Evidence map›Paper›PMID 41794998›Full record

ArticleCommunications biology2026

Protocadherin γC4 regulates neuronal survival and dendritic self-avoidance.

Ryuon Higuchi, Masaki Tatara, Satoko Horino, Shota Katori, Makoto Sanbo, Masumi Hirabayashi, Masahiko Watanabe, Ayumu Konno, Hirokazu Hirai, Yoshichika Yoshioka and 4 more

Abstract read
In one paragraph

Article in Communications biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Ryuon HiguchiKOKORO-Biology Group, Laboratories for Integrated Biology, Graduate School of Frontier Biosciences, The University of Osaka, Suita, Osaka, Japan.ORCID http://orcid.org/0009-0007-1433-7463
Masaki TataraKOKORO-Biology Group, Laboratories for Integrated Biology, Graduate School of Frontier Biosciences, The University of Osaka, Suita, Osaka, Japan.
Satoko HorinoKOKORO-Biology Group, Laboratories for Integrated Biology, Graduate School of Frontier Biosciences, The University of Osaka, Suita, Osaka, Japan.
Shota KatoriKOKORO-Biology Group, Laboratories for Integrated Biology, Graduate School of Frontier Biosciences, The University of Osaka, Suita, Osaka, Japan.
Makoto SanboDivision of Mammalian Embryogenesis, Department of Homeostatic Regulation, National Institute for Physiological Sciences, Okazaki, Aichi, Japan.ORCID http://orcid.org/0000-0001-8806-1745
Masumi HirabayashiDivision of Mammalian Embryogenesis, Department of Homeostatic Regulation, National Institute for Physiological Sciences, Okazaki, Aichi, Japan.ORCID http://orcid.org/0000-0002-1059-5883
Masahiko WatanabeDepartment of Anatomy, Faculty of Medicine, Hokkaido University, Kita-ku, Sapporo, Japan.
Ayumu KonnoDepartment of Neurophysiology and Neural Repair, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan.ORCID http://orcid.org/0000-0001-9382-396X
Hirokazu HiraiDepartment of Neurophysiology and Neural Repair, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan.ORCID http://orcid.org/0000-0002-0721-4293
Yoshichika YoshiokaInstitute for Biomedical Sciences, Iwate Medical University, Yahaba, Iwate, Japan.
Takahiro HirabayashiClinical Medicine Research Laboratory, Shonan University of Medical Sciences, Totsuka-ku, Yokohama, Japan.
Toshihiro KobayashiDivision of Mammalian Embryogenesis, Department of Homeostatic Regulation, National Institute for Physiological Sciences, Okazaki, Aichi, Japan.ORCID http://orcid.org/0000-0001-8019-0008
Ryosuke KanekoKOKORO-Biology Group, Laboratories for Integrated Biology, Graduate School of Frontier Biosciences, The University of Osaka, Suita, Osaka, Japan.
Takeshi YagiKOKORO-Biology Group, Laboratories for Integrated Biology, Graduate School of Frontier Biosciences, The University of Osaka, Suita, Osaka, Japan. yagi.takeshi.fbs@osaka-u.ac.jp.ORCID http://orcid.org/0000-0002-6604-0318

Funding

MEXT | Japan Society for the Promotion of Science (JSPS) 22H05498MEXT | Japan Society for the Promotion of Science (JSPS) 24H01237MEXT | Japan Society for the Promotion of Science (JSPS) 25H02501
6 · The paper itself

Abstract

Animal models are indispensable for linking human genetic findings to disease mechanisms. Mutations in protocadherin gamma C4 (γC4), one of the 22 isoforms encoded by the protocadherin-γ (Pcdh-γ) gene cluster, cause a human neurodevelopmental syndrome with progressive microcephaly, seizures, and intellectual disability. Here, we established a γC4 mutant mouse model that exhibits motor dysfunction, seizures, reduced brain size, and increased embryonic neuronal apoptosis. Using DOMINO (Double Mutation-Induced Open Reading Frame Switch), a two-step CRISPR/Cas9-based genome-editing strategy, we also generated γC4fl-only mice that retain full-length γC4 while truncating the other 21 Pcdh-γ isoforms. Unlike Pcdh-γ cluster-deficient mice, γC4fl-only mice were viable and fertile. Furthermore, we show that the γC4 constant region (γCR) contributes to the regulation of Purkinje cell dendritic architecture and self-avoidance. Together, these findings indicate that γCR-containing γC4 is required for neuronal survival and dendritic patterning, supporting γC4 as a principal functional isoform within the Pcdh-γ gene cluster.

Indexed as

CadherinsDendritesNeuronsAnimalsCadherin Related ProteinsCell SurvivalMiceMutationProtocadherinsPurkinje CellsCadherin Related ProteinsCadherinsGamma-protocadherinsProtocadherins

Identifiers

PMID41794998
PMCPMC13096477

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.