Abstract
Transcription factors are frequent cancer driver genes, exhibiting noted specificity based on the precise cell of origin. We demonstrate that ZIC1 exhibits loss-of-function (LOF) somatic events in group 4 (G4) medulloblastoma through recurrent point mutations, subchromosomal deletions and mono-allelic epigenetic repression (60% of G4 medulloblastoma). In contrast, highly similar SHH medulloblastoma exhibits distinct and diametrically opposed gain-of-function mutations and copy number gains (20% of SHH medulloblastoma). Overexpression of ZIC1 suppresses the growth of group 3 medulloblastoma models, whereas it promotes the proliferation of SHH medulloblastoma precursor cells. SHH medulloblastoma ZIC1 mutants show increased activity versus wild-type ZIC1, whereas G4 medulloblastoma ZIC1 mutants exhibit LOF phenotypes. Distinct ZIC1 mutations affect cells of the rhombic lip in diametrically opposed ways, suggesting that ZIC1 is a critical developmental transcriptional regulator in both the normal and transformed rhombic lip and identifying ZIC1 as an exquisitely context-dependent driver gene in medulloblastoma.
| Original language | English |
|---|---|
| Article number | 1749 |
| Pages (from-to) | 88-102 |
| Number of pages | 15 |
| Journal | Nature genetics |
| Volume | 57 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - Jan 2025 |
Keywords
- Animals
- Loss of Function Mutation
- Humans
- Medulloblastoma/genetics
- Gene Expression Regulation, Neoplastic
- Cell Line, Tumor
- Cerebellar Neoplasms/genetics
- Metencephalon/embryology
- Transcription Factors/genetics
- Mice
- Mutation
- Embryonic Structures
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