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首页> 外文期刊>The Australian journal of forensic sciences >Nucleotide sequence analysis of mitochondrial DNA hypervariable region II and inter HVR in Thais
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Nucleotide sequence analysis of mitochondrial DNA hypervariable region II and inter HVR in Thais

机译:ThaIS中线粒体DNA高变区II和ICL中的核苷酸序列分析

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摘要

In this study, the nucleotide sequences of the mitochondrial DNA hypervariable region II (HVRII) and inter HVR in the Thai population were investigated. Buccal swab samples were randomly collected from 100 unrelated healthy individuals residing in Thailand. The analysis of HVRII revealed a total of 65 different haplotypes of which 47 were unique and 18 were found in more than one individual. The most frequent haplotype observed was A73G-A249D-A263G-309.1C-315.1C (7%). Nucleotide transition from adenine (A) to guanine (G) was the most frequent substitution. Nucleotide transversions were also observed but with a lower frequency compared to nucleotide transitions. Insertions of C (57%), CC (14%), and CCC (1%) were found at position 309. Twenty-six samples were found to exhibit nucleotide deletion at position 249. The haplotype diversity, random match probability, and discrimination power were calculated to be 0.9859, 0.0240, and 0.976 respectively. In addition, the outside HVR fragment within the control region at positions 16381-72 (inter HVRI/HVRII) and 341-437 (inter HVRII/HVRIII) were sequenced in order to examine the polymorphic sites. High polymorphism was found at positions 16519, 150, 249, and 309. It was concluded that the nucleotide sequence variations in HVRII and inter HVRI/HVRII would be useful for forensic identification.
机译:在这项研究中,研究了泰国人群中线粒体DNA高变区II(HVRII)和HVR间的核苷酸序列。从居住在泰国的100名无关健康人中随机采集口腔拭子样本。对HVRII的分析显示,共有65种不同的单倍型,其中47种是独特的,18种是在多个个体中发现的。观察到的最常见单倍型为A73G-A249D-A263G-309.1C-315.1C(7%)。从腺嘌呤(A)到鸟嘌呤(G)的核苷酸转换是最常见的替换。也观察到了核苷酸转换,但与核苷酸转换相比频率较低。在309位发现C(57%)、CC(14%)和CCC(1%)的插入。发现26个样本在249位出现核苷酸缺失。单倍型多样性、随机匹配概率和分辨力分别为0.9859、0.0240和0.976。此外,对控制区16381-72位(HVRI间/HVRII)和341-437位(HVRII间/HVRIII)的外部HVR片段进行测序,以检测多态性位点。在16519、150、249和309位点发现了高多态性。结论:HVRII和HVRI/HVRII间的核苷酸序列变异有助于法医学鉴定。

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