TraitGenetics GmbH, Gatersleben, Germany.
PLoS One. 2011;6(12):e28334. doi: 10.1371/journal.pone.0028334. Epub 2011 Dec 8.
SNP genotyping arrays have been useful for many applications that require a large number of molecular markers such as high-density genetic mapping, genome-wide association studies (GWAS), and genomic selection. We report the establishment of a large maize SNP array and its use for diversity analysis and high density linkage mapping. The markers, taken from more than 800,000 SNPs, were selected to be preferentially located in genes and evenly distributed across the genome. The array was tested with a set of maize germplasm including North American and European inbred lines, parent/F1 combinations, and distantly related teosinte material. A total of 49,585 markers, including 33,417 within 17,520 different genes and 16,168 outside genes, were of good quality for genotyping, with an average failure rate of 4% and rates up to 8% in specific germplasm. To demonstrate this array's use in genetic mapping and for the independent validation of the B73 sequence assembly, two intermated maize recombinant inbred line populations - IBM (B73×Mo17) and LHRF (F2×F252) - were genotyped to establish two high density linkage maps with 20,913 and 14,524 markers respectively. 172 mapped markers were absent in the current B73 assembly and their placement can be used for future improvements of the B73 reference sequence. Colinearity of the genetic and physical maps was mostly conserved with some exceptions that suggest errors in the B73 assembly. Five major regions containing non-colinearities were identified on chromosomes 2, 3, 6, 7 and 9, and are supported by both independent genetic maps. Four additional non-colinear regions were found on the LHRF map only; they may be due to a lower density of IBM markers in those regions or to true structural rearrangements between lines. Given the array's high quality, it will be a valuable resource for maize genetics and many aspects of maize breeding.
SNP 基因分型阵列在许多需要大量分子标记的应用中非常有用,例如高密度遗传作图、全基因组关联研究(GWAS)和基因组选择。我们报告了一个大型玉米 SNP 阵列的建立及其用于多样性分析和高密度连锁作图的应用。这些标记来自超过 80 万个 SNP,被优先选择位于基因中,并均匀分布在基因组中。该阵列经过了一组包括北美和欧洲自交系、亲本/F1 组合以及远缘玉米材料的玉米种质的测试。共有 49,585 个标记,包括 33,417 个位于 17,520 个不同基因内和 16,168 个基因外的标记,用于基因分型的质量良好,平均失败率为 4%,在特定种质中高达 8%。为了展示该阵列在遗传作图中的用途以及独立验证 B73 序列组装,我们对两个互交玉米重组自交系群体 IBM(B73×Mo17)和 LHRF(F2×F252)进行了基因分型,分别建立了两个高密度连锁图谱,分别包含 20,913 个和 14,524 个标记。在当前的 B73 组装中,有 172 个标记缺失,它们的位置可用于未来改进 B73 参考序列。遗传图谱和物理图谱的共线性大部分得到了保留,但也有一些例外,表明 B73 组装存在错误。在染色体 2、3、6、7 和 9 上鉴定出了五个包含非共线性的主要区域,这两个独立的遗传图谱都支持这些区域。在 LHRF 图谱中仅发现了另外四个非共线性区域;它们可能是由于 IBM 标记在这些区域的密度较低,或者是由于品系之间的真实结构重排所致。鉴于该阵列的高质量,它将成为玉米遗传学和玉米许多方面的重要资源。