Detecting errors in mtDNA data by phylogenetic analysis

被引:160
作者
Bandelt, HJ
Lahermo, P
Richards, M
Macaulay, V
机构
[1] Univ Oxford, Dept Stat, Oxford OX1 3TG, England
[2] Univ Hamburg, Fachbereich Math, D-20146 Hamburg, Germany
[3] Univ Helsinki, Finnish Genome Ctr, Helsinki, Finland
[4] Univ Huddersfield, Dept Chem & Biol Sci, Huddersfield HD1 3DH, W Yorkshire, England
关键词
mitochondrial DNA; error detection; sequence data; phylogenetic analysis; types of error;
D O I
10.1007/s004140100228
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
Sequencing and documenting a sample of homologous DNA stretches is prone to copying errors in a way rather analogous to the biological replication process. Previous attempts at obtaining representative mtDNA sequences, typically of the control region, for evolutionary studies or forensic purposes have yielded rather unsatisfactory results in many cases. The key ingredient in pin-pointing problems with given data is the phylogenetic analysis of closely related mtDNAs within the framework of an established worldwide phylogeny that is supported by coding region information. We develop some general rules by which likely errors in data tables can readily be detected without rereading whole sequences repeatedly. Following these guidelines, one can expect to lower the error rate by at least an order of magnitude, although it will still be hard to beat the mitochondrial gamma polymerase in precision.
引用
收藏
页码:64 / 69
页数:6
相关论文
共 47 条
[1]   The ancestry of Brazilian mtDNA lineages [J].
Alves-Silva, J ;
Santos, MD ;
Guimaraes, PEM ;
Ferreira, ACS ;
Bandelt, HJ ;
Pena, SDJ ;
Prado, VF .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (02) :444-461
[2]   SEQUENCE AND ORGANIZATION OF THE HUMAN MITOCHONDRIAL GENOME [J].
ANDERSON, S ;
BANKIER, AT ;
BARRELL, BG ;
DEBRUIJN, MHL ;
COULSON, AR ;
DROUIN, J ;
EPERON, IC ;
NIERLICH, DP ;
ROE, BA ;
SANGER, F ;
SCHREIER, PH ;
SMITH, AJH ;
STADEN, R ;
YOUNG, IG .
NATURE, 1981, 290 (5806) :457-465
[3]   Median networks: Speedy construction and greedy reduction, one simulation, and two case studies from human mtDNA [J].
Bandelt, HJ ;
Macaulay, V ;
Richards, M .
MOLECULAR PHYLOGENETICS AND EVOLUTION, 2000, 16 (01) :8-28
[4]  
BANDELT HJ, 1995, GENETICS, V141, P743
[5]   DNA Commission of the International Society for Forensic Genetics:: Guidelines for mitochondrial DNA typing [J].
Bär, W ;
Brinkmann, B ;
Budowle, B ;
Carracedo, A ;
Gill, P ;
Holland, M ;
Lincoln, PJ ;
Mayr, W ;
Morling, N ;
Olaisen, B ;
Schneider, PM ;
Tully, G ;
Wilson, M .
INTERNATIONAL JOURNAL OF LEGAL MEDICINE, 2000, 113 (04) :193-196
[6]   From Asia to Europe: Mitochondrial DNA sequence variability in Bulgarians and Turks [J].
Calafell, F ;
Underhill, P ;
Tolun, A ;
Angelicheva, D ;
Kalaydjieva, L .
ANNALS OF HUMAN GENETICS, 1996, 60 :35-49
[7]   Forensic evaluation of mtDNA in a population from south west Switzerland [J].
Dimo-Simonin, N ;
Grange, F ;
Taroni, F ;
Brandt-Casadevall, C ;
Mangin, P .
INTERNATIONAL JOURNAL OF LEGAL MEDICINE, 2000, 113 (02) :89-97
[8]  
Easton RD, 1996, AM J HUM GENET, V59, P213
[9]   How clonal are human mitochondria? [J].
Eyre-Walker, A ;
Smith, NH ;
Smith, JM .
PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1999, 266 (1418) :477-483
[10]   Evidence for mitochondrial DNA recombination in a human population of island Melanesia:: correction [J].
Hagelberg, E ;
Goldman, N ;
Liò, P ;
Whelan, S ;
Schiefenhövel, W ;
Clegg, JB ;
Bowden, DK .
PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2000, 267 (1452) :1595-1596