We have uncovered a novel genetic pathway that determines adult lifespan in the nematodeCaenorhabditis elegans. This pathway encodes components of DNA damage/cell cycle checkpoints, whichare known to prevent inappropriate cell division. However, because non-dividing cells comprise the C.elegans adult soma, it appears that these checkpoint proteins also control the survival of cells in a postmitoticstate. Down-regulation of checkpoint functions in adult C. elegans renders them very stress resistantand extends their lifespan. Through a whole genome RNA interference screen, we determined that manynovel genes encode checkpoint functions and influence lifespan. We now propose to determine themechanism(s) by which these genes act during aging and survival, and whether their functions areconserved in mammals. We will determine the role of lifespan-modulating checkpoint proteins in the survivalof nematode neurons, which are crucial regulators of nematode lifespan, mouse cortical neurons, anddopaminergic neurons derived from human embryonic stem cells. We will modulate checkpoint functions inthese post-mitotic cells and determine their resistance genotoxic and cytotoxic insults. We will identifychemical compounds that modulate survival through checkpoints, with a view to developing novelinterventions into aging and neurological disease. This interdisciplinary project requires expertise ininvertebrate aging, mammalian neuroscience, high throughout screening, chemical biology, moleculargenetics and stem cell biology.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Linked Research project Grant (RL1)
Project #
1RL1ES016655-01
Application #
7466585
Study Section
Special Emphasis Panel (ZRR1-SRC (99))
Program Officer
Balshaw, David M
Project Start
2007-09-30
Project End
2012-06-30
Budget Start
2007-09-30
Budget End
2008-06-30
Support Year
1
Fiscal Year
2007
Total Cost
$388,000
Indirect Cost
Name
Buck Institute for Age Research
Department
Type
DUNS #
786502351
City
Novato
State
CA
Country
United States
Zip Code
94945
Lucanic, Mark; Lithgow, Gordon J; Alavez, Silvestre (2013) Pharmacological lifespan extension of invertebrates. Ageing Res Rev 12:445-58
Monroy, Adriana; Lithgow, Gordon J; Alavez, Silvestre (2013) Curcumin and neurodegenerative diseases. Biofactors 39:122-32
Alavez, Silvestre; Lithgow, Gordon J (2012) Pharmacological maintenance of protein homeostasis could postpone age-related disease. Aging Cell 11:187-91
Campisi, Judith (2011) Cellular senescence: putting the paradoxes in perspective. Curr Opin Genet Dev 21:107-12
Alavez, Silvestre; Vantipalli, Maithili C; Zucker, David J S et al. (2011) Amyloid-binding compounds maintain protein homeostasis during ageing and extend lifespan. Nature 472:226-9
McColl, Gawain; Rogers, Aric N; Alavez, Silvestre et al. (2010) Insulin-like signaling determines survival during stress via posttranscriptional mechanisms in C. elegans. Cell Metab 12:260-72
Bhaumik, Dipa; Scott, Gary K; Schokrpur, Shiruyeh et al. (2009) MicroRNAs miR-146a/b negatively modulate the senescence-associated inflammatory mediators IL-6 and IL-8. Aging (Albany NY) 1:402-11