IgA肾病患者核心1β3-半乳糖基转移酶基因编码区序列分析
The sequence analysis of core 1 β3-Galactosyltransferase gene coding region in IgA nephropathy
-
摘要: 目的: 测定核心1β3-半乳糖基转移酶基因的DNA序列,试图在IgA肾病(IgAN)患者中发现该基因编码区DNA序列的异常。方法: 应用双脱氧末端终止DNA测序技术,对核心1β3-半乳糖基转移酶基因外显子的PCR扩增产物进行直接测序,通过病例-对照研究方法,比较IgA肾病患者(50例)和正常对照(50例)之间核心1β3-半乳糖基转移酶基因组序列之间的差异。结果: 两者的核心1β3-半乳糖基转移酶基因编码区序列无差异。结论: 未发现IgA肾病患者有核心1β3-半乳糖基转移酶基因序列的异常,提示该基因编码区与IgA肾病患者IgA1的O-糖基化异常可能无关。Abstract: Objective: To sequence core 1 β3-Galactosyltransferase gene in order to sought an abnormality in coding region sequence of the sequence in IgA nephropathy(IgAN).Methods: We used dideoxy-sequencing of the PCR-amplified exons of core 1 β3-Galactosyltransferase gene to compare the sequences in IgA nephropathy(50 patients) and controls(50 persons). (Results: The) sequence of core 1 β3-Galactosyltransferase gene coding region was identical in IgAN and controls. Conclusion: We found no abnormality in coding region sequence of core 1 β3-galactosyltransferase gene, suggesting that this coding region probably not contribute to the decreased activity of core 1 β3-galactosyltransferase.
下载: