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Construction of a 10,000-Marker Ultradense Genetic Recombination Map of Potato: Providing a Framework for Accelerated Gene Isolation and a Genomewide Physical Map

机译:10,000标记的马铃薯超高密度遗传重组图的构建:提供加速的基因分离框架和全基因组物理图谱

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摘要

An ultradense genetic linkage map with >10,000 AFLP loci was constructed from a heterozygous diploid potato population. To our knowledge, this is the densest meiotic recombination map ever constructed. A fast marker-ordering algorithm was used, based on the minimization of the total number of recombination events within a given marker order in combination with genotyping error-detection software. This resulted in “skeleton bin maps,” which can be viewed as the most parsimonious marker order. The unit of distance is not expressed in centimorgans but in “bins.” A bin is a position on the genetic map with a unique segregation pattern that is separated from adjacent bins by a single recombination event. Putative centromeres were identified by a strong clustering of markers, probably due to cold spots for recombination. Conversely, recombination hot spots resulted in large intervals of up to 15 cM without markers. The current level of marker saturation suggests that marker density is proportional to physical distance and independent of recombination frequency. Most chromatids (92%) recombined once or never, suggesting strong chiasma interference. Absolute chiasma interference within a chromosome arm could not be demonstrated. Two examples of contig construction and map-based cloning have demonstrated that the marker spacing was in accordance with the expected physical distance: approximately one marker per BAC length. Currently, the markers are used for genetic anchoring of a physical map of potato to deliver a sequence-ready minimal tiling path of BAC contigs of specific chromosomal regions for the potato genome sequencing consortium (http://www.potatogenome.net).
机译:从杂合二倍体马铃薯群体构建了具有> 10,000个AFLP位点的超致密遗传连锁图。据我们所知,这是有史以来最密集的减数分裂重组图。基于基因标记错误检测软件,基于给定标记顺序内重组事件总数的最小化,使用了快速标记排序算法。这产生了“骨架箱图”,可以将其视为最简约的标记顺序。距离的单位不是用厘摩来表示,而是用“箱”来表示。仓是遗传图谱上具有独特分离模式的位置,该分离模式通过单个重组事件与相邻仓分开。推测的着丝粒通过标记物的强聚集来鉴定,可能是由于重组的冷点。相反,重组热点导致无标记的间隔高达15 cM。标记物饱和度的当前水平表明,标记物密度与物理距离成正比,并且与重组频率无关。大多数染色单体(92%)重组一次或从未重组,表明强烈的交叉瘤干扰。不能证明染色体臂内的绝对嵌合体干扰。重叠群构建和基于图谱的克隆的两个例子表明,标记间距与预期的物理距离一致:每BAC长度大约一个标记。当前,标记物用于马铃薯的物理图谱的遗传锚定,以为马铃薯基因组测序联盟(http://www.potatogenome.net)提供特定染色体区域的BAC重叠群的序列就绪最小平铺路径。

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