Department of Dermatology, Yamagata University School of Medicine, Yamagata, Japan.
J Dermatol Sci. 2011 Dec;64(3):217-22. doi: 10.1016/j.jdermsci.2011.09.005. Epub 2011 Sep 24.
Oculocutaneous albinism (OCA) type 3 caused by mutations of the TYRP1 gene is an autosomal recessive disorder of pigmentation characterized by reduced biosynthesis of melanin pigment in the skin, hair, and eye. The clinical phenotype has been reported as mild in Caucasian OCA3 patients.
We had the opportunity to examine a Japanese girl with OCA3 and investigated activity of TYRP1 protein derived from the mutant allele detected in the patient.
Mutation search for OCA responsible genes was done. A mutant allele with a missense mutation was analyzed using melanocyte cultures (b cells) established from a mouse model of OCA3.
Compound heterozygous mutations, p.C30R and p.367fsX384, were detected in the Japanese girl. Then we revealed that the missense mutation, p.C30R, was functionally incapable of melanin synthesis with in vitro experiments.
This is the first report of the occurrence of OCA3 in Japanese population.
TYRP1 基因突变导致的眼皮肤白化病 3 型(OCA3)是一种常染色体隐性色素沉着紊乱疾病,其特征是皮肤、头发和眼睛中黑色素的生物合成减少。据报道,白种人 OCA3 患者的临床表型为轻度。
我们有机会检查了一位日本女孩的 OCA3,并研究了从患者中检测到的突变等位基因衍生的 TYRP1 蛋白的活性。
对 OCA 相关基因进行突变搜索。使用从 OCA3 小鼠模型中建立的黑素细胞培养物(b 细胞)分析具有错义突变的突变等位基因。
在日本女孩中检测到复合杂合突变 p.C30R 和 p.367fsX384。然后,我们通过体外实验揭示了错义突变 p.C30R 无法进行黑色素合成。
这是日本人群中 OCA3 发生的首例报告。