4.5 Article

ERK-regulated differential expression of the Mitf 6a/b splicing isoforms in melanoma

Journal

PIGMENT CELL & MELANOMA RESEARCH
Volume 23, Issue 1, Pages 93-102

Publisher

WILEY
DOI: 10.1111/j.1755-148X.2009.00652.x

Keywords

Mitf; melanoma; splice-form; MAPKinase pathway

Funding

  1. Ligue National contre le Cancer - Comites Departementaux du Grand Ouest
  2. Marie Curie Cancer Care
  3. CNRS
  4. MRE

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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.

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