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干血斑标本珠蛋白生成障碍性贫血基因检测方法的建立

Development of a thalassemia gene diagnosis method for dried blood spots

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【作者】 骆明勇; 胡听听; 王继成; 袁腾龙; 张艳霞; 王奕霞; 杜丽; 梁驹卿; 尹爱华;

【Author】 Luo Mingyong;Hu Tingting;Wang Jicheng;Yuan Tenglong;Zhang Yanxia;Wang Yixia;Du Li;Liang Juqing;Yin Aihua;Center of Medical Genetics,Guangdong Women and Children Hospital/Maternal and Children Metabolic-Genetic Key Laboratory of Guangdong;

【机构】 广东省妇幼保健院医学遗传中心/广东省妇幼代谢与遗传病重点实验室;

【摘要】 目的建立并优化干血斑标本基因组DNA提取方法和流程,以适用于临床进行珠蛋白生成障碍性贫血(又称地中海贫血,以下简称"地贫")基因诊断,并对干血斑打孔标本间可能的交叉污染和保存的稳定性进行分析。方法收集150份血液标本制备干血斑后,采用打孔仪打孔,用洗脱裂解液对血斑进行洗脱,并对洗脱方法进行优化,采用磁珠法提取血斑DNA,再进行地贫基因检测,判断干血斑和全血的地贫基因检测结果是否相符。干血斑采用2种地贫基因检测方法进行检测,以验证其是否适用于多种方法。地贫阳性标本间打空白孔,对空白孔进行地贫基因检测确定打孔是否存在交叉污染。将干血斑常温干燥保存6、9个月后进行地贫基因检测,以判断其稳定性。结果采用5个3mm直径的干血斑在55℃振荡洗脱1h,可以获得DNA浓度10~20ng/μL(50μL DNA溶解液),DNA质量好。干血斑和全血的地贫基因检测结果完全一致,干血斑的2种地贫基因检测方法的结果也完全一致。打孔仪连续对干血斑打孔,地贫基因未检测出交叉污染。干血斑标本存放6、9个月后依然能够稳定地进行地贫基因检测。结论干血斑标本可以准确、方便、稳定地进行地贫基因检测,是地贫基因检测标本转诊的理想方式。

【Abstract】 Objective To devolope a method for extracting DNA from dried blood spots(DBS)and optimizing the operating procedure,which could be applied to clinical gene diagnosis of thalassemia.And the cross contamination of DBS punching and the storage stability of DBS were studied.Methods A total of 150 blood specimens were collected,and DBS were prepared.Circles(3mm in diameter)were punched in the DBS,and eluted with lysis buffer.The eluting method and operating procedure were optimized.Genomic DNA extracted from the elution solution by magnetic beads,and were performed thalassemia gene test.Finally judging whether the results of DBS and whole blood were consistent.Two methods of thalassemia gene test were used in DBS and the compatibility of DBS processing method was verified.Judging whether there was cross contamination of DBS punching by the thalassemia gene test results of blank hole which were punched in the blank filter paper between thalassemia positive DBS.The DBS storage stability in thalassemia gene test was verified by detecting the DBS which were dry stored at room temperature for 6and 9months.Results 5circles(3mm in diameter)DBS were vibrating eluted at 55℃for 1hour,the DNA concentration extracted from the elution solution was 10-20ng/μL,which was dissolved in 50μL solution,and the DNA quality was good.The thalassemia gene test results of DBS and whole blood were the same,and the DBS results of two thalassemia gene test methods were the same too.The cross contamination of DBS punching was not detected in thalassemia gene test.The DBS which were dry stored at room temperature for 6and 9months could be stably performed thalassemia gene test.Conclusion DBS could be used to perform thalassemia gene test,which is accurate,convenient and stable.It is an ideal way for specimen referral of thalassemia gene test.

【基金】 广东省省级科技计划项目(2013B022000019);广东省医学科学技术研究基金项目(A2014094)
  • 【文献出处】 国际检验医学杂志 ,International Journal of Laboratory Medicine , 编辑部邮箱 ,2015年19期
  • 【分类号】R556
  • 【被引频次】4
  • 【下载频次】131
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