摘要
目的探讨bcl-2、bcl-x和bax基因中7个多态位点同系统性红斑狼疮()是否存在SLE相关性。方法采用引物引入限制性内切酶分析(PIRA-PCR)、四引物扩增阻滞突变系统以及单链构象多态性(SSCP)技术,分析100名正常人和88例SLE患者bcl-2基因的3个单核苷酸多态性(SNP)位点(dbSNP:rs1800477,rs1801018,rs1564483)、bcl-x基因的3个SNP位点(dbSNP:rs6060900,rs6089046,rs5841091)及bax基因的1个微卫星位点。以Logistic回归分析统计实验数据。结果SLE患者组bcl-2基因rs1800477位点的GG基因型频率高于正常人群(P=0.013),rs1564483位点GG基因型频率则低于正常人群(P=0.024);rs1801018位点则无统计学意义。bcl-x和bax的所选位点均没有表现出多态性。结论bcl-2基因rs1800477和rs1564483两位点多态性可能与SLE相关。
Objective To explore the correlation of 7 polymorphism loci in bcl-2, bcl-x and bax genes with systemic lupus erythematosus (SLE). Method Primer-introduced restriction analysis PCR (PIRA-PCR), tetra-primers amplification refractory mutation system (ARMS) and single strand conformational polymorphism (SSCP) were applied to detect 3 single nuclear polymorphysm (SNP) loci in bcl-2 gene (dbSNP: rs1800477, rs1801018, rs1564483), 3 SNP loci (dbSNP: rs6060900, rs6089046, rs5841091) in bcl-x gene and a microsatellite in bax gene. Data was analysised with Logistic regression. Result In SLE cases, frequency of GG genotype of rs1800477 was higher than the healthy control (P=0.013) while that of GG genotype of rs1800477 was lower than controls(P=0.024), and rs1801018 had no significant difference between the two groups. But it seemed that the selected loci in bcl-x and bax genes had no polymorphism characteristics. Conclusion Two polymorphism loci, rs1800477 together with rs1564483, probablly correlate to SLE, although the latter lies out of the CDS region.
出处
《中华风湿病学杂志》
CAS
CSCD
2005年第5期265-268,共4页
Chinese Journal of Rheumatology
基金
美国纽约中华医学基金会资助项目(CMB98-675)
云南省自然科学基金资助项目(2000C009Z)