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首页> 外文期刊>BMC Genomics >Genome-wide SNP identification in multiple morphotypes of allohexaploid tall fescue (Festuca arundinacea Schreb)
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Genome-wide SNP identification in multiple morphotypes of allohexaploid tall fescue (Festuca arundinacea Schreb)

机译:全基因组SNP鉴定同种六倍体高羊茅(Festuca arundinacea Schreb)的多种形态类型

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Background Single nucleotide polymorphisms (SNPs) provide essential tools for the advancement of research in plant genomics, and the development of SNP resources for many species has been accelerated by the capabilities of second-generation sequencing technologies. The current study aimed to develop and use a novel bioinformatic pipeline to generate a comprehensive collection of SNP markers within the agriculturally important pasture grass tall fescue; an outbreeding allopolyploid species displaying three distinct morphotypes: Continental, Mediterranean and rhizomatous. Results A bioinformatic pipeline was developed that successfully identified SNPs within genotypes from distinct tall fescue morphotypes, following the sequencing of 414 polymerase chain reaction (PCR) – generated amplicons using 454 GS FLX technology. Equivalent amplicon sets were derived from representative genotypes of each morphotype, including six Continental, five Mediterranean and one rhizomatous. A total of 8,584 and 2,292 SNPs were identified with high confidence within the Continental and Mediterranean morphotypes respectively. The success of the bioinformatic approach was demonstrated through validation (at a rate of 70%) of a subset of 141 SNPs using both SNaPshot? and GoldenGate? assay chemistries. Furthermore, the quantitative genotyping capability of the GoldenGate? assay revealed that approximately 30% of the putative SNPs were accessible to co-dominant scoring, despite the hexaploid genome structure. The sub-genome-specific origin of each SNP validated from Continental tall fescue was predicted using a phylogenetic approach based on comparison with orthologous sequences from predicted progenitor species. Conclusions Using the appropriate bioinformatic approach, amplicon resequencing based on 454 GS FLX technology is an effective method for the identification of polymorphic SNPs within the genomes of Continental and Mediterranean tall fescue. The GoldenGate? assay is capable of high-throughput co-dominant SNP allele detection, and minimises the problems associated with SNP genotyping in a polyploid by effectively reducing the complexity to a diploid system. This SNP collection may now be refined and used in applications such as cultivar identification, genetic linkage map construction, genome-wide association studies and genomic selection in tall fescue. The bioinformatic pipeline described here represents an effective general method for SNP discovery within outbreeding allopolyploid species.
机译:背景技术单核苷酸多态性(SNP)为植物基因组学研究的发展提供了必不可少的工具,并且第二代测序技术的能力已加速了许多物种SNP资源的开发。当前的研究旨在开发和使用新型的生物信息学管道,以在农业上重要的牧草高羊茅内产生全面的SNP标记物。异源多倍体物种,表现出三种不同的形态型:大陆型,地中海型和根茎型。结果开发了一条生物信息学流水线,通过414聚合酶链反应(PCR)测序-使用454 GS FLX技术对成功扩增出的扩增子进行了测序,从而成功地从不同的羊茅高形态型中鉴定出了SNP。等效扩增子集来自每种形态型的代表性基因型,包括六种大陆型,五种地中海型和一种根状。分别在大陆型和地中海型中鉴定出总共8584个和2292个SNP。通过使用两个SNaPshot对141个SNP的子集进行验证(以70%的比率),证明了生物信息学方法的成功。和GoldenGate?分析化学。此外,GoldenGate的定量基因分型能力?分析表明,尽管六倍体基因组结构,大约30%的推定SNP仍可进行共计得分。基于与来自预测的祖先物种的直系同源序列的比较,使用系统发育方法来预测从大陆高羊茅验证的每个SNP的亚基因组特异性起源。结论使用适当的生物信息学方法,基于454 GS FLX技术的扩增子重测序是鉴定大陆和地中海高羊茅基因组内多态性SNP的有效方法。金门?该测定法能够检测高通量的SNP等位基因,并通过有效降低二倍体系统的复杂性,将与多倍体中SNP基因分型有关的问题降到最低。现在可以完善此SNP集合并将其用于诸如品种鉴定,遗传连锁图谱构建,全基因组关联研究和高羊茅基因组选择等应用。这里描述的生物信息学管道代表了在异源多倍体物种中发现SNP的有效通用方法。

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