An elt-3/elt-5/elt-6 GATA transcription circuit guides aging in C-elegans

被引:188
作者
Budovskaya, Yelena V. [1 ]
Wu, Kendall [1 ,3 ]
Southworth, Lucinda K. [2 ]
Jiang, Min [1 ]
Tedesco, Patricia [4 ]
Johnson, Thomas E. [4 ]
Kim, Stuart K. [1 ,2 ]
机构
[1] Stanford Univ, Med Ctr, Dept Dev Biol, Stanford, CA 94305 USA
[2] Stanford Univ, Med Ctr, Stanford Med Informat, Stanford, CA 94305 USA
[3] Affymetrix Inc, Santa Clara, CA 95051 USA
[4] Univ Colorado, Inst Behav Genet, Dept Integrat Physiol, Boulder, CO 80309 USA
关键词
D O I
10.1016/j.cell.2008.05.044
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
To define the C. elegans aging process at the molecular level, we used DNA microarray experiments to identify a set of 1294 age-regulated genes and found that the GATA transcription factors ELT-3, ELT-5, and ELT-6 are responsible for age regulation of a large fraction of these genes. Expression of elt-5 and elt-6 increases during normal aging, and both of these GATA factors repress expression of elt-3, which shows a corresponding decrease in expression in old worms. elt-3 regulates a large number of downstream genes that change expression in old age, including ugt- 9, col-144, and sod-3. elt-5( RNAi) and elt-6( RNAi) worms have extended longevity, indicating that elt-3, elt-5, and elt-6 play an important functional role in the aging process. These results identify a transcriptional circuit that guides the rapid aging process in C. elegans and indicate that this circuit is driven by drift of developmental pathways rather than accumulation of damage.
引用
收藏
页码:291 / 303
页数:13
相关论文
共 68 条
[1]  
[Anonymous], 2004, IMAGEJ COMPUTER PROG
[2]   Mitochondrial influence on aging rate in Caenorhabditis elegans [J].
Anson, RM ;
Hansford, RG .
AGING CELL, 2004, 3 (01) :29-34
[3]   Regulation of lifespan by sensory perception in Caenorhabditis elegans [J].
Apfeld, J ;
Kenyon, C .
NATURE, 1999, 402 (6763) :804-809
[4]  
Aviv A., 2004, SCI AGING KNOWLEDGE, V2004, pp, DOI DOI 10.1126/SAGEKE.2004.51.PE43
[5]   Signalling shutdown strategies in aging immune cells [J].
Ayub, K ;
Hallett, MB .
AGING CELL, 2004, 3 (04) :145-149
[6]   The epigenetic regulation of mammalian telomeres [J].
Blasco, Maria A. .
NATURE REVIEWS GENETICS, 2007, 8 (04) :299-309
[7]   Increased Wnt signaling during aging alters muscle stem cell fate and increases fibrosis [J].
Brack, Andrew S. ;
Conboy, Michael J. ;
Roy, Sudeep ;
Lee, Mark ;
Kuo, Calvin J. ;
Keller, Charles ;
Rando, Thomas A. .
SCIENCE, 2007, 317 (5839) :807-810
[8]  
BRENNER S, 1974, GENETICS, V77, P71
[9]   Genome sequence of the nematode C-elegans:: A platform for investigating biology [J].
不详 .
SCIENCE, 1998, 282 (5396) :2012-2018
[10]   Concerted assembly and cloning of multiple DNA segments using in vitro site-specific recombination: Functional analysis of multi-segment expression clones [J].
Cheo, DL ;
Titus, SA ;
Byrd, DRN ;
Hartley, JL ;
Temple, GF ;
Brasch, MA .
GENOME RESEARCH, 2004, 14 (10B) :2111-2120