Alternative lengthening of telomeres in molecular subgroups of paediatric high-grade glioma.
Simone MinasiCaterina BaldiFrancesca GiannoManila AntonelliAnna Maria BuccolieroTorsten PietschMaura MassiminoFrancesca Romana ButtarelliPublished in: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery (2020)
Our results show a strong association between H3.3 mutations and ALT, and highlight the different telomeric profiles in histone-defined subgroups: H3.3-G34R mutants always trigger ALT to maintain telomere length, irrespective of ATRX status, whereas only some H3.3-K27M tumours activate ALT. These findings suggest that acquiring the gly34 mutation on H3.3 might suffice to trigger the ALT mechanism.