腓骨肌萎缩症1A型基因重组热点区和多态性研究

A study of the recombination hotspot and polymorphisms of Charcot Marie Tooth disease type 1A in Chinese patients

  • 摘要: 目的:了解中国人腓骨肌萎缩症1A型(CMT1A)重组交换热点区和远端REP3795bp位置的多态性。方法:应用PCR酶切分析和短串联重复序列(STR)分析检测30例CMT1患者的17p112-12基因重复,根据特异性融合片段的检出率判断基因重复者交换的热点区是否位于1.7Kb区域;通过PCR产物的酶切证实多态性情况。结果:70% CMT1A患者交换断点位于1.7Kb区域;国人远端REP 3795bp位置的多态性为63.8%。结论:中国大多数CMT1A患者的交换断点位于1.7Kb区域,该区域为交换的热点区。特异性融合片段的存在可做为临床诊断CMT1A基因重复的筛选方法。

     

    Abstract: Objective: To study the recombination hotspot and polymorphisms of distal REP at position 3795 of Charcot.Marie.Tooth disease type 1A(CMT1A) in Chinese patients. Methods: Polymerase chain reaction combined with restriction enzyme digestion and analysis of Short Tandem Repeat(STR) sequence were used to detect gene duplications on chromosome 17p11.2-12 in 30 CMT1 patients.Whether a 1.7kb region was the recombination hotspot was determined by the detecting rate of novel junction fragments in duplication patients. Polymorphisms was identified by restriction analysis of PCR products. Results: A hotspot was observed through the detection of novel junction fragments in 70% of 21 unrelated CMT1A patients. The polymorphisms of distal REP at position 3795 was 63.8%. Conclusion: The crossover breakpoints of most Chinese CMT1A patients occurs in a 1.7kb region which is the recombination hotspot. The novel junction fragments can be used as screening method to diagnose CMT1A duplications clinically

     

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