Related Experiment Video
Updated: Jun 18, 2026

Detection of Alternative Splicing During Epithelial-Mesenchymal Transition
Published on: October 9, 2014
ERK-regulated differential expression of the Mitf 6a/b splicing isoforms in melanoma
Aline Primot1, Ariane Mogha, Sébastien Corre
1CNRS-UMR6061, RTO-Team/Rennes-1 University, Rennes, France.
Abstract:
The master regulator of the melanocyte lineage Mitf is intimately involved in development as well as melanoma, controlling cell survival, differentiation, proliferation and metastasis/migration. Consistent with its central role, Mitf expression and Mitf post-translational modifications are tightly regulated. An additional potential level of regulation is afforded by differential splicing of Mitf exon-6 leading to the generation of two isoforms that differ by the presence of six amino-acids in the Mitf (+) isoform and which have differential effects on cell cycle progression. However, whether the ratio of the two isoforms is regulated and whether their expression correlates with melanoma progression is not known. Here, we show that the differential expression of the Mitf 6a/b isoforms is dependent on the MAPKinase signalling, being linked to the activation of MEK1-ERK2, but not to N-RAS/B-RAF mutation status. In addition, quantification of Mitf 6a/b splicing forms in 86 melanoma samples revealed substantially increased levels of the Mitf (-) form in a subset of metastatic melanomas. The results suggest that differential expression of the Mitf 6a/b isoforms may represent an additional mechanism for regulating Mitf function and melanoma biology.
Insights
Differential splicing of the Mitf gene creates two isoforms impacting cell cycle. Their ratio is regulated by MAPKinase signaling and altered levels of Mitf (-) correlate with metastatic melanoma progression.
Area of Science:
- Molecular biology
- Cancer research
- Cell biology
Background:
- The Mitf gene is a master regulator of melanocyte development and melanoma.
- Mitf controls crucial cellular processes including survival, differentiation, proliferation, and metastasis.
- Mitf expression and post-translational modifications are tightly regulated.
Purpose of the Study:
- To investigate the regulation of Mitf alternative splicing.
- To determine if Mitf isoform ratios correlate with melanoma progression.
Main Methods:
- Analysis of Mitf exon-6 splicing in melanoma cells.
- Correlation of Mitf isoform expression with MAPKinase signaling pathways (MEK1-ERK2, N-RAS/B-RAF).
- Quantification of Mitf 6a/b isoforms in 86 melanoma patient samples.
Main Results:
- Differential expression of Mitf 6a/b isoforms is regulated by MEK1-ERK2 signaling, independent of N-RAS/B-RAF mutation status.
- Increased levels of the Mitf (-) isoform were observed in a subset of metastatic melanomas.
- The ratio of Mitf 6a/b isoforms is not fixed and can be modulated.
Conclusions:
- Mitf alternative splicing represents a novel regulatory mechanism for Mitf function.
- Altered Mitf isoform expression may contribute to melanoma progression and metastasis.
- MAPKinase signaling plays a role in regulating Mitf alternative splicing.
Related Concept Videos
RNA Splicing
Master Transcription Regulators
Alternative RNA Splicing
There are five types of alternative RNA splicing that vary in the ways the pre-mRNA segments are removed or retained in the mature mRNA. The first...

