Sirtuins in stress response: guardians of the genome

被引:79
作者
Bosch-Presegue, L. [1 ]
Vaquero, A. [1 ]
机构
[1] Inst Invest Biomed Bellvitge IDIBEL, Canc Epigenet & Biol Program PEBC, Chromatin Biol Lab, Barcelona, Spain
关键词
Sirtuins; genome stability; stress response; SIRT1-7; epigenetics; METHYL-TRANSFERASE SUV39H1; FOXO TRANSCRIPTION FACTORS; HISTONE DEACETYLASE SIRT6; FATTY-ACID OXIDATION; DNA-DAMAGE RESPONSE; TUMOR-SUPPRESSOR; GENE-EXPRESSION; CALORIE RESTRICTION; TELOMERE LENGTH; HOMOLOGOUS RECOMBINATION;
D O I
10.1038/onc.2013.344
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sirtuins, a family of NAD(+)-dependent deacetylases, help organisms to respond to metabolic and genotoxic stress through diverse pathways, including metabolic homeostasis, cell survival pathways and cell-cycle control. Evidence accumulated over the past decade, including recent descriptions of mouse knockout models for each of the seven mammalian Sirtuins, suggests that protection of genome stability is among the most important roles of Sirtuins during stress response. Our current knowledge suggests that Sirtuins promote genome integrity through a variety of mechanisms, the majority of which involve a direct role in chromatin-related functions. Here, we review these mechanisms and discuss their implications for cell physiology and tumorigenesis.
引用
收藏
页码:3764 / 3775
页数:12
相关论文
共 179 条
[51]   Parp-1 protects homologous recombination from interference by Ku and ligase IV in vertebrate cells [J].
Hochegger, H ;
Dejsuphong, D ;
Fukushima, T ;
Morrison, C ;
Sonoda, E ;
Schreiber, V ;
Zhao, GY ;
Saberi, A ;
Masutani, M ;
Adachi, N ;
Koyama, H ;
de Murcia, G ;
Takeda, S .
EMBO JOURNAL, 2006, 25 (06) :1305-1314
[52]   Sirtuins as regulators of metabolism and healthspan [J].
Houtkooper, Riekelt H. ;
Pirinen, Eija ;
Auwerx, Johan .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2012, 13 (04) :225-238
[53]   Cancer cell metabolism: Warburg and beyond [J].
Hsu, Peggy P. ;
Sabatini, David M. .
CELL, 2008, 134 (05) :703-707
[54]   Involvement of the TIP60 histone acetylase complex in DNA repair and apoptosis [J].
Ikura, T ;
Ogryzko, VV ;
Grigoriev, M ;
Groisman, R ;
Wang, J ;
Horikoshi, M ;
Scully, R ;
Qin, J ;
Nakatani, Y .
CELL, 2000, 102 (04) :463-473
[55]   Transcriptional silencing and longevity protein Sir2 is an NAD-dependent histone deacetylase [J].
Imai, S ;
Armstrong, CM ;
Kaeberlein, M ;
Guarente, L .
NATURE, 2000, 403 (6771) :795-800
[56]   SIRT2, a tubulin deacetylase, acts to block the entry to chromosome condensation in response to mitotic stress [J].
Inoue, T. ;
Hiratsuka, M. ;
Osaki, M. ;
Yamada, H. ;
Kishimoto, I. ;
Yamaguchi, S. ;
Nakano, S. ;
Katoh, M. ;
Ito, H. ;
Oshimura, M. .
ONCOGENE, 2007, 26 (07) :945-957
[57]   The molecular biology of mammalian SIRT proteins - SIRT2 in cell cycle regulation [J].
Inoue, Toshiaki ;
Hiratsuka, Masaharu ;
Osaki, Mitsuhiko ;
Oshimura, Mitsuo .
CELL CYCLE, 2007, 6 (09) :1011-1018
[58]   SIRT3 Functions in the Nucleus in the Control of Stress-Related Gene Expression [J].
Iwahara, Toshinori ;
Bonasio, Roberto ;
Narendra, Varun ;
Reinberg, Danny .
MOLECULAR AND CELLULAR BIOLOGY, 2012, 32 (24) :5022-5034
[59]   DNA repair: PARP - another guardian angel? [J].
Jeggo, PA .
CURRENT BIOLOGY, 1998, 8 (02) :R49-R51
[60]   Translating the histone code [J].
Jenuwein, T ;
Allis, CD .
SCIENCE, 2001, 293 (5532) :1074-1080