Characteristic sequences in the upstream region of the human tyrosinase gene

Author(s):  
Hideaki Kikuchi ◽  
Hirohito Miura ◽  
Hiroali Yamamoto ◽  
Takuji Takeuchi ◽  
Toshio Dei ◽  
...  
2012 ◽  
Vol 80 (6) ◽  
pp. 953-960
Author(s):  
Jiradej Manosroi ◽  
Narinthorn Khositsuntiwong ◽  
Friedrich Götz ◽  
Rolf G. Werner ◽  
Worapaka Manosroi ◽  
...  

1998 ◽  
Vol 16 ◽  
pp. S149
Author(s):  
Jun Matsunaga ◽  
Muneo Tanita ◽  
Miwako Dakeishi-Hara ◽  
Eriko Nakamura ◽  
Yoshinori Miyamura ◽  
...  

1994 ◽  
Vol 14 (12) ◽  
pp. 8058-8070 ◽  
Author(s):  
K Yasumoto ◽  
K Yokoyama ◽  
K Shibata ◽  
Y Tomita ◽  
S Shibahara

Tyrosinase is a rate-limiting enzyme in melanin biosynthesis and is specifically expressed in differentiated melanocytes. We have identified the enhancer element in the 5'-flanking region of the human tyrosinase gene that is responsible for its pigment cell-specific transcription and have termed it tyrosinase distal element (TDE) (positions -1861 to -1842). Transient expression assays showed that TDE confers efficient expression of a firefly luciferase reporter gene linked to the tyrosinase gene promoter in MeWo pigmented melanoma cells but not in HeLa cells, which do not express tyrosinase. TDE was specifically bound by nuclear proteins of MeWo and HeLa cells, the binding properties of which were indistinguishable in gel mobility shift assays. TDE contains the CATGTG motif in its center, and mutation analysis indicates that the CA dinucleotides of this motif are crucial for protein binding and pigment cell-specific enhancer function. The CATGTG motif is consistent with the consensus sequence recognized by a large family of transcription factors with a basic helix-loop-helix structure, which prompted us to examine the possible involvement of a ubiquitous transcription factor, USF, and a novel factor, microphthalmia-associated transcription factor (MITF), recently cloned as the human homolog of the mouse microphthalmia (mi) gene product. The mi phenotype is associated with a mutant mi locus and characterized by small eyes and loss of melanin pigments. Both USF and MITF are predicted to contain a basic helix-loop-helix structure and a leucine zipper structure. We provide evidence that USF binds to TDE, whereas we were unable to detect the DNA-binding activity of MITF. Transient coexpression assays showed that MITF specifically transactivates the promoter activity of the tyrosinase gene through the CATGTG motif of TDE but not the promoter of the ubiquitously expressed heme oxygenase gene, while USF is able to activate both promoters. These results indicate that MITF is a cell-type-specific factor that is capable of activating transcription of the tyrosinase gene.


2001 ◽  
Vol 46 (No. 7–8) ◽  
pp. 199-204 ◽  
Author(s):  
P. Pohlreich ◽  
J. Stříbrná ◽  
Z. Kleibl ◽  
V. Horák ◽  
J. Klaudy

Tyrosine, a key enzyme of melanin biosynthesis, is widely used as a specific marker for the detection of dissemination or metastatic melanoma cells in peripheral blood and other tissues like lymph node or bone marrow, which are normally tyrosinase negative. The amplification of tyrosinase-specific mRNA by means of RT-PCR is a sensitive technique capable of detecting a single tumour cell in 5&ndash;10 ml of whole blood. We have utilised this method to analyse the peripheral blood of laboratory miniature pigs with advanced cutaneous melanoma for the presence of tumor cells. This highly invasive hereditary malignancy can serve as an experimental model for the study of melanoma development and dissemination. For amplification of porcine gene, oligonucleotide primers derived from the sequence of human tyrosinase were used. These primers amplified fragment of the predicted length and restriction enzyme digestion confirmed their homology with the sequences of human tyrosinase gene. After the second round of amplification, tyrosinase could be detected up to the amount of 1 &times; 10<sup>&ndash;5</sup> &micro;g of total RNA isolated from porcine melanoma per 1 &micro;g of control RNA. Blood samples from eight animals with advanced melanoma and from five non-melanoma control animals were examined for tyrosinase expression. Tyrosinase mRNA was detected in five samples from animals with malignant melanoma. Non-melanoma control animals gave negative results.


1995 ◽  
Vol 15 (3) ◽  
pp. 1833-1833 ◽  
Author(s):  
K Yasumoto ◽  
K Yokoyama ◽  
K Shibata ◽  
Y Tomita ◽  
S Shibahara

2004 ◽  
Vol 14 (4) ◽  
pp. A5-A6
Author(s):  
A. Anichini ◽  
R. Mortarini ◽  
P. Baldassari ◽  
C. Carlo-Stella ◽  
A. Guidetti ◽  
...  

1995 ◽  
Vol 7 (1) ◽  
pp. 34
Author(s):  
Kyoung Chan Park ◽  
Kyu Han Kim

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