Age-related behaviors have distinct transcriptional profiles in Caenorhabditis elegans

被引:62
|
作者
Golden, Tamara R. [1 ]
Hubbard, Alan [2 ]
Dando, Caroline [3 ]
Herren, Michael A. [3 ]
Melov, Simon [1 ]
机构
[1] Buck Inst Age Res, Novato, CA 94945 USA
[2] Univ Calif Berkeley, Sch Publ Hlth, Div Biostat, Berkeley, CA 94720 USA
[3] Fluidigm Corp, San Francisco, CA 94080 USA
关键词
bio-marker; aging; gene-expression; lifespan; Caenorhabditis elegans;
D O I
10.1111/j.1474-9726.2008.00433.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
There has been a great deal of interest in identifying potential biomarkers of aging. Biomarkers of aging would be useful to predict potential vulnerabilities in an individual that may arise well before they are chronologically expected, due to idiosyncratic aging rates that occur between individuals. Prior attempts to identify biomarkers of aging have often relied on the comparisons of long-lived animals to a wild-type control. However, the effect of interventions in model systems that prolong lifespan (such as single gene mutations or caloric restriction) can sometimes be difficult to interpret due to the manipulation itself having multiple unforeseen consequences on physiology, unrelated to aging itself. The search for predictive biomarkers of aging therefore is problematic, and the identification of metrics that can be used to predict either physiological or chronological age would be of great value. One methodology that has been used to identify biomarkers for numerous pathologies is gene expression profiling. Here, we report whole-genome expression profiles of individual wild-type Caenorhabditis elegans covering the entire wild-type nematode lifespan. Individual nematodes were scored for either age-related behavioral phenotypes, or survival, and then subsequently associated with their respective gene expression profiles. This facilitated the identification of transcriptional profiles that were highly associated with either physiological or chronological age. Overall, our approach serves as a paradigm for identifying potential biomarkers of aging in higher organisms that can be repeatedly sampled throughout their lifespan.
引用
收藏
页码:850 / 865
页数:16
相关论文
共 50 条
  • [31] Effects of Fisetin, a Plant-Derived Flavonoid, on Response to Oxidative Stress, Aging, and Age-Related Diseases in Caenorhabditis elegans
    Park, Suhyeon
    Kim, Bo-Kyoung
    Park, Sang-Kyu
    PHARMACEUTICALS, 2022, 15 (12)
  • [32] Septins and a formin have distinct functions in anaphase chiral cortical rotation in the Caenorhabditis elegans zygote
    Zaatri, Adhham
    Perry, Jenna A.
    Maddox, Amy Shaub
    MOLECULAR BIOLOGY OF THE CELL, 2021, 32 (14) : 1283 - 1292
  • [33] Methylation profiles in age-related macular degeneration
    van Leeuwen, Elisa
    Colijn, Johanna Maria
    Uitterlinden, Andre G.
    van Meurs, Joyce
    Hofman, Albert
    Vingerling, Johannes R.
    Klaver, Caroline
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2017, 58 (08)
  • [34] Cur2004-8, a synthetic curcumin derivative, extends lifespan and modulates age-related physiological changes in Caenorhabditis elegans
    Kim, Bo-Kyoung
    Kim, Sung-A
    Baek, Sun-Mi
    Lee, Eun Young
    Lee, Eun Soo
    Chung, Choon Hee
    Ahn, Chan Mug
    Park, Sang-Kyu
    DRUG DISCOVERIES AND THERAPEUTICS, 2019, 13 (04): : 198 - 206
  • [35] Morphochemical age-related changes in the nematode Caenorhabditis elegans:: immunoperoxidase localization of cytokine- and growth factor-like molecules
    Franchini, A
    Peruzzi, E
    Ottaviani, E
    EUROPEAN JOURNAL OF HISTOCHEMISTRY, 2003, 47 (01): : 75 - 80
  • [36] Distinct Aqueous Humour Cytokine Profiles of Patients with Pachychoroid Neovasculopathy and Neovascular Age-related Macular Degeneration
    Nobuhiro Terao
    Hideki Koizumi
    Kentaro Kojima
    Tetsuya Yamagishi
    Yuji Yamamoto
    Kengo Yoshii
    Koji Kitazawa
    Asako Hiraga
    Munetoyo Toda
    Shigeru Kinoshita
    Chie Sotozono
    Junji Hamuro
    Scientific Reports, 8
  • [37] Pharmacological assays reveal age-related changes in synaptic transmission at the Caenorhabditis elegans neuromuscular junction that are modified by reduced insulin signalling
    Mulcahy, Ben
    Holden-Dye, Lindy
    O'Connor, Vincent
    JOURNAL OF EXPERIMENTAL BIOLOGY, 2013, 216 (03): : 492 - 501
  • [38] Mitochonic acid 5 attenuates age-related neuromuscular dysfunction associated with mitochondrial Ca2+ overload in Caenorhabditis elegans
    XinTong Wu
    Miku Seida
    Takaaki Abe
    Atsushi Higashitani
    npj Aging, 9
  • [39] Age-related phosphorylation and fragmentation events influence the distribution profiles of distinct tau isoforms in mouse brain
    Bahr, BA
    Vicente, JS
    JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1998, 57 (02): : 111 - 121
  • [40] Distinct Aqueous Humour Cytokine Profiles of Patients with Pachychoroid Neovasculopathy and Neovascular Age-related Macular Degeneration
    Terao, Nobuhiro
    Koizumi, Hideki
    Kojima, Kentaro
    Yamagishi, Tetsuya
    Yamamoto, Yuji
    Yoshii, Kengo
    Kitazawa, Koji
    Hiraga, Asako
    Toda, Munetoyo
    Kinoshita, Shigeru
    Sotozono, Chie
    Hamuro, Junji
    SCIENTIFIC REPORTS, 2018, 8