Micale Lucia, Augello Bartolomeo, Fusco Carmela, Turturo Maria Giuseppina, Granatiero Matteo, Piemontese Maria Rosaria, Zelante Leopoldo, Cecconi Antonella, Merla Giuseppe
Medical Genetics Unit, IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy.
Genet Test Mol Biomarkers. 2009 Aug;13(4):527-31. doi: 10.1089/gtmb.2009.0030.
X-linked ocular albinism type 1 (OA1) is caused by mutations in G protein-coupled receptor 143 (GPR143) gene, which encodes a membrane glycoprotein localized to melanosomes. GPR143 mainly affects pigment production in the eye, resulting in optic changes associated with albinism, including hypopigmentation of the retina, nystagmus, strabismus, foveal hypoplasia, abnormal crossing of the optic fibers, and reduced visual acuity. We report the mutational analysis of the GPR143 gene on two unrelated families with OA1 using direct sequencing and real-time quantitative polymerase chain reaction. We identified the c.564_565delCT, a 2-bp deletion in family 1, and we mapped the breakpoints at nucleotide level of the novel intragenic deletion g.5360_6371del1012, encompassing exon 2, in family 2. Our results confirm that GPR143 is the major locus for OA1 and that exon 2 is a region of high susceptibility to deletions. Finally, we emphasize the quantitative polymerase chain reaction as a valid tool for diagnosis of deletions in the GPR143 gene.
X连锁1型眼白化病(OA1)由G蛋白偶联受体143(GPR143)基因突变引起,该基因编码一种定位于黑素小体的膜糖蛋白。GPR143主要影响眼部色素生成,导致与白化病相关的视觉变化,包括视网膜色素减退、眼球震颤、斜视、黄斑发育不全、视神经纤维交叉异常以及视力下降。我们使用直接测序和实时定量聚合酶链反应对两个无关的OA1家系的GPR143基因进行了突变分析。我们在家族1中鉴定出c.564_565delCT,这是一个2碱基缺失;在家族2中,我们在核苷酸水平上定位了新的基因内缺失g.5360_6371del1012的断点,该缺失包含外显子2。我们的结果证实GPR143是OA1的主要基因座,外显子2是易发生缺失的高敏感区域。最后,我们强调定量聚合酶链反应是诊断GPR143基因缺失的有效工具。