斑马鱼
黑素体
生物
等位基因
杂合子丢失
遗传学
突变体
外显子
基因
细胞生物学
黑色素
作者
Rebecca L. Lamason,Manzoor-Ali P.K. Mohideen,Jason R. Mest,Andrew C. Wong,Heather 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 Makałowska,Paul McKeigue,David O’Donnell,Rick A. Kittles,Esteban J. Parra
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2005-12-15
卷期号:310 (5755): 1782-1786
被引量:1049
标识
DOI:10.1126/science.1116238
摘要
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.
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