| Abstract: |
The miR-17 similar to 92 cluster family is composed of three members encoding microRNAs that share seed sequences. To assess their role in cerebellar and medulloblastoma (MB) development, we deleted the miR-17 similar to 92 cluster family in Nestin-positive neural progenitors and in mice heterozygous for the Sonic Hedgehog (SHH) receptor Patched 1 (Ptch1(+/-)). We show that mice in which we conditionally deleted the miR-17,92 cluster (miR-17 similar to 92(floxed/floxed); Nestin-Cre(+)) alone or together with the complete loss of the miR-106b similar to 25 cluster (miR-106b similar to 25(-/-)) were born alive but with small brains and reduced cerebellar foliation. Remarkably, deletion of the miR-17 similar to 92 cluster abolished the development of SHH-MB in Ptch1(+/-) mice. Using an orthotopic transplant approach, we showed that granule neuron precursors (GNPs) purified from the cerebella of postnatal day 7 (P7) Ptch1(+/-); miR-106b similar to 25(-/-) mice and overexpressing Mycn induced MBs in the cortices of naive recipient mice. In contrast, GNPs purified from the cerebella of P7 Ptch1(+/-); miR-17 similar to 92(floxed/floxed); Nestin-Cre(+) animals and overexpressing Mycn failed to induce tumors in recipient animals. Taken together, our findings demonstrate that the miR-17 similar to 92 cluster is dispensable for cerebellar development, but required for SHH-MB development. |
