Modulated microRNA expression during adult lifespan in Caenorhabditis elegans

被引:163
作者
Ibanez-Ventoso, Carolina
Yang, Maocheng
Guo, Suzhen
Robins, Harlan
Padgett, Richard W.
Driscoll, Monica
机构
[1] Rutgers State Univ, Dept Mol Biol & Biochem, Nelson Biol Labs, Piscataway, NJ 08854 USA
[2] Rutgers State Univ, Inst Canc, Waksman Inst, Piscataway, NJ 08854 USA
[3] Inst Adv Study, Princeton, NJ 08540 USA
来源
AGING CELL | 2006年 / 5卷 / 03期
关键词
aging; longevity; microarray; translational control;
D O I
10.1111/j.1474-9726.2006.00210.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
MicroRNAs (miRNAs) are small, abundant transcripts that can bind partially homologous target messages to inhibit their translation in animal cells. miRNAs have been shown to affect a broad spectrum of biological activities, including developmental fate determination, cell signaling and oncogenesis. Little is known, however, of miRNA contributions to aging. We examined the expression of 114 identified Caenorhabditis elegans miRNAs during the adult lifespan and find that 34 miRNAs exhibit changes in expression during adulthood (P <= 0.05), 31 with more than a twofold level change. The majority of age-regulated miRNAs decline in relative abundance as animals grow older. Expression profiles of developmental timing regulators lin-4 and let-7 miRNAs, as well as conserved muscle miRNA miR-1, show regulation during adulthood. We also used bioinformatic approaches to predict miRNA targets encoded in the C. elegans genome and we highlight candidate miRNA-regulated genes among C. elegans genes previously shown to affect longevity, genes encoding insulin-like ligands, and genes preferentially expressed in C. elegans muscle. Our observations identify miRNAs as potential modulators of age-related decline and suggest a general reduction of message-specific translational inhibition during aging, a previously undescribed feature of C. elegans aging. Since many C. elegans age-regulated miRNAs are conserved across species, our observations identify candidate age-regulating miRNAs in both nematodes and humans.
引用
收藏
页码:235 / 246
页数:12
相关论文
共 71 条
[61]   Mesodermally expressed Drosophila microRNA-1 is regulated by Twist and is required in muscles during larval growth [J].
Sokol, NS ;
Ambros, V .
GENES & DEVELOPMENT, 2005, 19 (19) :2343-2354
[62]   Identification of Drosophila MicroRNA targets [J].
Stark, A ;
Brennecke, J ;
Russell, RB ;
Cohen, SM .
PLOS BIOLOGY, 2003, 1 (03) :397-409
[63]   The endocrine regulation of aging by insulin-like signals [J].
Tatar, M ;
Bartke, A ;
Antebi, A .
SCIENCE, 2003, 299 (5611) :1346-1351
[64]   Model organisms as a guide to mammalian aging [J].
Tissenbaum, HA ;
Guarente, L .
DEVELOPMENTAL CELL, 2002, 2 (01) :9-19
[65]   Computational analysis of microRNA targets in Caenorhabditis elegans [J].
Watanabe, Y ;
Yachie, N ;
Numata, K ;
Saito, R ;
Kanai, A ;
Tomita, M .
GENE, 2006, 365 :2-10
[66]   Gene expression profiling of aging using DNA microarrays [J].
Weindruch, R ;
Kayo, T ;
Lee, CK ;
Prolla, TA .
MECHANISMS OF AGEING AND DEVELOPMENT, 2002, 123 (2-3) :177-193
[67]   MicroRNA expression in zebrafish embryonic development [J].
Wienholds, E ;
Kloosterman, WP ;
Miska, E ;
Alvarez-Saavedra, E ;
Berezikov, E ;
de Bruijn, E ;
Horvitz, HR ;
Kauppinen, S ;
Plasterk, RHA .
SCIENCE, 2005, 309 (5732) :310-311
[68]   POSTTRANSCRIPTIONAL REGULATION OF THE HETEROCHRONIC GENE LIN-14 BY LIN-4 MEDIATES TEMPORAL PATTERN-FORMATION IN C-ELEGANS [J].
WIGHTMAN, B ;
HA, I ;
RUVKUN, G .
CELL, 1993, 75 (05) :855-862
[69]   MicroRNAs: Small regulators with a big impact [J].
Yang, MC ;
Li, Y ;
Padgett, RW .
CYTOKINE & GROWTH FACTOR REVIEWS, 2005, 16 (4-5) :387-393
[70]   MicroRNA-directed cleavage of HOXB8 mRNA [J].
Yekta, S ;
Shih, IH ;
Bartel, DP .
SCIENCE, 2004, 304 (5670) :594-596