Expression of genes for microphthalmia isoforms, Pax3 and MSG1, in human melanomas
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Microphthalmia (MITF) gene product, a transcription factor of the basic-helix-loop-helix type, is thought to play a role in the regulation of genes encoding the enzymes necessary for melanogenesis. These include tyrosinase, TRP-1 and TRP-2. Melanocyte-specific isoform of microphthalmia, MITF-M, is expressed in normal and malignant melanocytes. The presence of two other isoforms of microphthalmia, MITF-A and MITF-H, which differ from MITF-M in the amino-terminus, was demonstrated also in some non-melanocytic lineages. Here we have analyzed the presence of all three known isoforms of MITF mRNA in a panel of 17 human melanoma cell lines by a reverse transcriptase-polymerase chain reaction using isoform-specific primers. While, as expected, the predominant form in melanoma cell lines was MITF-M, low amounts of MITF-A mRNA was found in almost all melanomas, as well as in most of 20 tumor cell lines of the non-melanocyte origin (lung and colon carcinomas, osteosarcomas and neuroblastomas). The expression of MITF-H was not detected, with a few exceptions, in the tested cell lines. Pax3 transcription factor was reported earlier to regulate positively the melanocyte-specific promoter of the MITF gene. We found here that the Pax 3 mRNA was expressed in all melanoma cell lines, even in those that had repressed the MITF-M and were amelanotic. This suggests that additional factors, besides Pax3, are required for the MITF expression. The MSG1 (melanocyte-specific gene 1), a gene originally isolated from melanocytes and containing a strong transcription activation domain, was also found expressed in all melanomas and most non-melanocyte tumor cell lines. Together, these data indicate that the MITF-M isoform is the major type of MITF mRNA present in human melanoma cell lines and show that the expression of the isoform MITF-A and the MSG1 is not restricted to malignant melanocytes and occurs in a wide range of tumor cell lines.
- MeSH
- DNA vazebné proteiny biosyntéza genetika MeSH
- lidé MeSH
- melaniny biosyntéza MeSH
- melanocyty metabolismus MeSH
- melanom genetika metabolismus MeSH
- messenger RNA biosyntéza MeSH
- nádorové buňky kultivované metabolismus MeSH
- nádorové kmenové buňky metabolismus MeSH
- nádorové proteiny biosyntéza genetika MeSH
- nádory metabolismus patologie MeSH
- polymerázová řetězová reakce s reverzní transkripcí MeSH
- protein - isoformy biosyntéza genetika MeSH
- regulace genové exprese u nádorů * MeSH
- RNA nádorová biosyntéza MeSH
- slinné proteiny a peptidy biosyntéza genetika MeSH
- transkripční faktor PAX3 MeSH
- transkripční faktor spojený s mikroftalmií MeSH
- transkripční faktory paired box MeSH
- transkripční faktory * MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Názvy látek
- DNA vazebné proteiny MeSH
- melaniny MeSH
- messenger RNA MeSH
- MITF protein, human MeSH Prohlížeč
- nádorové proteiny MeSH
- PAX3 protein, human MeSH Prohlížeč
- Pax3 protein, mouse MeSH Prohlížeč
- protein - isoformy MeSH
- RNA nádorová MeSH
- slinné proteiny a peptidy MeSH
- Smr3a protein, mouse MeSH Prohlížeč
- transkripční faktor PAX3 MeSH
- transkripční faktor spojený s mikroftalmií MeSH
- transkripční faktory paired box MeSH
- transkripční faktory * MeSH