The application of mitochondrial DNA typing to the study of white Caucasian genetic identification (original) (raw)
References
Orrego C, King MC (1990) Determination of familial relationships. In: Innis MA, Gelfand DH, Sninsky JJ, White TJ (eds) PCR protocols: A guide to methods and applications. Academic press, London and San Diego, pp 416–426 Google Scholar
Hopgood R, Sullivan KM, Gill P (1992) Strategies for automated sequencing of human mitochondrial DNA directly from PCR products. Biotechniques 13:82–92 PubMed Google Scholar
Sullivan KM, Hopgood R, Gill P (1992) Identification of human remains by amplification and automated sequencing of mitochondrial DNA. Int J Leg Med 105:83–86 Google Scholar
Sullivan KM, Hopgood R, Lang B, Gill P (1991) Automated amplification and sequencing of human mitochondrial DNA. Electrophoresis 12:17–21 PubMed Google Scholar
Stoneking M, Hedgecock D, Higuchi RG, Vigilant L, Erlich HA (1991) Population variation of human mtDNA control region sequences detected by enzymatic amplification and sequence specific oligonucleotide probes. Am J Hum Genet 48:370–382 PubMed Google Scholar
Ginther C, Issel-Tarver L, King M (1992) Identifying individuals by sequencing mitochondrial DNA from teeth. Nat Genet 2:135–138 PubMed Google Scholar
Wrischnik LA, Higuchi RG, Stoneking M, Erlich HA, Arnheim N, Wilson AC (1987) Length mutations in human mtDNA: direct sequencing of enzymatically amplified DNA. Nucleic Acids Res 15:529–542 PubMed Google Scholar
Hess JF, Parisi MA, Bennett JL, Clayton DA (1991) Impairment of mitochondrial transcription termination by a point mutation associated with the MELAS subgroup of mitochondrial encephalmoyopathies. Nature 351:236–239 PubMed Google Scholar
McShane MA, Hammans SR, Sweeney M, Holt IJ, Beattie TJ, Brett EM, Harding AE (1991) Pearson Syndrome and mitochondrial encephalomyopathy in a patient with a deletion of mtDNA. Am J Hum Genet 48:39–42 PubMed Google Scholar
Lestienne P (1992) Mitochondrial DNA mutations in human diseases: a review. Biochimie 74:123–130 PubMed Google Scholar
Trischler H-J, Andreetta F, Moreas CT, Bonilla E, Arnaudo E, Danon MJ, Glass S, Zelaya BM, Vamos E, Telerman-Toppet N, Shanske S, Kadenbach B, DiMauro S, Schon EA (1992) Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA. Neurology 42:209–217 PubMed Google Scholar
Aquadro CF, Greenberg BD (1983) Human mitochondrial DNA variation and evolution: analysis of nucleotide sequences from seven individuals. Genetics 103:287–312 PubMed Google Scholar
Kocher TD, Wilson AC (1991) Sequence evolution of mitochondrial DNA in humans and chimpanzees: control region and a protein-coding regoin. In: Osawa S, Honjo T (eds) Evolution of life. Springer, Tokyo. pp 391–413 Google Scholar
Lundstrom R, Tavare S, Ward RH (1992) Estimating substitution rates from molecular data using the coalescent. Proc Natl Acid Sci USA 89:5961–5965 Google Scholar
Hasegawa M, Horai S (1991) Time of the deepest root for polymorphism in human mitochondrial DNA. J Mol Evol 32:37–42 PubMed Google Scholar
Pesole G, Sbisa E, Preparata G, Saccone C (1992) The evolution of the mitochondrial D-loop region and the origin of modern man. Mol Biol Evol 9:587–598 PubMed Google Scholar
Vigilant L, Stoneking M, Harpending H, Hawkes K, Wilson AC (1991) African populations and the evolution of human mitochondrial DNA. Science 253:1503–1507 PubMed Google Scholar
Thomas WK, Beckenbach AT (1989) Variation on Salmonid mitochondrial DNA: evolutionary constraints and mechanisms of substitution. J Mol Evol 29:233–245 PubMed Google Scholar
Horei S, Matsunaga E (1986) MtDNA polymorphism in Japanese. Hum Genet 72:105–117 PubMed Google Scholar
Merriwether DA, Clark AG, Ballinger SW, Schutt TG, Soodyall H, Jenkins T, Sherry ST, Wallace DC (1991) The structure of human mitochondrial DNA variation. J Mol Evol 33:543–555 PubMed Google Scholar
Brega A, Gardella R, Semino S, Morpurgo G, Astaldi Ricotti GB, Wallace DC, Santachiara Benerecetti AS (1986) Genetic studies on the Tharu population of Nepal: restriction endonuclease polymorphisms of mtDNA. Am J Hum Genet 39:502–512 PubMed Google Scholar
Denaro M, Blanc H, Johnson MJ, Chen KH, Wilmsen E, Cavalli-Sforza LL, Wallace DC (1981) Ethnic variation in Hpa I endonuclease cleavage patterns of human mitochondrial DNA. Proc Natl Acad Sci USA 78:5768–5772 PubMed Google Scholar
Bonné-Tamir B, Johnson MJ, Natali A, Wallace DC, CavalliSforza LL (1986) Human mtDNA types in two Israeli populations - a comparative study at the DNA level. Am J Hum Genet 38:341–351 PubMed Google Scholar
Vigilant L, Pennington R, Harpending H, Kocher TD (1989) Mitochondrial DNA sequences in single hairs from a Southern African population. Proc Natl Acad Sci USA 86:9350–9354 PubMed Google Scholar
Di Rienzo A, Wilson AC (1991) Branching pattern in the evolutionary tree for human mitochondrial DNA. Proc Natl Acad Sci USA 88:1597–1601 PubMed Google Scholar
Irwin DM, Kocher TD, Wilson AC (1991) Evolution of the cytochrome b gene of mammals. J Mol Evol 32:128–144 PubMed Google Scholar
Horai S, Kondo R, Murayama K, Hayashi S, Koike H, Nakai N (1991) Phylogenetic affiliation of ancient and contemporary humans inferred from mitochondrial DNA. Philos Trans R Soc Lond [Biol] 33:409–417 Google Scholar
Maddison DR (1991) African origin of human mitochondrial DNA reexamined. Syst Zool 40:355–363 Google Scholar
Templeton AR, Hedges SB, Kumar S, Tamura K, Stoneking M (1991) Human origins and analysis of mitochondrial DNA sequences. Science 255:737 Google Scholar
Cann RL, Stoneking M, Wilson AC (1987) Mitochondrial DNA and human evolution. Nature 325:457–465 Google Scholar
Nei M (1982) Evolution of human races at the gene level. In: Human genetics part A: The unfolding genome. Alan R. Liss, New York, pp 167–181 Google Scholar
Anderson S, Bankier AT, Barrell BG, de Brujin MHL, Coulson AR, Drouin J, Eperon IC, Nierlich DP, Roe BA, Sanger F, Schreier PH, Smith AJH, Staden R, Young IG (1981) Sequence and organisation of the human mitochondrial genome. Nature 290:457–465 PubMed Google Scholar
Greenberg BD, Newbold JE, Sugino A (1983) Intraspecific nucleotide sequence variability surrounding the origin of replication in human mitochondrial DNA. Gene 21:33–49 PubMed Google Scholar
Swofford DL (1989) PAUP, Phylogenetic Analysis Using Parsimony. Illinois Natural History Survey, Champaign, USA. Version 3.0 g Google Scholar