Song Qijian, Jenkins Jerry, Jia Gaofeng, Hyten David L, Pantalone Vince, Jackson Scott A, Schmutz Jeremy, Cregan Perry B
USDA-ARS, Soybean Genomics and Improvement Lab, Beltsville, MD, 20705, USA.
HudsonAlpha Institute for Biotechnology, Huntsville, Alabama, 35806, USA.
BMC Genomics. 2016 Jan 6;17:33. doi: 10.1186/s12864-015-2344-0.
A landmark in soybean research, Glyma1.01, the first whole genome sequence of variety Williams 82 (Glycine max L. Merr.) was completed in 2010 and is widely used. However, because the assembly was primarily built based on the linkage maps constructed with a limited number of markers and recombinant inbred lines (RILs), the assembled sequence, especially in some genomic regions with sparse numbers of anchoring markers, needs to be improved. Molecular markers are being used by researchers in the soybean community, however, with the updating of the Glyma1.01 build based on the high-resolution linkage maps resulting from this research, the genome positions of these markers need to be mapped.
Two high density genetic linkage maps were constructed based on 21,478 single nucleotide polymorphism loci mapped in the Williams 82 x G. soja (Sieb. & Zucc.) PI479752 population with 1083 RILs and 11,922 loci mapped in the Essex x Williams 82 population with 922 RILs. There were 37 regions or single markers where marker order in the two populations was in agreement but was not consistent with the physical position in the Glyma1.01 build. In addition, 28 previously unanchored scaffolds were positioned. Map data were used to identify false joins in the Glyma1.01 assembly and the corresponding scaffolds were broken and reassembled to the new assembly, Wm82.a2.v1. Based upon the plots of the genetic on physical distance of the loci, the euchromatic and heterochromatic regions along each chromosome in the new assembly were delimited. Genomic positions of the commonly used markers contained in BARCSOYSSR_1.0 database and the SoySNP50K BeadChip were updated based upon the Wm82.a2.v1 assembly.
The information will facilitate the study of recombination hot spots in the soybean genome, identification of genes or quantitative trait loci controlling yield, seed quality and resistance to biotic or abiotic stresses as well as other genetic or genomic research.
大豆研究中的一个里程碑,即大豆品种威廉姆斯82(Glycine max L. Merr.)的首个全基因组序列Glyma1.01于2010年完成并得到广泛应用。然而,由于该组装主要基于由有限数量的标记和重组自交系(RILs)构建的连锁图谱,所组装的序列,尤其是在一些锚定标记数量稀少的基因组区域,需要改进。大豆研究领域的研究人员正在使用分子标记,然而,随着基于本研究产生的高分辨率连锁图谱对Glyma1.01版本进行更新,这些标记的基因组位置需要进行定位。
基于在威廉姆斯82×野生大豆(Sieb. & Zucc.)PI479752群体(含1083个RILs)中定位的21478个单核苷酸多态性位点以及在埃塞克斯×威廉姆斯82群体(含922个RILs)中定位的11922个位点,构建了两张高密度遗传连锁图谱。在37个区域或单个标记处,两个群体中的标记顺序一致,但与Glyma1.01版本中的物理位置不一致。此外,定位了28个先前未锚定的支架。图谱数据用于识别Glyma1.01组装中的错误连接,并将相应的支架打断并重新组装到新的组装版本Wm82.a2.v1中。基于基因座的遗传距离与物理距离的图谱,界定了新组装版本中每条染色体上的常染色质和异染色质区域。基于Wm82.a2.v1组装版本,更新了BARCSOYSSR_1.0数据库和SoySNP50K BeadChip中常用标记的基因组位置。
这些信息将有助于大豆基因组中重组热点的研究、控制产量、种子质量以及对生物或非生物胁迫抗性的基因或数量性状位点的鉴定,以及其他遗传或基因组研究。