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Page 1: Genomic studies of speciation and gene flowevomicsorg.wpengine.netdna-cdn.com/.../02/Chris... · Some sub-species clearly in stage 1 lWing pattern “races” of Heliconius melpomene

Genomic studies of speciation and gene flow

Page 2: Genomic studies of speciation and gene flowevomicsorg.wpengine.netdna-cdn.com/.../02/Chris... · Some sub-species clearly in stage 1 lWing pattern “races” of Heliconius melpomene

Why study speciation genomics?

Page 3: Genomic studies of speciation and gene flowevomicsorg.wpengine.netdna-cdn.com/.../02/Chris... · Some sub-species clearly in stage 1 lWing pattern “races” of Heliconius melpomene

Why study speciation genomics?

Long-standing questions (role of geography/gene flow)

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Why study speciation genomics?

How do genomes diverge?

Long-standing questions (role of geography/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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Genomic divergence during speciation

evolution.berkeley.edu

1. Speciation as a bi-product of physical isolation

2. Speciation due to selection – without isolation

80 100 120 140 160 180

0.0

0.4

0.8

Transect position (km)

Sd

frequ

ency

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

80 100 120 140 160 180

0.0

0.4

0.8

b fre

quen

cy

19862011

n11050

80 100 120 140 160 180

0.0

0.4

0.8

D fr

eque

ncy

80 100 120 140 160 180

0.0

0.4

0.8

N fr

eque

ncy

80 100 120 140 160 180

0.0

0.4

0.8

Transect position (km)

Yb

frequ

ency

80 100 120 140 160 180

0.0

0.4

0.8

D fr

eque

ncy 1986

2011n11050

80 100 120 140 160 180

0.0

0.4

0.8

Cr

frequ

ency

80 100 120 140 160 180

0.0

0.4

0.8

Transect position (km)

Sd

frequ

ency

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 here is a recent example with multiple islands

Malinsky et al., Science 350, 1493 (2015).

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And here is a recent example with multiple islands

Malinsky et al., Science 350, 1493 (2015).

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And here is a recent 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…

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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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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

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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

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Explicit tests for gene flow: ABBA-BABA test

Green et al. 2010 Science 328:710-722

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OBSERVE: 103612 ABBA 94029 BABA

Gene flow

Explicit tests for gene flow: ABBA-BABA test

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EXPECT: 50% ABBA 50% BABA

OBSERVE: 103612 ABBA 94029 BABA

Gene flow

Green et al. 2010 Science 328:710-722

Explicit tests for gene flow: ABBA-BABA test

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EXPECT: 50% ABBA 50% BABA

OBSERVE: 103612 ABBA 94029 BABA

Gene flow

Green et al. 2010 Science 328:710-722

Explicit tests for gene flow: ABBA-BABA test

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Explicit tests for gene flow: ABBA-BABA test

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Explicit tests for gene flow: Combining multiple signals

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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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Explicit tests for gene flow: Heliconius butterflies

!

Martin et al., Genome Research 2013

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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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Explicit tests for gene flow: Heliconius butterflies

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Explicit tests for gene flow: Heliconius butterflies

• Much larger proportion of genome is flowing as compared to Neanderthals

• Similarly strong effect on sex chromosome

F

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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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So far models have mostly just estimated genome-wide parameters…assuming the genome is homogenous

Where we need to go next is to incorporate genome heterogeneity in selection and recombination

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So far models have mostly just estimated genome-wide parameters…assuming the genome is homogenous

Where we need to go next is to incorporate genome heterogeneity in selection and recombination

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High density linkage maps to map the recombination landscape

Chromosome length (Megabases)

0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19

1

00.

788

2.37

53.

163

3.95

4.73

8

6.32

5

7.91

38.

706

9.5

10.6

8611

.872

12.6

5913

.446

14.2

3415

.021

15.8

0916

.596

17.3

8418

.171

19.7

58

21.3

4622

.133

22.9

3323

.734

29.5

2530

.319

31.1

1331

.932

.688

34.2

9935

.616

46.7

73

48.3

2249

.109

50.6

96

52.2

8453

.071

54.6

59

56.2

4657

.034

57.8

21

59.4

0860

.196

60.9

83

63.3

8464

.171

64.9

5965

.746

66.5

33

71.4

5472

.248

73.0

42

74.6

29

76.2

1777

.004

77.7

92

79.3

7980

.166

80.9

6781

.767

82.5

55

85.7

8286

.569

87.3

5788

.144

88.9

3189

.719

91.3

0692

.094

92.8

81

99.6

21

102.

09

2

00.

787

1.57

5

4.80

25.

589

6.37

7

7.96

4

9.55

2

11.1

39

12.7

2613

.514

14.3

01

20.9

78

23.3

7824

.166

27.3

93

29.7

9330

.581

31.3

6832

.156

32.9

43

34.5

335

.318

36.9

0537

.693

38.4

8639

.28

40.8

6841

.655

42.4

4243

.23

44.8

1745

.617

46.4

1647

.203

47.9

9148

.778

51.1

7951

.967

52.7

5553

.542

54.3

29

55.9

2456

.705

57.4

92

60.7

19

62.3

1363

.094

63.8

88

65.5

0266

.282

67.0

767

.857

69.4

45

71.0

32

72.6

273

.407

74.9

94

3

00.

787

1.57

5

3.97

54.

763

5.55

6.33

7

10.4

0511

.19

13.5

8914

.376

15.9

6416

.751

19.2

1220

.02

20.8

07

23.2

08

24.7

9525

.583

27.9

8328

.774

29.5

6430

.352

31.1

3931

.927

32.7

1433

.502

35.0

89

36.6

77

38.2

6639

.056

40.6

4341

.426

43.0

09

44.6

0645

.384

46.9

7147

.759

49.3

46

50.9

3451

.721

54.1

2154

.909

55.7

0956

.509

58.0

97

62.3

863

.019

63.8

19

65.4

2

68.6

46

71.0

4771

.834

74.2

35

75.8

2676

.61

78.1

98

80.5

98

82.2

1282

.999

84.1

8585

.371

86.9

5887

.746

90.9

7391

.773

92.5

73

94.1

6194

.948

4

00.

787

1.57

52.

362

3.15

5.55

6.33

87.

125

7.91

28.

79.

494

10.2

8711

.075

11.8

6212

.65

13.4

37

15.8

37

18.2

38

19.8

2520

.619

21.4

13

22.9

42

25.4

7226

.265

27.0

6627

.86

28.6

4729

.435

30.2

22

31.8

4332

.61

35.8

536

.637

43.3

14

44.9

01

46.4

8947

.276

48.0

64

50.4

6451

.248

52.8

3953

.626

55.2

1456

.001

56.7

89

58.3

6

62.5

3763

.337

64.1

38

65.7

2566

.519

67.3

1368

.168

.887

69.6

7570

.462

72.0

5372

.843

75.2

77

76.8

64

78.4

5279

.239

80.8

27

82.4

14

84.0

02

85.5

8986

.376

87.1

49

88.7

7789

.564

5

0

1.58

8

3.98

84.

775

7.17

6

11.2

4312

.031

12.8

1813

.605

15.1

9315

.98

19.2

0719

.995

21.5

82

24.8

0925

.626

.387

27.9

7728

.785

30.3

7231

.159

31.9

4732

.747

33.5

4834

.335

35.1

22

38.3

49

48.7

01

51.1

0251

.889

52.6

7653

.464

54.2

5155

.039

55.8

26

59.8

9360

.681

61.4

6862

.256

63.8

43

65.4

3

67.8

7868

.657

70.2

5571

.033

71.8

2472

.616

73.4

03

75.8

0476

.591

77.3

7978

.166

78.9

5479

.741

82.1

4282

.93

83.7

1784

.505

85.2

9286

.08

86.8

67

6

0

1.58

7

3.17

5

4.76

25.

556.

337

7.92

5

9.51

2

11.1

1911

.912

13.5

15.0

87

16.6

75

18.2

6219

.05

19.8

3720

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21.4

12

24.6

3925

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27.0

39

29.4

4

31.0

27

32.6

15

34.2

0234

.989

35.7

7736

.564

38.1

5538

.933

40.5

2741

.315

42.1

02

44.5

0345

.29

47.4

7

51.9

67

54.3

6755

.154

57.5

958

.381

65.9

5866

.746

67.5

3368

.321

69.1

0869

.895

70.6

83

72.2

773

.058

73.8

4574

.632

77.0

33

78.6

2

86.1

9886

.972

88.5

46

90.6

8191

.727

92.5

14

94.9

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96.4

9697

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101.

354

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276

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677

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44

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028

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1313

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16.7

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519

.147

19.9

44

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0723

.894

25.4

8126

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28.6

69

30.2

5731

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35.9

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38.3

41

41.5

6842

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44.7

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47.1

32

48.7

2649

.507

52.7

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.52

54.3

08

56.7

08

59.1

0959

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60.6

8461

.471

62.2

5863

.046

63.8

464

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65.4

2166

.208

68.6

0969

.396

73.4

6374

.251

75.0

3875

.826

77.4

13

79.0

0779

.788

80.5

76

84.6

4385

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86.2

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824

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938

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.282

17.9

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19.5

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24.2

62

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5

28.2

5

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5131

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32.2

3833

.026

33.8

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35.4

0136

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36.9

7537

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38.5

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2540

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44.2

0744

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46.5

6847

.355

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24

51.5

1252

.313

53.1

13

54.7

55.4

8856

.275

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6957

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61.0

9

63.4

9

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78

66.6

65

68.2

49

70.6

5371

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72.2

2873

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0374

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766

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45

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95

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8228

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47.5

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50.7

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48

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46

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.883

80.5

6

82.1

4782

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83.7

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1

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9787

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0

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175

3.96

24.

75

6.33

7

7.92

58.

712

9.5

10.2

8711

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11.8

6212

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13.4

3714

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.799

16.5

86

18.9

87

20.5

7821

.362

22.9

4923

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25.3

2426

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27.6

9928

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29.2

74

30.8

6131

.649

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36

34.8

2435

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24

39.3

9640

.461

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7842

.836

43.6

3

45.2

3646

.024

46.8

1147

.599

48.3

8649

.174

50.7

6151

.548

52.3

3653

.123

54.7

1155

.498

56.2

9657

.094

58.6

82

60.2

6961

.056

65.1

2465

.911

66.7

0867

.499

68.2

8669

.074

69.8

6170

.648

71.4

3672

.223

73.8

1174

.753

78.6

5579

.443

81.0

381

.818

84.2

1885

.006

88.2

32

89.8

290

.607

91.3

9592

.182

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The effect of background selection on introgression in humans

Harris and Nielson Biorxiv 2015

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The effect of background selection on introgression in humans

Harris and Nielson Biorxiv 2015

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 shameless plug….

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And finally a shameless plug….

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Adaptive introgression

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Photo credit Andrei Sourakov

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Photo credit Andrei Sourakov

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Photo credit Andrei Sourakov

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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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Several major loci control Heliconius patterns

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Several major loci control Heliconius patterns

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Several major loci control Heliconius patterns

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Several major loci control Heliconius patterns

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Several major loci control Heliconius patterns

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Several major loci control Heliconius patterns

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Reed et al., 2011 Science

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E

Richard Wallbank

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Cross-species sharing

Heliconius Genome Consortium Nature 2012

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Cross-species sharing

Heliconius Genome Consortium Nature 2012

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Cross-species sharing

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

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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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

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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 heurippa

NNBB

Mavarez et al., Nature 2006

Camilo Salazar

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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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optix100kb

Wallbank et al., PLoS Biology 2016

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Red

optix100kb

Wallbank et al., PLoS Biology 2016

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RedBlue

optix100kb

Wallbank et al., PLoS Biology 2016

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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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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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What about behaviour?

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What about behaviour?

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H. melpomene X H. cydno

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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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Mate preference segregates withforewing colour in backcross hybrids

Rel

ativ

e pr

obab

ility

of c

ourti

ngH

. mel

pom

ene

fem

ales

Merrill et al. Proc Roy Soc B, 2011

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Mate preference segregates withforewing colour in backcross hybrids

Rel

ativ

e pr

obab

ility

of c

ourti

ngH

. mel

pom

ene

fem

ales

Merrill et al. Proc Roy Soc B, 2011

H. melpomene measured preference

H. cydnomeasured preference

Large effect: 35% of thedifference betweenparental species

G = 58.64, P << 0.001

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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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Now working on QTL maps of species differences in behaviour:

01234

LOD

sco

re

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 X

01234

LOD

sco

re

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 X

01234

Chromosome

LOD

sco

re

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 X

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Lamichhaney et al., Nature 2015

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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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Explicit tests for gene flow: ABBA-BABA test

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Explicit tests for gene flow: ABBA-BABA test

Green et al. 2010 Science 328:710-722

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D is quite dependent on the number of informative sites (the denominator)

Martin et al., MBE 2014

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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

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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

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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

Martin et al., MBE 2014

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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?