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Updated: Mar 31, 2026

Mapping the Structure-Function Relationships of Disordered Oncogenic Transcription Factors Using Transcriptomic Analysis
Published on: June 27, 2020
MEF2 transcription factors: developmental regulators and emerging cancer genes
Julia R Pon1, Marco A Marra1,2
1Canada's Michael Smith Genome Sciences Centre, BC Cancer Agency, Vancouver, Canada.
Abstract:
The MEF2 transcription factors have roles in muscle, cardiac, skeletal, vascular, neural, blood and immune system cell development through their effects on cell differentiation, proliferation, apoptosis, migration, shape and metabolism. Altered MEF2 activity plays a role in human diseases and has recently been implicated in the development of several cancer types. In particular, MEF2B, the most divergent and least studied protein of the MEF2 family, has a role unique from its paralogs in non-Hodgkin lymphomas. The use of genome-scale technologies has enabled comprehensive MEF2 target gene sets to be identified, contributing to our understanding of MEF2 proteins as nodes in complex regulatory networks. This review surveys the molecular interactions of MEF2 proteins and their effects on cellular and organismal phenotypes. We include a discussion of the emerging roles of MEF2 proteins as oncogenes and tumor suppressors of cancer. Throughout this article we highlight similarities and differences between the MEF2 family proteins, including a focus on functions of MEF2B.
Insights
Myocyte enhancer factor 2 (MEF2) transcription factors regulate cell development and metabolism. Dysregulated MEF2 activity contributes to human diseases, including various cancers, with MEF2B having unique roles in lymphomas.
Area of Science:
- Molecular Biology
- Genetics
- Cancer Research
Background:
- Myocyte enhancer factor 2 (MEF2) transcription factors are crucial regulators of cell differentiation, proliferation, apoptosis, migration, shape, and metabolism.
- These factors are involved in the development of multiple cell types, including muscle, cardiac, skeletal, vascular, neural, blood, and immune cells.
- Altered MEF2 activity is implicated in human diseases and has emerged as a factor in cancer development.
Purpose of the Study:
- To review the molecular interactions of MEF2 proteins and their impact on cellular and organismal phenotypes.
- To discuss the emerging roles of MEF2 proteins as oncogenes and tumor suppressors in cancer.
- To highlight similarities and differences among MEF2 family proteins, with a specific focus on MEF2B functions.
Main Methods:
- Survey of molecular interactions of MEF2 proteins.
- Analysis of MEF2 effects on cellular and organismal phenotypes.
- Review of genome-scale technologies for identifying MEF2 target gene sets.
Main Results:
- MEF2 proteins function as critical nodes in complex regulatory networks.
- MEF2B exhibits unique functions compared to its paralogs, particularly in non-Hodgkin lymphomas.
- Comprehensive MEF2 target gene sets have been identified, enhancing understanding of their regulatory roles.
Conclusions:
- MEF2 proteins play diverse roles in normal cellular development and are implicated in disease pathogenesis.
- The dual role of MEF2 proteins as oncogenes and tumor suppressors in cancer warrants further investigation.
- MEF2B's distinct functions highlight the need for family-specific analysis in understanding MEF2 roles in health and disease.
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