Sirtuins in stress response: guardians of the genome

被引:78
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
[1]   A role for the mitochondrial deacetylase Sirt3 in regulating energy homeostasis [J].
Ahn, Bong-Hyun ;
Kim, Hyun-Seok ;
Song, Shiwei ;
Lee, In Hye ;
Liu, Jie ;
Vassilopoulos, Athanassios ;
Deng, Chu-Xia ;
Finkel, Toren .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (38) :14447-14452
[2]   SIRT3 is pro-apoptotic and participates in distinct basal apoptotic pathways [J].
Allison, Simon J. ;
Milner, Jo .
CELL CYCLE, 2007, 6 (21) :2669-2677
[3]   Notch signaling in leukemia [J].
Aster, Jon C. ;
Pear, Warren S. ;
Blacklow, Stephen C. .
ANNUAL REVIEW OF PATHOLOGY-MECHANISMS OF DISEASE, 2008, 3 :587-613
[4]   Increased levels of superoxide and H2O2 mediate the differential susceptibility of cancer cells versus normal cells to glucose deprivation [J].
Aykin-Burns, Nukhet ;
Ahmad, Iman M. ;
Zhu, Yueming ;
Oberley, Larry W. ;
Spitz, Douglas R. .
BIOCHEMICAL JOURNAL, 2009, 418 :29-37
[5]   Human histone deacetylase SIRT2 interacts with the homeobox transcription factor HOXA10 [J].
Bae, NS ;
Swanson, MJ ;
Vassilev, A ;
Howard, BH .
JOURNAL OF BIOCHEMISTRY, 2004, 135 (06) :695-700
[6]   SIRT7 links H3K18 deacetylation to maintenance of oncogenic transformation [J].
Barber, Matthew F. ;
Michishita-Kioi, Eriko ;
Xi, Yuanxin ;
Tasselli, Luisa ;
Kioi, Mitomu ;
Moqtaderi, Zarmik ;
Tennen, Ruth I. ;
Paredes, Silvana ;
Young, Nicolas L. ;
Chen, Kaifu ;
Struhl, Kevin ;
Garcia, Benjamin A. ;
Gozani, Or ;
Li, Wei ;
Chua, Katrin F. .
NATURE, 2012, 487 (7405) :114-+
[7]   SIRT1 negatively regulates HDAC1-dependent transcriptional repression by the RBP1 family of proteins [J].
Binda, O. ;
Nassif, C. ;
Branton, P. E. .
ONCOGENE, 2008, 27 (24) :3384-3392
[8]   Telomere shortening and tumor formation by mouse cells lacking telomerase RNA [J].
Blasco, MA ;
Lee, HW ;
Hande, MP ;
Samper, E ;
Lansdorp, PM ;
DePinho, RA ;
Greider, CW .
CELL, 1997, 91 (01) :25-34
[9]   SirT1 Regulates Energy Metabolism and Response to Caloric Restriction in Mice [J].
Boily, Gino ;
Seifert, Erin L. ;
Bevilacqua, Lisa ;
He, Xiao Hong ;
Sabourin, Guillaume ;
Estey, Carmen ;
Moffat, Cynthia ;
Crawford, Sean ;
Saliba, Sarah ;
Jardine, Karen ;
Xuan, Jian ;
Evans, Meredith ;
Harper, Mary-Ellen ;
McBurney, Michael W. .
PLOS ONE, 2008, 3 (03)
[10]   Sirt1 regulates insulin secretion by repressing UCP2 in pancreatic β cells [J].
Bordone, L ;
Motta, MC ;
Picard, F ;
Robinson, A ;
Jhala, US ;
Apfeld, J ;
McDonagh, T ;
Lemieux, M ;
McBurney, M ;
Szilvasi, A ;
Easlon, EJ ;
Lin, SJ ;
Guarente, L .
PLOS BIOLOGY, 2006, 4 (02) :210-220