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利用代表性寡核苷酸微阵列分析进行高通量遗传标记物的鉴定。

High-throughput identification of genetic markers using representational oligonucleotide microarray analysis.

机构信息

Max Planck Institute for Molecular Genetics, Ihnestr. 63-73, 14195, Berlin, Germany.

出版信息

Theor Appl Genet. 2010 Aug;121(3):549-65. doi: 10.1007/s00122-010-1329-2. Epub 2010 Apr 9.

Abstract

We describe a novel approach for high-throughput development of genetic markers using representational oligonucleotide microarray analysis. We test the performance of the method in sugar beet (Beta vulgaris L.) as a model for crop plants with little sequence information available. Genomic representations of both parents of a mapping population were hybridized on microarrays containing in total 146,554 custom made oligonucleotides based on sugar beet bacterial artificial chromosome (BAC) end sequences and expressed sequence tags (ESTs). Oligonucleotides showing a signal with one parental line only, were selected as potential marker candidates and placed onto an array, designed for genotyping of 184 F(2) individuals from the mapping population. Utilizing known co-dominant anchor markers we obtained 511 new dominant markers (392 derived from BAC end sequences, and 119 from ESTs) distributed over all nine sugar beet linkage groups and calculated genetic maps. Further improvements for large-scale application of the approach are discussed and its feasibility for the cost-effective and flexible generation of genetic markers is presented.

摘要

我们描述了一种使用代表性寡核苷酸微阵列分析高通量开发遗传标记的新方法。我们以甜菜(Beta vulgaris L.)作为模型作物植物进行了方法性能测试,这些植物可用的序列信息很少。在微阵列上杂交了一个作图群体的两个亲本的基因组表示,该微阵列总共包含了基于甜菜细菌人工染色体(BAC)末端序列和表达序列标签(EST)的 146,554 个定制的寡核苷酸。仅与一个亲本系显示信号的寡核苷酸被选为潜在的标记候选物,并放置在设计用于对来自作图群体的 184 个 F2 个体进行基因分型的阵列上。利用已知的共显性锚定标记,我们获得了 511 个新的显性标记(392 个源自 BAC 末端序列,119 个源自 EST),分布在所有 9 个甜菜连锁群上,并计算了遗传图谱。进一步讨论了大规模应用该方法的改进措施,并展示了其用于经济高效且灵活地生成遗传标记的可行性。

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