基因6P21-22与白癜风易感性的研究

摘要

Objective To identify the disease-causing gene for vitiligo in 163 members of 38 Chinese Han family in Guangdong area. Methods The clinical data and peripheral blood samples were collected from patients with vitiligo and their family members. Genomic DNA was extracted from the blood samples. A genome-wide scan was performed using primers labelled with fluorescent stain. The sequencing results and microsatellite markers were analyzed by the Genescan and Genotype. Linkage analysis was conducted by the Linkage software to define the region of the disease-causing gene. Results The maximum linkage value was found at the disease-causing gene with microsatellite marker D6s289-D6S1584 ( NPL = 4.74, P= 0.000023, HLOD = 3.99, and α = 42％ ).Conclusion The susceptibily gene for vitiligo gene may locate at the chromosome 6P21-22 in Guangdong Han population.%目的 对收集的广东汉族白癜风38家系183人进行基因精细定位，以期识别白癜风的致病基因。方法 收集白癜风患者及其家系成员的临床资料及血液样本，抽提外周血基因组DNA,选用荧光标记引物及微卫星标记，用Genescan和Genotyper软件进行基因分型，用Linkage软件包进行连锁分析，明确致病基因的区域，并对6P21-22进行精细定位。结果 定位结果 发现白癜风致病基因与微卫星标记D6s289-D6S1584处获得最大连锁值(NPL=4.74,P=0.000023,HLOD=3.99,α=42％)。结论 染色体6P21-22上可能存在广东汉族人的白癜风易感基因。