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Partial FMRP expression is sufficient to normalize neuronal hyperactivity in Fragile X neurons
Author(s) -
Graef John D.,
Wu Hao,
Ng Carrie,
Sun Chicheng,
Villegas Vivian,
Qadir Deena,
Jesseman Kimberly,
Warren Stephen T.,
Jaenisch Rudolf,
Cacace Angela,
Wallace Owen
Publication year - 2020
Publication title -
european journal of neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.346
H-Index - 206
eISSN - 1460-9568
pISSN - 0953-816X
DOI - 10.1111/ejn.14660
Subject(s) - fragile x syndrome , fmr1 , neuroscience , gene silencing , phenotype , biology , fragile x , intellectual disability , epigenetics , excitatory postsynaptic potential , genetics , gene , inhibitory postsynaptic potential
Fragile X syndrome (FXS) is the most common genetic form of intellectual disability caused by a CGG repeat expansion in the 5′‐UTR of the Fragile X mental retardation gene FMR1 , triggering epigenetic silencing and the subsequent absence of the protein, FMRP . Reactivation of FMR1 represents an attractive therapeutic strategy targeting the genetic root cause of FXS. However, largely missing in the FXS field is an understanding of how much FMR1 reactivation is required to rescue FMRP‐dependent mutant phenotypes. Here, we utilize FXS patient‐derived excitatory neurons to model FXS in vitro and confirm that the absence of FMRP leads to neuronal hyperactivity. We further determined the levels of FMRP and the percentage of FMRP‐positive cells necessary to correct this phenotype utilizing a mixed and mosaic neuronal culture system and a combination of CRISPR, antisense and expression technologies to titrate FMRP in FXS and WT neurons. Our data demonstrate that restoration of greater than 5% of overall FMRP expression levels or greater than 20% FMRP‐expressing neurons in a mosaic pattern is sufficient to normalize a FMRP‐dependent, hyperactive phenotype in FXS iPSC‐derived neurons.