JollyAdelaide Medical School, The University of Adelaide, Adelaide, SA, Australia.
Isabel Martinez-GarayDivision of Neuroscience, School of Biosciences, Cardiff University, Cardiff, Wales, United Kingdom.ORCID 0000-0001-6849-7496
Ian W J FoxDivision of Neuroscience, School of Biosciences, Cardiff University, Cardiff, Wales, United Kingdom.
Karthik Shantharam KamathAustralian Proteome Analysis Facility, Macquarie University, Macquarie Park, NSW, Australia.
Raman KumarAdelaide Medical School, The University of Adelaide, Adelaide, SA, Australia.ORCID 0000-0001-7976-8386
Jozef GeczAdelaide Medical School, The University of Adelaide, Adelaide, SA, Australia. jozef.gecz@adelaide.edu.au.ORCID 0000-0002-7884-6861

Funding

Department of Health | National Health and Medical Research Council (NHMRC) 2010562Hospital Research Foundation (The Hospital Research Foundation) C-MCF-48-2019-
6 · The paper itself

Abstract

Clustering Epilepsy (CE) is a neurological disorder caused by pathogenic variants of the Protocadherin 19 (PCDH19) gene. PCDH19 encodes a protein involved in cell adhesion and Estrogen Receptor α mediated-gene regulation. To gain further insights into the molecular role of PCDH19 in the brain, we investigated the PCDH19 interactome in the developing mouse hippocampus and cortex. Combined with a meta-analysis of all reported PCDH19 interacting proteins, our results show that PCDH19 interacts with proteins involved in actin, microtubule, and gene regulation. We report CAPZA1, αN-catenin and, importantly, β-catenin as novel PCDH19 interacting proteins. Furthermore, we show that PCDH19 is a regulator of β-catenin transcriptional activity, and that this pathway is disrupted in CE individuals. Overall, our results support the involvement of PCDH19 in the cytoskeletal network and point to signalling pathways where PCDH19 plays critical roles.

Indexed as

beta CateninBrainCadherinsHippocampusProteomicsProtocadherinsWnt Signaling PathwayAnimalsCerebral CortexEpilepsyHumansMiceMice, Inbred C57BLbeta CateninCadherinsPCDH19 protein, humanPcdh19 protein, mouseProtocadherins

Identifiers

PMID38454084
PMCPMC11408250

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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.