AGE-DEPENDENT COVALENT DNA ALTERATIONS (I-COMPOUNDS) IN RAT-LIVER MITOCHONDRIAL-DNA

被引:31
作者
GUPTA, KP [1 ]
VANGOLEN, KL [1 ]
RANDERATH, E [1 ]
RANDERATH, K [1 ]
机构
[1] BAYLOR UNIV,DEPT PHARMACOL,DIV TOXICOL,1 BAYLOR PLAZA,HOUSTON,TX 77030
来源
MUTATION RESEARCH | 1990年 / 237卷 / 01期
关键词
!sup]32[!/sup]P-Postlabeling assay; DNA modifications; I-compounds; Mitochondria; Mitochondrial DNA; Nuclear DNA;
D O I
10.1016/0921-8734(90)90028-P
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Rat liver mitochondrial (mt) DNA was investigated for the presence of I-compounds, a recently discovered type of DNA modifications which is detected and measured via 32P-postlabeling. These DNA modifications were previously shown to accumulate in an age-dependent manner in total cellular DNA of various tissues of untreated rodents. In the present work, mt DNA of 1-, 3-, 6-, and 9-month-old female Sprague-Dawley rats was found by 32P-postlabeling also to contain I-compounds that increase with age. Most of the I-compounds were identical for mt and nuclear (nu) DNA. A cluster of 2 non-polar I-spots (termed M-compounds) was mitochondria-specific and increased about 8-fold from 1 to 9 months, attaining a RAL value of 44 × 10-9 or 1 modification in 2.3 × 107 DNA nucleotides at 9 months. Quantitative differences between chromatographically identical spots were seen mainly for a low-polarity fraction of I-compounds, which exhibited 2 times higher overall levels in mt DNA versus nu DNA over the age range studied. Total I-compound levels increased during this time 6.9- and 5.1-fold in nuclei and mitochondria, respectively. The M-compound level was close to 10% of total mt DNA I-compound levels. M-compounds may conceivably be derived from potentially DNA-reactive electron carriers of the mt electron-transport chain, while I-compounds common to both mt and nu DNA presumaly originate in extramitochondrial sources. The similarity of mitochondrial and nuclear I-compound profiles and amounts implies possible regulatory mechanisms in I-compound formation and repair. Mt DNA maps showed additional 32P-labeled material which may have been associated with DNA damage caused by oxygen free radicals known to be generated by the mt electron-transport chain. Age-dependent increases of mt DNA modifications are potentially related to mt mutations and may be linked to age-related degenerative changes in mitochondria. © 1990.
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页码:17 / 27
页数:11
相关论文
共 49 条
[1]  
ALLAN JA, 1980, NATURE, V287, P244
[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]   MITOCHONDRIAL-DNA IS A MAJOR CELLULAR TARGET FOR A DIHYDRODIOL-EPOXIDE DERIVATIVE OF BENZO[A]PYRENE [J].
BACKER, JM ;
WEINSTEIN, IB .
SCIENCE, 1980, 209 (4453) :297-299
[4]  
Brown W.M., 1983, P62
[5]   MITOCHONDRIAL-DNA SEQUENCES OF PRIMATES - TEMPO AND MODE OF EVOLUTION [J].
BROWN, WM ;
PRAGER, EM ;
WANG, A ;
WILSON, AC .
JOURNAL OF MOLECULAR EVOLUTION, 1982, 18 (04) :225-239
[6]   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
[7]  
CLAYTON DA, 1984, ANNU REV BIOCHEM, V53, P573
[8]   REPLICATION OF ANIMAL MITOCHONDRIAL-DNA [J].
CLAYTON, DA .
CELL, 1982, 28 (04) :693-705
[9]   OXYGEN RADICALS AND HUMAN-DISEASE [J].
CROSS, CE ;
HALLIWELL, B ;
BORISH, ET ;
PRYOR, WA ;
AMES, BN ;
SAUL, RL ;
MCCORD, JM ;
HARMAN, D .
ANNALS OF INTERNAL MEDICINE, 1987, 107 (04) :526-545
[10]  
CUTLER RG, 1985, MOL BIOL AGING GENE, P307