Life span is subject to genetic modification in yeasts, nematodes, fru
it flies, mice, humans, and other vertebrates and invertebrates. There
are a few single-gene mutants known that extend life span in yeast an
d nematodes; in other experimental systems the chat-deter is treated q
uantitatively, and generally has a low to moderate heritability. Life
span responds to artificial selection in Drosophila and Caenorhabditis
. There are many candidate genes presently under investigation, includ
ing the anti-oxidizing enzymes and heat-shock proteins. The main evolu
tionary models of senescence are antagonistic pleiotropy and mutation
accumulation, neither of which has substantial experimental support. T
he incorporation of analytical techniques from demography is playing a
n increasing role in research on aging.