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讲 座 提 纲. 1 什么是分子育种 2 历史回顾 3 全基因组策略 4 基因型鉴定 5 表现型鉴定 6 环境 型鉴定 ( etyping ) 7 标记 - 性状关联分析 8 标记 辅助 选择 9 决策支撑系统 10 展望. Marker-Assisted Selection Models. I. Major gene introgression (target genes only) 2 -10 markers for each trait
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讲 座 提 纲 1 什么是分子育种 2 历史回顾 3 全基因组策略 4 基因型鉴定 5 表现型鉴定 6 环境型鉴定 (etyping) 7 标记-性状关联分析 8 标记辅助选择 9 决策支撑系统 10 展望
Marker-Assisted Selection Models I. Major gene introgression (target genes only) 2 -10 markers for each trait Single trait introgression Multiple trait introgression A few markers for hundreds of plants II. Marker-assisted backcrossing (target genes plus background) 2 -10 markers for each trait 200-500 markers for background selection A few hundreds of markers for hundreds of plants III. Whole genome selection 500 to several thousands or millions of markers for hundreds or thousands of plants/lines
Marker-Assisted Selection Methods Xu et al 2012 Mol Breed 29:833–854
Genomic Selection • Phenotypic selection for complex traits is difficult and slow; traditional MAS is ineffective. • Genomic selection, as an example for genomewide selection, is poised to revolutionize plant breeding, because it • uses marker data to predict breeding line performance in one analysis • analyzes the breeding populations directly • includes all markers in the model so that effect estimates are unbiased and small effect QTL can be accounted for
Genomic Selection in a Plant Breeding Program Heffner et al 2010 Crop Science 49:1-12 Genomic selection reduces cycle time & cost by reducing frequency of phenotypingTraining
Key factors Affecting Genomic Selection • Number of markers and genome coverage • Markers types: single, haplotypes • Population structure • Population size • Relationship between training and breeding populations • Involvement of known genes and their markers • Precision of phenotyping for training model development • Heritability of target traits
Genetic Gain under Whole Genome Strategies Genetic gain: concept development from quantitative genetics to molecular breeding Genetic gain per unit time can be defined as R = Vg1/2 h2i t Vg: genetic variance h2: heritability i: selection intensity t: cycle time
Vg Unlocking genetic variation from original ecotypes of cultivated species and their wild relatives Single markers • Structure variation • Haplotypes Across elite lines Across ecotypes Across wild relatives Within-gene haplotypes Within-chromosome haplotypes Within-genome haplotypes
h2 Improvement of heritability estimation Precision phenotyping: more replications, MET Etyping and environmental error control i Increasing population size and thus the selection intensity Selection with seed DNA Selection in tissue culture Selection in gametophytic stage Selection in greenhouse phytotron, growth chamber Using of model plants
t Shorten cycle time through MAS Increasing selection efficiency and accuracy using MAS Speeding up pure-breeding process (DH etc) Speeding up growth and development Using greenhouse etc Moving to the breeding objective quickly See examples for marker development and application from B.M. Prasanna (2014)