Lecture 20 Flashcards

1
Q

Aging/Senescence

A
  • Progressive decline in somatic function reflected in reductions in fertility as well as survivorship
  • Caused by progressive degeneration of soma
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2
Q

Manifestations of aging

A
  • General degradation of soma
    • Impaired function
    • Increased disease
  • Increasing mortality rate
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3
Q

Costs of reproduction

A
  • High reproductive rates will accelerate senescence and shorten life span
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4
Q

Comparative study for costs of reproduction

A
  • Approach: Quantify reproductive effort and assess relationship between effort and lifespan, controlling for size
  • Result: Greater reproductive effort is associated with reduced lifespan. Reproductive cost appear to be greater for big dogs
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5
Q

Experimental study on female water striders

A
  • Hypothesis: High reproductive rates accelerate senescence and thereby shorten life span
  • Design: Manipulate the reproductive rate of females by changing food abundance
  • Results: There are costs to reproduction, increased rate of reproduction comes at cost of reduced longevity
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6
Q

Evolutionary explanations of aging

A
  • Some evidence to support the idea that reproduction influences longevity
  • Mutation accumulation: mutations with late-life deleterious effects accumulate in genome of a species over evolutionary time
  • Antagonistic pleiotropy: mutations with beneficial effects early in life may be favored even if those mutations have negative effects late in life
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7
Q

Reproductive value

A
  • Expected contribution of offspring to future generations of individuals of age x
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8
Q

Cohort of individuals

A
  • A: Early life acting deleterious mutation
  • B: Neutral mutations
  • C: Late-life acting deleterious mutation
  • Big difference in reproductive success (A vs. B and C)
  • Small difference in reproductive success (B vs. C)
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9
Q

Mutation accumulation theory

A
  • Few survive to older age and those that do are likely to have already reproduced
  • Strength of selection declines with age
  • Late acting deleterious mutations are not under strong selection and accumulate in genome over evolutionary time
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10
Q

Diseases caused by single genes

A
  • Severe diseases that act early in life are rare: 7%
  • Most such diseases act during or after reproduction: 93%
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11
Q

Antagonistic Pleiotropy Theory

A
  • Few survive to old age, and those that do are likely to have reproduced
  • Strength of selection declines with age
  • Genes with beneficial effects early in life will be favored in spite of negative effects late in life
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12
Q

Experimental evolution of aging

A
  • Hypothesis: Increasing importance of late-life reproduction should generate selection to maintain soma for longer
  • Natural reproduction(N): Eggs from young females used to start next generation. Life past day 14 is irrelevant
  • Old age reproduction (O): Eggs from old females are used to start the next generation
  • Predictions: O lines will evolve greater longevity, O lines will evolve greater late life fecundity
  • Conclusions: Rate of senescence can evolve. Antagonistic pleiotropy appears to play a role
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