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SOX11 regulates SWI/SNF complex components as member of the adrenergic neuroblastoma core regulatory circuitry.

Bieke DecaestekerAmber LouwaigeSiebe LoontiensFanny De VloedSarah-Lee BekaertJuliette RoelsSuzanne VanhauwaertSara De BrouwerEllen SandersAlla BerezovskayaGeertrui DeneckerEva D'haeneStéphane Van HaverWouter Van LoockeJo Van DorpeDavid CreytensNadine Van RoyTim PietersChristophe Van NesteMatthias FischerPieter Van VlierbergheStephen S RobertsJohannes Hubertus SchulteSara EkRogier VersteegJan KosterJohan van NesMark W ZimmermanKatleen De PreterFrank Speleman
Published in: Nature communications (2023)
The pediatric extra-cranial tumor neuroblastoma displays a low mutational burden while recurrent copy number alterations are present in most high-risk cases. Here, we identify SOX11 as a dependency transcription factor in adrenergic neuroblastoma based on recurrent chromosome 2p focal gains and amplifications, specific expression in the normal sympatho-adrenal lineage and adrenergic neuroblastoma, regulation by multiple adrenergic specific (super-)enhancers and strong dependency on high SOX11 expression in adrenergic neuroblastomas. SOX11 regulated direct targets include genes implicated in epigenetic control, cytoskeleton and neurodevelopment. Most notably, SOX11 controls chromatin regulatory complexes, including 10 SWI/SNF core components among which SMARCC1, SMARCA4/BRG1 and ARID1A. Additionally, the histone deacetylase HDAC2, PRC1 complex component CBX2, chromatin-modifying enzyme KDM1A/LSD1 and pioneer factor c-MYB are regulated by SOX11. Finally, SOX11 is identified as a core transcription factor of the core regulatory circuitry (CRC) in adrenergic high-risk neuroblastoma with a potential role as epigenetic master regulator upstream of the CRC.
Keyphrases
  • transcription factor
  • copy number
  • dna binding
  • genome wide identification
  • histone deacetylase
  • dna methylation
  • poor prognosis
  • gene expression
  • mitochondrial dna
  • stem cells
  • risk factors
  • binding protein