Gamma-ray Induced Double-strand Breaks in DNA Resulting from Randomly-inflicted Single-strand Breaks: Temporal Local Denaturation, a New Radiation Phenomenon?

Author(s):  
G.P. van der Schans
Genetics ◽  
1974 ◽  
Vol 78 (1) ◽  
pp. 139-148
Author(s):  
R B Painter

ABSTRACT Damage in DNA after irradiation can be classified into five kinds: base damage, single-strand breaks, double-strand breaks, DNA-DNA cross-linking, and DNA-protein cross-linking. Of these, repair of base damage is the best understood. In eukaryotes, at least three repair systems are known that can deal with base damage: photoreactivation, excision repair, and post-replication repair. Photoreactivation is specific for UV-induced damage and occurs widely throughout the biosphere, although it seems to be absent from placental mammals. Excision repair is present in prokaryotes and in animals but does not seem to be present in plants. Post-replication repair is poorly understood. Recent reports indicate that growing points in mammalian DNA simply skip past UV-induced lesions, leaving gaps in newly made DNA that are subsequently filled in by de novo synthesis. Evidence that this concept is oversimplified or incorrect is presented.—Single-strand breaks are induced by ionizing radiation but most cells can rapidly repair most or all of them, even after supralethal doses. The chemistry of the fragments formed when breaks are induced by ionizing radiation is complex and poorly understood. Therefore, the intermediate steps in the repair of single-strand breaks are unknown. Double-strand breaks and the two kinds of cross-linking have been studied very little and almost nothing is known about their mechanisms for repair.—The role of mammalian DNA repair in mutations is not known. Although there is evidence that defective repair can lead to cancer and/or premature aging in humans, the relationship between the molecular defects and the diseased state remains obscure.


Biopolymers ◽  
1969 ◽  
Vol 7 (5) ◽  
pp. 681-693 ◽  
Author(s):  
David Freifelder ◽  
Bruce Trumbo

2000 ◽  
Vol 66 (1) ◽  
pp. 199-205 ◽  
Author(s):  
Tony A. Slieman ◽  
Wayne L. Nicholson

ABSTRACT The loss of stratospheric ozone and the accompanying increase in solar UV flux have led to concerns regarding decreases in global microbial productivity. Central to understanding this process is determining the types and amounts of DNA damage in microbes caused by solar UV irradiation. While UV irradiation of dormant Bacillus subtilis endospores results mainly in formation of the “spore photoproduct” 5-thyminyl-5,6-dihydrothymine, genetic evidence indicates that an additional DNA photoproduct(s) may be formed in spores exposed to solar UV-B and UV-A radiation (Y. Xue and W. L. Nicholson, Appl. Environ. Microbiol. 62:2221–2227, 1996). We examined the occurrence of double-strand breaks, single-strand breaks, cyclobutane pyrimidine dimers, and apurinic-apyrimidinic sites in spore DNA under several UV irradiation conditions by using enzymatic probes and neutral or alkaline agarose gel electrophoresis. DNA from spores irradiated with artificial 254-nm UV-C radiation accumulated single-strand breaks, double-strand breaks, and cyclobutane pyrimidine dimers, while DNA from spores exposed to artificial UV-B radiation (wavelengths, 290 to 310 nm) accumulated only cyclobutane pyrimidine dimers. DNA from spores exposed to full-spectrum sunlight (UV-B and UV-A radiation) accumulated single-strand breaks, double-strand breaks, and cyclobutane pyrimidine dimers, whereas DNA from spores exposed to sunlight from which the UV-B component had been removed with a filter (“UV-A sunlight”) accumulated only single-strand breaks and double-strand breaks. Apurinic-apyrimidinic sites were not detected in spore DNA under any of the irradiation conditions used. Our data indicate that there is a complex spectrum of UV photoproducts in DNA of bacterial spores exposed to solar UV irradiation in the environment.


1971 ◽  
Vol 17 (5) ◽  
pp. 575-583 ◽  
Author(s):  
David L. Dugle ◽  
Janet R. Dugle

Evidence is presented for the isolation of DNA having a molecular weight of 31 ± 5 × 108 from Bacillus subtilis strain 23 Thy− cells. This accounts for the total DNA content of the genome. Single-strand and double-strand breaks induced by 60Co gamma rays were measured by sucrose density centrifugation. The occurrence of repair of single-strand and possibly double-strand breaks at 0 °C is inferred from survival data and the effects of pre- or post-irradiation heating.


1970 ◽  
Vol 25 (9) ◽  
pp. 1037-1042 ◽  
Author(s):  
G. Stephan ◽  
H. G. Miltenburger ◽  
G. Hotz

Phage Tl and BU-Τ1 (phage DNA substituted with 5-bromouracil) were inactivated by UV-light (2537 A). After irradiation DNA was extracted and its sedimentation behaviour studied by zone centrifugation in neutral and alkaline sucrose gradients, respectively. In the DNA of unsubstituted phage no double-strand breaks and only a small number of single-strand breaks per inactivation dose could be detected after high UV-doses. However, after irradiation of phage BU-T1 double- and single-strand breaks were observed at an increased rate. UV-irradiation in the presence of a radical scavenger (0.01 M cysteamine) prevented the occurrence of double- but not of single strand breaks. The relevance of these breaks attributable to BU-incorporation for the biological activity (plaque forming ability) of the phage and the site of action of cysteamine are discussed.


1969 ◽  
Vol 24 (12) ◽  
pp. 1565-1573 ◽  
Author(s):  
H. Jung, ◽  
U. Hagen, ◽  
M. Ullrich, ◽  
E. E. Petersen

The action of hydrogen atoms — generated in an electrodeless high frequency gas discharge — on calf thymus DNA in aqueous solution was investigated. The loss of priming activity was compared with the appearance of single strand breaks in native and denatured DNA, double strand breaks, denatured zones, base damage and rupture of hydrogen bonds. The primary lesions after exposure to H atoms and gamma radiation, respectively, are single strand breaks and base damage. Double strand breaks originating from accumulation of single breaks, and rupture of hydrogen bonds caused by single breaks and base damage, were identified as secondary lesions. In relation to strand breaks arising from radical attack on the sugar-phosphate backbone of the DNA molecule, base damage is about 12.5 times more frequent after Η-exposure than after γ-irradiation. It is concluded from this observation, that single strand breaks are the predominant critical lesions responsible for the loss of the functional activity of DNA.


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