Related Experiment Video
Updated: Sep 27, 2025

Identification of MyoD Interactome Using Tandem Affinity Purification Coupled to Mass Spectrometry
Published on: May 17, 2016
Polycomb group ring finger protein 6 suppresses Myc-induced lymphomagenesis
Nina Tanaskovic1, Mattia Dalsass1, Marco Filipuzzi1
1European Institute of Oncology (IEO) - IRCCS, Milan, Italy.
Abstract:
Max is an obligate dimerization partner for the Myc transcription factors and for several repressors, such as Mnt, Mxd1-4, and Mga, collectively thought to antagonize Myc function in transcription and oncogenesis. Mga, in particular, is part of the variant Polycomb group repressive complex PRC1.6. Here, we show that ablation of the distinct PRC1.6 subunit Pcgf6-but not Mga-accelerates Myc-induced lymphomagenesis in Eµ-myc transgenic mice. Unexpectedly, however, Pcgf6 loss shows no significant impact on transcriptional profiles, in neither pre-tumoral B-cells, nor lymphomas. Altogether, these data unravel an unforeseen, Mga- and PRC1.6-independent tumor suppressor activity of Pcgf6.
Insights
Pcgf6, a subunit of Polycomb repressive complex PRC1.6, unexpectedly suppresses Myc-driven lymphomagenesis independently of Mga and PRC1.6. Its loss accelerates tumor development without altering transcriptional profiles.
Area of Science:
- Molecular Biology
- Cancer Research
- Epigenetics
Background:
- Max protein partners with Myc transcription factors and repressors like Mnt, Mxd1-4, and Mga.
- Mga is a component of the variant Polycomb repressive complex PRC1.6.
- PRC1.6 is implicated in antagonizing Myc's role in transcription and oncogenesis.
Purpose of the Study:
- To investigate the role of Pcgf6, a PRC1.6 subunit, in Myc-induced lymphomagenesis.
- To determine if Pcgf6's function is dependent on Mga or PRC1.6 in lymphomagenesis.
- To elucidate the tumor suppressor activity of Pcgf6.
Main Methods:
- Utilizing Eµ-myc transgenic mice to study lymphomagenesis.
- Ablation of the Pcgf6 gene in mice.
- Analysis of transcriptional profiles in pre-tumoral B-cells and lymphomas.
Main Results:
- Ablation of Pcgf6, but not Mga, accelerated Myc-induced lymphomagenesis.
- Pcgf6 loss did not significantly impact transcriptional profiles in B-cells or lymphomas.
- These findings suggest a novel tumor suppressor role for Pcgf6.
Conclusions:
- Pcgf6 exhibits an unexpected tumor suppressor activity.
- This tumor suppressor function of Pcgf6 is independent of Mga and PRC1.6.
- Pcgf6 represents a potential new target for cancer therapies.
More Related Videos
Related Concept Videos
Abnormal Proliferation
Induced Pluripotent Stem Cells
Somatic...
Master Transcription Regulators
Negative Regulator Molecules
Combinatorial Gene Control
The expression of more than 30,000 genes is controlled by approximately 2000-3000 transcription factors. This is possible because a single transcription factor can recognize more than one regulatory sequence. The specificity in gene...
Loss of Tumor Suppressor Gene Functions
When the tumor suppressor genes develop mutations or are lost, cells start growing out of control, leading to cancer. However, a single functional copy of the tumor suppressor gene is enough for the cells to maintain their normal functions and cell...

