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    Please use this identifier to cite or link to this item: http://asiair.asia.edu.tw/ir/handle/310904400/16305


    Title: Analysis of ERCC2/XPD functional polymorphisms in systemic lupus erythematosus.
    Authors: 萬磊;Lei Wan;林應如;Ying-Ju Lin;許晉銓;Jinn-Chyuan Sheu;黃春明;Chung-Ming Huang;蔡育勳;Yuhsin Tsai;蔡長海;Chang-Hai Tsai;Wong W;蔡輔仁;Fuu-Jen Tsai
    Contributors: 生物科技學系
    Date: 2009-02
    Issue Date: 2012-11-23 17:11:14 (UTC+8)
    Abstract: Sunlight/ultraviolet (UV) irradiation has been recognized as an important risk factor for developing systemic lupus erythematosus (SLE). However, the interpretation of genetic variations involved in UV-light sensitivity is largely unknown. Recent studies indicated that two genetic variations of ERCC2/XPD gene (rs1799793 in exon 10 and rs13181 in exon 23) have been found to exert negative influences on nucleotide excision repair system. To analyse the possible contribution of the ERCC2/XPD functional single nucleotide polymorphisms in genetic susceptibility to SLE, the rs13181 and rs1799793 SNPs in ERCC2/XPD were genotyped by polymerase chain reaction followed by restriction fragment length polymorphism analysis. Association was studied by case-control analyses using samples from 172 SLE patients and 160 healthy controls. Haplotype analysis was performed to detect the association with genetic predisposition to SLE and the clinical features. Although these two functional genetic variations are linked to several immune dysfunction-induced diseases, no statistically significant differences in allele or genotype frequencies were observed between SLE patients and controls. Haplotype analysis showed that none of ERCC2/XPD haplotypes was associated with the incidence of SLE disease, nor the preference of clinical features. In conclusion, the ERCC2/XPD functional polymorphisms analysed in this study showed no association in genetic susceptibility to SLE.
    Relation: International Journal of Immunogenetics,36(1):33-37.
    Appears in Collections:[生物科技學系] 期刊論文

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