SEARCH

SEARCH BY CITATION

References

  • Arnheiter, H., Hou, L., Nguyen, M.T.T., Bismuth, K., Csermely, T., Murakami, H., Skuntz, S., Liu, W., and Bharti, K. (2006). Mitf – A matter of life and death for the developing melanocyte. In From Melanocytes to Malignant Melanoma, V.Hearing, and S.P.L.Leong, eds. (Totowa, NJ: Humana Press). pp 2749.
  • Bauer, G.L., Praetorius, C., Bergsteinsdottir, K. et al. (2009). The role of MITF phosphorylation sites during coat color and eye development in mice analyzed by bacterial artificial chromosome transgene rescue. Genetics 183, 581594.
  • Beechey, C.V., and Harrison, M.A. (1994). A new spontaneous W allele, W36H. Mouse Genome 92, 502.
  • Bharti, K., Liu, W., Csermely, T., Bertuzzi, S., and Arnheiter, H. (2008). Alternative promoter use in eye development: the complex role and regulation of the transcription factor MITF. Development (Cambridge, England) 135, 11691178.
  • Cheli, Y., Ohanna, M., Ballotti, R., and Bertolotto, C. (2010). Fifteen-year quest for microphthalmia-associated transcription factor target genes. Pigment Cell Melanoma Res. 23, 2740.
  • Diwakar, G., Zhang, D., Jiang, S., and Hornyak, T.J. (2008). Neurofibromin as a regulator of melanocyte development and differentiation. J. Cell Sci. 121, 167177.
  • Ebi, Y., Kasugai, T., Seino, Y., Onoue, H., Kanemoto, T., and Kitamura, Y. (1990). Mechanism of mast cell deficiency in mutant mice of mi/mi genotype: an analysis by co-culture of mast cells and fibroblasts. Blood 75, 12471251.
  • Gerstengarbe, S. (2003). . kenntnisreich, überlegt, kritisch gut veranlagt und von guter Darstellungsgabe – die Genetikerin Paula Hertwig. BIOspektrum 4/2003, 378380.
  • Grüneberg, H. (1948). Some observations on the microphthalmia gene in the mouse. J Genet 49, 113.
  • Hallsson, J.H., Haflidadottir, B.S., Stivers, C., Odenwald, W., Arnheiter, H., Pignoni, F., and Steingrimsson, E. (2004). The basic helix-loop-helix leucine zipper transcription factor Mitf is conserved in Drosophila and functions in eye development. Genetics 167, 233241.
  • Hemesath, T.J., Steingrimsson, E., McGill, G., Hansen, M.J., Vaught, J., Hodgkinson, C.A., Arnheiter, H., Copeland, N.G., Jenkins, N.A., and Fisher, D.E. (1994). microphthalmia, a critical factor in melanocyte development, defines a discrete transcription factor family. Genes Dev. 8, 27702780.
  • Hertwig, P. (1942). Neue Mutationen und Kopplungsgruppen bei der Hausmaus. Z. Indukt. Abstammungs- u. Vererbungsl. 80, 220246.
  • Hodgkinson, C.A., Moore, K.J., Nakayama, A., Steingrimsson, E., Copeland, N.G., Jenkins, N.A., and Arnheiter, H. (1993). Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein. Cell 74, 395404.
  • Hodgkinson, C.A., Nakayama, A., Li, H., Swenson, L.B., Opdecamp, K., Asher, J.H. Jr, Arnheiter, H., and Glaser, T. (1998). Mutation at the anophthalmic white locus in Syrian hamsters: haploinsufficiency in the Mitf gene mimics human Waardenburg syndrome type 2. Hum. Mol. Genet. 7, 703708.
  • Hoek, K.S., and Goding, C.R. (2010). Cancer stem cells versus phenotype-switching in melanoma. Pigment Cell Res. doi: 10.1111/j.1755-148X.2010.00757.x
  • Hollander, W.F. (1968). Complementary alleles at the mi-locus in the mouse. Genetics 60, 189.
  • Hou, L., Panthier, J.J., and Arnheiter, H. (2000). Signaling and transcriptional regulation in the neural crest-derived melanocyte lineage: interactions between KIT and MITF. Development (Cambridge, England) 127, 53795389.
  • Hughes, M.J., Lingrel, J.B., Krakowsky, J.M., and Anderson, K.P. (1993). A helix-loop-helix transcription factor-like gene is located at the mi locus. J. Biol. Chem. 268, 2068720690.
  • Karlsson, E.K., Baranowska, I., Wade, C.M. et al. (2007). Efficient mapping of mendelian traits in dogs through genome-wide association. Nat. Genet. 39, 13211328.
  • Konyukhov, B.V., and Osipov, V.V. (1968). Interallelic complementation of microphthalmia and white genes in mice. Genetika 4, 6576.
  • Kozmik, Z., Ruzickova, J., Jonasova, K. et al. (2008). Assembly of the cnidarian camera-type eye from vertebrate-like components. Proc. Natl. Acad. Sci. U S A 105, 89898993.
  • Lister, J.A., Robertson, C.P., Lepage, T., Johnson, S.L., and Raible, D.W. (1999). nacre encodes a zebrafish microphthalmia-related protein that regulates neural-crest-derived pigment cell fate. Development (Cambridge, England) 126, 37573767.
  • Liu, J.J., and Fisher, D.E. (2010). Lighting a path to pigmentation: mechanisms of MITF induction by UV. Pigment Cell Melanoma Res. doi: 10.1111/j.1755-148X.2010.00775.x
  • Mankoo, B.S., Skuntz, S., Harrigan, I., Grigorieva, E., Candia, A., Wright, C.V., Arnheiter, H., and Pachnis, V. (2003). The concerted action of Meox homeobox genes is required upstream of genetic pathways essential for the formation, patterning and differentiation of somites. Development (Cambridge, England) 130, 46554664.
  • Mochii, M., Ono, T., Matsubara, Y., and Eguchi, G. (1998). Spontaneous transdifferentiation of quail pigmented epithelial cell is accompanied by a mutation in the Mitf gene. Dev. Biol. 196, 145159.
  • Nakayama, A., Nguyen, M.T., Chen, C.C., Opdecamp, K., Hodgkinson, C.A., and Arnheiter, H. (1998). Mutations in microphthalmia, the mouse homolog of the human deafness gene MITF, affect neuroepithelial and neural crest-derived melanocytes differently. Mech. Dev. 70, 155166.
  • Nguyen, M., and Arnheiter, H. (2000). Signaling and transcriptional regulation in early mammalian eye development: a link between FGF and MITF. Development (Cambridge, England) 127, 35813591.
  • Opdecamp, K., Nakayama, A., Nguyen, M.T., Hodgkinson, C.A., Pavan, W.J., and Arnheiter, H. (1997). Melanocyte development in vivo and in neural crest cell cultures: crucial dependence on the Mitf basic-helix-loop-helix-zipper transcription factor. Development (Cambridge, England) 124, 23772386.
  • Opdecamp, K., Vanvooren, P., Riviere, M., Arnheiter, H., Motta, R., Szpirer, J., and Szpirer, C. (1998). The rat microphthalmia-associated transcription factor gene (Mitf) maps at 4q34-q41 and is mutated in the mib rats. Mamm. Genome 9, 617621.
  • Rehli, M., Den Elzen, N., Cassady, A.I., Ostrowski, M.C., and Hume, D.A. (1999). Cloning and characterization of the murine genes for bHLH-ZIP transcription factors TFEC and TFEB reveal a common gene organization for all MiT subfamily members. Genomics 56, 111120.
  • Skuntz, S., Mankoo, B., Nguyen, M.T., Hustert, E., Nakayama, A., Tournier-Lasserve, E., Wright, C.V., Pachnis, V., Bharti, K., and Arnheiter, H. (2009). Lack of the mesodermal homeodomain protein MEOX1 disrupts sclerotome polarity and leads to a remodeling of the cranio-cervical joints of the axial skeleton. Dev. Biol. 332, 383395.
  • Steel, K.P., Barkway, C., and Bock, G.R. (1987). Strial dysfunction in mice with cochleo-saccular abnormalities. Hear. Res. 27, 1126.
  • Steingrímsson, E. (2010). Interpretation of complex phenotypes: lessons from the Mitf gene. Pigment Cell Melanoma Res. doi: 10.1111/j.1755-148X.2010.00769.x
  • Steingrimsson, E., Arnheiter, H., Hallsson, J.H., Lamoreux, M.L., Copeland, N.G., and Jenkins, N.A. (2003). Interallelic complementation at the mouse Mitf locus. Genetics 163, 267276.
  • Steingrimsson, E., Copeland, N.G., and Jenkins, N.A. (2004). Melanocytes and the microphthalmia transcription factor network. Annu. Rev. Genet. 38, 365411.
  • Steingrímsson, E., Moore, K.J., Lamoreux, M.L. et al. (1994). Molecular basis of mouse microphthalmia (mi) mutations helps explain their developmental and phenotypic consequences [see comments]. Nat. Genet. 8, 256263.
  • Tachibana, M., Hara, Y., Vyas, D., Hodgkinson, C., Fex, J., Grundfast, K., and Arnheiter, H. (1992). Cochlear disorder associated with melanocyte anomaly in mice with a transgenic insertional mutation. Mol. Cell. Neurosci. 3, 433445.
  • Tachibana, M., Perez-Jurado, L.A., Nakayama, A., Hodgkinson, C.A., Li, X., Schneider, M., Miki, T., Fex, J., Francke, U., and Arnheiter, H. (1994). Cloning of MITF, the human homolog of the mouse microphthalmia gene and assignment to chromosome 3p14.1-p12.3. Hum. Mol. Genet. 3, 553557.
  • Tassabehji, M., Newton, V.E., and Read, A.P. (1994). Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene. Nat. Genet. 8, 251255.
  • Tomita, M., Itoh, H., Ishikawa, N., Higa, A., Ide, H., Murakumo, Y., Maruyama, H., Koga, Y., and Nawa, Y. (1995). Molecular cloning of mouse intestinal trefoil factor and its expression during goblet cell changes. Biochem J 311(Pt 1), 293297.
  • Tsujimura, T., Hashimoto, K., Morii, E., Tunio, G.M., Tsujino, K., Kondo, T., Kanakura, Y., and Kitamura, Y. (1997). Involvement of transcription factor encoded by the mouse mi locus (MITF) in apoptosis of cultured mast cells induced by removal of interleukin-3. Am. J. Pathol. 151, 10431051.
  • Weilbaecher, K.N., Hershey, C.L., Takemoto, C.M., Horstmann, M.A., Hemesath, T.J., Tashjian, A.H., and Fisher, D.E. (1998). Age-resolving osteopetrosis: a rat model implicating microphthalmia and the related transcription factor TFE3. J. Exp. Med. 187, 775785.
  • Wen, B., Chen, Y., Li, H. et al. (2010). Allele-specific genetic interactions between Mitf and Kit affect melanocyte development. Pigment Cell Melanoma Res. 23, 441447.
  • Wolfe, H.G., and Coleman, D.L. (1964). Mi-spotted: a mutation in the mouse. Genet. Res. Camb. 5, 432440.