Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2003-5-19
pubmed:abstractText
Recent population studies have demonstrated an association with the red-hair and fair-skin phenotype with variant alleles of the melanocortin-1 receptor (MC1R) which result in amino acid substitutions within the coding region leading to an altered receptor activity. In particular, Arg151Cys, Arg160Trp and Asp294His were the most commonly associated variants seen in the south-east Queensland population with at least one of these alleles found in 93% of those with red hair. In order to study the individual effects of these variants on melanocyte biology and melanocytic pigmentation, we established a series of human melanocyte strains genotyped for the MC1R receptor which included wild-type consensus, variant heterozygotes, compound heterozygotes and homozygotes for Arg151Cys, Arg160Trp, Val60Leu and Val92Met alleles. These strains ranged from darkly pigmented to amelanotic, with all strains of consensus sequence having dark pigmentation. UV sensitivity was found not to be associated with either MC1R genotype or the level of pigmentation with a range of sensitivities seen across all genotypes. Ultrastructural analysis demonstrated that while consensus strains contained stage IV melanosomes in their terminal dendrites, Arg151Cys and Arg160Trp homozygote strains contained only stage II melanosomes. This was despite being able to show expression of tyrosinase and tyrosinase-related protein-1 markers, although at reduced levels and an ability to convert exogenous 3,4-dihydroxyphenyl-alanine (DOPA) to melanin in these strains.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0893-5785
pubmed:author
pubmed:issnType
Print
pubmed:volume
16
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
198-207
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:12753386-Alleles, pubmed-meshheading:12753386-Antigens, pubmed-meshheading:12753386-Arginine, pubmed-meshheading:12753386-Cell Survival, pubmed-meshheading:12753386-Cells, Cultured, pubmed-meshheading:12753386-Cystine, pubmed-meshheading:12753386-DNA, pubmed-meshheading:12753386-Dihydroxyphenylalanine, pubmed-meshheading:12753386-Genetic Markers, pubmed-meshheading:12753386-Genotype, pubmed-meshheading:12753386-Heterozygote, pubmed-meshheading:12753386-Homozygote, pubmed-meshheading:12753386-Humans, pubmed-meshheading:12753386-Male, pubmed-meshheading:12753386-Melanins, pubmed-meshheading:12753386-Melanocytes, pubmed-meshheading:12753386-Melanoma, pubmed-meshheading:12753386-Melanosomes, pubmed-meshheading:12753386-Microscopy, Electron, pubmed-meshheading:12753386-Microscopy, Fluorescence, pubmed-meshheading:12753386-Monophenol Monooxygenase, pubmed-meshheading:12753386-Phenotype, pubmed-meshheading:12753386-Pigmentation, pubmed-meshheading:12753386-Tryptophan, pubmed-meshheading:12753386-Ultraviolet Rays, pubmed-meshheading:12753386-alpha-MSH
pubmed:year
2003
pubmed:articleTitle
Screening of human primary melanocytes of defined melanocortin-1 receptor genotype: pigmentation marker, ultrastructural and UV-survival studies.
pubmed:affiliation
Queensland Radium Institute Research Unit, Queensland Institute of Medical Research, Herston, Brisbane, Queensland, Australia.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't