Bacterial Nitric Oxide Extends the Lifespan of C. elegans

被引:146
作者
Gusarov, Ivan [1 ]
Gautier, Laurent [1 ]
Smolentseva, Olga [1 ]
Shamovsky, Ilya [1 ]
Eremina, Svetlana [2 ]
Mironov, Alexander [2 ]
Nudler, Evgeny [1 ]
机构
[1] NYU, Sch Med, Dept Biochem & Mol Pharmacol, New York, NY 10016 USA
[2] State Res Inst Genet & Select Ind Microorganisms, Moscow 117545, Russia
关键词
HEAT-SHOCK FACTOR; CAENORHABDITIS-ELEGANS; GENE-EXPRESSION; OXIDATIVE STRESS; S-NITROSYLATION; RNA-SEQ; LONGEVITY; DISEASE; POPULATIONS; EXTENSION;
D O I
10.1016/j.cell.2012.12.043
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
Nitric oxide (NO) is an important signaling molecule in multicellular organisms. Most animals produce NO from L-arginine via a family of dedicated enzymes known as NO synthases (NOSes). A rare exception is the roundworm Caenorhabditis elegans, which lacks its own NOS. However, in its natural environment, C. elegans feeds on Bacilli that possess functional NOS. Here, we demonstrate that bacterially derived NO enhances C. elegans longevity and stress resistance via a defined group of genes that function under the dual control of HSF-1 and DAF-16 transcription factors. Our work provides an example of interspecies signaling by a small molecule and illustrates the lifelong value of commensal bacteria to their host.
引用
收藏
页码:818 / 830
页数:13
相关论文
共 65 条
[1]   Regulation of HSF1 Function in the Heat Stress Response: Implications in Aging and Disease [J].
Anckar, Julius ;
Sistonen, Lea .
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 80, 2011, 80 :1089-1115
[2]   Regulation of lifespan by sensory perception in Caenorhabditis elegans [J].
Apfeld, J ;
Kenyon, C .
NATURE, 1999, 402 (6763) :804-809
[3]  
BRENNER S, 1974, GENETICS, V77, P71
[4]   Opposing activities protect against age-onset proteotoxicity [J].
Cohen, Ehud ;
Bieschke, Jan ;
Perciavalle, Rhonda M. ;
Kelly, Jeffery W. ;
Dillin, Andrew .
SCIENCE, 2006, 313 (5793) :1604-1610
[5]   Bacterial Nitric Oxide Synthases [J].
Crane, Brian R. ;
Sudhamsu, Jawahar ;
Patel, Bhumit A. .
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 79, 2010, 79 :445-470
[6]   Toxicogenomic analysis of Caenorhabditis elegans reveals novel genes and pathways involved in the resistance to cadmium toxicity [J].
Cui, Yuxia ;
McBride, Sandra J. ;
Boyd, Windy A. ;
Alper, Scott ;
Freedman, Jonathan H. .
GENOME BIOLOGY, 2007, 8 (06)
[7]   Timing requirements for insulin/IGF-1 signaling in C-elegans [J].
Dillin, A ;
Crawford, DK ;
Kenyon, C .
SCIENCE, 2002, 298 (5594) :830-834
[8]   Quantitative mass spectrometry identifies insulin signaling targets in C-elegans [J].
Dong, Meng-Qiu ;
Venable, John D. ;
Au, Nora ;
Xu, Tao ;
Park, Sung Kyu ;
Cociorva, Daniel ;
Johnson, Jeffrey R. ;
Dillin, Andrew ;
Yates, John R., III .
SCIENCE, 2007, 317 (5838) :660-663
[9]   PRODUCTION OF AGE-SYNCHRONOUS MASS-CULTURES OF CAENORHABDITIS-ELEGANS [J].
FABIAN, TJ ;
JOHNSON, TE .
JOURNALS OF GERONTOLOGY, 1994, 49 (04) :B145-B156
[10]   Population dynamics and habitat sharing of natural populations of Caenorhabditis elegans and C. briggsae [J].
Felix, Marie-Anne ;
Duveau, Fabien .
BMC BIOLOGY, 2012, 10