文献类型：期刊文章

作　　者：王俊岭[1] 沈璐[1,2] 雷立芳[1,2] 徐倩[1] 周洁[1] 刘玉涛[1] 关文娟[1] 潘乾[3] 夏昆[3] 唐北沙[1,2,3] 江泓[1,2]

机构地区：[1]中南大学湘雅医院神经内科,长沙410008 [2]中南大学神经退行性疾病研究中心,长沙410008 [3]中国医学遗传学国家重点实验室,长沙410078

出　　处：《中南大学学报（医学版）》

基　　金：supported by Projects in the National Science and Technology Pillar Program in the Eleventh Five-year Plan Period(2006BAI05A07);National High-Tech Research and Development Program of China(863 Program)(2006AA02A408);Major State Basic Research Development Program of China(973 Program)(2006cb500700);National Key Technologies Research and Development Program of China(2004BA720A03);National Natural Science Foundation of China(30400262,30470619,30710303061,30871354,30971585);New Century Excellent Talents in University of Department of Education;Key Project of Natural Science Foundation of Hunan Province(08JJ3048);Graduate Degree Thesis Innovation Foundation of Central South University(2008yb030)

年　　份：2011

卷　　号：36

期　　号：6

起止页码：482-489

语　　种：中文

收录情况：BDHX、BDHX2008、CAS、CSCD、CSCD2011_2012、PUBMED、SCOPUS、ZGKJHX、核心刊

摘　　要：目的:了解中国大陆汉族人群常染色体显性遗传和散发脊髓小脑性共济失调(SCA)中最新基因频率分布。方法:采用聚合酶链反应(PCR)和DNA直接测序(DNA sequenc ing)方法对430例常染色体显性遗传SCA(AD-SCA)家系先证者和237例散发患者进行了SCA1,SCA2,SCA3/M JD,SCA6,SCA7,SCA8,SCA10,SCA12,SCA17亚型和齿状核红核苍白球路易体萎缩(DRPLA)亚型致病基因核苷酸重复突变检测分析,然后采用聚合酶链反应-变性高效液相色谱(PCR-DHPLC),多重连接探针扩增(MLPA)和DNA直接测序方法对91例排除了以上SCA亚型突变的ADCA家系先证者和196例散发患者进行了SCA5,SCA11,SCA13,SCA14,SCA15/16/29,SCA27,SCA31和SCA35亚型的点突变及插入缺失突变检测。结果:在430个AD-SCA家系中,发现有25个SCA1家系(5.81%)、27个SCA2家系(5.81%)、267个SCA3/M JD家系(62.09%)、8个SCA6家系(1.86%)、8个SCA7家系(1.86%)、1个SCA12家系(0.23%)、1个SCA17家系(0.23%)和2个SCA35家系(0.47%),91个ADCA家系未明确基因分型(21.16%);在237例散发SCA患者中,发现有6例SCA1患者(2.53%)、9例SCA2患者(3.80%)、23例SCA3/M JD患者(9.70%)和3例SCA6患者(1.27%),196例SCA患者未明确基因分型(82.7%);未发现SCA8,SCA10和DRPLA亚型核苷酸重复突变和SCA5,SCA11,SCA13,SCA14,SCA15/16/29,SCA27和SCA31亚型点突变或插入缺失突变。结论:在中国汉族人群中SCA3/M JD为最常见的SCA亚型,其次为SCA2,SCA1,SCA6和SCA7亚型,SCA12,SCA17和SCA35亚型比较少见,SCA5,SCA8,SCA10,SCA11,SCA13,SCA14,SCA15/16/29,SCA27,SCA31和DRPLA亚型罕见。在AD-CA家系和散发患者中存在一定比例基因型暂不明的病例,说明SCA的遗传异质性,可能是由于部分ADCA家系存在其他致病基因的作用,大部分散发SCA患者除遗传因素外还存在其他致病因素。

关 键 词：脊髓小脑性共济失调 核苷酸重复  点突变 基因突变分析

分 类 号：R744]