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人类基因组DNA定量系统,H-Quant:用于法医案件工作的开发与验证

Human genomic DNA quantitation system, H-Quant: development and validation for use in forensic casework.

作者信息

Shewale Jaiprakash G, Schneida Elaine, Wilson Jonathan, Walker Jerilyn A, Batzer Mark A, Sinha Sudhir K

机构信息

ReliaGene Technologies, Inc., 5525 Mounes St. Suite 101, New Orleans, LA 70123, USA.

出版信息

J Forensic Sci. 2007 Mar;52(2):364-70. doi: 10.1111/j.1556-4029.2006.00369.x.

Abstract

The human DNA quantification (H-Quant) system, developed for use in human identification, enables quantitation of human genomic DNA in biological samples. The assay is based on real-time amplification of AluYb8 insertions in hominoid primates. The relatively high copy number of subfamily-specific Alu repeats in the human genome enables quantification of very small amounts of human DNA. The oligonucleotide primers present in H-Quant are specific for human DNA and closely related great apes. During the real-time PCR, the SYBR Green I dye binds to the DNA that is synthesized by the human-specific AluYb8 oligonucleotide primers. The fluorescence of the bound SYBR Green I dye is measured at the end of each PCR cycle. The cycle at which the fluorescence crosses the chosen threshold correlates to the quantity of amplifiable DNA in that sample. The minimal sensitivity of the H-Quant system is 7.6 pg/microL of human DNA. The amplicon generated in the H-Quant assay is 216 bp, which is within the same range of the common amplifiable short tandem repeat (STR) amplicons. This size amplicon enables quantitation of amplifiable DNA as opposed to a quantitation of degraded or nonamplifiable DNA of smaller sizes. Development and validation studies were performed on the 7500 real-time PCR system following the Quality Assurance Standards for Forensic DNA Testing Laboratories.

摘要

人类DNA定量(H-Quant)系统是为人类身份识别而开发的,能够对生物样本中的人类基因组DNA进行定量。该检测基于对类人猿灵长类动物中AluYb8插入序列的实时扩增。人类基因组中亚家族特异性Alu重复序列的相对高拷贝数使得能够对极少量的人类DNA进行定量。H-Quant中存在的寡核苷酸引物对人类DNA和与之密切相关的大型猿类具有特异性。在实时PCR过程中,SYBR Green I染料与由人类特异性AluYb8寡核苷酸引物合成的DNA结合。在每个PCR循环结束时测量结合的SYBR Green I染料的荧光。荧光超过选定阈值的循环与该样本中可扩增DNA的量相关。H-Quant系统的最低灵敏度为7.6 pg/μL人类DNA。H-Quant检测中产生的扩增子为216 bp,与常见的可扩增短串联重复序列(STR)扩增子在同一范围内。这种大小的扩增子能够对可扩增DNA进行定量,而不是对较小尺寸的降解或不可扩增DNA进行定量。按照法医DNA检测实验室质量保证标准,在7500实时PCR系统上进行了开发和验证研究。

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