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Introgression and the origin of maize 
in Mexico and the Southwest US 
Jeffrey Ross-Ibarra 
@jrossibarra • www.rilab.org 
Dept. Plant Sciences • Center for Population Biology • Genome Center 
University of California Davis
acknowledgements 
Matt Hufford 
(Iowa State) 
Rute Fonseca 
(Copenhagen) 
Joost van Heerwaarden 
(Wageningen) 
Tom Gilbert (Copenhagen) John Doebley (Wisconsin)
maize origins
maize origins
maize origins
Meyerowitz 1994 Current Biology 
Duvick et al. 1999 US 6639132 B1 
maize origins 
Tripsacum extinct maize
Meyerowitz 1994 Current Biology 
Duvick et al. 1999 US 6639132 B1 
maize origins 
Tripsacum F1 extinct maize
Meyerowitz 1994 Current Biology 
Duvick et al. 1999 US 6639132 B1 
maize origins 
Tripsacum F1 extinct maize
Meyerowitz 1994 Current Biology 
Duvick et al. 1999 US 6639132 B1 
maize origins 
F1 Tripsacum F1 extinct maize
single origin from teosinte 
Matsuoka et al. 2002 PNAS 
Piperno et al. 2009 PNAS 
mays 
parv 
mex
paradox of maize ancestry 
Fig. 2. A view of the enormous boulder that formed the Xihuatoxtla Shelter. 
Matsuoka et al. 2002 PNAS 
Piperno et al. 2009 PNAS 
mays 
parv 
mex 
1,400 mm annually with over 90% falling during the June-to- 
October rainy season. The potential vegetation of the region is 
tropical deciduous forest, seen today in remnants scattered 
throughout the region. Vegetational reconstructions indicate 
that a species-diverse seasonal tropical forest flourished there 
B.P.), but the reworking of the rock shelter deposits in the early 
20th century has left them thoroughly mixed over most of the 
site. At a fourth site, the Temaxcalapa Shelter, we recovered a 
large number of chipped stone artifacts from the eroded slope in 
front of the shelter, including preceramic-aged spear points.We 
SEE COMMENTARY
landrace and teosinte sampling 
van Heerwaarden et al. 2011 PNAS
SNPs show highland similarity to teosinte 
van Heerwaarden et al. 2011 PNAS
admixture explains patterns of diversity 
mexicana parviglumis South/Caribbean West Highland 
2500 
2000 
m 
1500 
1000 
500 
0 
van Heerwaarden et al. 2011 PNAS
admixture explains patterns of diversity 
H Genetic distance to parviglumis Heterozygosity 
0.0 0.2 0.4 0.6 0.8 1.0 
0.20 0.25 0.30 0.35 0.40 0.45 
admixture proportion 
F 
van Heerwaarden et al. 2011 PNAS 
0.0 0.2 0.4 0.6 0.8 1.0 
0.25 0.26 0.27 0.28 0.29 
admixture proportion 
observed 
observed
Pesach Lubinsky 
Norm Ellstrand 
hybrids commonly observed 
Pesach Lubinsky
admixture along the genome 
maize 
mexicana 
Mb 
% population admixed 
Chromosome 4 
Hufford et al. 2013 PLoS Genetics
El Porvenir 
Opopeo 
Santa Clara 
Nabogame 
Puruandiro 
Xochimilco 
Tenango del Aire 
San Pedro 
Ixtlan 
Allopatric 
admixture localized, asymmetric 
El Porvenir 
Opopeo 
Santa Clara 
Nabogame 
Puruandiro 
Xochimilco 
Tenango del Aire 
San Pedro 
Ixtlan 
Allopatric 
Hufford et al. 2013 PLoS Genetics 
Pyhäjärvi et al. 2013 GBE
El Porvenir 
Opopeo 
Santa Clara 
Nabogame 
Puruandiro 
Xochimilco 
Tenango del Aire 
San Pedro 
Ixtlan 
Allopatric 
admixture localized, asymmetric 
El Porvenir 
Opopeo 
Santa Clara 
Nabogame 
Puruandiro 
Xochimilco 
Tenango del Aire 
San Pedro 
Ixtlan 
Allopatric 
Inv4n 
Hufford et al. 2013 PLoS Genetics 
Pyhäjärvi et al. 2013 GBE
El Porvenir 
Opopeo 
Santa Clara 
Nabogame 
Puruandiro 
Xochimilco 
Tenango del Aire 
San Pedro 
Ixtlan 
Allopatric 
admixture localized, asymmetric 
El Porvenir 
Opopeo 
Santa Clara 
Nabogame 
Puruandiro 
Xochimilco 
Tenango del Aire 
San Pedro 
Ixtlan 
Allopatric 
Inv4n 
Hufford et al. 2013 PLoS Genetics 
Pyhäjärvi et al. 2013 GBE
El Porvenir 
Opopeo 
Santa Clara 
Nabogame 
Puruandiro 
Xochimilco 
Tenango del Aire 
San Pedro 
Ixtlan 
Allopatric 
admixture localized, asymmetric 
El Porvenir 
Opopeo 
Santa Clara 
Nabogame 
Puruandiro 
Xochimilco 
Tenango del Aire 
San Pedro 
Ixtlan 
Allopatric 
* 
* 
* 
* * 
Inv4n 
Hufford et al. 2013 PLoS Genetics 
Pyhäjärvi et al. 2013 GBE
introgressions overlap with mexicana QTL 
Lauter et al. 2004 Genetics 
Moose et al. 2004 Genetics 
b1 in maize 
Inv4n 
Hufford et al. 2013 PLoS Genetics
introgressions show mexicana phenotypes 
Introgression No Introgression 
Hufford et al. 2013 PLoS Genetics 
macrohairs 
pigmentaton
introgressions grow faster at low temp 
Introgressed 
Not 
Introgressed 
Hufford et al. 2013 PLoS Genetics
admixture confounds ancestral inference 
compare to wild ancestor 
inferred origin 
origin
admixture confounds ancestral inference 
compare to wild ancestor 
inferred origin 
origin 
compare to wild ancestor 
origin 
gene flow 
inferred origin
Gene frequency 
a solution: ancestral reconstruction 
Nicholson et al 2002 J Roy Stat Soc. B 
wild ancestor 
1 
0
origin 
Gene frequency 
a solution: ancestral reconstruction 
Nicholson et al 2002 J Roy Stat Soc. B 
wild ancestor 
1 
0 
1 
0
wild ancestor origin 
derivative 1 derivative 2 
Gene frequency 
a solution: ancestral reconstruction 
1 
drift 
1 
drift 
Nicholson et al 2002 J Roy Stat Soc. B 
1 
0 
1 
0 
0 
0
ancestral reconstruction resolves origins 
wild ancestor 
origin 
gene flow 
inferred origin
ancestral reconstruction resolves origins 
ancestral reconstruction 
origin 
inferred origin 
gene flow 
wild ancestor 
origin 
gene flow 
inferred origin
because the adaptive differences between highland and lowland 
maize are profound (14, 29). In other crops, uncertainty about 
ancestral allele frequen-cies. 
frequencies observed in parviglumis 
because the adaptive differences between highland and maize are profound (14, 29). In other crops, uncertainty 0.1 0.2 0.3 0.4 
maize origins in lowland west Mexico 
frequen-cies. 
parviglumis 
B A B C 
Compared to wild teosinte Compared to ancestral maize 
0.1 0.2 0.3 0.4 0.1 0.2 0.3 0.4 
Lowland 
Lowland 
0.3 0.4 0.1 0.2 0.3 0.4 
0.1 0.2 0.3 0.4 
Genetic distance from ancestor 
density 
F F 
F F 
F 
parameter F for 10 genetic groups with respect to (A) mexicana and (B) parviglumis. Only lowland included. van (Heerwaarden C) Drift of all et 10 al. genetic 2011 PNAS 
groups with respect to inferred ancestral frequencies. Light blue represents between lowlands (<1,500 m, solid line) and highlands (>2,000 m). 
C 
genetic groups with respect to (A) mexicana and (B) parviglumis. Only lowland accessions of 
genetic groups with respect to inferred ancestral frequencies. Light blue represents West 
m, solid line) and highlands (>2,000 m).
maize origins in lowland west Mexico 
1750m 1250m 
van Heerwaarden et al. 2011 PNAS
how did maize arrive and adapt to SW US? 
J. ROSS-IBARRA / UC DAVIS 
2. Coastal route 
1. Highland route 
SW 
Mexico 
Fonseca et al. 2015 Nature Plants 
Ronald Humeyestewa
ancient cobs to investigate chronology 
Fonseca et al. 2015 Nature Plants 
Hufford et al. 2012 Nature Genetics
DNA capture to enrich for subset of genome 
J. ROSS-IBARRA / UC DAVIS 
Fonseca et al. 2015 Nature Plants
ancient DNA data analysis: ANGSD 
J. ROSS-IBARRA / UC DAVIS 
error rate 
Fonseca et al. 2015 Nature Plants
SW shares ancestry with highland Mexico 
J. ROSS-IBARRA / UC DAVIS 
6. Barplots of STRUCTURE q-matrices (2310 modern maize landraces and 
teosinte) from k=3 to k=10 where k is the number of groups assigned. Each individual 
Figure group is sorted from low to high elevation (top to bottom). The high elevation groups in 
the SW, Mexico and Guatemala share ancestry with each other and to varying extents 
parviglumis 
mexicana 
S. America 
C. America 
Mexico 
SWUS 
Fonseca et al. 2015 Nature Plants 
US
allele counts support both hypotheses 
SWUS highland coast teosinte 
HUFFORD ET AL. 2012 PLOS GENETICS 
VAN HEERWAARDEN ET AL 2011 PNAS 
Fonseca et al. 2015 Nature Plants J. ROSS-IBARRA / UC DAVIS
allele counts support both hypotheses 
SWUS highland coast teosinte 
K=5 
a b c 
TMx25 
TMx08 
TPa06 
TPa10 
Ancient Mexico 
Reventador 
Chapalote 
Highlands 
Mex35 
Mex25 
Mex31 
Mex30 
Mex29 
SW3K 
SW2K 
SW750 
USA17 
0.00 0.05 0.10 0.15 0.20 
Teosintes 
USA 
Mexico 
Central/South America 
Chile 
Z. m. mexicana 
Z. m. parviglumis 
Coastal 
Drift parameter 
USA 
Mexico 
SW3K 
SW2K 
SW750 
USA17 
-0.2 -0.1 0.0 0.1 0.2 
D 
Coastal 
Highlands 
Outgroup 
SW 
Coastal 
Highlands 
Outgroup 
SW 
HUFFORD ET AL. 2012 PLOS GENETICS 
VAN HEERWAARDEN ET AL 2011 PNAS 
Figure 1 
Fonseca et al. 2015 Nature Plants J. ROSS-IBARRA / UC DAVIS
tree, admixture analyses support results 
K=5 
TMx25 
TMx08 
TPa06 
TPa10 
Ancient Mexico 
Reventador 
Chapalote 
Highlands 
Mex35 
Mex25 
Mex31 
Mex30 
Mex29 
SW3K 
SW2K 
SW750 
USA17 
0.00 0.05 0.10 0.15 0.20 
Teosintes 
USA 
Mexico 
Central/South America 
Chile 
Z. m. mexicana 
Z. m. parviglumis 
Coastal 
Drift parameter 
USA 
Coastal 
Highlands 
SW 
0.1 0.2 
b c 
Figure 1 
Fonseca et al. 2015 Nature Plants J. ROSS-IBARRA / UC DAVIS
ancient population genomics 
J. ROSS-IBARRA / UC DAVIS 
~2000 years b.p. 
n=10 
Changes in 
shape and size 
~750 years b.p. 
n=12 
Fonseca et al. 2015 Nature Plants
selection affects patterns of diversity
selection affects patterns of diversity 
SFS 
Proportion 
SNPs 
0.7 
0.525 
0.35 
0.175 
0 
1 2 3 4 
Individuals 
Proportion 
SNPs 
0.7 
0.525 
0.35 
0.175 
0 
1 2 3 4 
Individuals 
Taj D = 0 
Taj D < 0
selection affects patterns of diversity 
SFS 
Proportion 
SNPs 
0.7 
0.525 
0.35 
0.175 
0 
1 2 3 4 
Individuals 
Proportion 
SNPs 
0.7 
0.525 
0.35 
0.175 
0 
1 2 3 4 
Individuals 
Taj D = 0 
Taj D < 0 
PBS 
2000yr 
700yr 
teosinte
methods identify known domestication loci 
J. ROSS-IBARRA / UC DAVIS 
median PBS values 
parviglumis 
SW750 SW2K 
dehyd1A 
parviglumis 
SW2K 
SW750 
a b 
Fonseca et al. 2015 Nature Plants Figure 2
domestication loci 
John Doebley 
median PBS values parviglumis 
parviglumis) 
PBS(SW750 SW2K 
dehyd1A 
zagl1 
su1 
parviglumis 
SW750 SW2K 
parviglumis 
parviglumis 
SW2K 
b 
Fonseca et al. 2015 Nature Plants J. ROSS-IBARRA / UC DAVIS Liu et al. 2013 PLOS Genetics
domestication loci 
John Doebley 
median PBS values parviglumis 
parviglumis) 
PBS(SW750 SW2K 
dehyd1A 
zagl1 
su1 
parviglumis 
SW750 SW2K 
parviglumis 
parviglumis 
SW2K 
b 
Fonseca et al. 2015 Nature Plants J. ROSS-IBARRA / UC DAVIS Liu et al. 2013 PLOS Genetics
Fonseca et al. 2015 Nature Plants J. ROSS-IBARRA / UC DAVIS 
PBS(parviglumis) 
parviglumis 
SW750 SW2K 
dehyd1A 
su1 
parviglumis 
SW750 SW2K 
parviglumis 
SW2K 
SW750 
parviglumis 
SW2K 
SW750 
Figure 2 
Liu et al. 2013 PLOS Genetics 
median PBS values 
PBS(parviglumis) 
parviglumis 
SW750 SW2K 
dehyd1A 
zagl1 
su1 
parviglumis 
SW750 SW2K 
parviglumis 
parviglumis 
SW2K 
b 
adaptation loci 
Bill Belknap 
John Doebley
chronology of selection on starch pathway 
Fonseca et al. 2015 Nature Plants J. ROSS-IBARRA / UC DAVIS
concluding thoughts 
• introgression confounds simple estimates of origin 
• ancestral reconstruction provides resolution 
• introgression adapted maize to highlands 
• Southwest US maize originated in highlands with 
subsequent gene flow from Pacific Coast 
• ancient DNA allows chronology of gene flow, 
adaptation

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Maize origins in Mexico and SW US revealed through ancestral reconstruction

  • 1. Introgression and the origin of maize in Mexico and the Southwest US Jeffrey Ross-Ibarra @jrossibarra • www.rilab.org Dept. Plant Sciences • Center for Population Biology • Genome Center University of California Davis
  • 2. acknowledgements Matt Hufford (Iowa State) Rute Fonseca (Copenhagen) Joost van Heerwaarden (Wageningen) Tom Gilbert (Copenhagen) John Doebley (Wisconsin)
  • 6. Meyerowitz 1994 Current Biology Duvick et al. 1999 US 6639132 B1 maize origins Tripsacum extinct maize
  • 7. Meyerowitz 1994 Current Biology Duvick et al. 1999 US 6639132 B1 maize origins Tripsacum F1 extinct maize
  • 8. Meyerowitz 1994 Current Biology Duvick et al. 1999 US 6639132 B1 maize origins Tripsacum F1 extinct maize
  • 9. Meyerowitz 1994 Current Biology Duvick et al. 1999 US 6639132 B1 maize origins F1 Tripsacum F1 extinct maize
  • 10. single origin from teosinte Matsuoka et al. 2002 PNAS Piperno et al. 2009 PNAS mays parv mex
  • 11. paradox of maize ancestry Fig. 2. A view of the enormous boulder that formed the Xihuatoxtla Shelter. Matsuoka et al. 2002 PNAS Piperno et al. 2009 PNAS mays parv mex 1,400 mm annually with over 90% falling during the June-to- October rainy season. The potential vegetation of the region is tropical deciduous forest, seen today in remnants scattered throughout the region. Vegetational reconstructions indicate that a species-diverse seasonal tropical forest flourished there B.P.), but the reworking of the rock shelter deposits in the early 20th century has left them thoroughly mixed over most of the site. At a fourth site, the Temaxcalapa Shelter, we recovered a large number of chipped stone artifacts from the eroded slope in front of the shelter, including preceramic-aged spear points.We SEE COMMENTARY
  • 12. landrace and teosinte sampling van Heerwaarden et al. 2011 PNAS
  • 13. SNPs show highland similarity to teosinte van Heerwaarden et al. 2011 PNAS
  • 14. admixture explains patterns of diversity mexicana parviglumis South/Caribbean West Highland 2500 2000 m 1500 1000 500 0 van Heerwaarden et al. 2011 PNAS
  • 15. admixture explains patterns of diversity H Genetic distance to parviglumis Heterozygosity 0.0 0.2 0.4 0.6 0.8 1.0 0.20 0.25 0.30 0.35 0.40 0.45 admixture proportion F van Heerwaarden et al. 2011 PNAS 0.0 0.2 0.4 0.6 0.8 1.0 0.25 0.26 0.27 0.28 0.29 admixture proportion observed observed
  • 16. Pesach Lubinsky Norm Ellstrand hybrids commonly observed Pesach Lubinsky
  • 17. admixture along the genome maize mexicana Mb % population admixed Chromosome 4 Hufford et al. 2013 PLoS Genetics
  • 18. El Porvenir Opopeo Santa Clara Nabogame Puruandiro Xochimilco Tenango del Aire San Pedro Ixtlan Allopatric admixture localized, asymmetric El Porvenir Opopeo Santa Clara Nabogame Puruandiro Xochimilco Tenango del Aire San Pedro Ixtlan Allopatric Hufford et al. 2013 PLoS Genetics Pyhäjärvi et al. 2013 GBE
  • 19. El Porvenir Opopeo Santa Clara Nabogame Puruandiro Xochimilco Tenango del Aire San Pedro Ixtlan Allopatric admixture localized, asymmetric El Porvenir Opopeo Santa Clara Nabogame Puruandiro Xochimilco Tenango del Aire San Pedro Ixtlan Allopatric Inv4n Hufford et al. 2013 PLoS Genetics Pyhäjärvi et al. 2013 GBE
  • 20. El Porvenir Opopeo Santa Clara Nabogame Puruandiro Xochimilco Tenango del Aire San Pedro Ixtlan Allopatric admixture localized, asymmetric El Porvenir Opopeo Santa Clara Nabogame Puruandiro Xochimilco Tenango del Aire San Pedro Ixtlan Allopatric Inv4n Hufford et al. 2013 PLoS Genetics Pyhäjärvi et al. 2013 GBE
  • 21. El Porvenir Opopeo Santa Clara Nabogame Puruandiro Xochimilco Tenango del Aire San Pedro Ixtlan Allopatric admixture localized, asymmetric El Porvenir Opopeo Santa Clara Nabogame Puruandiro Xochimilco Tenango del Aire San Pedro Ixtlan Allopatric * * * * * Inv4n Hufford et al. 2013 PLoS Genetics Pyhäjärvi et al. 2013 GBE
  • 22. introgressions overlap with mexicana QTL Lauter et al. 2004 Genetics Moose et al. 2004 Genetics b1 in maize Inv4n Hufford et al. 2013 PLoS Genetics
  • 23. introgressions show mexicana phenotypes Introgression No Introgression Hufford et al. 2013 PLoS Genetics macrohairs pigmentaton
  • 24. introgressions grow faster at low temp Introgressed Not Introgressed Hufford et al. 2013 PLoS Genetics
  • 25. admixture confounds ancestral inference compare to wild ancestor inferred origin origin
  • 26. admixture confounds ancestral inference compare to wild ancestor inferred origin origin compare to wild ancestor origin gene flow inferred origin
  • 27. Gene frequency a solution: ancestral reconstruction Nicholson et al 2002 J Roy Stat Soc. B wild ancestor 1 0
  • 28. origin Gene frequency a solution: ancestral reconstruction Nicholson et al 2002 J Roy Stat Soc. B wild ancestor 1 0 1 0
  • 29. wild ancestor origin derivative 1 derivative 2 Gene frequency a solution: ancestral reconstruction 1 drift 1 drift Nicholson et al 2002 J Roy Stat Soc. B 1 0 1 0 0 0
  • 30. ancestral reconstruction resolves origins wild ancestor origin gene flow inferred origin
  • 31. ancestral reconstruction resolves origins ancestral reconstruction origin inferred origin gene flow wild ancestor origin gene flow inferred origin
  • 32. because the adaptive differences between highland and lowland maize are profound (14, 29). In other crops, uncertainty about ancestral allele frequen-cies. frequencies observed in parviglumis because the adaptive differences between highland and maize are profound (14, 29). In other crops, uncertainty 0.1 0.2 0.3 0.4 maize origins in lowland west Mexico frequen-cies. parviglumis B A B C Compared to wild teosinte Compared to ancestral maize 0.1 0.2 0.3 0.4 0.1 0.2 0.3 0.4 Lowland Lowland 0.3 0.4 0.1 0.2 0.3 0.4 0.1 0.2 0.3 0.4 Genetic distance from ancestor density F F F F F parameter F for 10 genetic groups with respect to (A) mexicana and (B) parviglumis. Only lowland included. van (Heerwaarden C) Drift of all et 10 al. genetic 2011 PNAS groups with respect to inferred ancestral frequencies. Light blue represents between lowlands (<1,500 m, solid line) and highlands (>2,000 m). C genetic groups with respect to (A) mexicana and (B) parviglumis. Only lowland accessions of genetic groups with respect to inferred ancestral frequencies. Light blue represents West m, solid line) and highlands (>2,000 m).
  • 33. maize origins in lowland west Mexico 1750m 1250m van Heerwaarden et al. 2011 PNAS
  • 34. how did maize arrive and adapt to SW US? J. ROSS-IBARRA / UC DAVIS 2. Coastal route 1. Highland route SW Mexico Fonseca et al. 2015 Nature Plants Ronald Humeyestewa
  • 35. ancient cobs to investigate chronology Fonseca et al. 2015 Nature Plants Hufford et al. 2012 Nature Genetics
  • 36. DNA capture to enrich for subset of genome J. ROSS-IBARRA / UC DAVIS Fonseca et al. 2015 Nature Plants
  • 37. ancient DNA data analysis: ANGSD J. ROSS-IBARRA / UC DAVIS error rate Fonseca et al. 2015 Nature Plants
  • 38. SW shares ancestry with highland Mexico J. ROSS-IBARRA / UC DAVIS 6. Barplots of STRUCTURE q-matrices (2310 modern maize landraces and teosinte) from k=3 to k=10 where k is the number of groups assigned. Each individual Figure group is sorted from low to high elevation (top to bottom). The high elevation groups in the SW, Mexico and Guatemala share ancestry with each other and to varying extents parviglumis mexicana S. America C. America Mexico SWUS Fonseca et al. 2015 Nature Plants US
  • 39. allele counts support both hypotheses SWUS highland coast teosinte HUFFORD ET AL. 2012 PLOS GENETICS VAN HEERWAARDEN ET AL 2011 PNAS Fonseca et al. 2015 Nature Plants J. ROSS-IBARRA / UC DAVIS
  • 40. allele counts support both hypotheses SWUS highland coast teosinte K=5 a b c TMx25 TMx08 TPa06 TPa10 Ancient Mexico Reventador Chapalote Highlands Mex35 Mex25 Mex31 Mex30 Mex29 SW3K SW2K SW750 USA17 0.00 0.05 0.10 0.15 0.20 Teosintes USA Mexico Central/South America Chile Z. m. mexicana Z. m. parviglumis Coastal Drift parameter USA Mexico SW3K SW2K SW750 USA17 -0.2 -0.1 0.0 0.1 0.2 D Coastal Highlands Outgroup SW Coastal Highlands Outgroup SW HUFFORD ET AL. 2012 PLOS GENETICS VAN HEERWAARDEN ET AL 2011 PNAS Figure 1 Fonseca et al. 2015 Nature Plants J. ROSS-IBARRA / UC DAVIS
  • 41. tree, admixture analyses support results K=5 TMx25 TMx08 TPa06 TPa10 Ancient Mexico Reventador Chapalote Highlands Mex35 Mex25 Mex31 Mex30 Mex29 SW3K SW2K SW750 USA17 0.00 0.05 0.10 0.15 0.20 Teosintes USA Mexico Central/South America Chile Z. m. mexicana Z. m. parviglumis Coastal Drift parameter USA Coastal Highlands SW 0.1 0.2 b c Figure 1 Fonseca et al. 2015 Nature Plants J. ROSS-IBARRA / UC DAVIS
  • 42. ancient population genomics J. ROSS-IBARRA / UC DAVIS ~2000 years b.p. n=10 Changes in shape and size ~750 years b.p. n=12 Fonseca et al. 2015 Nature Plants
  • 44. selection affects patterns of diversity SFS Proportion SNPs 0.7 0.525 0.35 0.175 0 1 2 3 4 Individuals Proportion SNPs 0.7 0.525 0.35 0.175 0 1 2 3 4 Individuals Taj D = 0 Taj D < 0
  • 45. selection affects patterns of diversity SFS Proportion SNPs 0.7 0.525 0.35 0.175 0 1 2 3 4 Individuals Proportion SNPs 0.7 0.525 0.35 0.175 0 1 2 3 4 Individuals Taj D = 0 Taj D < 0 PBS 2000yr 700yr teosinte
  • 46. methods identify known domestication loci J. ROSS-IBARRA / UC DAVIS median PBS values parviglumis SW750 SW2K dehyd1A parviglumis SW2K SW750 a b Fonseca et al. 2015 Nature Plants Figure 2
  • 47. domestication loci John Doebley median PBS values parviglumis parviglumis) PBS(SW750 SW2K dehyd1A zagl1 su1 parviglumis SW750 SW2K parviglumis parviglumis SW2K b Fonseca et al. 2015 Nature Plants J. ROSS-IBARRA / UC DAVIS Liu et al. 2013 PLOS Genetics
  • 48. domestication loci John Doebley median PBS values parviglumis parviglumis) PBS(SW750 SW2K dehyd1A zagl1 su1 parviglumis SW750 SW2K parviglumis parviglumis SW2K b Fonseca et al. 2015 Nature Plants J. ROSS-IBARRA / UC DAVIS Liu et al. 2013 PLOS Genetics
  • 49. Fonseca et al. 2015 Nature Plants J. ROSS-IBARRA / UC DAVIS PBS(parviglumis) parviglumis SW750 SW2K dehyd1A su1 parviglumis SW750 SW2K parviglumis SW2K SW750 parviglumis SW2K SW750 Figure 2 Liu et al. 2013 PLOS Genetics median PBS values PBS(parviglumis) parviglumis SW750 SW2K dehyd1A zagl1 su1 parviglumis SW750 SW2K parviglumis parviglumis SW2K b adaptation loci Bill Belknap John Doebley
  • 50. chronology of selection on starch pathway Fonseca et al. 2015 Nature Plants J. ROSS-IBARRA / UC DAVIS
  • 51. concluding thoughts • introgression confounds simple estimates of origin • ancestral reconstruction provides resolution • introgression adapted maize to highlands • Southwest US maize originated in highlands with subsequent gene flow from Pacific Coast • ancient DNA allows chronology of gene flow, adaptation