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SAMEER KHANAL
DEPARTMENT OF CROP AND SOIL SCIENCES
THE UNIVERSITY OF GEORGIA
DEVELOPMENT OF AN A-GENOME DIPLOID MODEL
FOR COMPARATIVE GENOMICS IN
PEANUT AND OTHER LEGUMES
BACKGROUN
D
OBJECTIVE
S
SUMMARY
IMPORTANCE OF PEANUT
Among food legumes, second in national and global economic importance
United States World
Crop Area
Harvested
(ha)
Production
(Mg)
Area
Harvested
(ha)
Production
(Mg)
Soybean 28,842,260 82,820,048 91,386,621 209,531,558
Peanut 650,340 2,112,700 25,217,201 36,492,147
Source: compiled from faostat.fao.org
PEANUT PRODUCTION CONSTRAINTS
Abiotic
Constraints
Drought
High Temperature
www.gapeanuts.com/news/2006/092906.asp
southeastfarmpress.com/news/091106-peanut-markets/
www.washingtonpost.com/wp-
dyn/content/article/2006/07/29/AR2006072900414_pf.html
Abiotic
Constraints
Drought
High Temperature
Biotic
Constraints
Diseases
Insect-Pests
PEANUT PRODUCTION CONSTRAINTS
Source: Diseases compiled from
plantpathology.tamu.edu/Texlab/Fiber/Peanuts/atlas-toc.html
edis.ifas.ufl.edu/IN176
Third most important source of vegetable protein
Among food legumes, second in national and global economic importance
IMPORTANCE OF PEANUT
Fourth most important source of vegetable oil
Twelfth most important food crop in the world
Source: ICRISAT (www.icrisat.org) and
the UN-FAO
PEANUT IMPROVEMENT CONSTRAINTS
• POLYPLOIDY (YOUNG ET AL., 1996)
• AUTOGAMY (HALWARD ET AL., 1991)
• NARROW GENETIC BASE (KNAUFT &
GORBET, 1989)
AA BBX
AB
AABB
PARENTS:
INTERSPECIFIC
HYBRIDIZATION
F1 HYBRID:
SPONTANEOUS
CHROMOSOME DOUBLING
ALLOTETRAPLOI
D
PEANUT :
LOW GENETIC VARIABILITY
PEANUT IMPROVEMENT CONSTRAINTS
LACK OF SOURCES OF RESISTANCE TO SEVERAL ABIOTIC/BIOTIC
STRESSES IN CULTIVATED PEANUT
Source: peanut.tamu.edu/peanut_photos.htm
PEANUT IMPROVEMENT CONSTRAINTS
DIFFICULT TO INTROGRESS RESISTANCE GENES FROM DIPLOID WILD
SPECIES
WARRANTS COMPLEX CROSSES OR GENETIC TRANSFORMATION
LAGGING IN GENOMIC RESOURCES AND APPLICATION OF MOLECULAR
BREEDING SOLUTIONS TO THE PERTINENT PROBLEMS
Source: peanut.tamu.edu/peanut_photos.htm
REALIZATIONS
- A CONSENSUS MAP FOR ARACHIS
- MAPPING PHENOTYPIC AND QUANTITATIVE TRAIT LOCI (QTLs)
- MARKERS LINKED TO THE GENES OF INTEREST FOR MARKER
ASSISTED SELECTION (MAS)
CROP IMPROVEMENT THROUGH MOLECULAR BREEDING TECHNIQUES
REQUIRE:
OBJECTIVES
INCREASING THE FREQUENCY OF HIGH-THROUGHPUT DNA MARKERS IN
THE A-GENOME
FIRST OBJECTIVE
GOAL
A MICROSATELLITE-ENRICHED LINKAGE MAP FOR A-GENOME
MICROSATELLITE-BASED LINKAGE MAP FOR
THE AA-GENOME
- DIPLOID RFLP MAP PRODUCED FROM AN INTERSPECIFIC (A. duranensis x A.
stenosperma) HYBRID (HALWARD ET AL., 1993)
- TETRAPLOID RFLP MAP PRODUCED FROM HYBRID BETWEEN A. hypogaea AND
A ‘SYNTHETIC’ AMPHIDIPLOID [A. batizocoi x A. diogoi)] (BUROW ET AL., 2002)
- RECENTLY FIRST MICROSATELLITE-BASED MAP IS PUBLISHED IN Arachis
(MORETZSOHN ET AL., 2005).
LINKAGE MAPPING IN DIFFERENT PEANUT SPECIES
MICROSATELLITE-BASED LINKAGE MAP FOR
THE AA-GENOME
MICROSATELLITES OR SIMPLE SEQUENCE REPEATS (SSRs) ARE MULTIPLE
REPEATING UNITS OF 1 TO 4 BASE PAIRS
EXAMPLE: (A)5, (AT)7, (CGG)9, (ACGG)6
- SCREENING SEQUENCES FROM GENOMIC LIBRARY
- SCREENING SSR ENRICHED LIBRARY
- SCREENING EST SEQUENCES
- SCREENING OF SSRs AGAINST DIFFERENT GENOTYPES
SSR DEFINITION
SSR DEVELOPMENT
POLYMORPHISM DETECTION
MICROSATELLITE-BASED LINKAGE MAP FOR
THE AA-GENOME
- 720 MARKERS SCREENED AMONG 18 ELITE AND 14 EXOTIC GERMPLAM
ACCESSIONS
- 556 SSR MARKERS FOUND POLYMORPHIC
- 336 (60.4%) WERE POLYMORPHIC IN (A. Kuhlmanii x A. diogoi)
- 82 OUT OF 336 HAVE ALREADY BEEN MAPPED (MORETZSOHN ET AL., 2005)
Source: Ma (Communication)
SCREENING AVAILABLE SSR MARKERS FOR
POLYMORPHISMS
MICROSATELLITE-BASED LINKAGE MAP FOR
THE AA-GENOME
- MAPPING POPULATION OF A. kuhlmanii X A. diogoi
- GENOTYPING 82 PREVIOUSLY MAPPED AND 254 PREVIOUSLY
UNMAPPED SSR MARKER LOCI
- THREE FOLD INCREASE IN THE DENSITY OF DNA MARKER LOCI IN THE
A-GENOME
RESEARCH OVERVIEW FOR THE FIRST OBJECTIVE
OBJECTIVES
GENETIC MAPPING OF NUCLEOTIDE BINDING SITE – LEUCINE RICH
REPEATS (NBS-LRR) REGISTANCE GENE CANDIDATE (RGC) LOCI
SECOND OBJECTIVE
GOAL
MAPPING OF 100-150 NBS-LRR RGCs
GENETIC MAPPING OF NBS-LRR RGC LOCI
- GROUPED INTO SEVERAL FAMILIES
- MOST R-GENE PROTEINS CHARACTERIZED BY NUCLEOTIDE BINDING
SITE LEUCINE RICH REPEATS
- 150 NBS-LRR-ENCODING GENES IN Arabidopsis thaliana AND >400 IN
Oryza sativa
Source: McHale et al. 2006
NBS LR
R
TIR/CCN C
RESISTANCE GENES IN PLANTS
GENETIC MAPPING OF NBS-LRR RGC
LOCI
INDEL AND SSCP MARKERS BEING DEVELOPED
NBS-LRR TEMPLETES: BERTIOLI ET AL. (2004), YUSKEL ET AL.
(2005), COOK ET AL. (UNPUBLISHED DATA)
SCREENING: 58 NBS-LRR TEMPLETES SCREENED SO FAR
EIGHT CULTIVATED PEANUT (AABB) : HIGHLY MONOMORPHIC
FOUR DIPLOID GENOTYPES: HIGHLY POLYMORPHIC
RGC7
RGC4
RGC8
DUR25
DUR35
BAT6
BAT8
HYP-GTC-9
HYP-A100
HYP-AEQ-2
HYP-PRV-1
HYP-Tifrunner
HYP-HIR-3
HYP-GTC-20
HYP-FST-3
DUR BAT
- AFLP-BASED MAPPING OF RESISTANCE TO
APHID VECTOR (HERSELMAN ET AL., 2004)
- THREE SMALL MAP SETS WITH MARKERS
FOR ROOT KNOT NEMATOD RESISTANCE
(JESUBATHAM AND BUROW, 2006)
RESISTANT GENE MAPPING IN PEANUT
MARKERS USED FOR MAPPING NBS-LRR RGC
LOCI
GENETIC MAPPING OF NBS-LRR RGC
LOCI
- MAPPING NBS-LRR RGC LOCI IN MAPPING POPULATION OF A.
kuhlmanii x A. diogoi F2 PROGENY
- SCREEN AND MAP AVAILABLE INDEL AND SSCP MARKERS FOR 50
NBS-LRR GENES
- DEVELOP, SCREEN AND MAP ADDITIONAL MARKERS FOR 50-150
ADDITIONAL NBS-LRR GENES
RESEARCH OVERVIEW FOR THE SECOND OBJECTIVE
OBJECTIVES
IDENTIFY NBS-LRR ALLELES INTROGRESSED FROM WILD DIPLOID INTO
CULTIVATED TETRAPLOID LINES
THIRD OBJECTIVE
GOAL
IDENTIFY AND CHARACTERIZE SEVERAL NBS-LRR GENES
Line P.I. Number Background Reference
  PI 262141 A. cardenasii Donor
  PI 261942 A. hypogaea Parent
  PI 261943 A. hypogaea Parent
GP-NC WS 1 PI 564844  Wild Introgression Line (WIL) Stalker and Beute (1993)
GP-NC WS 2 PI 564845  WIL Stalker and Beute (1993)
GP-NC WS 3 PI 564846  WIL Stalker and Beute (1993)
GP-NC WS 4 PI 564847  WIL Stalker and Beute (1993)
TXAG-6 PI 565287  WIL Simpson et al. (1993)
TXAG-7 PI 565288  WIL Simpson et al. (1993)
ICGV 86699 PI 591815 (A. batizocoi/A. duranensis)//NC 2 Reddy et al. (1996)
ICGV 87165 PI 594923 WIL Moss et al. (1997)
ICGV SM 86715 PI 598133  WIL Moss et al. (1998)
COAN PI 610452  WIL Simpson and Starr (2001)
GP-NC WS 5 PI 619169 WIL Stalker et al. (2002a)
GP-NC WS 6 PI 619170 WIL Stalker et al. (2002a)
GP-NC WS 7 PI 619171 WIL Stalker and Lynch (2002)
GP-NC WS 8 PI 619172 WIL Stalker and Lynch (2002)
GP-NC WS 9 PI 619173 WIL Stalker and Lynch (2002)
GP-NC WS 10 PI 619174  WIL Stalker and Lynch (2002)
GP-NC WS 11 PI 619175 (NC 6//NC Ac 3033)/GP-NC WS 1 Stalker et al. (2002b)
GP-NC WS 12 PI 619176 (NC 6//NC Ac 3033)/GP-NC WS 1 Stalker et al. (2002b)
GP-NC WS 13 PI 619177 (NC 5//PI 270806)/GP-NC WS 4 Stalker et al. (2002b)
GP-NC WS 14 PI 619178 WIL Stalker et al. (2002b)
GP-NC WS 15 PI 619179 WIL Stalker et al. (2002b)
NR 0817 PI 639266 AT-108/GP-NC WS 5 Anderson et a. (2006)
NR 0812 PI 639267 AT-108/GP-NC WS 5 Anderson et a. (2006)
N96076L PI 641950 N90004/GP-NC WS 13 Isleib et al. (2006)
IDENTIFICATION AND
CHARACTERIZATION OF NBS-LRR
GENES
IDENTIFICATION AND
CHARACTERIZATION OF NBS-LRR
GENES
-SCREENING AVAILABLE LINES FOR R-GENE INTROGRESSION
-IDENTIFYING INTROGRESSED NBS-LRR ALLELES
- CHARACTERIZING NOVEL NBS-LRR ALLELES
RESEARCH OVERVIEW FOR THE THIRD OBJECTIVE
SUMMARY
• WILD RELATIVES OF CULTIVATED PEANUT ARE THE
SOURCES OF NOVEL RESISTANCE GENES
• MOLECULAR BREEDING TOOLS FACILITATE TO TRANSFER
USEFUL GENES FROM WILD DIPLOID TO CULTIVATED
PEANUT SPECIES
• SSR-ENRICHED LINKAGE MAP WILL BE DEVELOPED FOR AA-
GENOME DIPLOID MODEL
• MORE THAN 100 NBS-LRR RGC LOCI WILL BE MAPPED WITH
SSCP AND INDEL MARKERS
• WILD INTROGRESSION LINES WILL BE SCREENED TO
IDENTIFY NBS-LRR ALLELE
END OF THE PRESENTATION
THANK YOU

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NBS-LRR proposal

  • 1. SAMEER KHANAL DEPARTMENT OF CROP AND SOIL SCIENCES THE UNIVERSITY OF GEORGIA DEVELOPMENT OF AN A-GENOME DIPLOID MODEL FOR COMPARATIVE GENOMICS IN PEANUT AND OTHER LEGUMES
  • 3. IMPORTANCE OF PEANUT Among food legumes, second in national and global economic importance United States World Crop Area Harvested (ha) Production (Mg) Area Harvested (ha) Production (Mg) Soybean 28,842,260 82,820,048 91,386,621 209,531,558 Peanut 650,340 2,112,700 25,217,201 36,492,147 Source: compiled from faostat.fao.org
  • 4. PEANUT PRODUCTION CONSTRAINTS Abiotic Constraints Drought High Temperature www.gapeanuts.com/news/2006/092906.asp southeastfarmpress.com/news/091106-peanut-markets/ www.washingtonpost.com/wp- dyn/content/article/2006/07/29/AR2006072900414_pf.html
  • 5. Abiotic Constraints Drought High Temperature Biotic Constraints Diseases Insect-Pests PEANUT PRODUCTION CONSTRAINTS Source: Diseases compiled from plantpathology.tamu.edu/Texlab/Fiber/Peanuts/atlas-toc.html edis.ifas.ufl.edu/IN176
  • 6. Third most important source of vegetable protein Among food legumes, second in national and global economic importance IMPORTANCE OF PEANUT Fourth most important source of vegetable oil Twelfth most important food crop in the world Source: ICRISAT (www.icrisat.org) and the UN-FAO
  • 7. PEANUT IMPROVEMENT CONSTRAINTS • POLYPLOIDY (YOUNG ET AL., 1996) • AUTOGAMY (HALWARD ET AL., 1991) • NARROW GENETIC BASE (KNAUFT & GORBET, 1989) AA BBX AB AABB PARENTS: INTERSPECIFIC HYBRIDIZATION F1 HYBRID: SPONTANEOUS CHROMOSOME DOUBLING ALLOTETRAPLOI D PEANUT : LOW GENETIC VARIABILITY
  • 8. PEANUT IMPROVEMENT CONSTRAINTS LACK OF SOURCES OF RESISTANCE TO SEVERAL ABIOTIC/BIOTIC STRESSES IN CULTIVATED PEANUT Source: peanut.tamu.edu/peanut_photos.htm
  • 9. PEANUT IMPROVEMENT CONSTRAINTS DIFFICULT TO INTROGRESS RESISTANCE GENES FROM DIPLOID WILD SPECIES WARRANTS COMPLEX CROSSES OR GENETIC TRANSFORMATION LAGGING IN GENOMIC RESOURCES AND APPLICATION OF MOLECULAR BREEDING SOLUTIONS TO THE PERTINENT PROBLEMS Source: peanut.tamu.edu/peanut_photos.htm
  • 10. REALIZATIONS - A CONSENSUS MAP FOR ARACHIS - MAPPING PHENOTYPIC AND QUANTITATIVE TRAIT LOCI (QTLs) - MARKERS LINKED TO THE GENES OF INTEREST FOR MARKER ASSISTED SELECTION (MAS) CROP IMPROVEMENT THROUGH MOLECULAR BREEDING TECHNIQUES REQUIRE:
  • 11. OBJECTIVES INCREASING THE FREQUENCY OF HIGH-THROUGHPUT DNA MARKERS IN THE A-GENOME FIRST OBJECTIVE GOAL A MICROSATELLITE-ENRICHED LINKAGE MAP FOR A-GENOME
  • 12. MICROSATELLITE-BASED LINKAGE MAP FOR THE AA-GENOME - DIPLOID RFLP MAP PRODUCED FROM AN INTERSPECIFIC (A. duranensis x A. stenosperma) HYBRID (HALWARD ET AL., 1993) - TETRAPLOID RFLP MAP PRODUCED FROM HYBRID BETWEEN A. hypogaea AND A ‘SYNTHETIC’ AMPHIDIPLOID [A. batizocoi x A. diogoi)] (BUROW ET AL., 2002) - RECENTLY FIRST MICROSATELLITE-BASED MAP IS PUBLISHED IN Arachis (MORETZSOHN ET AL., 2005). LINKAGE MAPPING IN DIFFERENT PEANUT SPECIES
  • 13. MICROSATELLITE-BASED LINKAGE MAP FOR THE AA-GENOME MICROSATELLITES OR SIMPLE SEQUENCE REPEATS (SSRs) ARE MULTIPLE REPEATING UNITS OF 1 TO 4 BASE PAIRS EXAMPLE: (A)5, (AT)7, (CGG)9, (ACGG)6 - SCREENING SEQUENCES FROM GENOMIC LIBRARY - SCREENING SSR ENRICHED LIBRARY - SCREENING EST SEQUENCES - SCREENING OF SSRs AGAINST DIFFERENT GENOTYPES SSR DEFINITION SSR DEVELOPMENT POLYMORPHISM DETECTION
  • 14. MICROSATELLITE-BASED LINKAGE MAP FOR THE AA-GENOME - 720 MARKERS SCREENED AMONG 18 ELITE AND 14 EXOTIC GERMPLAM ACCESSIONS - 556 SSR MARKERS FOUND POLYMORPHIC - 336 (60.4%) WERE POLYMORPHIC IN (A. Kuhlmanii x A. diogoi) - 82 OUT OF 336 HAVE ALREADY BEEN MAPPED (MORETZSOHN ET AL., 2005) Source: Ma (Communication) SCREENING AVAILABLE SSR MARKERS FOR POLYMORPHISMS
  • 15. MICROSATELLITE-BASED LINKAGE MAP FOR THE AA-GENOME - MAPPING POPULATION OF A. kuhlmanii X A. diogoi - GENOTYPING 82 PREVIOUSLY MAPPED AND 254 PREVIOUSLY UNMAPPED SSR MARKER LOCI - THREE FOLD INCREASE IN THE DENSITY OF DNA MARKER LOCI IN THE A-GENOME RESEARCH OVERVIEW FOR THE FIRST OBJECTIVE
  • 16. OBJECTIVES GENETIC MAPPING OF NUCLEOTIDE BINDING SITE – LEUCINE RICH REPEATS (NBS-LRR) REGISTANCE GENE CANDIDATE (RGC) LOCI SECOND OBJECTIVE GOAL MAPPING OF 100-150 NBS-LRR RGCs
  • 17. GENETIC MAPPING OF NBS-LRR RGC LOCI - GROUPED INTO SEVERAL FAMILIES - MOST R-GENE PROTEINS CHARACTERIZED BY NUCLEOTIDE BINDING SITE LEUCINE RICH REPEATS - 150 NBS-LRR-ENCODING GENES IN Arabidopsis thaliana AND >400 IN Oryza sativa Source: McHale et al. 2006 NBS LR R TIR/CCN C RESISTANCE GENES IN PLANTS
  • 18. GENETIC MAPPING OF NBS-LRR RGC LOCI INDEL AND SSCP MARKERS BEING DEVELOPED NBS-LRR TEMPLETES: BERTIOLI ET AL. (2004), YUSKEL ET AL. (2005), COOK ET AL. (UNPUBLISHED DATA) SCREENING: 58 NBS-LRR TEMPLETES SCREENED SO FAR EIGHT CULTIVATED PEANUT (AABB) : HIGHLY MONOMORPHIC FOUR DIPLOID GENOTYPES: HIGHLY POLYMORPHIC RGC7 RGC4 RGC8 DUR25 DUR35 BAT6 BAT8 HYP-GTC-9 HYP-A100 HYP-AEQ-2 HYP-PRV-1 HYP-Tifrunner HYP-HIR-3 HYP-GTC-20 HYP-FST-3 DUR BAT - AFLP-BASED MAPPING OF RESISTANCE TO APHID VECTOR (HERSELMAN ET AL., 2004) - THREE SMALL MAP SETS WITH MARKERS FOR ROOT KNOT NEMATOD RESISTANCE (JESUBATHAM AND BUROW, 2006) RESISTANT GENE MAPPING IN PEANUT MARKERS USED FOR MAPPING NBS-LRR RGC LOCI
  • 19. GENETIC MAPPING OF NBS-LRR RGC LOCI - MAPPING NBS-LRR RGC LOCI IN MAPPING POPULATION OF A. kuhlmanii x A. diogoi F2 PROGENY - SCREEN AND MAP AVAILABLE INDEL AND SSCP MARKERS FOR 50 NBS-LRR GENES - DEVELOP, SCREEN AND MAP ADDITIONAL MARKERS FOR 50-150 ADDITIONAL NBS-LRR GENES RESEARCH OVERVIEW FOR THE SECOND OBJECTIVE
  • 20. OBJECTIVES IDENTIFY NBS-LRR ALLELES INTROGRESSED FROM WILD DIPLOID INTO CULTIVATED TETRAPLOID LINES THIRD OBJECTIVE GOAL IDENTIFY AND CHARACTERIZE SEVERAL NBS-LRR GENES
  • 21. Line P.I. Number Background Reference   PI 262141 A. cardenasii Donor   PI 261942 A. hypogaea Parent   PI 261943 A. hypogaea Parent GP-NC WS 1 PI 564844  Wild Introgression Line (WIL) Stalker and Beute (1993) GP-NC WS 2 PI 564845  WIL Stalker and Beute (1993) GP-NC WS 3 PI 564846  WIL Stalker and Beute (1993) GP-NC WS 4 PI 564847  WIL Stalker and Beute (1993) TXAG-6 PI 565287  WIL Simpson et al. (1993) TXAG-7 PI 565288  WIL Simpson et al. (1993) ICGV 86699 PI 591815 (A. batizocoi/A. duranensis)//NC 2 Reddy et al. (1996) ICGV 87165 PI 594923 WIL Moss et al. (1997) ICGV SM 86715 PI 598133  WIL Moss et al. (1998) COAN PI 610452  WIL Simpson and Starr (2001) GP-NC WS 5 PI 619169 WIL Stalker et al. (2002a) GP-NC WS 6 PI 619170 WIL Stalker et al. (2002a) GP-NC WS 7 PI 619171 WIL Stalker and Lynch (2002) GP-NC WS 8 PI 619172 WIL Stalker and Lynch (2002) GP-NC WS 9 PI 619173 WIL Stalker and Lynch (2002) GP-NC WS 10 PI 619174  WIL Stalker and Lynch (2002) GP-NC WS 11 PI 619175 (NC 6//NC Ac 3033)/GP-NC WS 1 Stalker et al. (2002b) GP-NC WS 12 PI 619176 (NC 6//NC Ac 3033)/GP-NC WS 1 Stalker et al. (2002b) GP-NC WS 13 PI 619177 (NC 5//PI 270806)/GP-NC WS 4 Stalker et al. (2002b) GP-NC WS 14 PI 619178 WIL Stalker et al. (2002b) GP-NC WS 15 PI 619179 WIL Stalker et al. (2002b) NR 0817 PI 639266 AT-108/GP-NC WS 5 Anderson et a. (2006) NR 0812 PI 639267 AT-108/GP-NC WS 5 Anderson et a. (2006) N96076L PI 641950 N90004/GP-NC WS 13 Isleib et al. (2006) IDENTIFICATION AND CHARACTERIZATION OF NBS-LRR GENES
  • 22. IDENTIFICATION AND CHARACTERIZATION OF NBS-LRR GENES -SCREENING AVAILABLE LINES FOR R-GENE INTROGRESSION -IDENTIFYING INTROGRESSED NBS-LRR ALLELES - CHARACTERIZING NOVEL NBS-LRR ALLELES RESEARCH OVERVIEW FOR THE THIRD OBJECTIVE
  • 23. SUMMARY • WILD RELATIVES OF CULTIVATED PEANUT ARE THE SOURCES OF NOVEL RESISTANCE GENES • MOLECULAR BREEDING TOOLS FACILITATE TO TRANSFER USEFUL GENES FROM WILD DIPLOID TO CULTIVATED PEANUT SPECIES • SSR-ENRICHED LINKAGE MAP WILL BE DEVELOPED FOR AA- GENOME DIPLOID MODEL • MORE THAN 100 NBS-LRR RGC LOCI WILL BE MAPPED WITH SSCP AND INDEL MARKERS • WILD INTROGRESSION LINES WILL BE SCREENED TO IDENTIFY NBS-LRR ALLELE
  • 24. END OF THE PRESENTATION THANK YOU