摘要
目的应用多重连接依赖性探针扩增（MLPA）技术对假肥大型肌营养不良（DMD及BMD）患者及其家系成员进行dystrophin基因分析，探讨MLPA定量技术在本病重复突变及携带者检测中的优势。方法以355例DMD及BMD患者、46名缺失型患者之母和8名重复型患者之母为研究对象，应用MLPA技术对dystrophin基因全长外显子进行分析，对于单一外显子缺失的样本采用PCR及测序进行验证。结果经MLPA分析，全部355例患者中190例为dystrophin基因缺失型患者，在其余非缺失型患者中检测出34例重复型突变。此外，在46名缺失型患者的母亲中发现了28名携带者，在8名重复型患者的母亲中发现了6名携带者，两组患者母亲携带者频率差异无统计学意义。经过测序验证，在1例单一外显子缺失的患者中发现17号外显子存在AGGGAACAGATCCTGGTAAAGCA小片段缺失。结论与传统的定量方法相比，MLPA定量技术可对DMD及BMD患者全长外显子区域同时进行缺失、重复分析，并能对患者家系成员的携带状态进行判定。此外，MLPA检测结果受模板DNA的浓度及纯度影响较小。
Objective To analyze the dystrophin gene in patients with Duchenne/Becker muscular dystrophy （DMD/BMD） and their family members by multiplex ligation-dependent probe amplification （MLPA） method and to evaluate the application of this method in the mutations detection. Methods The whole dystrophin gene （79 exons） was analyzed by MLPA in 355 patients with DMD/BMD, the mothers of 46 patients with deletion mutation and the mothers of 8 patients with duplication mutation. The results were verified by PCR and sequencing when single exon deletion was found. Results One hundred and ninety cases were found to have deletion of one or more dystrophin exons, and 34 patients were identified to have duplication mutations. In 46 mothers of patients with deletion mutations, 28 were identified the mutations ; and of 8 mothers of patients with duplication mutations, 6 were identified the mutations. There was no statistical significance between the carrier incidences in the 2 groups. A 23 bp deletion of ＂AGGGAACAGATCCTGGTAAAGCA＂ fragment in exon 17 was found in a patient. Conclusions Comparing with the traditional quantitative methods, MLPA can detect the deletion and duplication mutation in all the 79 exons of dystrophin gene in DMD/BMD patients, and can identify the carrier status in their family members. Furthermore, MLPA is not apt to be interfered by the concentration and purity of DNA template.
出处
《中华神经科杂志》
CAS
CSCD
北大核心
2011年第8期568-573,共6页
Chinese Journal of Neurology
基金
福建省科技计划资助项目（2009D064）
