Cerebral organoids expressing mutant actin genes reveal cellular mechanism underlying microcephaly

Actins are cytoskeletal proteins that are essential for multiple cellular processes. Mutations in the ACTB and ACTG1 genes, encoding the ubiquitous beta- and gamma-cytoskeletal actin isoforms, respectively, cause a broad spectrum of neurodevelopmental disorders, with microcephaly as the most frequent one. To investigate the pathogenesis underlying this cortical malformation, we studied patient-derived cerebral organoids from induced pluripotent stem cells of individuals with the Baraitser-Winter-CerebroFrontoFacial syndrome (BWCFF-S) carrying an ACTB/ACTG1 missense mutation. These organoids were reduced in size, showing a thinner ventricular zone (VZ) due to reduced VZ progenitor abundance. Strikingly, VZ progenitors in BWCFF-S cerebral organoids displayed a shift in the orientation of their cleavage plane from a predominantly vertical to a majoritarian horizontal orientation. The latter cleavage plane orientation is incompatible with increasing VZ progenitor abundance and instead promotes basal progenitor generation. Various cytoskeletal and morphological irregularities of BWCFF-S VZ progenitors, notably in the apical region, seemingly contribute to this change in cleavage plane orientation. Our results provide insight into the cell biological basis of the microcephaly associated with BWCFF-S caused by actin mutations.

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Journal
EMBO Reports
Published
2025-12-10
DOI
https://doi.org/10.1038/s44319-025-00647-7
Citations
3
Primary Topic
Neurogenesis and neuroplasticity mechanisms
Type
article
Field-Weighted Citation Impact
3.96
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article

Cerebral organoids expressing mutant actin genes reveal cellular mechanism underlying microcephaly

Nataliya Di Donato, Alexandra Haase, Velena Radošević, Marija Milković Periša et al.
3 citations
EMBO Reports
Neurogenesis and neuroplasticity mechanisms
3.96
article

Cerebral organoids expressing mutant actin genes reveal cellular mechanism underlying microcephaly

Nataliya Di Donato, Alexandra Haase, Velena Radošević, Marija Milković Periša, Michael Heide, Wieland Β. Huttner, Michaela Wilsch‐Bräuninger, Fabian Rost, Felipe Mora‐Bermúdez, Nataša Jovanov Milošević, Evelin Schröck, Noreen Walker, Katrin Neumann, Pauline Wimberger, Indra Niehaus, Mariasavina Severino, Mihaela Bobić‐Rasonja, Karolina Kuenzel, Kaomei Guan, Ulrich Martin
article en
3 citations

Abstract

Actins are cytoskeletal proteins that are essential for multiple cellular processes. Mutations in the ACTB and ACTG1 genes, encoding the ubiquitous beta- and gamma-cytoskeletal actin isoforms, respectively, cause a broad spectrum of neurodevelopmental disorders, with microcephaly as the most frequent one. To investigate the pathogenesis underlying this cortical malformation, we studied patient-derived cerebral organoids from induced pluripotent stem cells of individuals with the Baraitser-Winter-CerebroFrontoFacial syndrome (BWCFF-S) carrying an ACTB/ACTG1 missense mutation. These organoids were reduced in size, showing a thinner ventricular zone (VZ) due to reduced VZ progenitor abundance. Strikingly, VZ progenitors in BWCFF-S cerebral organoids displayed a shift in the orientation of their cleavage plane from a predominantly vertical to a majoritarian horizontal orientation. The latter cleavage plane orientation is incompatible with increasing VZ progenitor abundance and instead promotes basal progenitor generation. Various cytoskeletal and morphological irregularities of BWCFF-S VZ progenitors, notably in the apical region, seemingly contribute to this change in cleavage plane orientation. Our results provide insight into the cell biological basis of the microcephaly associated with BWCFF-S caused by actin mutations.

EMBO ReportsVol. 27(2)
University Hospital Centre Zagreb (HR), University of Zagreb (HR), Istituto Giannina Gaslini (IT), German Primate Center (DE), Medizinische Hochschule Hannover (DE), Center for Systems Biology Dresden (DE), Max Planck Institute of Molecular Cell Biology and Genetics (DE), Technische Universität Dresden (DE)
Openalex Percentile: Top 6%
Neurogenesis and neuroplasticity mechanisms
3.96
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