首页 | 本学科首页   官方微博 | 高级检索  
     检索      

人体组织在非缓冲福尔马林固定剂中的STR检测时限
引用本文:柳燕,李莉,赵珍敏,林源,阙庭志.人体组织在非缓冲福尔马林固定剂中的STR检测时限[J].中国法医学杂志,2010,25(1).
作者姓名:柳燕  李莉  赵珍敏  林源  阙庭志
作者单位:司法部司法鉴定科学技术研究所,上海市法医学重点实验室,上海,200063
基金项目:中央级科研院所社会公益研究资助项目(GY0804)
摘    要:目的评估经非缓冲福尔马林固定不同时间后的人体组织STR分型有效性,了解各种人体组织在非缓冲福尔马林固定剂中可获得完全STR分型位点的时限。方法市售40%福尔马林溶液经1∶9稀释后在室温(15~20℃)下固定人体组织,不同时间后取样。以QIAamp DNA法和IQTMDNA System法提取DNA,用quantifiler humanTaqman探针法进行DNA定量,用常规16 STR位点的AmpFSTR identifiler kit和短小片段9 STR位点的AmpFSTR Min-iFiler kit进行PCR扩增,在3100遗传分析仪进行扩增DNA片段长度检测,用GeneMapper ID v3.2对STR位点检出率进行分析。结果福尔马林固定时间、组织类型以及DNA提取方法、PCR的DNA模板终浓度均影响非缓冲福尔马林固定后人体组织STR分型效能。DNA提取用QIAgen法为优,DNA模板终浓度的最佳范围在1~3ng/μL。各类型组织在非缓冲福尔马林固定剂中的降解速率有差异,肺组织的降解速率最慢,肝、肠组织最快。固定时间在4d内的组织可以获得常规STR的完整位点数;固定时间在15d内的组织可以获得miniSTR的完整位点数。结论非缓冲福尔马林固定人体组织时间是影响STR分型的最主要因素,其次组织类型、提取方法、DNA模板浓度及STR基因座的选择也是此类降解样品成功检测的关键因素。

关 键 词:法医物证学  非缓冲福尔马林固定剂  STR分型  降解

The detectable time limit of intact STR profile for human tissues in unbuffered formalin
LIU Yan,LI Li,ZHAO Zhenmin,LIN Yuan,QUE Tingzhi.The detectable time limit of intact STR profile for human tissues in unbuffered formalin[J].Chinese Journal of Forensic Medicine,2010,25(1).
Authors:LIU Yan  LI Li  ZHAO Zhenmin  LIN Yuan  QUE Tingzhi
Institution:LIU Yan;LI Li;ZHAO Zhenmin;LIN Yuan;QUE Tingzhi/Shanghai Key Laboratory of Forensic Medicine;Institute of Forensic Science;Ministry of Justice;P.R.China;Shanghai 200063;China
Abstract:Objective To evaluate the STR profiling availability of formalin-fixed tissues and the detectable time limit of intact STR profile.Methods The different human tissues were fixed with 10-fold diluted commercial 40%formalin fixative for different duration under 15~20℃,and then DNA was extracted using the method of QIAamp~(R)DNA and IQ~(TM) DNA System.The extracted DNA was quantified with QuantifilerTM kit and amplified by both AmpFSTR identifiler kit and AmpFSTR MiniFiler kit.The STR profile was analyzed by GeneMapper ID v3.2 on 3100-Avant.Resuls The STR profiling availability of formalin-fixed tissues was relevant to the formalin fixing duration mainly.as well as the type of tissues and the template concentration and protocol of DNA extracting.The optimal ranges of template concentration is 1~3ng/μL and the QIAamp extracting method was preferable.There are differences in the degradation rate between various types of tissues in the unbuffered formalin fixative,and the lung tissue showed the slowest rate and liver and intestine tissues the fastest.Intact miniSTR profile of all the tissues detected could be obtained within 15 days duration of formalin fixing while intact STR profile could be obtained within 4 days.Conclusion The major factor that impact the availability of STR profiling of formalin-fixed tissues is the fixing duration in unbuffered formalin,as well as the type of tissues,method of extraction,concentration of PCR template and the kinds of STR loci.
Keywords:forensic biology  unbuffered formalin fixative  STR profiling  degradation  
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号