McNevin Dennis, Wilson-Wilde Linzi, Robertson James, Kyd Jennelle, Lennard Chris
Division of Health, Design and Science, University of Canberra, ACT 2601, Australia.
Forensic Sci Int. 2005 Oct 29;153(2-3):237-46. doi: 10.1016/j.forsciint.2005.05.006.
We present a review of the literature on procedures for obtaining short tandem repeat (STR) genotypes from keratinised hair, being either hair shaft or telogen phase (naturally shed) hairs without associated scalp, follicle or sheath cells. Both the hair shaft and the telogen hair club have been subjected to the DNA-degrading keratinisation process and are more likely to be found at a crime scene than anagen (plucked) or catagen phase hairs. We discuss human hair structure, the human hair growth cycle, the keratinisation process and their implications for DNA extraction procedures, PCR amplification strategies and the interpretation of STR genotypes. Knowledge gaps and areas requiring research are identified and are the subject of a second article in this series.
我们对从角化毛发(即毛干或休止期(自然脱落)毛发,无相关头皮、毛囊或鞘细胞)获取短串联重复序列(STR)基因型的程序相关文献进行了综述。毛干和休止期毛球均经历了DNA降解的角化过程,并且比生长期(拔取)或退行期毛发更有可能在犯罪现场被发现。我们讨论了人类毛发结构、人类毛发生长周期、角化过程及其对DNA提取程序、PCR扩增策略和STR基因型解读的影响。确定了知识空白和需要研究的领域,这些是本系列第二篇文章的主题。