摘要
目的研究非综合征型耳聋（nonsyndromic hearing loss，NSHL）患者SLC26A4基因的突变情况，为临床上NSHL患者基因诊断提供指导。方法PCR分别扩增SLC26A4基因的21个外显子及其侧翼序列，所得目的片段用变性高效液相色谱（denaturing high—performance liquid chromatorgraphy,DHPLC）进行突变筛查，有异常峰形的样本进行DNA测序。结果在所选30例无血缘关系且GJB2基因检测未发现突变的NSHL患者中，共检测出10种SLC26A4基因变异，其中包括7种已知突变，2种未见报道的新突变（F572L和D87Y），及一种已知多态（Ivs11＋47T〉C），其中Ivs7—2A〉G是最常见的突变，约占总突变的40％。结论SLC26A4基因为仅次于GJB2的导致NSHL的相关基因，在GJB2基因检测未发现突变的NSHL人群中SLC26A4基因的检出率达到23．3％，其中Ivs7—2A〉G是其最常见的突变。
Objective To study the SLC26A4 gene mutations in patients with nonsyndromic hearing loss （NSHL） and provide the clinical guidance of gene diagnosis. Methods PCR and denaturing highperformance liquid chromatography （DHPLC） were used to screen the 21 exons and their flanking regions of the SLC26A4 gene. Samples with abnormal DHPLC wave patterns were sequenced to identify the variations. Results Among the 30 unrelated NSHL patients in whom no deafness-causing mutations of the GJB2 gene were identified, 10 types of variations were detected, including 7 known mutations, 2 novel mutations （F572L and D87Y）, and 1 known polymorphism （Ivs11＋47T〉C）. The Ivs7-2A〉G is the most common type of variation, accounting for 40% of all the mutations. Conclusion SLC26A4 mutation is a major cause of NSHL, just next to the GJB2 mutations. For NSHL patients without deafness-causing GJB2 mutations, the SLC26A4 mutation rate was 23. 3%, and the IvsT-2A〉G was the most common mutation.
出处
《中华医学遗传学杂志》
CAS
CSCD
北大核心
2009年第1期21-25,共5页
Chinese Journal of Medical Genetics
基金
国家自然科学基金（30571021）
十一五国家科技支撑计划课题（2006BA105A08）
国家863计划（2007AA022445）
关键词
SLC26A4基因
突变
耳聋
变性高效液相色谱
SLC26A4 gene
mutation
deafness
denaturing high-performance liquidchromatography
