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基于新一代双酶切限制性位点关联DNA测序(ddRADseq)大规模开发标记构建栽培花生的单核苷酸多态性(SNP)遗传连锁图谱。

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).

作者信息

Zhou Xiaojing, Xia Youlin, Ren Xiaoping, Chen Yulin, Huang Li, Huang Shunmou, Liao Boshou, Lei Yong, Yan Liyin, Jiang Huifang

机构信息

Key Laboratory of Biology and Genetic Improvement of Oil Crops, Ministry of Agriculture, Oil Crops Research Institute of the Chinese Academy of Agricultural Sciences, Wuhan 430062, Hubei, People's Republic of China.

出版信息

BMC Genomics. 2014 May 9;15(1):351. doi: 10.1186/1471-2164-15-351.

Abstract

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.

摘要

背景

栽培花生,即落花生(Arachis hypogaea L.),是一种重要的油料作物,具有异源四倍体基因组(AABB,2n = 4x = 40)。近年来,人们为构建栽培花生的连锁图谱付出了诸多努力,但几乎所有这些图谱都是使用低通量分子标记构建的,且大多数图谱密度较低,直接影响了其应用价值。随着下一代测序(NGS)技术的发展,以经济高效且快速的方式构建高密度遗传图谱已变得更具可行性。本研究的目的是通过分析下一代双酶切限制性位点关联DNA测序(ddRADseq)读数,为栽培花生建立一个基于单核苷酸多态性(SNP)的高密度遗传图谱。

结果

我们使用ddRADseq技术为两个花生品系及其166个重组自交系(RIL)后代构建了简化代表性文库(RRL)。经Solexa测序后,获得了约175千兆碱基的数据,包含952,679,665对末端读数。挖掘该数据集,在亲本之间检测到53,257个SNP,其中在群体中也检测到14,663个SNP,获得的1,765个多态性标记满足用于构建遗传图谱的要求。在50个随机选择的电子SNP中,47个能够成功验证。构建了一个连锁图谱,其由1,685个标记位点组成,包括1,621个SNP和64个简单序列重复(SSR)标记。该图谱显示标记分布在20个连锁群(LGs A01 - A10和B01 - B10)中,跨度为1,446.7 cM。将此图谱的LGs与先前整合的花生共识图谱进行了比较展示。

结论

本研究表明,ddRAD文库与NGS相结合能够在栽培花生中快速发现大量SNP。生成了首个基于A. hypogaea的高密度SNP连锁图谱,可作为栽培花生属物种的参考图谱,并将有助于遗传作图。我们的结果为现有的分子标记资源以及花生参考基因组序列的组装做出了贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91dd/4035077/d7aa799bf3dd/12864_2013_6048_Fig1_HTML.jpg

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