Genomic studies of speciation and gene flowevomicsorg.wpengine.netdna-cdn.com/wp-content/... ·...
Transcript of Genomic studies of speciation and gene flowevomicsorg.wpengine.netdna-cdn.com/wp-content/... ·...
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Genomic studies of speciation and gene flow
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Why study speciation genomics?
Find speciation genes
How do genomes diverge?
Long-standing questions (role of geography/gene flow)
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Genomic divergence during speciation
evolution.berkeley.edu
1. Speciation as a bi-product of physical isolation
2. Speciation due to selection – without isolation
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Genomic divergence during speciation
evolution.berkeley.edu
1. Speciation as a bi-product of physical isolation
2. Speciation due to selection – without isolation
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Cline theory - e.g. Barton and Gale 1993
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Genomic divergence during speciation
evolution.berkeley.edu Wu 2001, JEB
1. Speciation as a bi-product of physical isolation
2. Speciation due to selection – without isolation
?
Time
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Stage 1 - one or few loci under disruptive selection
Genome
FST
Gene under
selection
Feder, Egan and Nosil TiG
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Stage 2 - Divergence hitchhiking
Genome
FST
Feder, Egan and Nosil TiG
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Stage 2b - Inversion
Genome
FST
Feder, Egan and Nosil TiG
Inversion links co-adapted alleles
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Stage 3 - Genome hitchhiking
Feder, Egan and Nosil TiG
Genome
FST
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Stage 4 - Genome wide isolation
Feder, Egan and Nosil TiG
Genome
FST
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Some sub-species clearly in stage 1lWing pattern “races” of Heliconius melpomene
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Heliconius erato Heliconius melpomene
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Some sub-species clearly in stage 1
S. H. Martin et al. Genome Res. 23, 1817–1828 (2013). O. Seehausen et al. Nat. Rev. Genet. 15, 176–92 (2014).
lWing pattern “races” of Heliconius melpomene
B (red/orange patterns) Yb (yellow/white patterns)
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Some sub-species clearly in stage 1lCarrion and hooded Crows
Poelstra, J. W. et al. Science 344, 1410–4 (2014).
FST
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And an example with multiple islands?
Malinsky et al., Science 350, 1493 (2015).
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Other species have islands…but are they real?
Ellegren, et al. Nature 491, 756- (2012).
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Anopheles gambiae and A. coluzzi Formerly M and S forms of A. gambiae
Clarkson et al. 2014 Nature Communications
Other species have islands…but are they real?
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Other species have islands…but are they real?
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Seehausen et al., Nature Reviews Genetics, 2014
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• Fst measures relative divergence
• Peaks indicate regions of higher than expected between population divergence, given the within population divergence
• Peaks can therefore result from reduced diversity within species
• This could be due to lower Ne within species (selective sweeps, background selection)
• So peaks NOT NECESSARILY due to reduced gene flow
What do patterns of Fst really mean?
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Note that sometimes sweeps within species = speciation genes
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Sweeps across the species barrier can also lead to Fst peaks
Double peaks??
Nicolas Bierne, Daniel Berner and others
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Anopheles M-S divergence
Relative divergence higher in low recombination regions - not significant for absolute divergence
see also: Charlesworth 1998 MBE Measures of divergence… More recently see papers by Reto Burri
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No evidence for higher Dxy in wing pattern loci
S. H. Martin et al. Genome Res. 23, 1817–1828 (2013). O. Seehausen et al. Nat. Rev. Genet. 15, 176–92 (2014).
lWing pattern “races” of Heliconius melpomene
B (red/orange patterns) Yb (yellow/white patterns)
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Suggestion that we use absolute measures of divergence?
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Understanding genomic divergence
No single statistic will capture the complex history of mutation, migration and selection
Patterns need to be interpreted in the specific context of the study species
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Much better to use explicit tests for gene flow
Need to design sampling so the expectations in the absence of gene flow are clear and testable
The key is to identify ‘control’ populations that are not influenced by admixture
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•Isolated DNA from bones 38,000 yrs old in Croatia •We diverged from Neanderthals around 270-440,000yrs ago
•Evidence for gene exchange with humans (1-4% of genome?)
Green et al., 328:710 Science 2010
Explicit tests for gene flow: Neanderthal genome
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Explicit tests for gene flow: ABBA-BABA test
Green et al. 2010 Science 328:710-722EXPECT: 50% ABBA 50% BABA
OBSERVE: 103612 ABBA 94029 BABA
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Explicit tests for gene flow: ABBA-BABA test
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Explicit tests for gene flow: ABBA-BABA test
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The genomic landscape of Neanderthal ancestry in present-day humans - Sankararaman et al. Nature 2014
1) Derived alleles at high frequency shared with Neanderthal 2) High divergence to Africa but low to Neanderthal 3) Long haplotype blocks
Explicit tests for gene flow: Combining multiple signals
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Sampled 10 complete high coverage genomes per population
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Explicit tests for gene flow: Heliconius butterflies
Many sources of reproductive isolation:
Female hybrids are sterile Different host plant use Different habitat preference Strong assortative mating
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Using Simon Martin’s Twisst method to characterise relationships
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cydmelG melW
Martin et al., MBE 2015
outgroup
Simon Martin
ABBA-BABA statistics
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Figure 2. Four-taxon maximum-likelihood trees for 100 kb windows
(A) Trees were superimposed using Densitree (Bouckaert 2010). There were 2848 trees for the H.
cydno – H. melpomene dataset (left) and 2453 for the H. timareta – H. melpomene dataset (right).
Tree-lengths were equalized so that all trees could be superimposed, and then a random jitter was
added to all branch lengths to show density. Trees supporting each of the four possible topologies
are coloured accordingly: blue for the species tree, red for the geography tree, green for the control
tree and black for unresolved trees. (B) The four topologies scored, along with the number and
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618
619
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Cold Spring Harbor Laboratory Press on September 18, 2013 - Published by genome.cshlp.orgDownloaded from
Figure 2. Four-taxon maximum-likelihood trees for 100 kb windows
(A) Trees were superimposed using Densitree (Bouckaert 2010). There were 2848 trees for the H.
cydno – H. melpomene dataset (left) and 2453 for the H. timareta – H. melpomene dataset (right).
Tree-lengths were equalized so that all trees could be superimposed, and then a random jitter was
added to all branch lengths to show density. Trees supporting each of the four possible topologies
are coloured accordingly: blue for the species tree, red for the geography tree, green for the control
tree and black for unresolved trees. (B) The four topologies scored, along with the number and
29
617
618
619
620
621
622
623
Cold Spring Harbor Laboratory Press on September 18, 2013 - Published by genome.cshlp.orgDownloaded from
Figure 2. Four-taxon maximum-likelihood trees for 100 kb windows
(A) Trees were superimposed using Densitree (Bouckaert 2010). There were 2848 trees for the H.
cydno – H. melpomene dataset (left) and 2453 for the H. timareta – H. melpomene dataset (right).
Tree-lengths were equalized so that all trees could be superimposed, and then a random jitter was
added to all branch lengths to show density. Trees supporting each of the four possible topologies
are coloured accordingly: blue for the species tree, red for the geography tree, green for the control
tree and black for unresolved trees. (B) The four topologies scored, along with the number and
29
617
618
619
620
621
622
623
Cold Spring Harbor Laboratory Press on September 18, 2013 - Published by genome.cshlp.orgDownloaded from
x x
Figure 2. Four-taxon maximum-likelihood trees for 100 kb windows
(A) Trees were superimposed using Densitree (Bouckaert 2010). There were 2848 trees for the H.
cydno – H. melpomene dataset (left) and 2453 for the H. timareta – H. melpomene dataset (right).
Tree-lengths were equalized so that all trees could be superimposed, and then a random jitter was
added to all branch lengths to show density. Trees supporting each of the four possible topologies
are coloured accordingly: blue for the species tree, red for the geography tree, green for the control
tree and black for unresolved trees. (B) The four topologies scored, along with the number and
29
617
618
619
620
621
622
623
Cold Spring Harbor Laboratory Press on September 18, 2013 - Published by genome.cshlp.orgDownloaded from
Figure 2. Four-taxon maximum-likelihood trees for 100 kb windows
(A) Trees were superimposed using Densitree (Bouckaert 2010). There were 2848 trees for the H.
cydno – H. melpomene dataset (left) and 2453 for the H. timareta – H. melpomene dataset (right).
Tree-lengths were equalized so that all trees could be superimposed, and then a random jitter was
added to all branch lengths to show density. Trees supporting each of the four possible topologies
are coloured accordingly: blue for the species tree, red for the geography tree, green for the control
tree and black for unresolved trees. (B) The four topologies scored, along with the number and
29
617
618
619
620
621
622
623
Cold Spring Harbor Laboratory Press on September 18, 2013 - Published by genome.cshlp.orgDownloaded from
x
Figure 2. Four-taxon maximum-likelihood trees for 100 kb windows
(A) Trees were superimposed using Densitree (Bouckaert 2010). There were 2848 trees for the H.
cydno – H. melpomene dataset (left) and 2453 for the H. timareta – H. melpomene dataset (right).
Tree-lengths were equalized so that all trees could be superimposed, and then a random jitter was
added to all branch lengths to show density. Trees supporting each of the four possible topologies
are coloured accordingly: blue for the species tree, red for the geography tree, green for the control
tree and black for unresolved trees. (B) The four topologies scored, along with the number and
29
617
618
619
620
621
622
623
Cold Spring Harbor Laboratory Press on September 18, 2013 - Published by genome.cshlp.orgDownloaded from
PstI RAD sequencing(site every ~10kb)
Linkage maps builtwith Lep-MAP
300+ offspring for each cross typeJohn Davey
Davey et al., Evol Letters 2017
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Recombination rate strongly correlated with admixture proportion
Simon Martin
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Short chromosomes have more admixture:
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And chromosome ends have more admixture:
Admixture tree
Species tree
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Burri et al., Genome Research 2015
Sequenced 20 individuals per population at 20x coverage
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An alternative is to take an explicit modelling approach
IM and IMa Jody Hey
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Martin et al., Biorxiv 2015
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The effect of background selection on introgression in humans
Harris and Nielson Genetics 2016, Juric, Aeschbacher and Coop 2016
Admixture is less in gene rich regions supporting this model…..
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Population and speciation genomics: Conclusions
• Great power to detect subtle signals of selection and gene flow
• Can make more general observations about genes and regions involved in adaptation
• BUT genomic processes complicate the picture
• Best approaches combine multiple signals to infer process
• Eventually we need to combine background selection, recombination, positive selection
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And finally a plug….
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Adaptive introgression
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Photo credit Andrei Sourakov
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43 s
peci
es 77 s
peci
es
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Fritz Müller
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–G-test:G=7.25,d.f.=1,p=0.007
Expected number
0
15
30
No.
Mod
els
Atta
cked
H. melpomene H. cydno F1 hybrid
Merrill et al., Proc. Roy. Soc 2012
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102 204 76
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van Belleghem et al., Nature Ecol Evol
Peaks of divergence correspond to wing pattern genes
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Reed et al., 2011 Science
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Expressed in larva and pupa
Cell cycle, related to fizzy (Nadeau et al., Nature
2016)Putative morphogen defines black-fated regions in larval disc (Arnaud
Martin & Bob Reed)
Transcription factor,
paints red in pupal wing(Richard Wallbank)
Yb - yellow patternsChromosome 15cortex
D - red patternsChromosome 18optix
Ac - band shapeChromosome 10WntA
Wing pattern controlled almost entirely by large effect loci
knockoutWild type
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4
5
6
7
8
9Day 1 Day 3 Day 5 Day 7
P HD P HD P HD P HD
hthD
P
Hw
H. m
elpo
men
e pl
esse
ni
D
P
Hw
H. m
elpo
men
e m
alle
ti
*
*
**
P HD P HD P HD P HD
Day 1 Day 3 Day 5 Day 7
5
6
7
8
9
10
11
12
optix
*
*
*
*
*
*
**
*
2
3
3.5
4
4.5
5
Day 1 Day 3 Day 5 Day 7
P HD P HD P HD P HD
cinnabar
*
*
*
PATTERN
COLOUR
A B
D
Rela
tive
expr
essi
on
Rela
tive
expr
essi
on
Rela
tive
expr
essi
on
Rela
tive
expr
essi
on
E
Heliconius
Drosophila
C
Richard Wallbank
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Adaptive introgression
Heliconius Genome Consortium Nature 2012
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Phylogenies across B/D
ML tree based on
50,000 bp
Heliconius Genome Consortium Nature 2012
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Phylogenies across B/D
ML tree based on
50,000 bp
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Phylogenies across B/D
ML tree based on
50,000 bp
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Phylogenies across B/D
ML tree based on
50,000 bp
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Phylogenies across B/D
ML tree based on
50,000 bp
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Okay, so introgression causes mimicry
But mimicry is weird, right?
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Novelty can arise through introgression and recombination
Heliconius cydno cordula
Heliconius melpomene melpomene
NNbb
nnBB
Heliconius heurippa
NNBB
Mavarez et al., Nature 2006
Camilo Salazar
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RedBlue
optix100kb
Wallbank et al., PLoS Biology 2016
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Wallbank et al., PLoS Biology 2016
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Generate dated trees using this node as a reference point
Wallbank et al., PLoS Biology 2016
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H. cydno
H. pachinus
H. heurippa
H. tristeroH. timareta
H. melpomene
H. elevatus
H. pardalinus
H. luciana
H. athis
H. hecale
H. ethilla
H. nattereri
H. besckei
H. ismenius
H. numata
Million Years Ago4 3 2 1 0
AB C D E
Wallbank et al., PLoS Biology 2016
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Stryjewski & Sorensen Nat Ecol Evol 2017
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What about behaviour?
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H. melpomene X H. cydno
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Backcross design:
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bb Bb
-10
010
2030
Genotype
Num
ber o
f app
roac
hes
Diff
eren
ce b
etw
een
appr
oach
es to
cyd
no a
nd
mel
ponm
ene
Richard Merrill
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5% genome-wide significance threshold
Significant QTL detected on three linkage groups
Z
Richard Merrill unpub.
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0.0
0.2
0.4
0.6
0.8
1.0
Rel
ativ
e pr
obab
ility
of c
ourti
ng ~
italic
(H. m
elpo
men
e)
CC CM CC CM CC CM CC|CC|CC CM|CM|CM
LG 1 LG 17 LG 18 All three
GenotypeatputativeQTL
Relative
pro
babi
lity
of c
ourt
ing
H. m
elpo
men
e
Together explain ~ 50% measured differences between H. melpomene and H. cydno
H. melpomenemales
H. cydnomales
Z
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Heliconius cydno cordula
Heliconius melpomene melpomene
NNbb
nnBBHeliconius heurippa
NNBB
Mavarez et al., Nature 2006
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cordula heurippa melpomene
010
2030
40
Num
ber o
f app
roac
hes
Melo et al., Evolution 2009
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Lamichhaney et al., Nature 2015
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Pointy
Blunt
ALX1 associated with beak shape
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Most of these studies use phenotype associations to identify introgressed loci
But can we identify them a priori using the ABBA-BABA method?
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Green et al. 2010 Science 328:710-722
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D is quite dependent on the number of informative sites (the denominator)
D is not at all good at detecting outlier windows
Martin et al., MBE 2014
Where s is numerator from the D equation f is the fraction of introgression compared to maximum possible
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Martin’s F
But Martin’s F is quite good at finding the introgression outliers
Martin et al., MBE 2014
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• Smith and Kronforst argued that introgression could be inferred where ABBA-BABA outliers showed lower Dxy compared to genome-wide average
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• Be wary of window based D statistics
• F is better than D…
• Sampling design is very important!
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Implications for tree-thinking
Archaea
Eukarya
Bacteria
The tree of life is reticulatedThe tree of life is reticulated
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Implications for tree-thinking
Mallet, Hahn and Besansky BioEssays 2015 Hahn and Nakhleh Evolution 2015
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Okay, so what have we learnt and where do we go from here?