Sir Peter Medawar proposed that aging is the byproduct of "late acting deleterious genes". Evolution is good at weeding out genetic mutations that are harmful at an young age, before the organism has a chance to reproduce, because the organism will not survive to pass on those genes (genes that are weeded out are genes that reduce fitness, confer disability and generally reduce chance of living long enough to reproduce). However, genes that exert their effect at a later age pass through the sieve of natural selection, because natural selection cannot act on them. According to Peter Medawar it's the accumulation of such late acting deleterious genes that causes aging.

I have two questions: What kind of "genes" are we talking about (whose accumulation in late age and its deleterious effects lead to ageing)? Genes with some essential function at young age: such as genes involved in reproduction, survival, functioning of organs etc - or "neutral" selfish genes (i.e genes that are "neutral"or have non-essential functions during the organism's youth, but individually mildly deleterious during late age) that kind of "hitched a ride" to the next generation? These kinds of "neutral genes" could arise over evolutionary time simply due to genetic drift?

Second question: What causes these late acting genes to become activated at late age (but not at young age)? Epigenetic landscape in late age, internal biochemistry? Is there any experimental evidence, and examples of such genes? I am guessing they are mildly deleterious on their own but collectively debilitating.

  • $\begingroup$ Austad, Steven N., and Jessica M. Hoffman. 2018. “Is Antagonistic Pleiotropy Ubiquitous in Aging Biology?” Evolution, Medicine, and Public Health 2018 (1): 287–94. doi.org/10.1093/emph/eoy033. $\endgroup$
    – Ben Bolker
    Dec 20, 2023 at 20:07

1 Answer 1


It's not that genes become 'activated' at late age, but that they aren't relevant until late age, so high performing versions aren't selected for and poor performing versions aren't selected against. As for which genes, we can see some in the answers to another question, What is the longest-lasting protein in a human body?

The accepted answer is crystallin, in the lens in your eye. These proteins eventually cross-link and degrade, leading to cataracts and blindness, which decreases fitness. Newts can regenerate their lenses, and more stable versions that take longer to degrade could presumably exist, so it's biologically possible to avoid this loss of fitness. However, doing so wouldn't affect the fitness in the first ~50 years of life, so selection can't maintain those mechanisms against genetic drift.

Crystallin is one example of long-lasting proteins, and those are just one example of how genes can have fitness costs that don't reveal themselves until late in life. When 'accumulation' is used in the context of Medawar's hypothesis, it refers to the accumulation in the population over many generations of these late-acting mutations, because natural selection can't remove them the way it can early-acting mutations.

  • 2
    $\begingroup$ Maybe more precisely, it isn't that the genes aren't relevant until late age, it's that the deleterious effects aren't relevant until late age. $\endgroup$
    – Bryan Krause
    Dec 15, 2023 at 16:49
  • 1
    $\begingroup$ I went back + forth on how to phrase that, and decided to be more focused on the OP's misunderstanding. Also, if we think of, e.g. "a gene to regenerate crystallin", it doesn't exist because it wouldn't be relevant to fitness until late age $\endgroup$
    – timeskull
    Dec 15, 2023 at 16:58
  • 1
    $\begingroup$ That's fair; I agree we do not need to get into all the detailed debates about what exactly a "gene" is for this Q&A. $\endgroup$
    – Bryan Krause
    Dec 15, 2023 at 18:04
  • $\begingroup$ I thought that it was mutations accumulated throughout life that affected genes. Which genes are responsible for ageing, and whether they are activated or their product is just changed, I have no idea, but I find an answer solely in terms of damage to long-lived proteins very constrained. Could you cite references that this is the modern interpretation of Medawar's hypothesis, and perhaps mention other ideas about ageing. $\endgroup$
    – David
    Dec 21, 2023 at 16:49

You must log in to answer this question.

Not the answer you're looking for? Browse other questions tagged .