| Literature DB >> 16357253 |
Rebecca L Lamason1, Manzoor-Ali P K Mohideen, Jason R Mest, Andrew C Wong, Heather L Norton, Michele C Aros, Michael J Jurynec, Xianyun Mao, Vanessa R Humphreville, Jasper E Humbert, Soniya Sinha, Jessica L Moore, Pudur Jagadeeswaran, Wei Zhao, Gang Ning, Izabela Makalowska, Paul M McKeigue, David O'donnell, Rick Kittles, Esteban J Parra, Nancy J Mangini, David J Grunwald, Mark D Shriver, Victor A Canfield, Keith C Cheng.
Abstract
Lighter variations of pigmentation in humans are associated with diminished number, size, and density of melanosomes, the pigmented organelles of melanocytes. Here we show that zebrafish golden mutants share these melanosomal changes and that golden encodes a putative cation exchanger slc24a5 (nckx5) that localizes to an intracellular membrane, likely the melanosome or its precursor. The human ortholog is highly similar in sequence and functional in zebrafish. The evolutionarily conserved ancestral allele of a human coding polymorphism predominates in African and East Asian populations. In contrast, the variant allele is nearly fixed in European populations, is associated with a substantial reduction in regional heterozygosity, and correlates with lighter skin pigmentation in admixed populations, suggesting a key role for the SLC24A5 gene in human pigmentation.Entities:
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Year: 2005 PMID： 16357253 DOI： 10.1126/science.1116238
Source DB: PubMed Journal: Science ISSN： 0036-8075 Impact factor: 47.728