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Multiscale modeling uncovers 7q11.23 copy number variation–dependent changes in ribosomal biogenesis and neuronal maturation and excitability
Marija Mihailovich, … , Michela Matteoli, Giuseppe Testa
Marija Mihailovich, … , Michela Matteoli, Giuseppe Testa
Published July 15, 2024
Citation Information: J Clin Invest. 2024;134(14):e168982. https://doi.org/10.1172/JCI168982.
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Research Article Neuroscience Article has an altmetric score of 8

Multiscale modeling uncovers 7q11.23 copy number variation–dependent changes in ribosomal biogenesis and neuronal maturation and excitability

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Abstract

Copy number variation (CNV) at 7q11.23 causes Williams-Beuren syndrome (WBS) and 7q microduplication syndrome (7Dup), neurodevelopmental disorders (NDDs) featuring intellectual disability accompanied by symmetrically opposite neurocognitive features. Although significant progress has been made in understanding the molecular mechanisms underlying 7q11.23-related pathophysiology, the propagation of CNV dosage across gene expression layers and their interplay remains elusive. Here we uncovered 7q11.23 dosage–dependent symmetrically opposite dynamics in neuronal differentiation and intrinsic excitability. By integrating transcriptomics, translatomics, and proteomics of patient-derived and isogenic induced neurons, we found that genes related to neuronal transmission follow 7q11.23 dosage and are transcriptionally controlled, while translational factors and ribosomal genes are posttranscriptionally buffered. Consistently, we found phosphorylated RPS6 (p-RPS6) downregulated in WBS and upregulated in 7Dup. Surprisingly, p-4EBP was changed in the opposite direction, reflecting dosage-specific changes in total 4EBP levels. This highlights different dosage-sensitive dyregulations of the mTOR pathway as well as distinct roles of p-RPS6 and p-4EBP during neurogenesis. Our work demonstrates the importance of multiscale disease modeling across molecular and functional layers, uncovers the pathophysiological relevance of ribosomal biogenesis in a paradigmatic pair of NDDs, and uncouples the roles of p-RPS6 and p-4EBP as mechanistically actionable relays in NDDs.

Authors

Marija Mihailovich, Pierre-Luc Germain, Reinald Shyti, Davide Pozzi, Roberta Noberini, Yansheng Liu, Davide Aprile, Erika Tenderini, Flavia Troglio, Sebastiano Trattaro, Sonia Fabris, Ummi Ciptasari, Marco Tullio Rigoli, Nicolò Caporale, Giuseppe D’Agostino, Filippo Mirabella, Alessandro Vitriolo, Daniele Capocefalo, Adrianos Skaros, Agnese Virginia Franchini, Sara Ricciardi, Ida Biunno, Antonino Neri, Nael Nadif Kasri, Tiziana Bonaldi, Rudolf Aebersold, Michela Matteoli, Giuseppe Testa

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Figure 3

Robust transcriptional changes in translation- and neural transmission–related genes.

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Robust transcriptional changes in translation- and neural transmission–r...
(A) Fold changes of DEGs in the merged analysis of isogenic and patient-derived lines (in either WBS vs. CTL, 7Dup vs. CTL, or regression on 7q11.23 copy number), showing robust transcriptional signatures that are largely symmetrically opposite between genotypes. SRP, signal recognition particle. (B) Enriched GO terms in the regression on 7q11.23 copy number. Similar terms are clustered (denoted by colors) and only the top term per cluster is shown. (C–E) Top DEGs associated with translation (C), ion channels and their regulation (D), or ASD (E). (F) Comparison of fold changes at the RNA and protein levels (for the union of genes found significant at either level), in each of the 3 comparisons performed. (G) Expression of the transcriptionally dysregulated translation genes that could also be measured at the proteome level, highlighting a buffering in 7Dup.

Copyright © 2025 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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