Abstract
In the past several decades the budding yeast Saccharomyces cerevisiae has emerged as a prominent model for aging research. The creation of a single-gene deletion collection covering the majority of open reading frames in the yeast genome and advances in genomic technologies have opened yeast research to genome-scale screens for a variety of phenotypes. A number of screens have been performed looking for genes that modify secondary age-associated phenotypes such as stress resistance or growth rate. More recently, moderate-throughput methods for measuring replicative life span and high-throughput methods for measuring chronological life span have allowed for the first unbiased screens aimed at directly identifying genes involved in determining yeast longevity. In this chapter we discuss large-scale life span studies performed in yeast and their implications for research related to the basic biology of aging.
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Abbreviations
- CCE:
-
counter flow centrifugation elutriation
- DR:
-
dietary restriction
- ERC:
-
extrachromosomal rDNA circles
- FNR:
-
false negative rate
- FPR:
-
false positive rate
- LL:
-
long-lived
- LLM:
-
long-lived mutant
- MEP:
-
mother enrichment program
- NLL:
-
not long-lived
- NSE:
-
no significant extension
- OD:
-
optical density
- ORF:
-
open reading frame
- PKA:
-
protein kinase A
- ROS:
-
reactive oxygen species
- SL:
-
short-lived
- SIR:
-
silent information regulator
- TOR:
-
target of rapamycin
- uORF:
-
upstream open reading frame
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Sutphin, G.L., Olsen, B.A., Kennedy, B.K., Kaeberlein, M. (2011). Genome-Wide Analysis of Yeast Aging. In: Breitenbach, M., Jazwinski, S., Laun, P. (eds) Aging Research in Yeast. Subcellular Biochemistry, vol 57. Springer, Dordrecht. https://doi.org/10.1007/978-94-007-2561-4_12
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