An enhanced MITOMAP with a global mtDNA mutational phylogeny

被引:476
作者
Ruiz-Pesini, Eduardo
Lott, Marie T.
Procaccio, Vincent
Poole, Jason C.
Brandon, Marty C.
Mishmar, Dan
Yi, Christina
Kreuziger, James
Baldi, Pierre
Wallace, Douglas C. [1 ]
机构
[1] Univ Calif Irvine, Ctr Mol & Mitochondrial Med & Genet, MAMMAG, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Biol Chem, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Dept Ecol & Evolut Biol, Irvine, CA 92697 USA
[4] Univ Calif Irvine, Dept Pediat, Irvine, CA 92697 USA
[5] Univ Zaragoza, Dept Bioquim Biol Mol & Celular, E-50009 Zaragoza, Spain
[6] Univ Calif Irvine, Sch Informat & Comp Sci, Irvine, CA 92697 USA
[7] Univ Calif Irvine, Inst Genom & Bioinformat, Irvine, CA 92697 USA
[8] Ben Gurion Univ Negev, Dept Life Sci, IL-84105 Beer Sheva, Israel
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
D O I
10.1093/nar/gkl927
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The MITOMAP (http://www.mitomap.org) data system for the human mitochondrial genome has been greatly enhanced by the addition of a navigable mutational mitochondrial DNA (mtDNA) phylogenetic tree of similar to 3000 mtDNA coding region sequences plus expanded pathogenic mutation tables and a nuclear-mtDNA pseudogene (NUMT) data base. The phylogeny reconstructs the entire mutational history of the human mtDNA, thus defining the mtDNA haplogroups and differentiating ancient from recent mtDNA mutations. Pathogenic mutations are classified by both genotype and phenotype, and the NUMT sequences permits detection of spurious inclusion of pseudogene variants during mutation analysis. These additions position MITOMAP for the implementation of our automated mtDNA sequence analysis system, Mitomaster.
引用
收藏
页码:D823 / D828
页数:6
相关论文
共 49 条
[1]   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
[2]  
[Anonymous], [No title captured]
[3]  
BALLINGER SW, 1992, GENETICS, V130, P139
[4]   Mitochondrial mutations in cancer [J].
Brandon, M. ;
Baldi, P. ;
Wallace, D. C. .
ONCOGENE, 2006, 25 (34) :4647-4662
[5]   mtDNA haplogroup X: An ancient link between Europe western Asia and North America? [J].
Brown, MD ;
Hosseini, SH ;
Torroni, A ;
Bandelt, HJ ;
Allen, JC ;
Schurr, TG ;
Scozzari, R ;
Cruciani, F ;
Wallace, DC .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (06) :1852-1861
[6]   The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J [J].
Brown, MD ;
Starikovskaya, E ;
Derbeneva, O ;
Hosseini, S ;
Allen, JC ;
Mikhailovskaya, IE ;
Sukernik, RI ;
Wallace, DC .
HUMAN GENETICS, 2002, 110 (02) :130-138
[7]  
Brown MD, 1997, AM J HUM GENET, V60, P381
[8]   MITOCHONDRIAL-DNA AND HUMAN-EVOLUTION [J].
CANN, RL ;
STONEKING, M ;
WILSON, AC .
NATURE, 1987, 325 (6099) :31-36
[9]   Mitochondrial DNA haplogroups and APOE4 allele are non-independent variables in sporadic Alzheimer's disease [J].
Carrieri, G ;
Bonafè, M ;
De Luca, M ;
Rose, G ;
Varcasia, O ;
Bruni, A ;
Maletta, R ;
Nacmias, B ;
Sorbi, S ;
Corsonello, F ;
Feraco, E ;
Andreev, KF ;
Yashin, AI ;
Franceschi, C ;
De Benedictis, G .
HUMAN GENETICS, 2001, 108 (03) :194-198
[10]  
Chagnon P, 1999, AM J MED GENET, V85, P20, DOI 10.1002/(SICI)1096-8628(19990702)85:1<20::AID-AJMG6>3.0.CO