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Second-hit mosaic mutation in mTORC1 repressor DEPDC5 causes focal cortical dysplasia–associated epilepsy
Théo Ribierre, … , Richard Miles, Stéphanie Baulac
Théo Ribierre, … , Richard Miles, Stéphanie Baulac
Published April 30, 2018
Citation Information: J Clin Invest. 2018;128(6):2452-2458. https://doi.org/10.1172/JCI99384.
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Concise Communication Genetics Neuroscience

Second-hit mosaic mutation in mTORC1 repressor DEPDC5 causes focal cortical dysplasia–associated epilepsy

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Abstract

DEP domain–containing 5 protein (DEPDC5) is a repressor of the recently recognized amino acid–sensing branch of the mTORC1 pathway. So far, its function in the brain remains largely unknown. Germline loss-of-function mutations in DEPDC5 have emerged as a major cause of familial refractory focal epilepsies, with case reports of sudden unexpected death in epilepsy (SUDEP). Remarkably, a fraction of patients also develop focal cortical dysplasia (FCD), a neurodevelopmental cortical malformation. We therefore hypothesized that a somatic second-hit mutation arising during brain development may support the focal nature of the dysplasia. Here, using postoperative human tissue, we provide the proof of concept that a biallelic 2-hit — brain somatic and germline — mutational mechanism in DEPDC5 causes focal epilepsy with FCD. We discovered a mutation gradient with a higher rate of mosaicism in the seizure-onset zone than in the surrounding epileptogenic zone. Furthermore, we demonstrate the causality of a Depdc5 brain mosaic inactivation using CRISPR-Cas9 editing and in utero electroporation in a mouse model recapitulating focal epilepsy with FCD and SUDEP-like events. We further unveil a key role of Depdc5 in shaping dendrite and spine morphology of excitatory neurons. This study reveals promising therapeutic avenues for treating drug-resistant focal epilepsies with mTORC1-targeting molecules.

Authors

Théo Ribierre, Charlotte Deleuze, Alexandre Bacq, Sara Baldassari, Elise Marsan, Mathilde Chipaux, Giuseppe Muraca, Delphine Roussel, Vincent Navarro, Eric Leguern, Richard Miles, Stéphanie Baulac

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Figure 4

Morphological and functional changes in Depdc5fKO neurons.

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Morphological and functional changes in Depdc5fKO neurons.
(A) Neuronal ...
(A) Neuronal reconstruction of representative control (n = 5) and Depdc5fKO-gRNA1 (n = 5) recorded neurons. Scale bars: 100 μm. (B) Quantification of branching complexity by Sholl analysis. ***P < 0.0001, by 2-way-ANOVA for group effects. Nb, number. (C) Apical tuft width of control (n = 5) and Depdc5fKO-gRNA1 (n = 5) neurons. ***P = 0.0079, by Mann-Whitney U test. (D) Representative images of level-2 basal dendrite. Scale bars: 5 μm. (E) Dot plot showing the distribution of spine head widths (μm). **P = 0.0072, by unpaired t test (n = 4 neurons/group; n = 200 spines/neuron). (F) Capacitance (Cm) and (G) input resistance (Rin) for control (n = 11) and Depdc5fKO (n = 12) neurons. ***P = 0.002, by Mann-Whitney U test (mean Cm: controls = 130.5 pF, Depdc5fKO-gRNA1 = 238.1 pF; mean Rin: controls = 95.6 MOhm, Depdc5fKO-gRNA1 = 67.6 MOhm). (H) Left: Firing pattern of control Depdc5fKO-gRNA1 cells for 250 pA and 300 pA current input, respectively. Right: Mean frequency-current curve. ***P < 0.0001, by 2-way-ANOVA for group effects. (I) Left: Representative traces of sEPSC events over a 1-minute period. Right: Cumulative frequency distribution and dot plot of sEPSC mean amplitude. Mean amplitude: controls (n = 10) = 11.07 ± 0.12 pA; Depdc5fKO-gRNA1 (n = 8) = 12.1 ± 0.52 pA. *P = 0.0219, by Mann-Whitney U test.

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