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Large-Scale Identification and Analysis of Genome-Wide Single-Nucleotide Polymorphisms for Mapping in Arabidopsis thaliana

机译:拟南芥基因组全基因组单核苷酸多态性的大规模鉴定和分析

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摘要

Genetic markers such as single nucleotide polymorphisms (SNPs) are essential tools for positional cloning, association, or quantitative trait locus mapping and the determination of genetic relationships between individuals. We identified and characterized a genome-wide set of SNP markers by generating 10,706 expressed sequence tags (ESTs) from cDNA libraries derived from 6 different accessions, and by analysis of 606 sequence tagged sites (STS) from up to 12 accessions of the model flowering plant Arabidopsis thaliana. The cDNA libraries for EST sequencing were made from individuals that were stressed by various means to enrich for transcripts from genes expressed under such conditions. SNPs discovered in these sequences may be useful markers for mapping genes involved in interactions with the biotic and abiotic environment. The STS loci are distributed randomly over the genome. By comparison with the Col-0 genome sequence, we identified a total of 8051 SNPs and 637 insertion/deletion polymorphisms (InDel). Analysis of STS-derived SNPs shows that most SNPs are rare, but that it is possible to identify intermediate frequency framework markers that can be used for genetic mapping in many different combinations of accessions. A substantial proportion of SNPs located in ORFs caused a change of the encoded amino acid. A comparison of the density of our SNP markers among accessions in both the EST and STS datasets, revealed that Cvi-0 is the most divergent accession from Col-0 among the 12 accessions studied. All of these markers are freely available via the internet.
机译:遗传标记(例如单核苷酸多态性(SNP))是用于位置克隆,关联或定量性状基因座作图以及确定个体之间遗传关系的重要工具。我们通过从6种不同种质来源的cDNA文库中生成10,706个表达的序列标签(EST),并通过分析模型开花的12种种质中的606个序列标签位点(STS),鉴定并表征了全基因组SNP标记植物拟南芥。用于EST测序的cDNA文库是由通过各种方式强调从这种条件下表达的基因中富集转录本的个体制成的。在这些序列中发现的SNP可能是有用的标记,可用于定位与生物和非生物环境相互作用中涉及的基因。 STS基因座随机分布在基因组上。通过与Col-0基因组序列进行比较,我们确定了总共8051个SNP和637个插入/缺失多态性(InDel)。对STS衍生的SNP的分析表明,大多数SNP很少见,但有可能鉴定出中频框架标记,这些标记可用于许多不同组合的遗传图谱中。位于ORF中的SNP的很大一部分引起了编码氨基酸的改变。在EST和STS数据集中,我们的SNP标记密度在种质之间的比较表明,在研究的12种种质中Cvi-0与Col-0的差异最大。所有这些标记都可以通过互联网免费获得。

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