A highly conserved neuronal microexon in DAAM1 controls actin dynamics, RHOA/ROCK signaling, and memory formation

Actin cytoskeleton dynamics is essential for proper nervous system development and function. A conserved set of neuronal-specific microexons influences multiple aspects of neurobiology; however, their roles in regulating the actin cytoskeleton are unknown. Here, we study a microexon in DAAM1, a form...

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Detalles Bibliográficos
Autores: Poliński, Patryk, Miret-Cuesta, Marta, Zamora Moratalla, Alfonsa, Mantica, Federica, Cantero Recasens, Gerard, 1984-, Viana, Carlotta, Sabariego Navarro, Miguel, Normanno, Davide, Iñiguez, Luis P., Bonnal, Sophie, Gómez-Riera, Raúl, Fanlo-Ucar, Hugo, Yap, Dominic S., Martínez de Lagrán Cabredo, María, Fernández-Blanco, Álvaro, Rodríguez-Marin, Cristina, Permanyer, Jon, Fölsz, Orsolya, Domínguez-Sala, Eduardo, Sierra, Cesar, Wojnacki, José, Musoles Lleo, Juan Luis, Cosma, Maria Pia, Muñoz López, Francisco José, 1964-, Dierssen, Mara, Irimia Martínez, Manuel
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2025
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:10230/70629
Acceso en línea:http://hdl.handle.net/10230/70629
http://dx.doi.org/10.1038/s41467-025-59430-w
Access Level:acceso abierto
Palabra clave:Biochemistry
Learning and memory
Molecular biology
Molecular neuroscience
RNA splicing
Descripción
Sumario:Actin cytoskeleton dynamics is essential for proper nervous system development and function. A conserved set of neuronal-specific microexons influences multiple aspects of neurobiology; however, their roles in regulating the actin cytoskeleton are unknown. Here, we study a microexon in DAAM1, a formin-homology-2 (FH2) domain protein involved in actin reorganization. Microexon inclusion extends the linker region of the DAAM1 FH2 domain, altering actin polymerization. Genomic deletion of the microexon leads to neuritogenesis defects and increased calcium influx in differentiated neurons. Mice with this deletion exhibit postsynaptic defects, fewer immature dendritic spines, impaired long-term potentiation, and deficits in memory formation. These phenotypes are associated with increased RHOA/ROCK signaling, which regulates actin-cytoskeleton dynamics, and are partially rescued by treatment with a ROCK inhibitor. This study highlights the role of a conserved neuronal microexon in regulating actin dynamics and cognitive functioning.

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