摘要
目的 建立以纸片末梢血筛查儿童铅毒性易感性的方法。方法 以Chelex 10 0为介质及氯仿法抽提基因组DNA ,并比较二者的DNA得率。PCR扩增σ aminolevulinatedehydratase(ALAD)基因片段 ,以限制性内切酶MspⅠ分析ALAD基因型。结果 以Chelex 10 0为介质抽提基因组DNA的得率为 17.1μg/ml,氯仿法抽提基因组DNA的得率为 17.5 μg/ml,两种之间的差异无显著性意义 (P >0 .0 5 )。以两种方法提取的DNA为模板扩增ALAD基因片段及进行ALAD基因型分析均具有较高的特异性 ,但以Chelex 10 0为介质抽提基因组DNA扩增时敏感性有所降低。
Objective To establish the method of screening the susceptibility to childhood lead poisoning by filter paper. Methods The genomic DNA from normal children was extracted with Chelex 100 (the filter paper method) and the chloroform method. The quantity of DNA recovered by the two methods were compared. A rapid PCR based method for precise σ aminolevulinate dehydratase (ALAD) genotyping was also established. Results The quantity of DNA recovered by the filter paper method (with Chelex 100) and the chloroform method was 17.1 μg/ml and 17.5 μg/ml , respectively. There was no difference between the two methods. Both the two methods were of great practical value in the screening of ALAD genotype in high risk people, but the filter paper method was less sensitive for PCR amplification than the chloroform method. Conclusions Technically the filter paper method might be more reliable in screening the susceptibility to childhood lead poisoning.
出处
《中国当代儿科杂志》
CAS
CSCD
2002年第5期351-353,共3页
Chinese Journal of Contemporary Pediatrics
基金
国家自然科学基金资助项目 (基金号 :3 9970 64 5 )