A MAFG~MITF complex drives melanoma phenotype switching and progression

Phenotype switching, a key driver of melanoma progression and therapy resistance, is governed by the lineage transcription factor MITF. Here, we identify the small MAF family transcription factor MAFG as a critical regulator of MITF activity and melanoma cell state plasticity. MAFG expression is frequently elevated in melanoma and correlates with poor patient survival. Mechanistically, MAFG binds MITF and redirects its genomic occupancy, thereby modulating transcriptional programs governed by MITF. Genetic perturbation studies in vitro and in vivo show that MAFG promotes a dedifferentiated cell state and accelerates melanoma progression through its direct interaction with MITF. Moreover, MAFG is required for melanoma cell proliferation and for the transition from nevi to melanoma in genetic mouse models. Together, these findings demonstrate that the MAFG~MITF complex orchestrates phenotype switching and tumor progression, uncovering an unrecognized mechanism of MITF regulation in melanoma.

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Publication Details

Journal
Nature Communications
Published
2026-05-21
DOI
https://doi.org/10.1038/s41467-026-73291-x
Primary Topic
Melanoma and MAPK Pathways
Type
article
Field-Weighted Citation Impact
0.00

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article

A MAFG~MITF complex drives melanoma phenotype switching and progression

Michael B. Major, Jane L. Messina, Ilah Bok, Florian A. Karreth et al.
Nature Communications
Melanoma and MAPK Pathways
article

A MAFG~MITF complex drives melanoma phenotype switching and progression

Michael B. Major, Jane L. Messina, Ilah Bok, Florian A. Karreth, Benjamin Posorske, Nicol Mecozzi, Manon Chadourne, Michael Martinez, Kaizhen Wang, Zulaida Soto-Vargas, Harini Murikipudi, Sara Ruiz-Buceta, Kenneth Y Tsai, Eric K. Lau, Yumi Kim, Qian Liu, Inmaculada Ibanez de Caceres, Xiaoqing Yu, Juan D. Ulloa Arrieta, Ariana Angarita, Xiaonan Xu, Olga Vera
article en

Abstract

Phenotype switching, a key driver of melanoma progression and therapy resistance, is governed by the lineage transcription factor MITF. Here, we identify the small MAF family transcription factor MAFG as a critical regulator of MITF activity and melanoma cell state plasticity. MAFG expression is frequently elevated in melanoma and correlates with poor patient survival. Mechanistically, MAFG binds MITF and redirects its genomic occupancy, thereby modulating transcriptional programs governed by MITF. Genetic perturbation studies in vitro and in vivo show that MAFG promotes a dedifferentiated cell state and accelerates melanoma progression through its direct interaction with MITF. Moreover, MAFG is required for melanoma cell proliferation and for the transition from nevi to melanoma in genetic mouse models. Together, these findings demonstrate that the MAFG~MITF complex orchestrates phenotype switching and tumor progression, uncovering an unrecognized mechanism of MITF regulation in melanoma.

Nature Communications
Inserm (FR), Oregon Health & Science University (US), Washington University in St. Louis (US), University of South Florida (US), Hospital Universitario La Paz (ES), Moffitt Cancer Center (US), Hospital La Paz Institute for Health Research (ES), Centre Méditerranéen de Médecine Moléculaire (FR), Molecular Oncology (United States) (US), A.T. Still University (US)
American Cancer Society, Melanoma Research Foundation, Melanoma Research Alliance, Moffitt Cancer Center, European Commission, National Institutes of Health, Instituto de Salud Carlos III, European Regional Development Fund, National Cancer Institute
No poverty
Openalex Percentile: Top 8%
Melanoma and MAPK Pathways
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