TY - JOUR
T1 - Expression profile of DNA damage signaling genes in 2 Gy proton exposed mouse brain
AU - Baluchamy, Sudhakar
AU - Zhang, Ye
AU - Ravichandran, Prabakaran
AU - Ramesh, Vani
AU - Sodipe, Ayodotun
AU - Hall, Joseph C.
AU - Jejelowo, Olufisayo
AU - Gridley, Daila S.
AU - Wu, Honglu
AU - Ramesh, Govindarajan T.
N1 - Funding Information:
Acknowledgements This work was supported by NASA funding NNX08BA47A: NCC-1-02038: NIH-1P20MD001822-1.
PY - 2010/8
Y1 - 2010/8
N2 - 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.
AB - 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.
KW - Caspase activity
KW - DNA damage
KW - Differential gene expression
KW - Proton
KW - Real-time RT PCR
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U2 - 10.1007/s11010-010-0451-4
DO - 10.1007/s11010-010-0451-4
M3 - Article
C2 - 20383738
SN - 0300-8177
VL - 341
SP - 207
EP - 215
JO - Molecular and Cellular Biochemistry
JF - Molecular and Cellular Biochemistry
IS - 1-2
ER -