Ultraviolet radiation mutations from

Acquired (or somatic) mutations occur in the DNA of individual cells at some time during a person s life. These changes can be caused by environmental factors such as ultraviolet radiation from the sun, or can occur if a mistake is made as DNA copies itself during cell division. Acquired mutations in somatic cells (cells other than sperm and egg cells) cannot be passed on to the next generation. 

Ultraviolet light produces pyrimidine dimers in human DNA, as it does in E. coli DNA. Furthermore, the repair mechanisms are similar. Studies of skin fibroblasts from patients with xeroderma pigmentosum have revealed a biochemical defect in one form of this disease. In normal fibro-blasts, half the pyrimidine dimers produced by ultraviolet radiation are excised in less than 24 hours. In contrast, almost no dimers are excised in this time interval in fibroblasts derived from patients with xeroderma pigmentosum. The results of these studies show that xeroderma pigmentosum can be produced by a defect in the excinuclease that hydrolyzes the DNA backbone near a pyrimidine dimer. The drastic clinical consequences of this enzymatic defect emphasize the critical importance of DNA-repair processes. The disease can also be caused by mutations in eight other genes for DNA repair, which attests to the complexity of repair processes. 

Melanomas develop from exposure of the skin to the ultraviolet rays of the sun. The ultraviolet radiation causes pyrimidine dimers to form in DNA. Mutations may result that produce melanomas, appearing as dark brown growths on the skin. 

Another important mutagen is ultraviolet light. Recent concern about the depletion of the atmospheric ozone layer by chlorofluorocarbon compounds (CFCs) is due to the role of the ozone in absorbing UV radiation before it can cause mutations in the organisms at the earth s surface. All the DNA bases efficiently absorb UV and become chemically reactive as a result. The formation of pyrimidine dimers from adjacent thymidine residues in DNA interferes with replication and transcription of DNA. See Figure 8-14. 

The hazards of an atomic bomb explosion include not only shock waves from the explosive pressure and tremendous heat, but also intense radiation in the form of alpha particles, beta particles, gamma rays, and ultraviolet rays. Gamma rays and X-rays can penetrate deeply into the body, causing burns, sterilization, and gene mutation, which can adversely affect future generations. Both radioactive fission products... 

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