Evidence map›Paper›PMID 40448601›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025

EFTUD2 Regulates Cortical Morphogenesis via Modulation of Caspase-3 and Aifm1 Splicing Pathways.

Liping Chen, Ying Li, Yan Yu, Mingze Cai, Hao Li, Minghe Huang, Guochao Yang, Jiageng Guo, Huailin Wang, Zhihong Song and 3 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

13 authors.

Liping ChenDepartment of Neurobiology, Beijing Institute of Basic Medical Sciences, Beijing, 100850, China.
Ying LiDepartment of Neurobiology, Beijing Institute of Basic Medical Sciences, Beijing, 100850, China.
Yan YuDepartment of Neurobiology, Beijing Institute of Basic Medical Sciences, Beijing, 100850, China.
Mingze CaiDepartment of Neurobiology, Beijing Institute of Basic Medical Sciences, Beijing, 100850, China.
Hao LiDepartment of Neurobiology, Beijing Institute of Basic Medical Sciences, Beijing, 100850, China.
Minghe HuangDepartment of Neurobiology, Beijing Institute of Basic Medical Sciences, Beijing, 100850, China.
Guochao YangDepartment of Neurobiology, Beijing Institute of Basic Medical Sciences, Beijing, 100850, China.
Jiageng GuoDepartment of Neurobiology, Beijing Institute of Basic Medical Sciences, Beijing, 100850, China.
Huailin WangDepartment of Neurobiology, Beijing Institute of Basic Medical Sciences, Beijing, 100850, China.
Zhihong SongDepartment of Neurobiology, Beijing Institute of Basic Medical Sciences, Beijing, 100850, China.
Wei ShenDepartment of Neurobiology, Beijing Institute of Basic Medical Sciences, Beijing, 100850, China.
Huihui JiangDepartment of Neurobiology, Beijing Institute of Basic Medical Sciences, Beijing, 100850, China.
Haitao WuDepartment of Neurobiology, Beijing Institute of Basic Medical Sciences, Beijing, 100850, China.ORCID https://orcid.org/0000-0001-8437-3194

Funding

Ministry of Science and Technology Innovation (STI) 2030-Major Projects 2021ZD0202500National Key Technologies Research and Development Program 2021YFA1101801National Natural Science Foundation of China 32171148National Science Fund for Distinguished Young Scholars 32325025
6 · The paper itself

Abstract

Elongation Factor Tu GTP-Binding Domain Containing 2 (EFTUD2), a core spliceosomal GTPase associated with Mandibulofacial Dysostosis with Microcephaly (MFDM), plays a mechanistically undefined role in cerebral development. To investigate its pathophysiological contributions, murine models are generated through conditional Eftud2 ablation and in utero electroporation of human pathogenic EFTUD2 variants into cortical neural stem cells (NSCs). Embryonic NSC-specific Eftud2 knockout resulted in cortical disorganization and microcephaly, while pathogenic variants led to significant neuronal loss. Integrative transcriptomic and immunofluorescence analyses revealed that Eftud2 deficiency triggers apoptotic pathways, contributing to cortical malformations. Mechanistic studies using RNA co-immunoprecipitation and full-length transcriptome sequencing demonstrated that Eftud2 directly interacts with Caspase3 and Aifm1 transcripts, regulating their alternative splicing to generate pro-apoptotic isoforms. Splicing assays functionally validated this regulatory mechanism, showing its role in activating cell death pathways and disrupting neurodevelopmental homeostasis. These findings elucidate EFTUD2's critical role in maintaining apoptotic balance during corticogenesis and identify defective splicing regulation as the molecular basis of MFDM. This study provides insights for advancing diagnostic frameworks and therapeutic strategies for neurodevelopmental disorders.

Indexed as

Apoptosis Inducing FactorCaspase 3Cerebral CortexMorphogenesisRibonucleoprotein, U5 Small NuclearAlternative SplicingAnimalsApoptosisHumansMiceMice, KnockoutMicrocephalyNeural Stem CellsPeptide Elongation FactorsAIFM1 protein, mouseApoptosis Inducing FactorCaspase 3EFTUD2 protein, humanPeptide Elongation FactorsRibonucleoprotein, U5 Small NuclearAifm1alternative splicingcortical morphogenesisEFTUD2mandibulofacial dysostosis‐microcephaly syndrome

Identifiers

PMID40448601
PMCPMC12407278

What OpenQuestion holds

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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.