Quantification of human mitochondrial DNA in a real time PCR

被引:49
作者
von Wurmb-Schwark, N [1 ]
Higuchi, R
Fenech, AP
Elfstroem, C
Meissner, C
Oehmichen, M
Cortopassi, GA
机构
[1] Univ Kiel, Inst Legal Med, D-24105 Kiel, Germany
[2] Roche Mol Syst, Alameda, CA 94501 USA
[3] Univ Calif Davis, Dept Stat, Davis, CA 95616 USA
[4] Med Univ Lubeck, Inst Legal Med, D-23562 Lubeck, Germany
基金
美国国家卫生研究院;
关键词
real time PCR; mtDNA; forensic; 4977; bp deletion;
D O I
10.1016/S0379-0738(02)00026-9
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
Recently, a moderately priced machine for real-time quantitative PCR has become available, the Perkin Elmer 5700. The rapid and quantitative assay of mitochondrial DNA (mtDNA) copy number is potentially useful in a variety of molecular, evolutionary and forensic fields. Using this new tool, we have evaluated the precision and reliability of the real time PCR to quantify undeleted mitochondrial genome copy number, and to determine the frequency of an age-associated deletion of 4977 base pairs in length, in 42 human iliopsoas muscle DNA samples from persons of known age. We have evaluated the accuracy with which age can be predicted, knowing only the frequency of this common 4977 bp deletion, and derived a statistical formula which describes the confidence with which the 4977 bp frequency predicts age. The results indicate that the mutation frequency Could be used to distinguish between tissue from young and old individuals. However in this data set. while there was considerable agreement of 4977 bp frequency among replicates from the same individual sample, there was Substantial diversity of mean mutation frequency between individuals of the same or similar ages. The simplest interpretation of these results is that there are biological modifiers of 4977 bp frequency that are age-independent, which are potentially interesting but may limit the usefulness of this deletion frequency alone as a "molecular forensic clock." (C) 2002 Published by Elsevier Science Ireland Ltd.
引用
收藏
页码:34 / 39
页数:6
相关论文
共 23 条
[1]  
Allen M, 1998, J FORENSIC SCI, V43, P453
[2]   DELETERIOUS MITOCHONDRIAL-DNA MUTATIONS ACCUMULATE IN AGING HUMAN TISSUES [J].
ARNHEIM, N ;
CORTOPASSI, G .
MUTATION RESEARCH, 1992, 275 (3-6) :157-167
[3]  
Ballinger SW, 1996, CANCER RES, V56, P5692
[4]   Singlet oxygen mediates the UVA-induced generation of the photoaging-associated mitochondrial common deletion [J].
Berneburg, M ;
Grether-Beck, S ;
Kürten, V ;
Ruzicka, T ;
Briviba, K ;
Sies, H ;
Krutmann, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (22) :15345-15349
[5]   MITOCHONDRIAL-DNA AND HUMAN-EVOLUTION [J].
CANN, RL ;
STONEKING, M ;
WILSON, AC .
NATURE, 1987, 325 (6099) :31-36
[6]   Reproducibility of mtDNA analysis between laboratories: a report of the European DNA profiling group (EDNAP) [J].
Carracedo, A ;
D'Aloja, E ;
Dupuy, B ;
Jangblad, A ;
Karjalainen, M ;
Lambert, C ;
Parson, W ;
Pfeiffer, H ;
Pfitzinger, H ;
Sabatier, M ;
Court, DS ;
Vide, C .
FORENSIC SCIENCE INTERNATIONAL, 1998, 97 (2-3) :165-170
[7]  
CORALLDEBRINSKI M, 1992, NAT GENET, V2, P324
[8]   DETECTION OF A SPECIFIC MITOCHONDRIAL-DNA DELETION IN TISSUES OF OLDER HUMANS [J].
CORTOPASSI, GA ;
ARNHEIM, N .
NUCLEIC ACIDS RESEARCH, 1990, 18 (23) :6927-6933
[9]   KINETIC PCR ANALYSIS - REAL-TIME MONITORING OF DNA AMPLIFICATION REACTIONS [J].
HIGUCHI, R ;
FOCKLER, C ;
DOLLINGER, G ;
WATSON, R .
BIO-TECHNOLOGY, 1993, 11 (09) :1026-1030
[10]  
HIGUCHI R, 1999, PCR APPL PROTOCOLS F, P263