TY - JOUR
T1 - Downstream region of the human tyrosinase-related protein gene enhances its promoter activity
AU - Shibata, Koushi
AU - Takeda, Kazuhisa
AU - Tomita, Yasushi
AU - Tagami, Hachiro
AU - Shibahara, Shigeki
PY - 1992/4/30
Y1 - 1992/4/30
N2 - We have cloned and sequenced the human genomic DNA segments encoding the 5′-flanking region and the first two exons of the tyrosinase-related protein (TRP) gene, a pigment cell-specific gene. Functional analysis of its promoter suggests that the downstream region of the TRP gene, including the first intron, enhances the transient expression of the luciferase gene under control of the TRP gene promoter about 16- to 20-fold. This enhancer-like activity is detected not only in melanoma cells but also in HeLa cells whose TRP gene expression is assumed to be repressed. We suggest a possibility that the downstream region is not sufficient to confer pigment cell-specific expression, but is required for efficient transcription of the TRP gene in pigment cells.
AB - We have cloned and sequenced the human genomic DNA segments encoding the 5′-flanking region and the first two exons of the tyrosinase-related protein (TRP) gene, a pigment cell-specific gene. Functional analysis of its promoter suggests that the downstream region of the TRP gene, including the first intron, enhances the transient expression of the luciferase gene under control of the TRP gene promoter about 16- to 20-fold. This enhancer-like activity is detected not only in melanoma cells but also in HeLa cells whose TRP gene expression is assumed to be repressed. We suggest a possibility that the downstream region is not sufficient to confer pigment cell-specific expression, but is required for efficient transcription of the TRP gene in pigment cells.
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U2 - 10.1016/0006-291X(92)90627-W
DO - 10.1016/0006-291X(92)90627-W
M3 - Article
C2 - 1575733
AN - SCOPUS:0026752605
SN - 0006-291X
VL - 184
SP - 568
EP - 575
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 2
ER -