Mis-splicing of a neuronal microexon promotes CPEB4 aggregation in ASD

The inclusion of microexons by alternative splicing occurs frequently in neuronal proteins. The roles of these sequences are largely unknown, and changes in their degree of inclusion are associated with neurodevelopmental disorders1. We have previously shown that decreased inclusion of a 24-nucleoti...

Descripción completa

Detalles Bibliográficos
Autores: Garcia-Cabau, Carla, Bartomeu, Anna, Tesei, Giulio, Cheung, Kai Chit, Pose-Utrilla, Julia, Picó, Sara, Balaceanu, Andreea, Duran-Arqué, Berta, Fernández-Alfara, Marcos, Martín, Judit, De Pace, Cesare, Ruiz-Pérez, Lorena, García, Jesús, Battaglia, Giuseppe, Lucas, José J., Hervás, Rubén, Lindorff-Larsen, Kresten, Méndez, Raúl, Salvatella, Xavier
Tipo de recurso: artículo
Fecha de publicación:2024
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/398161
Acceso en línea:http://hdl.handle.net/10261/398161
Access Level:acceso abierto
Descripción
Sumario:The inclusion of microexons by alternative splicing occurs frequently in neuronal proteins. The roles of these sequences are largely unknown, and changes in their degree of inclusion are associated with neurodevelopmental disorders1. We have previously shown that decreased inclusion of a 24-nucleotide neuron-specific microexon in CPEB4, a RNA-binding protein that regulates translation through cytoplasmic changes in poly(A) tail length, is linked to idiopathic autism spectrum disorder (ASD)2. Why this microexon is required and how small changes in its degree of inclusion have a dominant-negative effect on the expression of ASD-linked genes is unclear. Here we show that neuronal CPEB4 forms condensates that dissolve after depolarization, a transition associated with a switch from translational repression to activation. Heterotypic interactions between the microexon and a cluster of histidine residues prevent the irreversible aggregation of CPEB4 by competing with homotypic interactions between histidine clusters. We conclude that the microexon is required in neuronal CPEB4 to preserve the reversible regulation of CPEB4-mediated gene expression in response to neuronal stimulation.

Similares en LA Referencia