Role of DNA-PK in the cellular response to DNA double-strand breaks

被引:174
作者
Burma, S [1 ]
Chen, DJ [1 ]
机构
[1] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Life Sci, Berkeley, CA 94720 USA
关键词
DNA-dependent protein kinase; DNA double-strand breaks; non-homologous end joining; phosphorylation; telomere maintenance; apoptosis; innate immunity;
D O I
10.1016/j.dnarep.2004.03.021
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The DNA-dependent protein kinase (DNA-PK) plays a critical role in DNA double-strand break (DSB) repair and in V(D)J recombination. DNA-PK also plays a very important role in triggering apoptosis in response to severe DNA damage or critically shortened telomeres. Paradoxically, components of the DNA-PK complex are present at the mammalian telomere where they function in capping chromosome ends to prevent them from being mistaken for double-strand breaks. In addition, DNA-PK appears to be involved in mounting an innate immune response to bacterial DNA and to viral infection. As DNA-PK localizes very rapidly to DNA breaks and phosphorylates itself and other damage-responsive proteins, it appears that DNA-PK serves as both a sensor and a transducer of DNA-damage signals. The many roles of DNA-PK in the mammalian cell are discussed in this review with particular emphasis on recent advances in our understanding of the phosphorylation events that take place during the activation of DNA-PK at DNA breaks. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:909 / 918
页数:10
相关论文
共 98 条
[41]   Ku acts in a unique way at the mammalian telomere to prevent end joining [J].
Hsu, HL ;
Gilley, D ;
Galande, SA ;
Hande, MP ;
Allen, B ;
Kim, SH ;
Li, GC ;
Campisi, J ;
Kohwi-Shigematsu, T ;
Chen, DJ .
GENES & DEVELOPMENT, 2000, 14 (22) :2807-2812
[42]   Ku is associated with the telomere in mammals [J].
Hsu, HL ;
Gilley, D ;
Blackburn, EH ;
Chen, DJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (22) :12454-12458
[43]   Defining interactions between DNA-PK and ligase IV/XRCC4 [J].
Hsu, HL ;
Yannone, SM ;
Chen, DJ .
DNA REPAIR, 2002, 1 (03) :225-235
[44]  
Huang LC, 1996, CANCER RES, V56, P2940
[45]   Potential role of phosphatidylinositol 3 kinase, rather than DNA-dependent protein kinase, in CpG DNA-induced immune activation [J].
Ishii, KJ ;
Takeshita, F ;
Gursel, I ;
Gursel, M ;
Conover, J ;
Nussenzweig, A ;
Klinman, DM .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (02) :269-274
[46]   The p53 response to DNA damage in vivo is independent of DNA-dependent protein kinase [J].
Jhappan, C ;
Yusufzai, TM ;
Anderson, S ;
Anver, MR ;
Merlino, G .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (11) :4075-4083
[47]   DNA-dependent protein kinase is not required for the p53-dependent response to DNA damage [J].
Jimenez, GS ;
Bryntesson, F ;
Torres-Arzayus, MI ;
Priestley, A ;
Beeche, M ;
Saito, S ;
Sakaguchi, K ;
Appella, E ;
Jeggo, PA ;
Taccioli, GE ;
Wahl, GM ;
Hubank, M .
NATURE, 1999, 400 (6739) :81-83
[48]   The ability of p53 to activate downstream genes p21WAF1/cip1 and MDM2, and cell cycle arrest following DNA damage is delayed and attenuated in scid cells deficient in the DNA-dependent protein [J].
Kachnic, LA ;
Wu, B ;
Wunsch, H ;
Mekeel, KL ;
DeFrank, JS ;
Tang, W ;
Powell, SN .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (19) :13111-13117
[49]   Werner protein is a target of DNA-dependent protein kinase in vivo and in vitro, and its catalytic activities are regulated by phosphorylation [J].
Karmakar, P ;
Piotrowski, J ;
Brosh, RM ;
Sommers, JA ;
Miller, SPL ;
Cheng, WH ;
Snowden, CM ;
Ramsden, DA ;
Bohr, VA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (21) :18291-18302
[50]   Interferon regulatory factor-3 is an in vivo target of DNA-PK [J].
Karpova, AY ;
Trost, M ;
Murray, JM ;
Cantley, LC ;
Howley, PM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (05) :2818-2823