MYCN
Identifiers
Aliases	MYCN, MODED, N-myc, NMYC, ODED, bHLHe37, v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog, MYCN proto-oncogene, bHLH transcription factor, MYCNsORF, MYCNsPEP
External IDs	OMIM: 164840; MGI: 97357; HomoloGene: 3922; GeneCards: MYCN; OMA:MYCN - orthologs
Gene location (Human) Chr. Chromosome 2 (human)[1] Band 2p24.3 Start 15,940,550 bp[1] End 15,947,007 bp[1]
Gene location (Mouse) Chr. Chromosome 12 (mouse)[2] Band 12 A1.1|12 6.14 cM Start 12,986,094 bp[2] End 12,991,915 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in ventricular zone embryo ganglionic eminence gonad placenta kidney tubule testicle middle temporal gyrus decidua Brodmann area 23 Top expressed in primitive streak epiblast hair follicle medial ganglionic eminence somite ventricular zone abdominal wall mandibular prominence maxillary prominence superior cervical ganglion More reference expression data BioGPS More reference expression data
Gene ontology Molecular function DNA binding protein dimerization activity DNA-binding transcription factor activity protein binding RNA polymerase II cis-regulatory region sequence-specific DNA binding DNA-binding transcription activator activity, RNA polymerase II-specific kinase binding DNA-binding transcription factor activity, RNA polymerase II-specific Cellular component chromatin nucleus nucleolus Biological process regulation of transcription, DNA-templated regulation of transcription by RNA polymerase II transcription, DNA-templated positive regulation of gene expression negative regulation of gene expression positive regulation of production of miRNAs involved in gene silencing by miRNA transcription by RNA polymerase II cartilage condensation positive regulation of mesenchymal cell proliferation positive regulation of cell population proliferation positive regulation of cell death lung development embryonic digit morphogenesis regulation of inner ear auditory receptor cell differentiation positive regulation of transcription, DNA-templated positive regulation of transcription by RNA polymerase II embryonic skeletal system morphogenesis negative regulation of astrocyte differentiation branching morphogenesis of an epithelial tube negative regulation of reactive oxygen species metabolic process Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 4613 18109 Ensembl ENSG00000134323 ENSMUSG00000037169 UniProt P04198 P03966 RefSeq (mRNA) NM_005378 NM_001293228 NM_001293231 NM_001293233 NM_008709 RefSeq (protein) NP_001280157 NP_001280160 NP_001280162 NP_005369 NP_032735 Location (UCSC) Chr 2: 15.94 – 15.95 Mb Chr 12: 12.99 – 12.99 Mb PubMed search [3] [4]
Wikidata
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N-myc proto-oncogene protein also known as N-Myc or basic helix-loop-helix protein 37 (bHLHe37), is a protein that in humans is encoded by the MYCN gene.

The MYCN gene is a member of the MYC family of transcription factors and encodes a protein with a basic helix-loop-helix (bHLH) domain. This protein is located in the cell nucleus and must dimerize with another bHLH protein in order to bind DNA.^[5] N-Myc is highly expressed in the fetal brain and is critical for normal brain development.^[6]

The MYCN gene has an antisense RNA, N-cym or MYCNOS, transcribed from the opposite strand which can be translated to form a protein product.^[7] N-Myc and MYCNOS are co-regulated both in normal development and in tumor cells, so it is possible that the two transcripts are functionally related.^[8] It has been shown that the antisense RNA encodes for a protein, named NCYM, that has originated de novo and is specific to human and chimpanzee. This NCYM protein inhibits GSK3b and thus prevents MYCN degradation. Transgenic mice that harbor human MYCN/NCYM pair often show neuroblastomas with distant metastasis, which are atypical for normal mice. Thus NCYM represents a rare example of a de novo gene that has acquired molecular function and plays a major role in oncogenesis.^[9]

Amplification and overexpression of N-Myc can lead to tumorigenesis. Excess N-Myc is associated with a variety of tumors, most notably neuroblastomas where patients with amplification of the N-Myc gene tend to have poor outcomes.^[10][11][12] MYCN can also be activated in neuroblastoma and other cancers through somatic mutation.^[13] Intriguingly, recent genome-wide H3K27ac profiling in patient-derived NB samples revealed four distinct SE-driven epigenetic subtypes, characterized by their own and specific master regulatory networks. Three of them are named after the known clinical groups: MYCN-amplified, MYCN non-amplified high-risk, and MYCN non-amplified low-risk NBs, while the fourth displays cellular features which resemble multipotent Schwann cell precursors. Interestingly, the cyclin gene CCND1 was regulated through distinct and shared SEs in the different subtypes, and, more importantly, some tumors showed signals belonging to multiple epigenetic signatures, suggesting that the epigenetic landscape is likely to contribute to intratumoral heterogeneity. ^[14]

N-Myc has been shown to interact with MAX.^[15][16]

N-Myc is also stabilized by aurora A which protects it from degradation.^[17] Drugs that target this interaction are under development, and are designed to change the conformation of aurora A. Conformational change in Aurora A leads to release of N-Myc, which is then degraded in a ubiquitin-dependent manner.^[18]

Being independent from MYCN/MAX interaction, MYCN is also a transcriptional co-regulator of p53 in MYCN-amplified neuroblastoma.^{[citation needed]} MYCN alters transcription of p53 target genes which regulate apoptosis responses and DNA damage repair in cell cycle. This MYCN-p53 interaction is through exclusive binding of MYCN to C-terminal domains of tetrameric p53. As a post-translational modification, MYCN binding to C-terminal domains of tetrameric p53 impacts p53 promoter selectivity and interferes other cofactors binding to this region.^[19]

• Myc

• MYCN+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)

This article incorporates text from the United States National Library of Medicine, which is in the public domain.