Mapping and linkage disequilibrium analysis with a genome-wide collection of SNPs that detect polymorphism in cultivated tomato

被引:60
|
作者
Robbins, Matthew D. [1 ]
Sim, Sung-Chur [1 ]
Yang, Wencai [2 ]
Van Deynze, Allen [3 ]
van der Knaap, Esther [1 ]
Joobeur, Tarek [4 ]
Francis, David M. [1 ]
机构
[1] Ohio State Univ, Dept Hort & Crop Sci, OARDC, Wooster, OH 44691 USA
[2] China Agr Univ, Coll Agron & Biotechnol, Dept Vegetable Sci, Beijing 100094, Peoples R China
[3] Univ Calif Davis, Seed Biotechnol Ctr, Davis, CA 95616 USA
[4] Ohio State Univ, Mol & Cellular Imaging Ctr, OARDC, Wooster, OH 44691 USA
关键词
Breeding; domestication; gametic phase; inter-chromosomal; selection; LYCOPERSICON-HIRSUTUM LA407; MAIZE DOMESTICATION; SEQUENCE DIVERSITY; GENETIC DIVERSITY; BACTERIAL SPOT; SHAPED TOMATO; QTL ANALYSIS; FRUIT SIZE; ESCULENTUM; RESISTANCE;
D O I
10.1093/jxb/erq367
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The history of tomato (Solanum lycopersicum L.) improvement includes genetic bottlenecks, wild species introgressions, and divergence into distinct market classes. This history makes tomato an excellent model to investigate the effects of selection on genome variation. A combination of linkage mapping in two F-2 populations and physical mapping with emerging genome sequence data was used to position 434 PCR-based markers including SNPs. Three-hundred-and-forty markers were used to genotype 102 tomato lines representing wild species, landraces, vintage cultivars, and contemporary (fresh market and processing) varieties. Principal component analysis confirmed genetic divergence between market classes of cultivated tomato (P < 0.0001). A genome-wide survey indicated that linkage disequilibrium (LD) decays over 6-8 cM when all cultivated tomatoes, including vintage and contemporary, were considered together. Within contemporary processing varieties, LD decayed over 6-14 cM, and decay was over 3-16 cM within fresh market varieties. Significant inter-chromosomal (gametic phase) LD was detected in both fresh market and processing varieties between chromosomes 2 and 3, and 2 and 4, but in distinct chromosomal locations for each market class. Additional LD was detected between chromosomes 3 and 4, 3 and 11, and 4 and 6 in fresh market varieties and chromosomes 3 and 12 in processing varieties. These results suggest that breeding practices for market specialization in tomato have led to a genetic divergence between fresh market and processing types.
引用
收藏
页码:1831 / 1845
页数:15
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