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Adapting Genotyping-by-Sequencing for Rice F2 Populations

机译:通过测序适应水稻F2群体的基因分型

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摘要

Rapid and cost-effective genotyping of large mapping populations can be achieved by sequencing a reduced representation of the genome of every individual in a given population, and using that information to generate genetic markers. A customized genotyping-by-sequencing (GBS) pipeline was developed to genotype a rice F2 population from a cross of Oryza sativa ssp. japonica cv. Nipponbare and the African wild rice species O. longistaminata. While most GBS pipelines aim to analyze mainly homozygous populations, we attempted to genotype a highly heterozygous F2 population. We show how species- and population-specific improvements of established protocols can drastically increase sample throughput and genotype quality. Using as few as 50,000 reads for some individuals (134,000 reads on average), we were able to generate up to 8154 informative SNP markers in 1081 F2 individuals. Additionally, the effects of enzyme choice, read coverage, and data postprocessing are evaluated. Using GBS-derived markers, we were able to assemble a genetic map of 1536 cM. To demonstrate the usefulness of our GBS pipeline, we determined quantitative trait loci (QTL) for the number of tillers. We were able to map four QTL to chromosomes 1, 3, 4, and 8, and partially confirm their effects using introgression lines. We provide an example of how to successfully use GBS with heterozygous F2 populations. By using the comparatively low-cost MiSeq platform, we show that the GBS method is flexible and cost-effective, even for smaller laboratories.
机译:通过对给定种群中每个个体的基因组的简化表示进行测序,然后使用该信息生成遗传标记,可以实现大型作图种群的快速且经济高效的基因分型。开发了定制的测序基因分型(GBS)管道,以对来自水稻(Oryza sativa ssp)杂交的水稻F2群体进行基因分型。粳稻Nipponbare和非洲野生稻种O. longistaminata。尽管大多数GBS管道主要用于分析纯合子种群,但我们尝试对高度杂合的F2种群进行基因分型。我们展示了已建立协议的物种和种群特定的改进如何能够大大提高样品通量和基因型质量。对于某些个体,使用少至50,000个读数(平均134,000个读数),我们就能够在1081个F2个体中生成多达8154个信息性SNP标记。此外,评估酶选择,读取覆盖率和数据后处理的效果。使用GBS衍生的标记,我们能够构建1536 cM的遗传图谱。为了证明我们的GBS管道的有用性,我们确定了分till数量的数量性状基因座(QTL)。我们能够将四个QTL映射到1、3、4和8号染色体,并使用渗入系部分证实了它们的作用。我们提供了一个示例,说明如何成功将GBS与杂合F2群体一起使用。通过使用成本相对较低的MiSeq平台,我们证明了GBS方法既灵活又具有成本效益,即使对于较小的实验室也是如此。

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