The yeast Saccharomyces cerevisiae possesses a finite life span simila
r in many attributes and implications to that of higher eukaryotes. He
re, the measure of the life span is the number of generations or divis
ions the yeast cell has undergone. The yeast cell is the organism, sim
plifying many aspects of aging research. Most importantly, the genetic
s of yeast is highly-developed and readily applicable to the dissectio
n of longevity. Two candidate longevity genes have already been identi
fied and are being characterized. Others will follow through the utili
zation of both the primary phenotype and the secondary phenotypes asso
ciated with aging in yeast. An ontogenetic theory of longevity that fo
llows from the evolutionary biology of aging is put forward in this ar
ticle. This theory has at its foundation the asymmetric reproduction o
f cells and organisms, and it makes specific predictions regarding the
genetics, molecular mechanisms, and phenotypic features of longevity
and senescence, including these: GTP-binding proteins will frequently
be involved in determining longevity, asymmetric cell division will be
often encountered during embryogenesis while binary fission will be m
ore characteristic of somatic cell division, tumor cells of somatic or
igin will not be totipotent, and organisms that reproduce symmetricall
y will not have intrinsic limits to their longevity.