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SMARCB1 loss interacts with neuronal differentiation state to block maturation and impact cell stability

Atypical teratoid rhabdoid tumors (ATRTs) are challenging pediatric brain cancers that are predominantly associated with inactivation of the gene SMARCB1, a conserved subunit of the chromatin remodeling BAF complex, which has known contributions to developmental processes. To identify potential inte...

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Bibliographische Detailangaben
Hauptverfasser: Parisian, Alison (VerfasserIn) , Koga, Tomoyuki (VerfasserIn) , Miki, Shunichiro (VerfasserIn) , Johann, Pascal-David (VerfasserIn) , Kool, Marcel (VerfasserIn) , Crawford, John R. (VerfasserIn) , Furnari, Frank B. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: September 10, 2020
In: Genes & development
Year: 2020, Jahrgang: 34, Heft: 19/20, Pages: 1316-1329
ISSN:1549-5477
DOI:10.1101/gad.339978.120
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1101/gad.339978.120
Verlag, lizenzpflichtig, Volltext: http://genesdev.cshlp.org/content/34/19-20/1316
Volltext
Verfasserangaben:Alison D. Parisian, Tomoyuki Koga, Shunichiro Miki, Pascal D. Johann, Marcel Kool, John R. Crawford, and Frank B. Furnari
Beschreibung
Zusammenfassung:Atypical teratoid rhabdoid tumors (ATRTs) are challenging pediatric brain cancers that are predominantly associated with inactivation of the gene SMARCB1, a conserved subunit of the chromatin remodeling BAF complex, which has known contributions to developmental processes. To identify potential interactions between SMARCB1 loss and the process of neural development, we introduced an inducible SMARCB1 loss-of-function system into human induced pluripotent stem cells (iPSCs) that were subjected to either directed neuronal differentiation or differentiation into cerebral organoids. Using this system, we identified substantial differences in the downstream effects of SMARCB1 loss depending on differentiation state and identified an interaction between SMARCB1 loss and neural differentiation pressure that causes a resistance to terminal differentiation and a defect in maintenance of a normal cell state. Our results provide insight into how SMARCB1 loss might interact with neural development in the process of ATRT tumorigenesis.
Beschreibung:Gesehen am 12.11.2020
Beschreibung:Online Resource
ISSN:1549-5477
DOI:10.1101/gad.339978.120

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