ASCL1 is a MYCN- and LMO1-dependent member of the adrenergic neuroblastoma core regulatory circuitry

Author:

Wang Lu,Tan Tze KingORCID,Durbin Adam D.ORCID,Zimmerman Mark W.ORCID,Abraham Brian J.ORCID,Tan Shi Hao,Ngoc Phuong Cao ThiORCID,Weichert-Leahey Nina,Akahane KoshiORCID,Lawton Lee N.,Rokita Jo LynneORCID,Maris John M.,Young Richard A.ORCID,Look A. Thomas,Sanda TakaomiORCID

Abstract

AbstractA 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.

Funder

U.S. Department of Health & Human Services | NIH | National Cancer Institute

National Research Foundation Singapore

Ministry of Education - Singapore

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

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