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Age-correlated DNA damage in human muscle tissue
R K Zahn1, J Reinmüller, R Beyer
1Physiologisch-Chemisches Institut der Johannes-Gutenberg-Universität, Mainz, F.R.G.
Abstract:
This investigation represents the largest study so far published on human DNA damage and aging. The subject of this investigation is damage, determined as DNA alterations which give rise to complete molecular breaks in the course of treatment of purified DNA solutions with single-strand-specific nucleases. The DNA is derived from milligram samples of human muscle of individuals mostly undergoing surgical treatment. Care has been taken to bring the muscle samples, once shut off from blood circulation to liquid nitrogen temperatures within few seconds. The DNA is prepared by a procedure keeping breaks by handling and by DNAase attack as low as possible, however pushing DNA purity, especially with respect to protein as high as possible. Highly purified DNA treated in this way has some sites which are susceptible to single-strand (ss) specific DNAase splitting (ss-events). Three different deoxyribonucleases have been used: Nuclease S1, Nuclease BAL31 and Pea Endo-Nuclease. They give very similar results, i.e. splitting of the DNA so as to yield DNA pieces of given distribution. The lengths of these double-strand (ds) pieces have been determined from their electron microscopical pictures, either by following the image contours with a magnetostrictive stylo of the projected photo on a pad, by following the contours with a mileage ruler, or by integrating the silver grains on the photo. The molecular weight averages of the ds DNA threads between two ss-events for each individual have been determined from 20 to 200 molecules. The 470 individuals contributing their data were from age groups from 1 to 91 years. The molecular weights show a considerable scatter with an average molecular weight of the DNA ds pieces between two ss-events of 43.93 MDa and a standard deviation of 17.99 MDa. Among the single-strand breaks (ssb) that split the DNA into such pieces is a fraction, the number of which increases in a highly significant fashion with the age of the donor. From this derives the fact that the average molecular weight of the DNA strand pieces between two ssb decreases with age. It is remarkable that the standard deviation of the molecular weights of such pieces increases with age significantly, too. On the basis of additional information mainly supplied by the DNA donor himself or by his parents the 470 members of the main group M where grouped according to their life-style, into: (1) abstinent people, essentially non-smokers and refraining from use of licit or illicit drugs, sub-group N.(ABSTRACT TRUNCATED AT 400 WORDS)
Insights
This study reveals that DNA damage, measured by single-strand breaks, increases significantly with age in humans. Consequently, the average molecular weight of DNA fragments decreases as individuals get older.
Area of Science:
- Molecular Biology
- Genetics
- Aging Research
Background:
- Human DNA damage is a critical factor in aging.
- Previous studies on DNA damage and aging have been limited in scope.
- Understanding DNA alterations is key to comprehending the aging process.
Purpose of the Study:
- To investigate the relationship between DNA damage and chronological aging in a large human cohort.
- To quantify DNA alterations in muscle tissue across a wide age range.
- To determine if lifestyle factors correlate with DNA damage levels.
Main Methods:
- Analysis of purified DNA from human muscle samples (N=470) across ages 1-91.
- Treatment of DNA with single-strand-specific nucleases (S1, BAL31, Pea Endo-Nuclease) to induce breaks.
- Measurement of double-strand DNA piece lengths between single-strand breaks using electron microscopy.
- Statistical analysis of DNA molecular weights in relation to donor age and lifestyle.
Main Results:
- A significant positive correlation was found between the number of single-strand breaks (ssb) and donor age.
- The average molecular weight of DNA fragments between ssb significantly decreased with increasing age.
- The standard deviation of DNA fragment molecular weights also significantly increased with age.
Conclusions:
- DNA damage, specifically single-strand breaks, accumulates with age in human muscle tissue.
- Aging is associated with a decrease in DNA integrity and an increase in DNA fragmentation.
- Further research into lifestyle impacts on DNA damage is warranted.