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作 者:王志刚[1,2] 李媛媛[2] 刘卓[2] 欧阳胜荣[2] 常会波[2] 吴建新[2]
机构地区:[1]北京协和医学院研究生院,北京100730 [2]首都儿科研究所生化研究室,北京100020
出 处:《现代生物医学进展》2011年第24期4861-4863,4848,共4页Progress in Modern Biomedicine
基 金:国家重点基础发展规划项目(973项目)(2007CB511903);国家自然科学基金(30671156);北京市自然科学基金(5072014)
摘 要:目的:通过对脊柱裂(spina bifida)胚胎脑组织中微卫星不稳定性(microsatellite instability,MSI)的分析,探讨遗传不稳定性是否为此疾病的特征之一,进而研究错配修复系统(mismatch repair,MMR)与脊柱裂发病的分子机制。方法:19例脊柱裂和19例非神经管畸形对照脑组织中提取DNA;尿素变性凝胶电泳法检测标本中MSI发生情况。结果:在19例脊柱裂脑组织中9例MSI阳性,阳性率47.4%。其中2例为高度微卫星不稳定(high frequency microsatellite instability,MSI-H),7例为低度微卫星不稳定(lowfrequency microsatellite instability,MSI-L),其余10例为微卫星稳定(microsatellite stable,MSS),对照组中未出现MSI。选择的5个微卫星位点MSI的阳性率分别为Bat34C4(10.5%)、Bat26(26.5%)、D2S123(10.5%)、D3S1611(5.3%),D2S119(5.3%)。结论:脊柱裂中存在MSI现象,提示MSI、错配修复系统可能与脊柱裂的发生有一定关系。Objective: To investigate microsatellite instability(MSI) in fetuses with spina bifida and explore whether genetic insta-bility is a feature of this disease,and to study the molecular mechanism between mismatch repair(MMR) and the occurrence of spina bifi-da.Methods: DNA was extracted from 19 cases of spina bifida and the control group.PCR-urea denaturing polyacrylamide gel elec-trophoresis was used to analyze MSI.Results: Of 19 cases of spina bifida,9 with MSI(47.4%),2 with MSI-H,7 with MSI-L and 10 with MSS.Positive cases of five microsatellite loci were 2 for Bat34C4(10.5%),5 for Bat26(26.5%),2 for D2S123(10.5%),1 for D3S1611(5.3%) and 1 for D2S119(5.3%) respectively.No MSI was found in normal group.Conclusion: The high incidence of MSI was found in fetuses with spina bifida,which indicated that MSI and MMR may be correlated with the occurrence of spina bifida.
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