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QTL Mapping
MSc ag (2) year
Agriculture Genetics and Plant Breeding
Deen Dayal Upadhyaya Gorakhpur University
Gorakhpur
Submitted by.
Shweta Kumari
Submitted to
Department of
Genetics and plant
breeding
Introduction
✩ QTL mapping
✩ QTL mapping is the process to identify the genomic region associated
with desirable quantitative trait with the help of DNA marker
✩ In this process DNA markers are tested throughout the genome which
are associated with QTLs.
Quantitative Traits Loci
✩ The loci controlling quantitative traits are called quantitative traits Ioci
( QTL)
✩ the term quantitative traits coined by Genderman.
✩ QTL is the region of genome which control quantitative trait
✩ QTL characteristics
✩ The QTLs are controlled by multiple genes ,each segregating according
to Mendel's Law.
✩ These traits also a ected by environment to varying degrees
✩ QTL can show dominant or co-dominant
Objective of QTL mapping
✩ The basic objective is to detect QTL
✩ To identify the region of genome that a ects the trait of interest
✩ To analyse the e ect of the QTL on the trait
✩ How much variation for the trait is caused by a specific region
✩ What is the gene action associated with the QTL?
✩ Which allele is associated with the favourable e ect.
Procedure for QTL mapping
✩ Selection of diverse parental lines
✩ Creation of mapping population
✩ Phenotyping of the progeny
✩ Genotyping of the progeny
✩ Construction of linkage map.
Types of mapping population
✩ Recombinant Inbred line(RIL)
✩ Backcross
✩ F2 population
✩ Double haploid
✩ Near isogenic line(NIL)
Backcross mapping population
✩ Advantages: It is easier to
identify QTL as there are less
epistatic and linkage drag
e ects; especially useful for
crosses with wild species.
✩ Disadvantages: Di cult or
impossible in species that are
highly heterozygous and
outcrossing.
✩ Use: best when inbred lines
are available
F2 mapping Population
✩ Advantage: Fast and easy to
construct.
✩ Disadvantage: F3 families are
still very heterozygous; so the
precision of the estimates can
be low (because of the high
standard error); can't be
replicated
Recombinant Inbred Line
✩ RILs are produced by
continuous selfing progeny of
individual member of an F2
population until complete
homozygous is achieved
✩ Advantages: fixed lines so can
be replicated across many
locations and/or years; can
eliminate problem of
background heterozygosity.
✩ Disadvantages: Can take a
long time to produce. (Some
species are not amenable)
Near Isogenic Line
✩ Advantage: Very precise and
statistically strong, as
background is constant;
especially useful for validation
experiments.
✩ Disadvantage: Can take time
to construct; only useful for
specific target QTL
Doubled Haploid Line
✩ Advantages: 1)Spontaneous
chromosome doubling of
✩ Haploid microspores in in vitro
culture
✩ 2)Homozygosity achieved in a single
step Plants.
✩ Disadvantages: Less recombination
between linked markers Not all
systems are amenable to in vitro
culture
Methods of QTL Detection
✩ Studying single markers one
at a time.
✩ The simplest method for QTL
analysis.
✩ Can be done by t-tests or
ANOVA.
✩ Does not require a complete
linkage map.
Simple Interval mapping
✩ Two markers at a time
(flanking markers).
✩ Based on linkage mapping of
markers.
✩ More accurate than
single-marker analysis.
Composite interval mapping
✩ For detection of a QTL more than two markers are used
✩ It is based on linkage mapping of the marker.
Thank you
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QTL mapping and analysis

  • 1. QTL Mapping MSc ag (2) year Agriculture Genetics and Plant Breeding Deen Dayal Upadhyaya Gorakhpur University Gorakhpur Submitted by. Shweta Kumari Submitted to Department of Genetics and plant breeding
  • 2. Introduction ✩ QTL mapping ✩ QTL mapping is the process to identify the genomic region associated with desirable quantitative trait with the help of DNA marker ✩ In this process DNA markers are tested throughout the genome which are associated with QTLs.
  • 3. Quantitative Traits Loci ✩ The loci controlling quantitative traits are called quantitative traits Ioci ( QTL) ✩ the term quantitative traits coined by Genderman. ✩ QTL is the region of genome which control quantitative trait ✩ QTL characteristics ✩ The QTLs are controlled by multiple genes ,each segregating according to Mendel's Law. ✩ These traits also a ected by environment to varying degrees ✩ QTL can show dominant or co-dominant
  • 4. Objective of QTL mapping ✩ The basic objective is to detect QTL ✩ To identify the region of genome that a ects the trait of interest ✩ To analyse the e ect of the QTL on the trait ✩ How much variation for the trait is caused by a specific region ✩ What is the gene action associated with the QTL? ✩ Which allele is associated with the favourable e ect.
  • 5. Procedure for QTL mapping ✩ Selection of diverse parental lines ✩ Creation of mapping population ✩ Phenotyping of the progeny ✩ Genotyping of the progeny ✩ Construction of linkage map.
  • 6. Types of mapping population ✩ Recombinant Inbred line(RIL) ✩ Backcross ✩ F2 population ✩ Double haploid ✩ Near isogenic line(NIL)
  • 7. Backcross mapping population ✩ Advantages: It is easier to identify QTL as there are less epistatic and linkage drag e ects; especially useful for crosses with wild species. ✩ Disadvantages: Di cult or impossible in species that are highly heterozygous and outcrossing. ✩ Use: best when inbred lines are available
  • 8. F2 mapping Population ✩ Advantage: Fast and easy to construct. ✩ Disadvantage: F3 families are still very heterozygous; so the precision of the estimates can be low (because of the high standard error); can't be replicated
  • 9. Recombinant Inbred Line ✩ RILs are produced by continuous selfing progeny of individual member of an F2 population until complete homozygous is achieved ✩ Advantages: fixed lines so can be replicated across many locations and/or years; can eliminate problem of background heterozygosity. ✩ Disadvantages: Can take a long time to produce. (Some species are not amenable)
  • 10. Near Isogenic Line ✩ Advantage: Very precise and statistically strong, as background is constant; especially useful for validation experiments. ✩ Disadvantage: Can take time to construct; only useful for specific target QTL
  • 11. Doubled Haploid Line ✩ Advantages: 1)Spontaneous chromosome doubling of ✩ Haploid microspores in in vitro culture ✩ 2)Homozygosity achieved in a single step Plants. ✩ Disadvantages: Less recombination between linked markers Not all systems are amenable to in vitro culture
  • 12. Methods of QTL Detection ✩ Studying single markers one at a time. ✩ The simplest method for QTL analysis. ✩ Can be done by t-tests or ANOVA. ✩ Does not require a complete linkage map.
  • 13. Simple Interval mapping ✩ Two markers at a time (flanking markers). ✩ Based on linkage mapping of markers. ✩ More accurate than single-marker analysis.
  • 14. Composite interval mapping ✩ For detection of a QTL more than two markers are used ✩ It is based on linkage mapping of the marker.
  • 16. Zoho Show To create beautiful presentations, download Zoho Show from Play Store https://zoho.to/cy7 QTL mapping.pdf (This PDF has been generated using Zoho Show)