Department of Natural Resources & Environmental Sciences, University of Illinois, Urbana, Illinois, United States of America.
PLoS One. 2012;7(11):e47864. doi: 10.1371/journal.pone.0047864. Epub 2012 Nov 5.
Genetic maps serve as frameworks for determining the genetic architecture of quantitative traits, assessing structure of a genome, as well as aid in pursuing association mapping and comparative genetic studies. In this study, a dense genetic map was constructed using a high-throughput 1,536 EST-derived SNP GoldenGate genotyping platform and a global consensus map established by combining the new genetic map with four existing reliable genetic maps of apple. The consensus map identified markers with both major and minor conflicts in positioning across all five maps. These major inconsistencies among marker positions were attributed either to structural variations within the apple genome, or among mapping populations, or genotyping technical errors. These also highlighted problems in assembly and anchorage of the reference draft apple genome sequence in regions with known segmental duplications. Markers common across all five apple genetic maps resulted in successful positioning of 2875 markers, consisting of 2033 SNPs and 843 SSRs as well as other specific markers, on the global consensus map. These markers were distributed across all 17 linkage groups, with an average of 169±33 marker per linkage group and with an average distance of 0.70±0.14 cM between markers. The total length of the consensus map was 1991.38 cM with an average length of 117.14±24.43 cM per linkage group. A total of 569 SNPs were mapped onto the genetic map, consisting of 140 recombinant individuals, from our recently developed apple Oligonucleotide pool assays (OPA). The new functional SNPs, along with the dense consensus genetic map, will be useful for high resolution QTL mapping of important traits in apple and for pursuing comparative genetic studies in Rosaceae.
遗传图谱可用于确定数量性状的遗传结构、评估基因组结构,以及辅助关联作图和比较遗传研究。本研究使用高通量 1536 个 EST 衍生 SNP GoldenGate 基因分型平台和一个综合了新的遗传图谱与苹果的 4 个可靠遗传图谱的全球共识图谱,构建了一个高密度遗传图谱。共识图谱确定了在所有 5 个图谱中定位存在主要和次要冲突的标记。这些标记位置的主要不一致性归因于苹果基因组内的结构变异、或作图群体间的结构变异、或基因分型技术错误。这也突显了参考苹果基因组序列在已知片段重复区域的组装和锚定问题。在所有 5 个苹果遗传图谱中通用的标记成功地将 2875 个标记定位于全球共识图谱上,包括 2033 个 SNP 和 843 个 SSR 以及其他特定标记。这些标记分布在所有 17 个连锁群上,每个连锁群平均有 169±33 个标记,标记间平均距离为 0.70±0.14 cM。共识图谱的总长度为 1991.38 cM,每个连锁群的平均长度为 117.14±24.43 cM。共有 569 个 SNP 被映射到遗传图谱上,包括来自我们最近开发的苹果寡核苷酸池分析(OPA)的 140 个重组个体。新的功能 SNP 以及高密度共识遗传图谱将有助于苹果重要性状的高分辨率 QTL 作图和蔷薇科比较遗传研究。