Suppr超能文献

牙釉蛋白和人类白细胞抗原DQα基因的共扩增:优化与验证

Co-amplification of the amelogenin and HLA DQ alpha genes: optimization and validation.

作者信息

Taylor M S, Challed-Spong A, Johnson E A

机构信息

Technical Associates, Inc., Altadena, CA, USA.

出版信息

J Forensic Sci. 1997 Jan;42(1):130-6.

PMID:8988587
Abstract

An optimized PCR-based system allowing the co-amplification of the HLA DQ alpha and the amelogenin genes has been developed and validated, enabling simultaneous identity testing and sex determination. Sensitivities below 100 pg of human DNA were obtained, using a convenient, high resolution agarose gel system and ethidium bromide staining. Comparison of several co-amplification methods revealed that the best sensitivities and most consistent results were obtained using a hotstart technique employing an inactivating antibody to Taq polymerase. HLA DQ alpha typing results were reliably obtained using the co-amplification process. The sensitivity and ease of this system rendered it directly applicable to forensic analyses. The optimized techniques described here have been validated and successfully applied to forensic cases including People vs. Trujillo, in which the California Superior Court accepted these techniques as scientifically reliable and admissible. Work currently in progress has demonstrated that the described protocol may also be used to co-amplify the amelogenin gene with the AmpliType PM (polymarker) system, allowing identity testing at six loci in addition to sex determination.

摘要

一种优化的基于聚合酶链反应(PCR)的系统已被开发并验证,该系统可共同扩增人类白细胞抗原(HLA)DQα基因和牙釉蛋白基因,从而能够同时进行身份鉴定和性别判定。使用便捷的高分辨率琼脂糖凝胶系统和溴化乙锭染色,可检测到低于100 pg的人类DNA。对几种共同扩增方法的比较表明,采用对Taq聚合酶具有灭活作用抗体的热启动技术,可获得最佳的灵敏度和最一致的结果。通过共同扩增过程能够可靠地获得HLA DQα分型结果。该系统的灵敏度和简便性使其直接适用于法医分析。本文所述的优化技术已经过验证,并成功应用于包括“加利福尼亚州人民诉特鲁希略案”在内的法医案件中,加利福尼亚州高等法院认可这些技术在科学上可靠且可采信。目前正在进行的工作表明,所描述的方案还可用于将牙釉蛋白基因与AmpliType PM(多标记)系统共同扩增,除性别判定外,还能在六个位点进行身份鉴定。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验