Department of Forest Mycology and Plant Pathology, Swedish University of Agricultural Sciences, Uppsala, Sweden.
PLoS One. 2012;7(11):e48347. doi: 10.1371/journal.pone.0048347. Epub 2012 Nov 5.
In this study, we present a 2(nd) generation genetic linkage map of a cross between the North American species Heterobasidion irregulare and H. occidentale, based on the alignment of the previously published 1(st) generation map to the parental genomes. We anchored 216 of the original 308 AFLP markers to their respective restriction sites using an in silico-approach. The map resolution was improved by adding 146 sequence-tagged microsatellite markers and 39 sequenced gene markers. The new markers confirmed the positions of the anchored AFLP markers, fused the original 39 linkage groups together into 17, and fully expanded 12 of these to single groups covering entire chromosomes. Map coverage of the genome increased from 55.3% to 92.8%, with 96.3% of 430 markers collinearly aligned with the genome sequence. The anchored map also improved the H. irregulare assembly considerably. It identified several errors in scaffold arrangements and assisted in reducing the total number of major scaffolds from 18 to 15. This denser, more comprehensive map allowed sequence-based mapping of three intersterility loci and one mating type locus. This demonstrates the possibility to utilize an in silico procedure to convert anonymous markers into sequence-tagged ones, as well as the power of a sequence-anchored linkage map and its usefulness in the assembly of a whole genome sequence.
在这项研究中,我们展示了北美物种 Heterobasidion irregulare 和 H. occidentale 杂交种的第二代遗传连锁图谱,该图谱基于先前发表的第一代图谱与亲本基因组的比对。我们使用计算机模拟方法将最初的 308 个 AFLP 标记中的 216 个锚定到它们各自的限制位点。通过添加 146 个序列标记的微卫星标记和 39 个测序基因标记,提高了图谱的分辨率。新标记证实了锚定 AFLP 标记的位置,将原来的 39 个连锁群融合成 17 个,并将其中的 12 个完全扩展成覆盖整个染色体的单个群体。基因组的图谱覆盖率从 55.3%增加到 92.8%,430 个标记中有 96.3%与基因组序列共线性排列。锚定图谱也大大改进了 H. irregulare 的组装。它确定了几个支架排列中的错误,并有助于将主要支架的总数从 18 个减少到 15 个。这个更密集、更全面的图谱允许基于序列的三个不亲和性位点和一个交配型位点的映射。这证明了可以利用计算机模拟程序将匿名标记转换为序列标记,以及序列锚定连锁图谱的强大功能及其在整个基因组序列组装中的有用性。