SPONTANEOUS DNA BREAKS IN THE RAT-BRAIN DURING DEVELOPMENT AND AGING

被引:32
作者
MULLAART, E
BOERRIGTER, METI
BOER, GJ
VIJG, J
机构
[1] TNO, INST EXPTL GERONTOL, DEPT MOLEC BIOL, POB 5815, 2280 HV RIJSWIJK, NETHERLANDS
[2] NETHERLANDS INST BRAIN RES, AMSTERDAM, NETHERLANDS
来源
MUTATION RESEARCH | 1990年 / 237卷 / 01期
关键词
Aging; Alkaline elution; Development; DNA single-strand breaks; Rat brain; Rat liver;
D O I
10.1016/0921-8734(90)90027-O
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The level of spontaneous DNA breaks in nuclei isolated from the cerebral cortex of rat embryos at 12, 15 and 19 days of gestation, and from cerebral cortex and cerebellum of 24-day-, 6-month- and 36-month-old rats was measured by alkaline elution. A constant low level of DNA breaks was found in brain DNA during development from an embryo at day 12 of gestation to a 24-day-old rat. During aging the level of DNA breaks remained at the same low level, as shown by comparing nuclei from the cerebral cortex and cerebellum of 6- and 36-month-old animals. By contrast, an almost 2-fold increase in the level of DNA breaks was observed in rat liver nuclei between 6 and 36 months of age, confirming our earlier findings on isolated liver cells. Although there were no changes in the level of DNA breaks in rat brain during development or during aging, breaks accumulated rapidly post mortem. The rate of this process was not age-dependent. Our data suggest that the level of spontaneous DNA breaks in the brain is not likely to be of fundamental importance in the complex cellular alterations associated with brain development and aging. © 1990.
引用
收藏
页码:9 / 15
页数:7
相关论文
共 26 条
[1]   QUIESCENT HUMAN PERIPHERAL-BLOOD LYMPHOCYTES DO NOT CONTAIN A SIZABLE AMOUNT OF PREEXISTENT DNA SINGLE-STRAND BREAKS [J].
BOERRIGTER, METI ;
MULLAART, E ;
VANDERSCHANS, GP ;
VIJG, J .
EXPERIMENTAL CELL RESEARCH, 1989, 180 (02) :569-573
[2]   MODIFIED PROCEDURE FOR ISOLATION OF ASTROCYTE-ENRICHED AND NEURON-ENRICHED FRACTIONS FROM RAT-BRAIN [J].
FAROOQ, M ;
NORTON, WT .
JOURNAL OF NEUROCHEMISTRY, 1978, 31 (04) :887-894
[3]   DNA STRAND BREAKS AND ADP-RIBOSYL TRANSFERASE ACTIVATION DURING CELL-DIFFERENTIATION [J].
FARZANEH, F ;
ZALIN, R ;
BRILL, D ;
SHALL, S .
NATURE, 1982, 300 (5890) :362-366
[4]   TRANSIENT FORMATION OF DNA STRAND BREAKS DURING THE INDUCED-DIFFERENTIATION OF A HUMAN PROMYELOCYTIC LEUKEMIC-CELL LINE, HL-60 [J].
FARZANEH, F ;
MELDRUM, R ;
SHALL, S .
NUCLEIC ACIDS RESEARCH, 1987, 15 (08) :3493-3502
[5]   DNA DAMAGE AS THE PRIMARY CAUSE OF AGING [J].
GENSLER, HL ;
BERNSTEIN, H .
QUARTERLY REVIEW OF BIOLOGY, 1981, 56 (03) :279-303
[6]   DNA STRAND BREAKS IN MURINE LYMPHOCYTES - INDUCTION BY PURINE AND PYRIMIDINE ANALOGS [J].
GREER, WL ;
KAPLAN, JG .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1983, 115 (03) :834-840
[7]   THE FUNCTIONAL-SIGNIFICANCE OF THE PENTOSE-PHOSPHATE PATHWAY IN SYNAPTOSOMES - PROTECTION AGAINST PEROXIDATIVE DAMAGE BY CATECHOLAMINES AND OXIDANTS [J].
HOTHERSALL, JS ;
GREENBAUM, AL ;
MCLEAN, P .
JOURNAL OF NEUROCHEMISTRY, 1982, 39 (05) :1325-1332
[8]   LIGATION AND SYNTHESIS OF CHROMATIN DEOXYRIBONUCLEIC-ACID INVITRO IN NEURONAL, GLIAL AND LIVER NUCLEI ISOLATED FROM ADULT GUINEA-PIG [J].
INOUE, N ;
ONO, T ;
KATO, T .
BIOCHEMICAL JOURNAL, 1979, 180 (03) :471-480
[9]   CHEMISTRY OF THE BRAIN [J].
IVERSEN, LL .
SCIENTIFIC AMERICAN, 1979, 241 (03) :134-&
[10]   ROLE OF DNA BREAKS AND ADP-RIBOSYL TRANSFERASE-ACTIVITY IN EUKARYOTIC DIFFERENTIATION DEMONSTRATED IN HUMAN-LYMPHOCYTES [J].
JOHNSTONE, AP ;
WILLIAMS, GT .
NATURE, 1982, 300 (5890) :368-370