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Mark E. Sorrells

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Title: Mark E. Sorrells


1
Genomic Tools for Oat Improvement
  • Mark E. Sorrells
  • Cornell Department of Plant Breeding Genetics

2
Presentation Overview
  • Background (Other crops already presented)
  • What are Genomic Tools and how are they used
  • Funding opportunities for Oat Improvement
  • Genomic selection for oat improvement

3
Background
  • For crops with adequate research support, genomic
    tools have evolved with technological innovation
    over time.
  • The availability of genomic tools is affected by
  • Public and private funding,
  • Complexity of the genome,
  • Importance of the crop domestically and
    internationally, and
  • Expertise and research focus of dedicated
    researchers
  • Specialty (minor, orphan) crops are less
    competitive for public funding because of
  • A lack of genomic tools
  • Limited fundamental knowledge about the biology
    of the species
  • Difficulty in transferring knowledge to and from
    model species

4
Useful Resources for Oat Genomics Research
  • Highly collaborative and open community of
    researchers
  • Abundant, inexpensive molecular markers (always
    need more)
  • Comparative genome maps (low resolution, old
    technology)
  • High density molecular marker QTL maps (Need
    more)
  • Large EST collection (Currently only 7,632 ESTs
    in GenBank)
  • BAC libraries (1 or 2?)
  • Physical map of genome (none)
  • Full length cDNAs (none?)

5
Useful Resources for Oat Genomics Research (cont.)
  • High quality phenotypic data collected in target
    environments (USDA Uniform Nurseries)
  • Rich collection of germplasm (Oat has 21,292
    Accessions)
  • Microarray development (none)
  • Transformation system (available)
  • Doubled haploid system (Maize pollinator or
    anther culture?)
  • Online curated database (GrainGenes)

6
Research Activities Benefiting from Molecular
Markers
  • Knowledge of genome structure function
  • Genomic relationships of primary germplasm
    resources
  • Location of important genes affecting traits of
    interest
  • Marker assisted breeding
  • QTL mapping studies
  • Physical map construction
  • Facilitate genome sequencing
  • Gene cloning
  • Fingerprinting

7
Funding Strategies for Developing Oat Genomic
Tools (U.S.)
  • Pool available public resources (International
    DArT consortium)
  • Limited to community resources not locked up by
    institutions
  • Most public researchers have very little
    flexibility with funds
  • Does not require justification to an agency
  • Benefits everyone
  • Lobby legislators to provide more opportunities
    for funding oat research
  • Historically, legislators are reluctant to
    support projects requiring new funding
  • Limited to states with powerful legislators in
    key positions
  • Often requires a crisis to generate interest
  • Difficult to convince legislators to invest in a
    relatively minor crop
  • Can be long term
  • Develop a USDA Coordinated Agriculture Project
    (CAP)
  • Extremely competitive
  • Only funds one crop per year
  • 4 to 5 year funding cycle
  • Builds strong collaboration within the community
    of researchers
  • Tight integration with all stakeholders

8
Funding Strategies for Developing Oat Genomic
Tools (cont.)
  • Identify fundamental research topics that might
    interest NSF
  • Challenging for a crop with limited genomic
    resources
  • Benefits few researchers if funded
  • Applied research topics are not competitive
  • Likely to generate novel and sometimes useful
    fundamental information
  • Could open new areas for research
  • Oat researchers, buyers and processors could
    establish a public/private research consortium
  • Challenging to build a united effort with common
    goals
  • Intellectual property issues often complicate
    research activities and slow progress
  • Benefits to industry are long term and diffuse
  • Can provide a stable, longer term funding
    resource
  • Can benefit the entire oat community
  • May help stabilize oat production
  • Likely to generate novel, high value, germplasm
    and varieties

9
How can we use genomic tools?
  • Germplasm resources
  • Identify novel germplasm
  • Improve sampling for phenotyping
  • Develop core collections of various types
  • Gene marker discovery
  • Reduce mapping costs
  • Enhance resolution
  • Characterize the value of alleles for important
    traits
  • Molecular Breeding
  • Marker assisted breeding
  • Genomic selection
  • Comparative mapping for transfer of information
    from other species
  • Cloning genes producing novel phenotypes in oat

10
Association Breeding for Oat Improvement
  • Breeding Progress depends on
  • Genetic variation for important traits
  • Development of genotypes with new or improved
    attributes due to superior combinations of
    alleles at multiple loci
  • Accurate selection of rare genotypes that possess
    the new improved characteristics

11
Association Breeding for Oat Improvement
  • Primary Goals
  • Allele discovery
  • Allele validation
  • Parental progeny selection

12
Association Analysis as a Breeding Strategy
  • Issues
  • Breeding programs are dynamic, complex genetic
    entities that require frequent evaluation of
    marker / phenotype relationships.
  • Accurate detection and estimation of QTL effects
    required
  • Pre-existing marker alleles may be linked to
    undesirable QTL alleles
  • Population structure can cause a high frequency
    of false positive associations between markers
    and QTL
  • Linkage disequilibrium is unknown and highly
    variable among populations

13
Strategies for Molecular Breeding
  • Marker Assisted Selection
  • Only significant markers are used for selection,
    usually qualitative traits
  • Association Breeding (Breseghello Sorrells
    2006)
  • Uses conventional hybridization/MAS/Testing for
    significant markers but allows for updating
    breeding values for alleles
  • Phenotyping and association analysis are used as
    often as necessary for allele discovery and
    validation
  • Genomic Selection (Meuwissen, Hayes Goddard
    2001)
  • Requires genome-wide markers that are used to
    estimate a breeding value for each individual
  • Marker/QTL effects are estimated and updated only
    after a generation is phenotyped

14
Application of Association Analysis in a Breeding
Program
Germplasm
Parental Selection
Hybridization
Genomic Selection
Elite germplasm feeds back into hybridization
nursery
New Populations
Marker Assisted Selection
Selection (Intermating)
Characterize Allelic Value Validate
QTL/Marker Allele Associations
New Synthetics, Lines, Varieties
Evaluation Trials
Elite Synthetics, Lines, Varieties
Genotypic Phenotypic data
  • MAS identifies desired segregates up front so
    selection pressure can be increased for other
    traits
  • Association breeding facilitates allele
    discovery and evaluation
  • Genomic selection reduces cycle time by reducing
    frequency of phenotyping

15
Genomic Selection Methodology
  • Genome-wide markers are used to explain all or
    nearly all of the genetic variance of the trait
  • One or more markers are assumed to be in LD with
    each QTL affecting the trait
  • A genomic estimated breeding value for each
    individual is obtained by summing the effects for
    that genotype
  • Genetic relationships and population structure
    are taken into account by the prediction equation
  • Multiple generations of selection can be imposed
    without phenotyping

Goddard Hayes 2007
16
Implementation of Genomic Selection
  • Discovery dataset -Large number of markers on
    moderate sized population that has been
    phenotyped (Discovery or Training Popn)
  • Derive prediction equations for predicting
    breeding values using random regression BLUP or
    Bayesian analysis.
  • Validate prediction equation using independent
    population and all or selected markers to reduce
    bias in estimates (Validation population)
  • A selection population is genotyped (no
    phenotyping) and the prediction equation is used
    to calculate genomic breeding values (Multiple
    generations of recurrent selection)
  • Update prediction equation periodically with
    phenotyping

17
Genomic Selection Marker Assisted Recurrent
Selection Schemes for Maize Inbred
Development Bernardo Yu 2008
Simulations QTL - 20, 40, 100 H2 - 0.2, 0.5,
0.8
Training Population to develop prediction
equations
Used computer simulation to compare Genomic
Selection to Marker Assisted Recurrent
Selection Varied number of QTL and h2
Off-season nurseries
18
Genomic Selection Marker Assisted Recurrent
Selection Schemes for Maize Inbred
Development Bernardo Yu 2008
Results of simulations Response to genomic
selection was 18-43 higher than MARS across
different population sizes, numbers of QTL and
heritabilities. Advantage of GS over MARS was
greatest for low h2 and many QTL.
  • Advantage of GS over MARS
  • QTL Heritability
  • 0.2 0.4 0.8
  • 130 121 118
  • 136 132 135
  • 100 143 128 130

19
SummaryAssociation Breeding and Genomic
Selection
  • Allelic values of previously identified alleles
    can be dynamically updated based on advanced
    trial data as desired
  • New alleles can be identified and characterized
    to determine their value
  • Predicted breeding values will improve with more
    markers however, the oat DArT markers provide an
    excellent start and supplemental markers can
    focus on specific QTL regions and candidate genes
  • Most important advantages are reductions in the
    length of the selection cycle and phenotyping cost

20
Acknowledgements
  • USDA Cooperative State Research, Education and
    Extension Service

The Quaker Oat Company for many years of support
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