| First Author | Grill C | Year | 2013 |
| Journal | Hum Mol Genet | Volume | 22 |
| Issue | 21 | Pages | 4357-67 |
| PubMed ID | 23787126 | Mgi Jnum | J:202281 |
| Mgi Id | MGI:5517771 | Doi | 10.1093/hmg/ddt285 |
| Citation | Grill C, et al. (2013) MITF mutations associated with pigment deficiency syndromes and melanoma have different effects on protein function. Hum Mol Genet 22(21):4357-67 |
| abstractText | The basic-helix-loop-helix-leucine zipper (bHLHZip) protein MITF (microphthalmia-associated transcription factor) is a master regulator of melanocyte development. Mutations in the MITF have been found in patients with the dominantly inherited hypopigmentation and deafness syndromes Waardenburg syndrome type 2A (WS2A) and Tietz syndrome (TS). Additionally, both somatic and germline mutations have been found in MITF in melanoma patients. Here, we characterize the DNA-binding and transcription activation properties of 24 MITF mutations found in WS2A, TS and melanoma patients. We show that most of the WS2A and TS mutations fail to bind DNA and activate expression from melanocyte-specific promoters. Some of the mutations, especially R203K and S298P, exhibit normal activity and may represent neutral variants. Mutations found in melanomas showed normal DNA-binding and minor variations in transcription activation properties; some showed increased potential to form colonies. Our results provide molecular insights into how mutations in a single gene can lead to such different phenotypes. |
