题名

粒線體MTATP6及MTATP8基因序列變化在粒線體DNA型別次分類與人別鑑定應用之評估

并列篇名

Evaluation of the Application of the MTATP6 and MTATP8 Sequence Variations on Subclassification of mtDNA Haplogroups and Human Identification

DOI

10.6134/tjfm.2012.040102.03

作者

陳嬿晴(Yen-Ching Chen);李俊億(James Chun-I Lee);林俊彥(Chun-Yen Lin);華筱玲(Hsiao-Lin Hwa)

关键词

MTATP6基因 ; MTATP8基因 ; 多型性 ; 單倍型 ; 單倍群 ; MTAP6 ; MTATP8 ; Polymorphism ; Haplotype ; Haplogroup

期刊名称

台灣法醫學誌

卷期/出版年月

4卷1&2期(2012 / 12 / 01)

页次

12 - 25

内容语文

繁體中文

中文摘要

人類粒線體DNA因為具有母系遺傳、高突變率、細胞內套數很多等特性,可應用於法醫學微量檢體作人身鑑別。粒線體DNA非轉譯區hypervariable region 1(HV1)及hypervariable region 2(HV2),為粒線體DNA變異頻率最高的區域,常被用來作為法醫學人身鑑別的工具,為了區分擁有相同HV1及HV2序列的無親屬關係之任何二人,本研究蒐集無親屬關係的167個台灣漢人個案,分析其MTATP6與MTATP8基因序列多型性,並與同一個檢體之D-loop、MTCYB、MTCOI基因序列比較,評估應用這些片段在法醫人身鑑別及型別分類的能力。在167個DNA檢體中,842個核酸序列中有62個序列點位與rCRS不同,共53種單倍型,haplotype diversity為0.8982 +/- 0.0168、nucleotide diversity為0.002751 +/- 0.001675、random match probability為10.72%、power of discrimination為0.8928。在單倍群型別分析中,分析D-loop、MTATP6及MTATP8、MTCOI、MTCYB之合併序列,有24%(25/102)的檢體合併D-loop以外之序列分析後其單倍群有改變。所有檢體的單倍群以M haplogroup為最多(28.4%,29/102),其中又以M7最多,佔18.6%(19/102),B haplogroup次之(22.5%,23/102),以B4最多,佔17.6%(18/102)。本研究利用台灣漢人MTATP6與MTATP8基因序列的多型性建立haplotype frequency,可能輔助目前常用的HV1及HV2序列分析的人身鑑別。在法醫人類學上,除了應用D-loop分類haplogroup外,MTATP6及MTATP8可能有助於建立haplogroup的次型別分類,使haplogroup的區分更為詳細,作為研究人類族群來源、遷移之依據。

英文摘要

The characteristics of human mitochondrial DNA (mtDNA), such as maternal inheritance, high mutation rate, and high copy number allow mtDNA to be applied to forensic trace samples for human identification. The hypervariable region 1 (HV1) and the hypervariable region 2 (HV2), with high frequency of variation, are often used as a tool for forensic human identification. In order to distinguish between two unrelated persons with the same HV1 and HV2 sequence, we collected DNA samples of 167 unrelated Taiwanese Han. The polymorphisms of the MTATP6 and MTATP8 genes were analyzed. Evaluation of the usefulness of the mtDNA region polymorphisms including D-loop, MTCYB, MTCOI, MTATP6 and MTATP8 for forensic human identification and haplogroup subclassification was performed. In these 167 DNA samples, there were 62 positions that varied form the rCRS with a total of 53 haplotypes found in the 842 nucleotide sequence of MTATP6 and MTATP8 genes. The haplotypes diversity, the nucleotide diversity, the power of discrimination and the random match probability (RMP) were 0.8982 +/- 0.0168, 002751 +/- 0.001675, 0.8928, and 10.72%, respectively. In the the haplogroup analysis of combinations of D-loop,MTATP6, MTATP8, MTCOI, and MTCYB sequence, 24% of the sample changed their haplogroup subclassification with additional sequence polymorphism outside D-loop. The M haplogroup was the most common haplogroup (28.4%), among which the M7 was the most common sub-haplogroup, accounting for 18.6%.The second common haplogroup was B haplogroup (22.5%), among which B4 was the most common (17.6%). In this study, polymorphisms of MTATP6 and MTATP8 in Taiwanese Han were analyzed. These polymorphisms may serve as an auxiliary of HV1 and HV2 sequence analysis for human identification. In forensic anthropology, in addition to the D-loop haplogroup, MTATP6 and MTATP8 may help to further subclassify the haplogroups for establishing the maternal lineage and migration of Taiwanese Han population.

主题分类 醫藥衛生 > 基礎醫學
社會科學 > 法律學
参考文献
  1. Akagi, M,Inui, K,Tsukamoto, H(2001).A point mutation of mitochondrial ATPase 6 gene in Leigh syndrome.Neuromuscul Disord,12,53-5.
  2. Brandstatter, A,Niederstatter, H,Parsson, W(2004).Monitoring the inheritance of heteroplasmy by computer-assisted detection of mixed basecalls in the entire human mitochondrial DNA control region.Int J Legal Med,118,47-54.
  3. Budowle, B,Allard, MW,Fisher, CL(2002).HVI and HVII mitochondrial DNA data in Apaches and Navajos.Int J Legal Med,116,212-5.
  4. Cann, RL,Stoneking, M,Wilson, AC(1987).Mitochondrial DNA and human evolution.Nature,325,31-6.
  5. Carrozzo, R,Tessa, A,Vazquez-Memije, ME(2001).The T9176G mtDNA mutation severely affects ATP production and results in Leigh syndrome.Neurology,56,687-90.
  6. Chen, YS,Torroni, A,Excoffier, L,Santachiara-Benerecetti, AS,Wallace, DC(1995).Analysis of mtDNA variation in African populations reveals the most ancient of all human continent-specific haplogroups.Am J Hum Genet,57,133-49.
  7. Coble, MD(2004).Washington, DC,The George Washington University.
  8. Gené, M,Borrego, N,Xifró, A,Piqué, E,Moreno, P,Huguet, E(1999).Haplotype frequencies of eight Y-chromosome STR loci in Barcelona (North-East Spain).Int J Legal Med,112,403-5.
  9. Horai, S,Hayasaka, K(1990).Intraspecific nucleotide sequence differences in the major noncoding region of human mitochondrial DNA.Am J Hum Genet,46,828-42.
  10. Hwa, HL,Ko, TM,Chen, YC(2012).Sequence polymorphisms of mtDNA HV1, HV2 and HV3 regions in eight population groups living in Taiwan.Australian J Forensic Sci,44,243-52.
  11. Hwa, HL,Lin, CY,Ko, TM(2011).Analysis of MTCOI and MTCYB sequence variations in eight population groups living in Taiwan.Rom J Leg Med,19,219-28.
  12. Ingman, M,Kaessmann, H,Pääbo, S,Gyllensten, U(2000).Mitochondrial genome variation and the origin of modern humans.Nature,408,708-13.
  13. Johns, DR(1995).Seminars in medicine of the Beth Israel Hospital, Boston. Mitochondrial DNA and disease.N Engl J Med,333,638-44.
  14. Kivisild, T,Tolk, HV,Parik, J(2002).The emerging limbs and twigs of the East Asian mtDNA tree.Mol Biol Evol,19,1737-51.
  15. Lutz, S,Weisser, HJ,Heizmann, J,Pollak, S(1998).Location and frequency of polymorphic positions in the human mtDNA control region of individuals from Germany.Int J Legal Med,111,67-77.
  16. Lutz-Bonengel, S,Schmidt, U,Schmitt, T,Pollak, S(2003).Sequence polymorphisms within the human mitochondrial genes MTATP6, MTATP8, and MTND4.Int J Leg Med,117,133-42.
  17. Nei, M(1987).Molecular Evolutionary Genetics.New York:Columbia University Press.
  18. Nei, M,Tajima, F(1983).Maximum likelihood estimation of the number of nucleotide substitutions from restriction sites data.Genetics,105,207-17.
  19. Poetsch, M,Wittig, H,Krause, D,Lignitz, E(2003).The impact of mtDNA analysis between positions nt8306 and nt9021 for forensic casework.Mitochondrion,3,133-7.
  20. Schurr, TG,Ballinger, SW,Gan, YY(1990).Amerindian mitochondrial DNAs have rare Asian mutations at high frequencies, suggesting they derived from four primary maternal lineages.Am J Hum Genet,46,613-23.
  21. Tajima, F(1989).Statistical method for testing the neutral mutation hypothesis by DNA polymorphism.Genetics,123,585-95.
  22. Tanaka, M,Cabrera, VM,González, AM(2004).Mitochondrial genome variation in eastern Asia and the peopling of Japan.Genome Res,14,1832-50.
  23. Torroni, A,Huoponen, K,Francalacci, P(1996).Classification of European mtDNAs from an analysis of three European populations.Genetics,144,1835-50.
  24. Torroni, A,Lott, MT,Cabell, MF,Chen, YS,Lavergne, L,Wallace, DC(1994).MtDNA and the origin of Caucasians: Identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region.Am J Hum Genet,55,760-76.
  25. Trejaut, JA,Kivisild, T,Loo, JH(2005).Traces of archaic mitochondrial lineages persist in Austronesian-speaking Formosan populations.PLoS Biol,3,e247.
  26. Tsai, LC,Lin, CY,Lee, JCI,Chang, JG,Linacre, A,Goodwin, W(2001).Sequence polymorphism of mitochondrial D-loop DNA in the Taiwanese Han population.Forensic Sci Int,119,239-47.
  27. Tzen, CY,Wu, TY,Liu, HF(2001).Sequence polymorphism in the coding region of mitochondrial genome encompassing position 8389-8865.Forensic Sci Int,120,204-9.
  28. Umetsu, K,Tanaka, M,Yuasa, I(2001).Multiplex amplified product-length polymorphism analysis for rapid detection of human mitochondrial DNA variations.Electrophoresis,22,3533-8.
  29. Yao, YG,Kong, QP,Bandelt, HJ,Kivisild, T,Zhang, YP(2002).Phylogeographic differentiation of mitochondrial DNA in Han Chinese.Am J Hum Genet,70,635-51.
  30. 林勝義、何顯榮(2001)。台灣─人類文明原鄉。台北市:台灣飛碟學會。