Abstract
Group3 medulloblastoma (MB(G3)) that predominantly occur in young children are usually associated with MYC amplification and/or overexpression, frequent metastasis and a dismal prognosis. Physiologically relevant MB(G3) models are currently lacking, making inferences related to their cellular origin thus far limited. Using in utero electroporation, we here report that MB(G3) mouse models can be developed in situ from different multipotent embryonic cerebellar progenitor cells via conditional expression of Myc and loss of Trp53 function in several Cre driver mouse lines. The Blbp-Cre driver that targets embryonic neural progenitors induced tumors exhibiting a large-cell/anaplastic histopathology adjacent to the fourth ventricle, recapitulating human MB(G3). Enforced co-expression of luciferase together with Myc and a dominant-negative form of Trp53 revealed that GABAergic neuronal progenitors as well as cerebellar granule cells give rise to MB(G3) with their distinct growth kinetics. Cross-species gene expression analysis revealed that these novel MB(G3) models shared molecular characteristics with human MB(G3), irrespective of their cellular origin. We here developed MB(G3) mouse models in their physiological environment and we show that oncogenic insults drive this MB subgroup in different cerebellar lineages rather than in a specific cell of origin.