4.5 Article

Molecular analysis of common polymorphisms within the human Tyrosinase locus and genetic association with pigmentation traits

Journal

PIGMENT CELL & MELANOMA RESEARCH
Volume 27, Issue 4, Pages -

Publisher

WILEY-BLACKWELL
DOI: 10.1111/pcmr.12253

Keywords

tyrosinase; pigmentation; melanocyte; albinism; melanin

Funding

  1. Australian Cancer Research Foundation (ACRF)/Institute for Molecular Bioscience Dynamic Imaging Facility for Cancer Biology
  2. Australian Research Council (ARC) Discovery Project [DP1094964]
  3. National Institutes of Health (NIH)/National Cancer Institute [CA88363]
  4. National Health and Medical Research Council of Australia (NHMRC)
  5. Australian Research Council Linkage [LP LP110100121]
  6. Identitas USA Inc. within the framework of the international Visigen consortium
  7. NHMRC
  8. Australian Research Council [DP1094964, LP110100121] Funding Source: Australian Research Council

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We have compared the melanogenic activities of cultured melanocytes carrying two common TYR alleles as homozygous 192S-402R wild-type, heterozygous and homozygous variant. This includes assays of TYR protein, DOPAoxidase activity, glycosylation and temperature sensitivity of protein and DOPAoxidase levels. Homozygous wild-type strains on average had higher levels of TYR protein and enzyme activity than other genotypes. Homozygous 402Q/Q melanocytes produced significantly less TYR protein, displayed altered trafficking and glycosylation, with reduced DOPAoxidase. However, near wild-type TYR activity levels could be recovered at lower growth temperature. In a sample population from Southeast Queensland, these two polymorphisms were present on four TYR haplotypes, designated as WT 192S-402R, 192Y-402R and 192S-402Q with a double-variant 192Y-402Q of low frequency at 1.9%. Based on cell culture findings and haplotype associations, we have used an additive model to assess the penetrance of the ten possible TYR genotypes derived from the combination of these haplotypes.

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