Construction of a SNP-based genetic linkage map in cultivated peanut based on large scale marker development using next-generation double-digest restriction-site-associated DNA sequencing (ddRADseq)

被引:96
|
作者
Zhou, Xiaojing [1 ]
Xia, Youlin [2 ]
Ren, Xiaoping [1 ]
Chen, Yulin [1 ]
Huang, Li [1 ]
Huang, Shunmou [1 ,3 ]
Liao, Boshou [1 ]
Lei, Yong [1 ]
Yan, Liyin [1 ]
Jiang, Huifang [1 ]
机构
[1] Chinese Acad Agr Sci, Oil Crops Res Inst, Minist Agr, Key Lab Biol & Genet Improvement Oil Crops, Wuhan 430062, Hubei, Peoples R China
[2] Nanchong Acad Agr Sci, Nanchong 637000, Sichuan, Peoples R China
[3] Databridge Technol Corp, Wuhan 430062, Hubei, Peoples R China
来源
BMC GENOMICS | 2014年 / 15卷
基金
中国国家自然科学基金;
关键词
Cultivated peanut; Linkage map; SNP; ddRADseq; ARACHIS-HYPOGAEA L; POLYPLOID BRASSICA-NAPUS; RAD-SEQ; DISCOVERY; GENOME; IDENTIFICATION; SEGREGATION; RESISTANCE; TOOL;
D O I
10.1186/1471-2164-15-351
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Cultivated peanut, or groundnut (Arachis hypogaea L.), is an important oilseed crop with an allotetraploid genome (AABB, 2n = 4x = 40). In recent years, many efforts have been made to construct linkage maps in cultivated peanut, but almost all of these maps were constructed using low-throughput molecular markers, and most show a low density, directly influencing the value of their applications. With advances in next-generation sequencing (NGS) technology, the construction of high-density genetic maps has become more achievable in a cost-effective and rapid manner. The objective of this study was to establish a high-density single nucleotide polymorphism (SNP)-based genetic map for cultivated peanut by analyzing next-generation double-digest restriction-site-associated DNA sequencing (ddRADseq) reads. Results: We constructed reduced representation libraries (RRLs) for two A. hypogaea lines and 166 of their recombinant inbred line (RIL) progenies using the ddRADseq technique. Approximately 175 gigabases of data containing 952,679,665 paired-end reads were obtained following Solexa sequencing. Mining this dataset, 53,257 SNPs were detected between the parents, of which 14,663 SNPs were also detected in the population, and 1,765 of the obtained polymorphic markers met the requirements for use in the construction of a genetic map. Among 50 randomly selected in silico SNPs, 47 were able to be successfully validated. One linkage map was constructed, which was comprised of 1,685 marker loci, including 1,621 SNPs and 64 simple sequence repeat (SSR) markers. The map displayed a distribution of the markers into 20 linkage groups (LGs A01-A10 and B01-B10), spanning a distance of 1,446.7 cM. The alignment of the LGs from this map was shown in comparison with a previously integrated consensus map from peanut. Conclusions: This study showed that the ddRAD library combined with NGS allowed the rapid discovery of a large number of SNPs in the cultivated peanut. The first high density SNP-based linkage map for A. hypogaea was generated that can serve as a reference map for cultivated Arachis species and will be useful in genetic mapping. Our results contribute to the available molecular marker resources and to the assembly of a reference genome sequence for the peanut.
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页数:14
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