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Expression profile of DNA damage signaling genes in 2 Gy proton exposed mouse brain. | LitMetric

Expression profile of DNA damage signaling genes in 2 Gy proton exposed mouse brain.

Mol Cell Biochem

Department of Biology, Molecular Toxicology Laboratory, Center for Biotechnology & Biomedical Sciences, Norfolk State University, Norfolk, VA 23504, USA.

Published: August 2010

AI Article Synopsis

  • Exposure to radiation causes various types of damage in living systems, primarily impacting genomic DNA and cell functions like proliferation.
  • This study focuses on the effects of proton radiation, revealing significant changes in gene expression related to DNA damage and apoptosis in mouse brain tissues exposed to 2 Gy of protons compared to control tissues.
  • Findings indicate that proton exposure leads to severe DNA damage and destabilizes chromatin stability, potentially triggering programmed cell death through altered gene expression.

Article Abstract

Exposure of living systems to radiation results in a wide assortment of lesions, the most significant of is damage to genomic DNA which alter specific cell functions including cell proliferation. The radiation induced DNA damage investigation is one of the important area in biology, but still the information available regarding the effects of proton is very limited. In this report, we investigated the differential gene expression pattern of DNA damage signaling genes such as damaged DNA binding, repair, cell cycle arrest, checkpoints and apoptosis using quantitative real-time RT-PCR in proton exposed mouse brain tissues. The expression profiles showed significant changes in DNA damage related genes in 2 Gy proton exposed mouse brain tissues as compared to control brain tissues. Furthermore, we also show that significantly increased levels of apoptotic related genes, caspase-3 and 8 activities in these cells, suggesting that in addition to differential expression of DNA damage genes, the alteration of apoptosis related genes may also contribute to the radiation induced DNA damage followed by programmed cell death. In summary, our findings suggest that proton exposed cells undergo severe DNA damage which in turn destabilize the chromatin stability.

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Source
http://dx.doi.org/10.1007/s11010-010-0451-4DOI Listing

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