DNA repair pathway stimulated by the forkhead transcription factor FOXO3a through the Gadd45 protein

被引:691
作者
Tran, H
Brunet, A
Grenier, JM
Datta, SR
Fornace, AJ
DiStefano, PS
Chiang, LW
Greenberg, ME [1 ]
机构
[1] Harvard Univ, Childrens Hosp, Sch Med, Div Neurosci, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Neurobiol, Boston, MA 02115 USA
[3] Millennium Pharmaceut Inc, Cambridge, MA 02139 USA
[4] NCI, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1126/science.1068712
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The signaling pathway from phosphoinositide 3-kinase to the protein kinase Akt controls organismal life-span in invertebrates and cell survival and proliferation in mammals by inhibiting the activity of members of the FOXO family of transcription factors. We show that mammalian FOXO3a also functions at the G(2) to M checkpoint in the cell cycle and triggers the repair of damaged DNA. By gene array analysis, FOXO3a was found to modulate the expression of several genes that regulate the cellular response to stress at the G(2)-M checkpoint. The growth arrest and DNA damage response gene Gadd45a appeared to be a direct target of FOXO3a that mediates part of FOXO3a's effects on DNA repair. These findings indicate that in mammals FOXO3a regulates the resistance of cells to stress by inducing DNA repair and thereby may also affect organismal life-span.
引用
收藏
页码:530 / 534
页数:5
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