PUBLICATION

Expression analysis of a tyrosinase promoter sequence in zebrafish

Authors
Camp, E., Badhwar, P., Mann, G.J., and Lardelli, M.
ID
ZDB-PUB-030319-14
Date
2003
Source
Pigment cell research   16(2): 117-126 (Journal)
Registered Authors
Camp, Esther, Lardelli, Michael
Keywords
none
MeSH Terms
  • Animals
  • Base Sequence/genetics
  • E-Box Elements/genetics
  • Embryo, Nonmammalian/cytology
  • Embryo, Nonmammalian/embryology*
  • Embryo, Nonmammalian/enzymology
  • Gene Expression Regulation, Developmental/genetics*
  • Gene Expression Regulation, Enzymologic/genetics*
  • Genes, Regulator/genetics
  • Humans
  • Melanins/biosynthesis*
  • Melanocytes/enzymology
  • Melanoma/enzymology
  • Melanoma/genetics
  • Molecular Sequence Data
  • Monophenol Monooxygenase/genetics*
  • Pigment Epithelium of Eye/cytology
  • Pigment Epithelium of Eye/embryology*
  • Pigment Epithelium of Eye/enzymology
  • Promoter Regions, Genetic/genetics*
  • Transcription Initiation Site/physiology
  • Tumor Cells, Cultured/enzymology
  • Zebrafish/embryology*
  • Zebrafish/genetics
  • Zebrafish/metabolism
PubMed
12622788 Full text @ Pig. Cell Res.
Abstract
Sequence comparisons and functional analysis of the 5' upstream regions of tyrosinase genes have revealed the importance of cis-regulatory elements acting to control the spatiotemporal expression of tyrosinase in the melanocytes and retinal pigmented epithelium of developing embryos. To date there are no reports addressing the control of tyrosinase gene transcription in zebrafish, a vertebrate model organism of increasing importance. To exploit the tyrosinase gene as a marker in zebrafish we set out to clone its promoter and analyse its regulation during embryogenesis. Amplification of a zebrafish tyrosinase complementary DNA fragment by reverse transcriptase polymerase chain reaction allowed us to isolate and sequence a 1041 nt genomic DNA fragment that includes a transcription initiation site and 73 nt of the open reading frame. Bioinformatic analysis of this genomic sequence revealed five E-box motifs, including one CATGTG type E-box present in a putative initiation region. These are conserved positive regulatory elements in vertebrate tyrosinase promoters. We show that a region of 814 nt upstream from the translation start site of the zebrafish tyrosinase gene can drive expression in retinal pigmented epithelium in transiently transgenic zebrafish embryos but that its activity is not restricted to melanin-producing cells. This region is unable to drive transcription in human melanoma cell lines. Ectopic expression from this zebrafish tyrosinase promoter fragment is probably due to the absence of positive and negative cis-regulatory elements, such as a tyrosinase distal element, which is known to function as a pigment cell-specific enhancer.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping