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作 者:周雅[1] 孙维[1] 肖冰[1] 韩旭[1] 龙飞[1] 蒋雯婷[1] 季星[1] 陶炯[1]
机构地区:[1]上海交通大学医学院附属新华医院,上海市儿科医学研究所,200092
出 处:《中华医学遗传学杂志》2011年第4期401-405,共5页Chinese Journal of Medical Genetics
基 金:上海市教委曙光计划项目(06SG21);上海市浦江人才计划项目(05PJ14062);上海市自然科学基金(10ZR1424500);上海市卫生局青年科研项目(2009Y113)
摘 要:目的通过优化PCR并结合毛细管电泳,建立高扩增效率、高分辨率的FMR1基因CGG重复序列异常扩增检测体系。方法选择标准样本和经Southern印迹技术确定(CGG)n的正常、前突变、全突变男性和女性样本15例,进行PCR检测体系的优化。优化的PCR扩增产物经琼脂糖凝胶电泳、聚丙烯酰胺凝胶电泳和毛细管电泳等多种方法进行结果比较。结果经优化的PCR体系可以检测出(CGG)n大于260个拷贝的全突变男性和(CGG)n达到183个拷贝的前突变女性。毛细管电泳能够清晰分辨出相差1个CGG的两个等位基因,结果具有良好的可重复性。结论该PCR检测体系大幅度提高了普通PCR方法的扩增效率和分辨率,明显降低了对于Southern印迹技术的依赖,可以作为临床筛查FMR1基因突变的首选方法。Objective To develop an efficient, high resolution PCR assay suitable for detection of the (CGG)n repeats of the fragile X mental retardation 1 (FMR1)gene by optimizing the PCR system in combination with capillary electrophoresis. Methods Three standard samples and twelve samples that were verified by Southern blot analysis including both male and female in the normal, pre- and full mutation range were used in this study to evaluate the enhanced PCR system. All amplicons were electrophoresed by agarose, polyacrylamide and capillary electrophoresis to compare the results. Results The enhanced PCR assay developed in this study was able to detect a full mutation with (CGG)n being larger than 260 repeats in a male. An expanded premutation allele with (CGG)n as large as 183 repeats in a female was also amplified. The capillary eleetrophoresis method used in this study was able to distinguish two alleles with 1 CGG repeat difference and the results were reproducible. Conclusion A high resolution PCR assay is developed, which is much more efficient than the general PCR systems. It is suitable for the clinical screening of FMR1 gene and will greatly reduce the number of Southern blot analysis needed in clinical application.
关 键 词:脆性X综合征 FMR1基因 CGG重复序列 聚合酶链反应 毛细管电泳
分 类 号:R749.94[医药卫生—神经病学与精神病学]
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