targeted mapping of loci conferring resistance to yellow rust in pavon-76/ borlaug ril population
DESCRIPTION
Abdulqader Jighly;Yaljarouka A; Nazari K; Tahir I; Abdalla O; Ogbonnaya FCTRANSCRIPT
TARGETED MAPPING OF LOCI CONFERRING RESISTANCE TO YELLOW RUST IN PAVON-76/ BORLAUG RIL POPULATION
IWSR Symposium ICARDA
Abdulqader Jighly;Yaljarouka A; Nazari K; Tahir I; Abdalla O; Ogbonnaya FC
ICARDA
OUTLINES
Introduction Serve epidemic 2009-10YR genes summaryYR genes – 2010
Aim of the study Study Plan Plant Material Progress so far Summary
INTRODUCTION Stripe rust, caused by Puccinia striiformis,
is one of the most globally important fungal diseases of wheat that cause significant annual yield losses.
In 2009-10, the breakdown of Yr27 has caused significant yield losses in Syria, Turkey, Iran, Uzbekistan, Morocco, Ethiopia, and Kenya, threatening the food security and livelihood of resource poor farmers (Hodson and Nazari 2010).
http://www.globalrust.org/traction?type=single&proj=Pathogen&sort=2&stickyparams=sort&rec=206
2009-10 STRIPE RUST SERVE EPIDEMIC IN SYRIA
Farmars field Idleb – Joubas
OPTIONS AVAILABLE FOR THE FARMERS
1. Fungicide
2. Disease Management
3.Using resistance varieties
Chromosome
GenesChromo.
CountGenome Count
1A YrDa1 1
1518.98%
2A Yr1, Yr8, Yr17, Yr32 43A YrTr2 14A YrHVII, YrMin, YrND 35A Yr34, Yr48 26A Yr42, YrD,YrDru2,YrH46 47A - 0
1BYr9, Yr10, Yr15, Yr21, Yr24, Yr26, Yr29, YrC143, YrAlp, YrH52, YrExp1, YrR212, YrCN17
13
4759.5%
2BYr5, Yr7, Yr27, Yr31, Yr41, Yr43, Yr44, YrCn19, YrZak, YrV23, YrSte, YrP81, YrS2199, YrSP
14
3B Yr4, Yr30, YrS, YrSte2, Yrns-B1 54B YrCle, YrMor, YrYam 35B Yr3, Yr19, Yr47, YrDru, YrExp2 56B Yr35, Yr36 27B Yr2,Yr6, Yr39, YrC591, YrZH84 51D Yr25 1
1721.52%
2D Yr16, Yr37, YrCK 33D Yr45 14D Yr22,Yr28,Yr46,YrAS2388 45D Yr40,YrDa2 26D Yr20, Yr23, YrTye, YrTr1 47D Yr18,Yr33 2Total 79 100%
SUMMARY OF YR GENES
DESIGNATED GENES FOR RESISTANCE TO STRIPE RUST 2010
Gene Chromo. Sources Linked
Markers Ref.
Yr4 3BS Avalon, Bolac, Emu S, Rubric AUS33333 (Bread wheat) Xcfb3530 Bansal et al.
2010
Yr43 2BL PI 591045, Lolo, many IDO377s derivatives (Spring Wheat)
Xwgp110, Xwgp113
Cheng and Chen 2009
Yr44 2BL PI 607839 (Spring Wheat) Xwgp100 Sui et al. 2009
Yr45 3DL PI 181434 (Spring Wheat) Xwp115, Xwp118
Li et al. 2010
Yr46 4D PI 250413 (common wheat) Xcfd71, Xbarc98
Herrera-Foessel et al. 2009
Yr47 5BS AUS28183 (common wheat)5 ± 2 cM
proximal to Lr52
Bansal U et al. 2011
Yr48 5AL PI 610750 (Bread wheat) Xwms291 Dubcovsky 2010
PREVIOUS WORK
The Pavon-76 variety (spring wheat) has been mapped before by (Williams et al. 2006) in the cross Pavon-76/Avocet with AFLP and SSR markers.
Based on the previous study, three locations (1BL, 3BS and 6BS) showed significant link to stripe rust resistance in Pavon-76 with some AFLP markers and only 1 SSR marker on 1BL.
The source of resistance (Pavon-76) showed a very good resistance level for the new stripe rust race.
AIM OF THE STUDY
Developing molecular markers which are more closely linked to those genomic locations and more useful for breeding programs and marker assisted selection than AFLP markers.
Discovering more genomic locations that linked to stripe rust resistance in this important gene pool.
THE STUDY PLAN
Field Scoring for two years in Tel-hadya. Bulk segregant analysis using molecular
markers with known link to different YR genes
Applying different kinds of molecular markers to construct a high resolution linkage map which are: SSR CAPs SNPs (based on NSF wheat SNP project) RGA EST-SSR
THE STUDY PLAN
The following link contains 5425 designed EST-SSR primers for wheat.
We search for RGA motifs with more than 70% identity in this file. The ESTs that contain high density of RGA motifs have been chosen to be requested.
CA707339http://wheat.pw.usda.gov/ITMI/EST-SSR/LaRota/table3_est-ssr%20designed%20primers.xls
PLANT MATERIALSStripe rust resistance has been
studied on 301 recombinant inbred lines (F7) of the cross Pavon-76/Borloug in 2009-10.
The source of resistance (Pavon-76) showed a very good resistance level
RESULTS SO FAR
PHENOTYPIC VARIATION 2009-10
0-4
5-9
10
-14
15
-19
20
-24
25
-29
30
-34
35
-39
40
-44
45
-49
50
-54
55
-59
60
-64
65
-70
71
-75
76
-80
0
5
10
15
20
25
R M S
33.67% 31.33% 35%
%
The score is according to CIMMYT coefficient
0-4 5-9 10-24 25-44 45-800
5
10
15
20
25
30
35
%
PHENOTYPIC VARIATION 2009-10
R M S
33.67% 31.33% 35%
PLANTING THE POPULATION AT ICARDA FIELD 2010-2011
Spreader
BULK DESCRIPTION The DNA of at least five lines that showed
similar resistant classification were used for bulk segregant analysis as follows: 10 MR 15 MR 20 MR 20 M * S
76 SSR (simple sequence repeat) and RGA (resistance gene analogue) markers should be applied on those bulked lines, 30 of them have been applied and the others have been requested.
BULK RESULTS Two markers on chromosome 1BL were
polymorphic between the bulks . Each marker seems to be linked to a
different gene because the first one –Xwmc631– showed coupling phase with the source of resistance (Pavon-76) and the other one –Xbarc181– showed a repulsion phase with the same parent.
The 1BL linkage group indicate that.
UP TO DATE
cfd48
barc181
barc137
gwm273wmc631
32.9
17.3
10.9
3.9
1BL
barc55
gwm148
16.8
2BS
0 2 4 6 8
cfd48
barc181
barc137
gwm273wmc631
LOD
0 5 10
Exp
Gro
up
1B
LU
nm
ap
pe
d
Le
ge
nd
« L
OD
» %
Exp
l.
Borl
Pavon
-76 *
S20
MR
20
M15
M
R10
M
R
Borl
Pavon
-76 *
S20
MR
20
M15
M
R10
M
R
UP TO DATE We also get a single markers on
chromosome 6BS –Xwmc487– which linked to stripe rust resistance but we weren’t able to construct a linkage group because of the lack of polymorphic markers.
The R2 value for this region was about 5%, this may increase if we add more markers.
380 SSR markers has been screened on the parental lines:92 markers of the whole set showed
polymorphic alleles.15 markers of those 92 polymorphic
ones have been applied on the whole population.
7 markers of those 15 have been mapped on two locations 1BL and 2BS
UP TO DATE
SUMMARY Pavon-76 showed a good level of
resistance to the new race of stripe rust.
Pavon-76/Borloug RIL population has been planted again in 2010-11.
Two QTLs on chromosome 1BL and one on 6BS has been detected so far based on some SSR markers.
Different molecular markers (EST-SSR, RGA, STS) are being applied on the population to identify markers for MAS.
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