Bhakta Mehul S, Jones Valerie A, Vallejos C Eduardo
Horticultural Sciences Department, University of Florida, Gainesville, Florida, United States of America.
Horticultural Sciences Department, University of Florida, Gainesville, Florida, United States of America; Plant Molecular and Cellular Biology Program, University of Florida, Gainesville, Florida, United States of America.
PLoS One. 2015 Jan 28;10(1):e0116822. doi: 10.1371/journal.pone.0116822. eCollection 2015.
High density genetic maps are a reliable tool for genetic dissection of complex plant traits. Mapping resolution is often hampered by the variable crossover and non-crossover events occurring across the genome, with pericentromeric regions (pCENR) showing highly suppressed recombination rates. The efficiency of linkage mapping can further be improved by characterizing and understanding the distribution of recombinational activity along individual chromosomes. In order to evaluate the genome wide recombination rate in common beans (Phaseolus vulgaris L.) we developed a SNP-based linkage map using the genotype-by-sequencing approach with a 188 recombinant inbred line family generated from an inter gene pool cross (Andean x Mesoamerican). We identified 1,112 SNPs that were subsequently used to construct a robust linkage map with 11 groups, comprising 513 recombinationally unique marker loci spanning 943 cM (LOD 3.0). Comparative analysis showed that the linkage map spanned >95% of the physical map, indicating that the map is almost saturated. Evaluation of genome-wide recombination rate indicated that at least 45% of the genome is highly recombinationally suppressed, and allowed us to estimate locations of pCENRs. We observed an average recombination rate of 0.25 cM/Mb in pCENRs as compared to the rest of genome that showed 3.72 cM/Mb. However, several hot spots of recombination were also detected with recombination rates reaching as high as 34 cM/Mb. Hotspots were mostly found towards the end of chromosomes, which also happened to be gene-rich regions. Analyzing relationships between linkage and physical map indicated a punctuated distribution of recombinational hot spots across the genome.
高密度遗传图谱是对复杂植物性状进行遗传剖析的可靠工具。全基因组中发生的可变交换和非交换事件常常会阻碍图谱的分辨率,着丝粒周围区域(pCENR)的重组率被高度抑制。通过表征和理解沿单个染色体的重组活性分布,可以进一步提高连锁图谱构建的效率。为了评估普通菜豆(Phaseolus vulgaris L.)的全基因组重组率,我们利用基因分型测序方法,基于一个由基因池间杂交(安第斯×中美洲)产生的包含188个重组自交系的家系,构建了一个基于单核苷酸多态性(SNP)的连锁图谱。我们鉴定出1112个SNP,随后利用这些SNP构建了一个稳健的连锁图谱,该图谱包含11个连锁群,由513个重组独特标记位点组成,跨度为943厘摩(LOD 3.0)。比较分析表明,该连锁图谱覆盖了物理图谱的>95%,表明该图谱几乎饱和。全基因组重组率评估表明,至少45%的基因组重组受到高度抑制,并使我们能够估计着丝粒周围区域(pCENR)的位置。我们观察到,与基因组其他区域平均3.72厘摩/兆碱基的重组率相比,着丝粒周围区域(pCENR)的平均重组率为0.25厘摩/兆碱基。然而,也检测到了几个重组热点,重组率高达34厘摩/兆碱基。热点大多位于染色体末端,而这些区域恰好也是基因丰富的区域。分析连锁图谱与物理图谱之间的关系表明,重组热点在全基因组中呈间断分布。