Nature Communications · 2019 · 99 citations · 37 references
Life SciencesGeneticsOncologyGene ExpressionGene RegulationTranscriptional RegulationGene-specific Transcriptional ControlMolecular NeurogeneticsMyc Family OncogenesOncogenic Signaling PathwaysTranscription Factor OncogenesTumor Suppressor GenesCo-transcriptional RegulationDevelopmental Regulatory ElementsDownstream Regulatory ElementsMyc In NeuroblastomaNeuroblastoma BiologyOncogene RegulationRegulatory SequencesRna Sequencing (Rna-seq)
A heritable polymorphism within regulatory sequences of the LMO1 gene is associated with its elevated expression and increased susceptibility to develop neuroblastoma, but the oncogenic pathways downstream of the LMO1 transcriptional co-regulatory protein are unknown. Our ChIP-seq and RNA-seq analyses reveal that a key gene directly regulated by LMO1 and MYCN is ASCL1, which encodes a basic helix-loop-helix transcription factor. Regulatory elements controlling ASCL1 expression are bound by LMO1, MYCN and the transcription factors GATA3, HAND2, PHOX2B, TBX2 and ISL1-all members of the adrenergic (ADRN) neuroblastoma core regulatory circuitry (CRC). ASCL1 is required for neuroblastoma cell growth and arrest of differentiation. ASCL1 and LMO1 directly regulate the expression of CRC genes, indicating that ASCL1 is a member and LMO1 is a coregulator of the ADRN neuroblastoma CRC.
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