PRC2 disruption in cerebellar progenitors produces cerebellar hypoplasia and aberrant myoid differentiation without blocking medulloblastoma growth

Cleveland, A. H.; Malawsky, D.; Churiwal, M.; Rodriguez, C.; Reed, F.; Schniederjan, M.; Velazquez Vega, J. E.; Davis, I.; Gershon, T. R.

doi:10.1101/2022.07.11.499567

bioRxiv · 10.1101/2022.07.11.499567

PRC2 disruption in cerebellar progenitors produces cerebellar hypoplasia and aberrant myoid differentiation without blocking medulloblastoma growth

Cleveland, A. H.·Malawsky, D.·Churiwal, M.·Rodriguez, C.·Reed, F.·Schniederjan, M.·Velazquez Vega, J. E.·Davis, I.·Gershon, T. R.

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Abstract

We show that the Polycomb Repressive Complex 2 (PRC2) maintains neural identity in Sonic Hedgehog (SHH)-driven cerebellar granule neuron progenitors (CGNPs) and SHH-driven medulloblastoma, a cancer of CGNPs. Proliferating CGNPs and medulloblastoma cells pass the neural fate commitment to their progeny through epigenetic mechanisms. The PRC2 mediates epigenetic regulation through histone methylation, and PRC2 inhibitors have been proposed for medulloblastoma therapy. We investigated PRC2 function in CGNPs and medulloblastoma by conditionally deleting PRC2 components Eed or Ezh2 in CGNPs and analyzing cerebellar growth, cellular gene expression (scRNA-seq), and tumorigenesis in medulloblastoma-prone Smo-mutant mice. Eed-deleted CGNPs showed reduced growth, with decreased proliferation, increased apoptosis and inappropriate myoid differentiation. Ezh2-deleted CGNPs also showed myoid differentiation without reduced growth. Eed-deleted and Ezh2-deleted medulloblastomas similarly demonstrated myoid differentiation, but progressed more rapidly than PRC2-intact controls. The PRC2 thus maintained neural fate in CGNPs and medulloblastoma, but PRC2 disruption did not block SHH medulloblastoma progression.

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Cleveland, A. H., Malawsky, D., Churiwal, M., Rodriguez, C., Reed, F., Schniederjan, M., Velazquez Vega, J. E., Davis, I., Gershon, T. R.. 2022-07-12. PRC2 disruption in cerebellar progenitors produces cerebellar hypoplasia and aberrant myoid differentiation without blocking medulloblastoma growth. https://doi.org/10.1101/2022.07.11.499567

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