An integrated genetic linkage map of cultivated peanut (Arachis hypogaea L.) constructed from two RIL populations

被引:79
|
作者
Qin, Hongde [2 ,3 ]
Feng, Suping [2 ,4 ]
Chen, Charles [5 ]
Guo, Yufang [6 ]
Knapp, Steven [6 ]
Culbreath, Albert [2 ]
He, Guohao [7 ]
Wang, Ming Li [8 ]
Zhang, Xinyou [9 ]
Holbrook, C. Corley [10 ]
Ozias-Akins, Peggy [11 ]
Guo, Baozhu [1 ]
机构
[1] ARS, Crop Protect & Management Res Unit, USDA, Tifton, GA USA
[2] Univ Georgia, Dept Plant Pathol, Tifton, GA 31793 USA
[3] Hubei Acad Agr Sci, Cash Crop Res Inst, Wuhan, Peoples R China
[4] Qiongzhou Univ, Coll Biosci & Biotechnolgy, Sanya, Hainan, Peoples R China
[5] ARS, Natl Peanut Res Lab, USDA, Dawson, GA USA
[6] Univ Georgia, Ctr Appl Genet Technol, Athens, GA 30602 USA
[7] Tuskegee Univ, Ctr Plant Biotechnol, Tuskegee, AL 36088 USA
[8] ARS, Plant Genet Resources Conservat Unit, USDA, Griffin, GA USA
[9] Henan Acad Agr Sci, Peanut Res Unit, Zhengzhou, Peoples R China
[10] ARS, Crop Genet & Breeding Res Unit, USDA, Tifton, GA USA
[11] Univ Georgia, Dept Hort, Tifton, GA USA
关键词
MARKERS; GENOME; SSR; IDENTIFICATION; RESISTANCE; RECOMBINATION; TRANSMISSION; REGISTRATION; DURANENSIS; EVOLUTION;
D O I
10.1007/s00122-011-1737-y
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Construction and improvement of a genetic map for peanut (Arachis hypogaea L.) continues to be an important task in order to facilitate quantitative trait locus (QTL) analysis and the development of tools for marker-assisted breeding. The objective of this study was to develop a comparative integrated map from two cultivated x cultivated recombinant inbred line (RIL) mapping populations and to apply in mapping Tomato spotted wilt virus (TSWV) resistance trait in peanut. A total of 4,576 simple sequence repeat (SSR) markers from three sources: published SSR markers, newly developed SSR markers from expressed sequence tags (EST) and from bacterial artificial chromosome end-sequences were used for screening polymorphisms. Two cleaved amplified polymorphic sequence markers were also included to differentiate ahFAD2A alleles and ahFAD2B alleles. A total of 324 markers were anchored on this integrated map covering 1,352.1 cM with 21 linkage groups (LGs). Combining information from duplicated loci between LGs and comparing with published diploid maps, seven homoeologous groups were defined and 17 LGs (A1-A10, B1-B4, B7, B8, and B9) were aligned to corresponding A-subgenome or B-subgenome of diploid progenitors. One reciprocal translocation was confirmed in the tetraploid-cultivated peanut genome. Several chromosomal rearrangements were observed by comparing with published cultivated peanut maps. High consistence with cultivated peanut maps derived from different populations may support this integrated map as a reliable reference map for peanut whole genome sequencing assembling. Further two major QTLs for TSWV resistance were identified for each RILs, which illustrated the application of this map.
引用
收藏
页码:653 / 664
页数:12
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