AGING-ASSOCIATED 5 KB DELETION IN HUMAN LIVER MITOCHONDRIAL-DNA

被引:229
作者
YEN, TC
SU, JH
KING, KL
WEI, YH
机构
[1] NATL YANG MING MED COLL,DEPT BIOCHEM,TAIPEI 11221,TAIWAN
[2] NATL YANG MING MED COLL,DEPT GEN SURG,TAIPEI 11221,TAIWAN
关键词
D O I
10.1016/0006-291X(91)91788-E
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
Using PCR technique and restriction mapping, we analyzed liver mitochondrial DNA(mtDNA) of 2 stillborn babies and 55 Chinese subjects from 27 to 86 years old and blood cell mtDNA from 20 subjects of various ages. An ageing-associated 4,977-bp deletion was detected between nucleotide position 8,469 and 13,447 (or between 8482 and 13460) in the liver mtDNA of older subjects. In the region containing the junction fragment, we observed a 13 bp repeat "ACCTCCCTCACCA". Moreover, the incidence of the deleted mtDNA of each of the study subjects was found to increase with age. The deletion was found in 5 out of 8 patients of the 31-40 age group and 9 out of 11 patients of the 41-50 age group, and in all the patients over 50 years old. The deletion was not observed in either the mtDNA of the liver of the still-birth or the blood cells of subjects of all the age groups. These results support our previous contention that liver mitochondrial respiratory functions decline with age and the hypothesis that continuous accumulation of mitochondrial DNA mutation is an important contributor to ageing process. © 1991.
引用
收藏
页码:124 / 131
页数:8
相关论文
共 32 条
[1]   DIETARY CARCINOGENS AND ANTICARCINOGENS - OXYGEN RADICALS AND DEGENERATIVE DISEASES [J].
AMES, BN .
SCIENCE, 1983, 221 (4617) :1256-1264
[2]   ENDOGENOUS DNA DAMAGE AS RELATED TO CANCER AND AGING [J].
AMES, BN .
MUTATION RESEARCH, 1989, 214 (01) :41-46
[3]   ENDOGENOUS OXIDATIVE DNA DAMAGE, AGING, AND CANCER [J].
AMES, BN .
FREE RADICAL RESEARCH COMMUNICATIONS, 1989, 7 (3-6) :121-128
[4]   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
[5]   MITOCHONDRIAL MUTATIONS MAY INCREASE OXIDATIVE STRESS - IMPLICATIONS FOR CARCINOGENESIS AND AGING [J].
BANDY, B ;
DAVISON, AJ .
FREE RADICAL BIOLOGY AND MEDICINE, 1990, 8 (06) :523-539
[6]   RAPID SHIFT IN GENOTYPE OF HUMAN MITOCHONDRIAL-DNA IN A FAMILY WITH LEBER HEREDITARY OPTIC NEUROPATHY [J].
BOLHUIS, PA ;
BLEEKERWAGEMAKERS, EM ;
PONNE, NJ ;
VANSCHOONEVELD, MJ ;
WESTERVELD, A ;
VANDENBOGERT, C ;
TABAK, HF .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 170 (03) :994-997
[7]   RAPID EVOLUTION OF ANIMAL MITOCHONDRIAL-DNA [J].
BROWN, WM ;
GEORGE, M ;
WILSON, AC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (04) :1967-1971
[8]   PROOXIDANT STATES AND TUMOR PROMOTION [J].
CERUTTI, PA .
SCIENCE, 1985, 227 (4685) :375-381
[9]   HETEROGENEITY OF MITOCHONDRIAL-DNA IN DIFFERENT TISSUES FROM THE SAME ANIMAL [J].
COOTE, JL ;
SZABADOS, G ;
WORK, TS .
FEBS LETTERS, 1979, 99 (02) :255-260
[10]   RESPIRATORY ACTIVITY OF ISOLATED RAT-LIVER MITOCHONDRIA FOLLOWING INVITRO EXPOSURE TO OXYGEN SPECIES - A THRESHOLD STUDY [J].
CORBISIER, P ;
RAES, M ;
MICHIELS, C ;
PIGEOLET, E ;
HOUBION, A ;
DELAIVE, E ;
REMACLE, J .
MECHANISMS OF AGEING AND DEVELOPMENT, 1990, 51 (03) :249-263