脊髓小脑共济失调
三核苷酸重复扩增
遗传学
基因座(遗传学)
生物
中国人口
微卫星
分子生物学
共济失调
医学
等位基因
人口
基因
基因型
环境卫生
神经科学
作者
Junling Wang,Yun-qin Wu,Lifang Lei,Lu Shen,Hong Jiang,Yafang Zhou,Jiping Yi,Jie Zhou,Xinxiang Yan,Qian Pan,Kun Xia,Beisha Tang
出处
期刊:PubMed
日期:2010-10-01
卷期号:27 (5): 501-5
被引量:21
标识
DOI:10.3760/cma.j.issn.1003-9406.2010.05.006
摘要
To assist the establishment of platform and provide the reference standard for mutation detection in spinocerebellar ataxia (SCA) subtypes 1, 2, 3, 6, 7, 8, 10, 12, 17 and dentatorubral-pallidoluysian atrophy (DRPLA) in Chinese Han population.The nucleotide repeat numbers of the 9 SCA subtypes and DRPLA were detected using fluorescence-PCR and capillary gel electrophoresis technique in 300 healthy Chinese Han individuals.Among the 300 healthy controls, the range of the CAG trinucleotide repeat number was 17 to 35 in SCA1, 14-28 in SCA2, 13-41 in SCA3/MJD, 4-16 in SCA6, 5-17 in SCA7, 5-21 in SCA12, 23-41 in SCA17, and 12-33 in DRPLA; and the range of CTA/CTG trinucleotide repeat number on SCA8 locus was 12-43 and the range of ATTCT pentanucleotide repeat number on SCA10 locus was 9-32. Of which, the 12 CTA/CTG repeats of SCA8, 9 ATTCT repeats of SCA10, 23 CAG repeats of SCA17 were the shortest normal repeat number, while the 41 CAG repeats of SCA3/MJD, 32 CAG repeats of SCA10 were the largest normal number that have not been reported.The normal ranges of polynucleotide repeats of different subtypes of SCA vary with geographical areas and ethnicities. It might be associated with the genetic and ethnic backgrounds. This is the first normal reference standard of polynucleotide repeat number of these ten SCA subtypes in Chinese Han.
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