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PXD011630

PXD011630 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleIdentification of neurodevelopmental abnormalities including COMT deficiency in an isogenic hPSC model of Fragile X syndrome
DescriptionFragile X Syndrome (FXS) is a neurodevelopmental disorder caused by epigenetic silencing of FMR1 and loss of FMRP expression. Here we describe the establishment of an isogenic human pluripotent embryonic stem cell model of FXS. Using CRISPR/Cas9 to introduce indels in exon 3 of FMR1 and result in complete loss of FMRP (FMR1KO). We show that FMRP-deficient neurons exhibit a number of phenotypic abnormalities including neurite outgrowth and branching deficits and impaired electrophysiological network activity as measured by multi-electrode arrays. RNA-Seq and proteome analysis of FMRP-deficient neurons revealed transcriptional dysregulation in pathways related to neurodevelopment, neurotransmission, and the cell cycle.
HostingRepositoryPRIDE
AnnounceDate2020-06-18
AnnouncementXMLSubmission_2020-06-17_23:04:27.xml
DigitalObjectIdentifier
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterNiels Henning Skotte
SpeciesList scientific name: Homo sapiens (Human); NCBI TaxID: 9606;
ModificationListNo PTMs are included in the dataset
InstrumentQ Exactive HF-X
Dataset History
RevisionDatetimeStatusChangeLog Entry
02018-11-08 06:08:15ID requested
12020-06-17 23:04:28announced
Publication List
Dataset with its publication pending
Keyword List
submitter keyword: FXS, Isogenic, hPSC, Neuron, Proteomics, HF, Human
Contact List
Mahmoud Pouladi
contact affiliationTranslational Laboratory in Genetic Medicine, Agency for Science, Technology and Research, Singapore (A*STAR), 8A Biomedical Grove, Immunos, Level 5, Singapore 138648
contact emailpouladi@thetlgm.com
lab head
Niels Henning Skotte
contact affiliationUniversity of Copenhagen
contact emailniels.skotte@cpr.ku.dk
dataset submitter
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Dataset FTP location
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PRIDE project URI
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