TY - JOUR
T1 - A Big Gene Linked to Small Eyes Encodes Multiple Mitf Isoforms
T2 - Many Promoters Make Light Work
AU - Yasumoto, Ken Ichi
AU - Amae, Shintaro
AU - Udono, Tetsuo
AU - Fuse, Nobuo
AU - Takeda, Kazuhisa
AU - Shibahara, Shigeki
PY - 1998/12
Y1 - 1998/12
N2 - Among more than 80 different loci related to mouse coat color, microphthalmia-associated transcription factor (Mitf) encoded at the mouse microphthalmia locus is one of the most exciting molecules that regulates the development and survival of many cell types, including melanocyte, retinal pigment epithelium (RPE), and mast cells. Mitf and its human homolog MITF consist of at least three isoforms, referred to as Mitf-A/MITF-A, the heart-type Mitf-H/MITF-H, and the melanocyte lineage-specific Mitf-M/MITF-M, respectively. These isoforms differ in the amino-terminal domains but share a transactivation domain and a basic helix-loop-helix and leucine-zipper structure that is required for DNA binding and dimerization. MITF-M is exclusively expressed in melanocytes and melanoma cells, but not in other cell types, including RPE cells. In contrast, MITF-A mRNA is widely expressed in many cell types. These three isoform mRNAs are possibly generated by differential usage of the gene promoters and by alternative splicing. We predict that the entire MITF gene spans about 200 kb of DNA. Like MITF-M, MITF-A is able to activate the two melanogenesis gene promoters, tyrosinase and tyrosinase-related protein 1. These results suggest that melanogenesis may be regulated by different MITF isoforms in melanocyte and RPE. Possible implications of the multiplicity in Mitf/MITF isoforms are discussed.
AB - Among more than 80 different loci related to mouse coat color, microphthalmia-associated transcription factor (Mitf) encoded at the mouse microphthalmia locus is one of the most exciting molecules that regulates the development and survival of many cell types, including melanocyte, retinal pigment epithelium (RPE), and mast cells. Mitf and its human homolog MITF consist of at least three isoforms, referred to as Mitf-A/MITF-A, the heart-type Mitf-H/MITF-H, and the melanocyte lineage-specific Mitf-M/MITF-M, respectively. These isoforms differ in the amino-terminal domains but share a transactivation domain and a basic helix-loop-helix and leucine-zipper structure that is required for DNA binding and dimerization. MITF-M is exclusively expressed in melanocytes and melanoma cells, but not in other cell types, including RPE cells. In contrast, MITF-A mRNA is widely expressed in many cell types. These three isoform mRNAs are possibly generated by differential usage of the gene promoters and by alternative splicing. We predict that the entire MITF gene spans about 200 kb of DNA. Like MITF-M, MITF-A is able to activate the two melanogenesis gene promoters, tyrosinase and tyrosinase-related protein 1. These results suggest that melanogenesis may be regulated by different MITF isoforms in melanocyte and RPE. Possible implications of the multiplicity in Mitf/MITF isoforms are discussed.
KW - Differentiation
KW - Melanocyte
KW - Microphthalmia
KW - Retinal Pigment epithelium
UR - http://www.scopus.com/inward/record.url?scp=0032248265&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0032248265&partnerID=8YFLogxK
U2 - 10.1111/j.1600-0749.1998.tb00491.x
DO - 10.1111/j.1600-0749.1998.tb00491.x
M3 - Review article
C2 - 9870544
AN - SCOPUS:0032248265
SN - 0893-5785
VL - 11
SP - 329
EP - 336
JO - Pigment Cell Research
JF - Pigment Cell Research
IS - 6
ER -