Increased abundance of translation machinery in stem cell–derived neural progenitor cells from four schizophrenia patients View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2015-10-20

AUTHORS

A Topol, J A English, E Flaherty, P Rajarajan, B J Hartley, S Gupta, F Desland, S Zhu, T Goff, L Friedman, J Rapoport, D Felsenfeld, G Cagney, A Mackay-Sim, J N Savas, B Aronow, G Fang, B Zhang, D Cotter, K J Brennand

ABSTRACT

The genetic and epigenetic factors contributing to risk for schizophrenia (SZ) remain unresolved. Here we demonstrate, for the first time, perturbed global protein translation in human-induced pluripotent stem cell (hiPSC)-derived forebrain neural progenitor cells (NPCs) from four SZ patients relative to six unaffected controls. We report increased total protein levels and protein synthesis, together with two independent sets of quantitative mass spectrometry evidence indicating markedly increased levels of ribosomal and translation initiation and elongation factor proteins, in SZ hiPSC NPCs. We posit that perturbed levels of global protein synthesis in SZ hiPSC NPCs represent a novel post-transcriptional mechanism that might contribute to disease progression. More... »

PAGES

e662-e662

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  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1038/tp.2015.118

    DOI

    http://dx.doi.org/10.1038/tp.2015.118

    DIMENSIONS

    https://app.dimensions.ai/details/publication/pub.1046771966

    PUBMED

    https://www.ncbi.nlm.nih.gov/pubmed/26485546


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