origins and dynamics of new self- incompatibility …anr-manege/agay/billiard.pdforigins and...
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Origins and dynamics of new Self-Incompatibility alleles in plantsAn example of diversification with coevolution
Camille Gervais, Vincent Castric, Adrienne Ressayre, Sylvain Billiard
Université Lille 1 / INRA Moulon - France
ANR MANEGE, 2011
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• Present in dozens Angiosperms families
(e.g. Solanaceae, Brassicaceae, ...)
introduction
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Self-Incompatibility in plants
• Molecular recognition that prevents selfing and some cross-fertilization
• Up to 200 SI haplotypes thanks to the advantage of the rare (Wright 1939)
(or negative frequency dependent-selection)
Proteins
S-locus
introduction
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Red phenotype is common
→ - potential mates
→ unfavored
introduction
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White is self-compatible and compatible with anyone
introduction
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The problem of S diversification
• Easy to understand how such a large diversity is maintained (Wright 1939)
• Hard to understand how it can be generated (sir R.A. Fisher 1961)
POLLEN PISTIL
POLLEN PISTIL
Mutation
Recognition: Self-Incompatible
Non- Recognition: Self-Compatible
Self-Compatible haplotype can invade → SI Loss → Coevolution is necessary
introduction
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Uyenoyama et al. (2001)’s model
POLLEN PISTIL
POLLEN PISTIL
POLLEN PISTILMUTATION 2
= compensatory mutation
MUTATION 1
Mutation
Ancestral
New S-haplotype
Intermediate Self-Compatible
introduction
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Uyenoyama et al. (2001)’s model
POLLEN PISTIL
POLLEN PISTIL
POLLEN PISTILMUTATION 2
= compensatory mutation
MUTATION 1
Mutation
Ancestral
New S-haplotype
Intermediate Self-CompatibleX
→ SI system remains unchanged
introduction
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Uyenoyama et al. (2001)’s model
POLLEN PISTIL
POLLEN PISTIL
POLLEN PISTIL
MUTATION 2
= compensatory mutation
MUTATION 1
Mutation
Ancestral
New S-haplotype
Intermediate Self-Compatible
X
→ SI system is lost
X
introduction
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The model (based on Uyenoyama et al.2001)
POLLEN PISTIL
ASSUMPTIONS-Unstructured population with S diploid individuals
- Bipartite S-locus
- Inbreeding depression δ = decreased viability of selfed offspring
- Self-pollination rate α
-Initial number of S-haplotypes n
-Max number of different alleles Kα 1-α
model
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POLLEN i PISTIL i
POLLEN j PISTIL j
POLLEN n PISTIL n
POLLEN n+1 PISTIL n
POLLEN n+1 PISTIL n+1
ii
j
n (ancestral)
b
n+1 (new)
model
Description
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POLLEN i PISTIL i
POLLEN j PISTIL j
POLLEN n PISTIL n
POLLEN n+1 PISTIL n
POLLEN n+1 PISTIL n+1
ii
j
n (ancestral)
b
n+1 (new)
model
What may happen...
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Reproduction+ Viability selection
RecurrentMutation
modelmodelmodel
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deterministic outcomes
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model: deterministic behaviour
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xuv
frequency of genotype uv
Suv
selfing rate of genotype uv
Nuv
proportion of compatible pollen received by genotype uv
pb frequency of allele b
p frequency of allele iW mean fitness (normalization term because of selection)
model
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deterministic outcomes
4 interesting equilibria
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n = 5
deterministic outcomes
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REPLACEMENT
SI LOSS
UNCHANGEDDIVERSIFICATION
n = 5
deterministic outcomes
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n = 3 n = 4 n = 5
n = 6 n = 7 n = 8
deterministic outcomes
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REPLACEMENT
SI LOSS
UNCHANGEDDIVERSIFICATION
stochastic outcomes
N = 5, K=20, u=5.10-7, S=5000
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Diversification probability in finite populations
100 replicates
n = 5
100% diversification
(n > 5)
0% diversification
(0 < n < 5)
stochastic outcomes
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n with time
α = 0.4
α = 0.2
α = 0.2
α = 0.2
stochastic outcomes
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back to data
e.g. In Solanaceae(Richman & Kohn 1999)
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e.g. In Brassicaceae (B. rapa)(Takuno et al. 2007)
back to data
POLLENPISTIL
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back to data
Allele number(Castric & Vekemans 2004)
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going further
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going further
Best model of diversification at the S-locus?
Decaying diversification rate with increasing diversity: a general property?
Best model of speciation(Morlon et al. 2010)
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Decaying diversification rate with increasing diversity: a general property?
Looking for analogs: speciation with coevolution?