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The evolution of sex and death Bdelloids: No sex for over 40 million years Science News 2000 “Methuselah” – 4767 years old.

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Presentation on theme: "The evolution of sex and death Bdelloids: No sex for over 40 million years Science News 2000 “Methuselah” – 4767 years old."— Presentation transcript:

1 The evolution of sex and death Bdelloids: No sex for over 40 million years Science News 2000 “Methuselah” – 4767 years old

2 Part I: The evolution of senescence The official world record for the oldest human: 122 years, 164 days -- Jeanne Calment of France 113’th birthday party Semi-official world record for oldest organism: "Methuselah" at 4,767 years.

3 What is senescence? Senescence – The late-life decline in an individuals fertility and probability of survival that occurs in all organisms in which germ cells and somatic cells are distinct.

4 Why not live forever? All else being equal, living forever would certainly maximize lifetime fitness! lxlx x 1 0 R 0 = ∑ l x m x = ∞

5 Even organisms that don’t age “die”! lxlx x 1 0

6 This is true even for real organisms Even if an organism could live forever… it wouldn’t! lxlx x 1 0 WHY?

7 Predation Crab spider eating skipper Tobacco hornworm with parasitoids

8 Disease/Parasitism Dutch elm disease (Ophiostoma ulmi) Trypanasoma brucei

9 Random chance https://www.youtube.com/watch?v=8bS4fOHzN1U#t=10

10 What are the consequences of this result? lxlx x 1 0 R 0 = ∑ l x m x An individuals ‘reproductive value’, R 0, declines with age because FUTURE reproduction is DISCOUNTED by mortality

11 A numerical example (60% survive in every generation) xlxlx mxmx lxmxlxmx 01.0000.000.000 10.6000.000.000 20.3601.000.360 30.2161.000.216 40.1301.000.130 50.0781.000.078 60.0471.000.047 70.0281.000.028 80.0171.000.017 90.0101.000.010 100.0061.000.006 What is the reproductive value, R 0, of an individual of age 1? R 0 (1) = 0 +.360 +.216 +.130 +.078 +.047 +.028 +.017 +.010 +.006 =.892

12 A numerical example What is the reproductive value, R 0, of an individual of age 6? R 0 =.047 +.028 +.017 +.010 +.006 =.108 xlxlx mxmx lxmxlxmx 01.0000.000.000 10.6000.000.000 20.3601.000.360 30.2161.000.216 40.1301.000.130 50.0781.000.078 60.0471.000.047 70.0281.000.028 80.0171.000.017 90.0101.000.010 100.0061.000.006

13 Why does it matter if R 0 decreases with age? The number of offspring an individual produces, R 0, is a measure of its lifetime fitness As a consequence, by age x, an individual has already accrued R x /R 0 of its lifetime fitness Age, x Fitness Accrued As a result, the strength of natural selection declines with advancing age

14 This leads to two evolutionary theories of aging Mutation accumulation – Deleterious mutations that affect later age classes accumulate to higher frequencies in populations than do mutations acting on earlier age classes because selection against them is weak (Medawar, 1952) Antagonistic pleiotropy – New mutations with beneficial effects in early age classes tend to accumulate even though these same mutations have deleterious effects in later age classes (Williams, 1957)

15 Mutation accumulation xlxlx mxmx lxmxlxmx 01.0000.000.000 10.6000.000.000 20.3601.000.360 30.2161.000.216 40.1301.000.130 50.0781.000.078 60.0471.000.047 70.0281.000.028 80.0171.000.017 90.0001.000.000 100.0001.000.000 Imagine a new mutation arises that causes death at age 9 As a result, R 0 decreases from.892 to.876 Because this represents very little change in R 0 this deleterious mutation will not be efficiently removed by selection Mutation causes early death here

16 Antagonistic pleiotropy xlxlx mxmx lxmxlxmx 01.0000.000.000 10.6001.000.600 20.3601.000.360 30.2161.000.216 40.1301.000.130 50.0781.000.078 60.0001.000.000 7 1.000.000 8 1.000.000 9 1.000.000 100.0001.000.000 Imagine a new mutation arises that leads to early fertility, but causes death at age 6 As a result, R 0 actually INCREASES from.892 to 1.384 Because this mutation increases fitness, this mutation is likely to reach a high frequency, even though it shortens life. Mutation causes early maturation here Mutation causes early death here

17 An experimental test of senescence theory Offspring from young parents Offspring from old parents Repeat for many generations

18 The result From Rose (1984) Standardized fecundity ‘Old’ selected lines The ‘Old’ selected lines have low fecundity in early age classes. Natural selection for increased early reproduction would therefore lead to a decline in later reproduction and fecundity, consistent with the AP hypothesis

19 So why do we age? Some empirical evidence supports the antagonistic pleiotropy model Some empirical evidence supports the mutation accumulation model These models are NOT mutually exclusive Suggests that both are important for the evolution of senescence

20 Practice Problem

21 Part II: Why have sex? Bdelloids: No sex for over 40 million years Science News 2000 Heuchera: Sex everyday

22 What is sex? For the purposes of this class at least… Sex is the union of two genomes, usually carried by gametes, followed at some later time by reduction, ordinarily through the process of meiosis 1n 2n 1n Meiosis & Recombination

23 The disadvantages of sex 1.Recombination breaks apart co-adapted gene complexes 2.Sex requires males AB X ab  AB ab & Ab aB Combinations favored by N.S. Combinations disfavored by N.S.

24 Sex breaks apart co-adapted gene complexes Fitness Genotype In a clonal population (i.e. no sex) only AABB and aabb genotypes would persist In a sexual population, however, recombination would continually re-generate the other less fit genotypes

25 Sex requires males SSAMM X X SMX SMX AA 20% asexual 33% asexual SMXSMXAAAA After just two generations the frequency of asexuals has increased from 20% to 50%!

26 And yet, the vast majority of eukaryotes are sexual WHY?

27 Hypotheses for the advantage of sex Fixation of rare beneficial mutations – Sex and recombination brings beneficial mutations that arise in different genomes together. Muller’s ratchet – Sex and recombination allows deleterious mutations to be more efficiently purged from the genome. The Red Queen – Sex and recombination generate new combinations of genes to which parasites are not adapted

28 Fixation of rare beneficial mutations “For, unless advantageous mutations occur so seldom that each has had time to become predominant before the next appears, they can only come to be simultaneously in the same gamete by means of recombination.” - R. A. Fisher (1930)

29 Fixation of rare beneficial mutations (In finite populations: The Hill-Robertson effect) ab aBaB aBaBaBaB AbAb aBaBaBaBaBaBaBaBAbAbAbAb aBaBaBaBaBaBaBaBaBaBaBaB Clone ab aBaB aBaBaBaB AbAb ABABaBaBaBaBaBaBAbAbAbAb ABABABABABABaBaBaBaBABAB Sexual The beneficial A mutation was lost Both beneficial mutations remain

30 The Red Queen All species are continually assaulted by a variety of parasites These parasites are continually adapting to the host population Sex and recombination may allow the host to produce genetically novel offspring to which the parasites are not adapted

31 The Red Queen Clonal hostSexual hostParasite ab AB ab AB Ab ab aBAB aBAb AB aB AB ab AB ab AB ab AB ab Ab aB Ab Parasite adaptation

32 The Red Queen and some famous snails Potamopyrgus antipodarum Some random lake in New Zealand where this snail lives A castrating trematode

33 The Red Queen and some famous snails Lively (2001)

34 So why do we have sex? The red queen hypothesis: May be important for some groups of organisms, but is not likely to be the general explanation for why so many species have so much sex Hill-Robertson effect: Currently the most likely explanation because it depends only on pervasive factors common to all populations: - Genetic drift - Advantageous mutations

35 Practice question


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