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Transcriptomic analysis of adrenergic and mesenchymal neuroblastoma cells using RNA-sequencing

ABSTRACT: Transcriptomic analysis of adrenergic and mesenchymal neuroblastoma cells using RNA-sequencing

PROVIDER: PRJNA695580 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR13575171.fastq.gz	Fastqsanger.gz
	SRR13575172.fastq.gz	Fastqsanger.gz
	SRR13575173.fastq.gz	Fastqsanger.gz
	SRR13575174.fastq.gz	Fastqsanger.gz
	SRR13575175.fastq.gz	Fastqsanger.gz

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Genome-wide maps of chromatin state in adrenergic and mesenchymal neuroblastoma cells

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Project description:Childhood neuroblastomas exhibit plasticity between an undifferentiated neural crest-like “mesenchymal” cell state and a more differentiated sympathetic “adrenergic” cell state. These cell states are governed by autoregulatory transcriptional loops called core regulatory circuitries (CRCs), which drive the early development of sympathetic neuronal progenitors from migratory neural crest cells during embryogenesis. The adrenergic cell identity of neuroblastoma requires LMO1 as a transcriptional co-factor. Both LMO1 expression levels and the risk of developing neuroblastoma in children are associated with a single nucleotide polymorphism G/T that affects a GATA motif in the first intron of LMO1. Here we showed that wild-type zebrafish with the GATA genotype developed adrenergic neuroblastoma, while knock-in of the protective TATA allele at this locus reduced the penetrance of MYCN-driven tumors, which were restricted to the mesenchymal cell state. Whole genome sequencing of childhood neuroblastomas demonstrated that TATA/TATA tumors also exhibited a mesenchymal cell state and were low risk at diagnosis. Thus, conversion of the regulatory GATA to a TATA allele in the first intron of LMO1 reduced the neuroblastoma initiation rate by preventing formation of the adrenergic cell state, a mechanism that was conserved over 400 million years of evolution separating zebrafish and humans.

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