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Focus Formation: A Cell-based Assay to Determine the Oncogenic Potential of a Gene
Published on: December 31, 2014
The Myc/Max/Mad network and the transcriptional control of cell behavior
C Grandori1, S M Cowley, L P James
1Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109-1024, USA. cgrnador@fhcrc.org
Abstract:
The Myc/Max/Mad network comprises a group of transcription factors whose distinct interactions result in gene-specific transcriptional activation or repression. A great deal of research indicates that the functions of the network play roles in cell proliferation, differentiation, and death. In this review we focus on the Myc and Mad protein families and attempt to relate their biological functions to their transcriptional activities and gene targets. Both Myc and Mad, as well as the more recently described Mnt and Mga proteins, form heterodimers with Max, permitting binding to specific DNA sequences. These DNA-bound heterodimers recruit coactivator or corepressor complexes that generate alterations in chromatin structure, which in turn modulate transcription. Initial identification of target genes suggests that the network regulates genes involved in the cell cycle, growth, life span, and morphology. Because Myc and Mad proteins are expressed in response to diverse signaling pathways, the network can be viewed as a functional module which acts to convert environmental signals into specific gene-regulatory programs.
Insights
The Myc/Max/Mad network regulates gene expression for cell functions. This review explores how Myc and Mad proteins control transcription, impacting cell growth, differentiation, and death.
Area of Science:
- Molecular Biology
- Genetics
- Cell Biology
Background:
- The Myc/Max/Mad network is crucial for regulating gene transcription.
- These transcription factors control fundamental cellular processes like proliferation, differentiation, and apoptosis.
Purpose of the Study:
- To review the Myc and Mad protein families within the Myc/Max/Mad network.
- To correlate their biological functions with specific transcriptional activities and gene targets.
Main Methods:
- Literature review focusing on Myc and Mad proteins.
- Analysis of heterodimer formation with Max and DNA binding.
- Examination of coactivator/corepressor recruitment and chromatin modulation.
Main Results:
- Myc and Mad proteins form heterodimers with Max, binding to DNA.
- These complexes recruit coactivators or corepressors to alter chromatin structure and modulate transcription.
- Identified target genes are involved in cell cycle, growth, lifespan, and morphology.
Conclusions:
- The Myc/Max/Mad network acts as a signaling module, converting environmental cues into gene regulatory programs.
- Myc and Mad proteins play a central role in orchestrating cellular responses through transcriptional control.
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