Related Experiment Video
Updated: Jun 21, 2026

Identification of MyoD Interactome Using Tandem Affinity Purification Coupled to Mass Spectrometry
Published on: May 17, 2016
Regulation of myocardin-related transcriptional coactivators through cofactor interactions in differentiation and
Dominique T Brandt1, Jianming Xu, Herbert Steinbeisser
1Institute of Pharmacology, University of Heidelberg, Heidelberg, Germany. robert.grosse@pharma.uni-heidelberg.de
Abstract:
Transcriptional signaling networks are orchestrated and fine-tuned through multiple interactions of transcription factors with subsets of cofactors thereby assembling multiprotein complexes to negatively or positively balance transcriptional output. These mechanisms account for the large diversity of target genes but also for time and tissue specific gene regulations through single transcription factors such as SRF. One family of SRF coactivators that has attracted much attention is represented by the myocardin-related transcription factors (MRTFs). MRTFs themselves are controlled through interactions with a growing number of cofactors and transcriptional regulators. We recently identified SCAI (suppressor of cancer cell invasion), which can associate with MAL (MRTF-A) to modulate invasive cancer cell migration through regulation of beta1-integrin expression and function. However, SCAI is likely to have additional functions depending on the tissue environment and signaling program. Interestingly, SCAI not only inhibits MRTF-A but can also regulate the activities of other MRTFs such as myocardin, or the oncogenic OTT-MAL fusion protein. Thus, SCAI may act in very different conditions such as during cancer progression, development or cell differentiation.
Insights
The suppressor of cancer cell invasion (SCAI) protein interacts with myocardin-related transcription factors (MRTFs), including MAL (MRTF-A). SCAI influences cell migration and gene regulation in various conditions like cancer and development.
Area of Science:
- Molecular Biology
- Cell Biology
- Cancer Research
Background:
- Transcriptional regulation relies on transcription factors and cofactors forming complexes.
- Myocardin-related transcription factors (MRTFs) are key coactivators for transcription factors like SRF.
- The role of novel cofactors in modulating MRTF activity is an area of active investigation.
Purpose of the Study:
- To investigate the function of SCAI (suppressor of cancer cell invasion) as a regulator of MRTF activity.
- To determine the interaction between SCAI and MAL (MRTF-A) and its impact on cancer cell migration.
- To explore the broader roles of SCAI in different cellular contexts and with other MRTF family members.
Main Methods:
- Co-immunoprecipitation assays to confirm protein interactions.
- Analysis of gene expression related to beta1-integrin.
- Functional assays assessing cancer cell migration and invasion.
- Studies involving different MRTF family members and oncogenic fusion proteins.
Main Results:
- SCAI associates with MAL (MRTF-A).
- SCAI modulates invasive cancer cell migration by regulating beta1-integrin expression and function.
- SCAI can inhibit MAL (MRTF-A) and also regulate other MRTFs like myocardin and the OTT-MAL fusion protein.
Conclusions:
- SCAI is a versatile regulator with functions extending beyond MAL (MRTF-A) inhibition.
- SCAI plays a role in cancer cell migration and potentially in development and differentiation.
- Further research is warranted to elucidate the full spectrum of SCAI functions in diverse biological settings.
Related Concept Videos
Master Transcription Regulators
Master Transcription Regulators
Co-activators and Co-repressors
Co-activators and Co-repressors
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...
Covalently Linked Protein Regulators
These groups modify specific amino acids in a protein.

