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  4. Modeling the functional impact of CPEB3 and CPEB4 dysregulation in autism: A theoretical–computational framework
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Modeling the functional impact of CPEB3 and CPEB4 dysregulation in autism: A theoretical–computational framework

Journal
Molecular and Cellular Neuroscience
ISSN
1095-9327
Publisher
Elsevier BV
Date Issued
2026
Author(s)
González-Paz, Lenin
Vivas, Alejandro
Cardozo-Urdaneta, Arlene
Lossada, Carla
Mendez, Anibal
Delgado, Ariana
Pérez-Castillo, Yunierkis
Alvarado, Ysaías J.
Type
text::journal::journal article
DOI
10.1016/j.mcn.2026.104072
URL
https://scripta.up.edu.mx/handle/20.500.12552/12799
Abstract
Autism spectrum disorder (ASD) involves impaired synaptic plasticity tightly coupled to local mRNA translation. Cytoplasmic polyadenylation element-binding proteins 3 and 4 (CPEB3 and CPEB4) are post-transcriptional regulators of neuronal mRNA translation that may contribute to ASD-related molecular alterations. In this theoretical–computational study, we develop a weighted functional impact model that integrates transcriptomic expression with intrinsic molecular constraints of CPEB3 and CPEB4 to estimate regional and cell type–specific vulnerability in ASD. Coarse-grained molecular dynamics (MD) simulations were quantitatively analyzed to assess aggregation, diffusion, and cluster stability under cell type–specific cytoplasmic conditions, with statistical uncertainty explicitly evaluated. The anterior cingulate cortex and thalamus emerged as primary vulnerability sites. Despite higher CPEB4 expression—mainly in glial cells—our weighted functional impact model predicted greater theoretical susceptibility linked to CPEB3 dysfunction, particularly in inhibitory and excitatory neurons. MD simulations revealed that CPEB3 forms transient diffusion-permissive aggregates, whereas CPEB4 tends to assemble into more stable condensates. These complementary behaviors suggest differential but interdependent regulation of neuronal and glial functions. Importantly, the proposed framework provides experimentally testable predictions on how protein–protein interactions, microexon loss, and cytoplasmic crowding influence translational control in ASD. This integrative approach provides a quantitative and biologically grounded framework to investigate how post-transcriptional regulators contribute to ASD-relevant molecular vulnerability. ©The authors ©Sciencedirect ©Elsevier.
Subjects

Autism

CPEB3

CPEB4

Post-transcriptional ...

Brain expression patt...

License
Acceso Restringido
URL License
https://creativecommons.org/licenses/by-nc-sa/4.0/
How to cite
González-Paz, L., Vivas, A., Cardozo-Urdaneta, A., Lossada, C., Mendez, A., Delgado, A., Marrero-Ponce, Y., Martinez-Rios, F., Pérez-Castillo, Y., & Alvarado, Y. J. (2026). Modeling the functional impact of CPEB3 and CPEB4 dysregulation in autism: A theoretical–computational framework. Molecular and Cellular Neuroscience, 136, 104072. https://doi.org/10.1016/j.mcn.2026.104072

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