harbouring the Fusarium head blight resistance QTL Qfhsifa5A Christian Wagner 1 Petra Schwarz 1 Maria Buerstmayr 1 Barbara Steiner 1 Klaus Brugger 1 Lisa Blazek 1 Delfina Barabaschi ID: 928536
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Slide1
High-resolution mapping of wheat chromosome arm 5AS
harbouring the Fusarium head blight resistance QTL Qfhs.ifa-5A
Christian Wagner
1, Petra Schwarz1, Maria Buerstmayr1, Barbara Steiner1, Klaus Brugger1, Lisa Blazek1, Delfina Barabaschi2, Andrea Volante2, Giampiero Vale2, Luigi Cativelli2, Hermann Buerstmayr1
1 BOKU-University of Natural Resources and Life Sciences Vienna, Department IFA-Tulln, Institute for Biotechnology in Plant Production, Konrad Lorenz Str. 20, A-3430 Tulln, Austria, 2 Council for Agricultural Research and Economics CREA , Genomics Research Centre, Via S. Protaso 302, 29017 Fiorenzuola d'Arda, Italy
Universität für Bodenkultur WienDepartment IFA-Tulln
Slide2Major disease caused by
Fusarium
species
Yield and quality lossesMycotoxin contaminationMany resistance QTL mapped in wheatQfhs.ifa-5A (Buerstmayr et al. 2002, 2003)Major Type 1 FHB resistance QTLCentromeric region of chromosome 5AS
Fusarium Head blight and Qfhs.ifa-5AConclusion
MethodAimDiscussionResultsIntroduction
Slide30
0.7
9.7
9.8
10.0
10.1
10.2
10.3
10.4
10.5
10.6
10.7
11.0
11.4
12.2
18.3
0.9
cM
- 9 bins
> 75% of 5AS
Linkage Mapping of
Qfhs.ifa-5A
Problems:
Centromeric position of
Qfhs.ifa-5A
Recombination
coldspot
NI-RIL population
NIL1 x NIL2
(
Qfhs.ifa-5A
) (susceptible)
3650 F
2
plants
70 recombinant
lines
Conclusion
Method
Aim
Discussion
Results
Introduction
Slide4http://www.biochemj.org/content/471/1/1
https://www.jic.ac.uk/staff/graham-moore/Wheat_meiosis.htmWheat Genome
Radiation induce double
stranded breaksrandomly and evenly distributed
recombination independentWheat tolerate large deletionshexaploid, 42 chromosmesviable in vivo plantsAim: increase map-resolution of 5AS via radiation mappingcreate deletion-mutants also for phenotyping
Radiation Hybrid mapping (Kumar et al. 2014)Conclusion MethodAimDiscussionResults
Introduction
Slide5mapping and
phenotyping
deletion mutations
for mapping only
Header
Chinese Spring
RH
1
M
2
=RS
1
M
3
=RS
2
1 or 2
selfing
generations
homozygous deletions
RS-NIL3 panel
Radiation
Selfing
RH-CS panel
Radiation Hybrid
5A
5B5B5B5D5D
only one
5A
->
hemizygous
RH
0
♂
5A
5B5D
♀
5B5B5D
X
CS fresh pollen
γ
-
irradiation
100
Gray
haploid cell
CS-N5AT5B
emasculated
haploid cell
5A5A
5B5B5D5D
M
1
=RS
0
NIL3 – Qfhs.ifa-5A
seeds
γ
-
irradiation
diploid cells 240-350
Gray
Seibersdorf
Department of
Plant Sciences
Conclusion
Method
Aim
Discussion
Results
Introduction
Slide6Prescreening plants for deletions with >15 markers
Plants with deletions on 5AS:
Genotyped with 102 5AS
specific markersRS-NIL3 panelSeed irradiation5157 plants screened80 informative plants
1.85% deletionsRH-CS panelPollen irradiation276 plants screened40 informative plants18% deletions
Deletion ScreeningConclusion MethodAimDiscussionResults
Introduction
Slide7Distributions of Deletions on 5AS
telomere, distal
proximal, centromere
RS-NIL3 panelRH-CS panel
Radiation Selfing
→ mostly small, intestitial deletions
Radiation Hybrid
→ mostly big, telomeric
deletions
Conclusion
Method
Aim
Discussion
Results
Introduction
= Deletion
marker order
Slide8RSH-consensus map
Cartha
Gène (De Givry et al., 2005)Genetic and radiation hybrid mappingCan merge populations
All data used for consensus map80 of RS-NIL3 panel40 of RH-CS panel = 120 in total102 5AS specific marker
http://www7.inra.fr/mia/T/CarthaGene/marker pattern: presence-absenceDeletion map:centi-Ray positions Conclusion MethodAimDiscussion
Results
Introduction
Slide9*5AS IWGSC physical length: ~250
Mbp
RSH-consensus map
Map length: 384.4 cR
Mapped
loci: 76
Map resolution: 0.65 Mb/cR
263.8
centromere
cR
0.0
3.1
6.3
14.4
15.9
19.0
20.5
22.0
26.6
32.7
34.1
37.0
38.5
68.0
74.5
76.1
80.9
87.3
88.8
92.0
96.7
106.4
109.6
112.7
114.2
119.0
125.4
126.9
128.5
131.5
133.0
141.1
142.6
158.3
162.7
165.5
171.8
180.3
181.9
190.4
203.7
209.3
212.9
220.1
221.8
235.1
238.6
240.3
248.9
255.5
257.1
272.7
276.2
281.8
283.6
287.3
291.0
294.7
296.6
298.4
302.1
307.8
313.3
315.1
327.2
331.0
336.8
338.8
349.5
358.3
365.1
367.3
374.6
376.9
384.4
gpg1293
cwem44c
gpg537
IWB62899
IWB4146
gpg2328
gpg2326
IWB29780
IWB68241
barc186
ldk243
IWB51518
ldk267
barc56
ldk284
gpg2162
gpg2163
gpg1438
barc117
gpg2168
gpg2038
IWB75561
jfio7
wmc150a
gwm293
gpg1440
gwm304
IWB8393
wmc150b
gpg2049
gpg2060
IWB10809
BE498768
ldk49
ldk2
gpg2233
gpg1763
gpg2092
gpg2072
gpg2126
IWB58275
ldk217
IWB33435
gpg574
gpg277
ldk218
ldk241
gpg1139
gpg1789
gpg2309
jfio4
gpg1994
gpg2250
ldk50
gpg2244
gpg2313
ldk16
ldk14
gpg2019
gpg2108
gpg1383
ldk242
gwm129
jfio2
ldk289
gpg2231
gpg2232
gpg2075
gpg2083
gpg2097
gwm415
gpg2121
gpg119
gpg35
gpg2336
gpg743
gpg1294
gpg2117
ldk113
gpg214
gpg2020
gpg2147
gpg2123
gpg2102
gpg1395
gpg2158
gpg1321
ldk215
gpg1777
gpg158
gpg2034
gpg2255
gpg2011
BE425161
gpg542
cfa2250
jfio6
gpg503
gwm443
IWB11440
gpg2
wmc654
telomere
Conclusion
Method
Aim
Discussion
Results
Introduction
Slide10Linkage vs RSH-consensus map
NI-RIL map
3650 NI-RILs
263.8
centromere
cR
0.0
3.1
6.3
14.4
15.9
19.0
20.5
22.0
26.6
32.7
34.1
37.0
38.5
68.0
74.5
76.1
80.9
87.3
88.8
92.0
96.7
106.4
109.6
112.7
114.2
119.0
125.4
126.9
128.5
131.5
133.0
141.1
142.6
158.3
162.7
165.5
171.8
180.3
181.9
190.4
203.7
209.3
212.9
220.1
221.8
235.1
238.6
240.3
248.9
255.5
257.1
272.7
276.2
281.8
283.6
287.3
291.0
294.7
296.6
298.4
302.1
307.8
313.3
315.1
327.2
331.0
336.8
338.8
349.5
358.3
365.1
367.3
374.6
376.9
384.4
gpg1293
cwem44c
gpg537
IWB62899
IWB4146
gpg2328
gpg2326
IWB29780
IWB68241
barc186
ldk243
IWB51518
ldk267
barc56
ldk284
gpg2162
gpg2163
gpg1438
barc117
gpg2168
gpg2038
IWB75561
jfio7
wmc150a
gwm293
gpg1440
gwm304
IWB8393
wmc150b
gpg2049
gpg2060
IWB10809
BE498768
ldk49
ldk2
gpg2233
gpg1763
gpg2092
gpg2072
gpg2126
IWB58275
ldk217
IWB33435
gpg574
gpg277
ldk218
ldk241
gpg1139
gpg1789
gpg2309
jfio4
gpg1994
gpg2250
ldk50
gpg2244
gpg2313
ldk16
ldk14
gpg2019
gpg2108
gpg1383
ldk242
gwm129
jfio2
ldk289
gpg2231
gpg2232
gpg2075
gpg2083
gpg2097
gwm415
gpg2121
gpg119
gpg35
gpg2336
gpg743
gpg1294
gpg2117
ldk113
gpg214
gpg2020
gpg2147
gpg2123
gpg2102
gpg1395
gpg2158
gpg1321
ldk215
gpg1777
gpg158
gpg2034
gpg2255
gpg2011
BE425161
gpg542
cfa2250
jfio6
gpg503
gwm443
IWB11440
gpg2
wmc654
cwem44c
6.3
wmc654
7.0
barc186
9.7
barc303
9.8
ldk267
10.0
gwm1057
10.1
barc56
10.2
barc117
wmc150a
gwm293
gwm304
10.3
ldk49
ldk2
ldk14
gwm129
gwm415
cfa2250
10.6
wmc705
10.7
barc1
11.0
barc180
11.4
wmc805
12.2
cM
10.4
10.5
RSH- consensus map
0.9 cM
342.2
cR
excellent resolution in centromeric region
380 fold map
improvement in
cR
/
cM
Conclusion
Method
Aim
Discussion
Results
Introduction
9 bins
66 bins
Centi
-Ray vs IWGSC-positions on 5AS
→
Confirms mapping data – match in marker order→ Breaks independent from chromosome position
ρ
=1r=0.99Conclusion MethodAimDiscussionResultsIntroduction
Centi
-Morgan
NIL-
map
telomere
centromere
ρ
=1
r
=0.55
*
centromere
Centi-Ray
RSH-map
telomere
centromere
Mbp IWGS
ref.sequ.V1
*
centromere
Slide12Radiation
Selfing
panel:
plants with deletions in QTL interval useable also for phenotypingFurther work:Backcrossing RS plants → minimize background mutationsPhenotype these lines in fieldRadiation Mapping rules in centromeric Regions
Genetic linkage mapping → low resolution
Radiation mapping → high resolution – even in centromeric regions→ Breaks evenly distributed→ Centi-Ray positions reflect true ratio of physical positionsConclusion Method
Aim
Discussion
Results
Introduction
Slide13Acknowledgement
xy
3.0
xy
16.0
5A_NILx10NI-RILsMorgane RothNoemie PratChristine UlzJohannes HeckmannNorman SchlatterLaura Hemmerling
Luigio
Cattivalli
Giampario
Vale
Delfina
Barabaschi
Andrea
Volante
providing RH panel and
marker sequences
Hermann Buerstmayr
Barbara Steiner
RH and RS panels
Petra Schwarz
Babor
Eshonkulov
Christian Wagner
Klaus
Brugger
Lisa Blazek
Anna Buerstmayr
Louise
Marteau
Marina
Roksandic
Kristina
BodischSimone ZimmerlShahryar Kianian and Ajay Kumarseed irradiation
Seibersdorf
Bradley J. TillMirta Matijevic
Department of Plant Sciences
This research project was funded through the Austrian Science Fund (FWF),
project number SFB F3711:
Functional genomics of Fusarium
resistance in wheat
Genotyping, Phenotyping
Slide14Thank You for Your Attention!
Are there any Questions?
christian.wagner@boku.ac.at
Slide15Further Information