Yim Young-Sun, Moak Patricia, Sanchez-Villeda Hector, Musket Theresa A, Close Pamela, Klein Patricia E, Mullet John E, McMullen Michael D, Fang Zheiwei, Schaeffer Mary L, Gardiner Jack M, Coe Edward H, Davis Georgia L
Division of Plant Sciences, University of Missouri, 1-31 Agriculture, Columbia, MO, USA.
BMC Genomics. 2007 Feb 9;8:47. doi: 10.1186/1471-2164-8-47.
Molecular markers serve three important functions in physical map assembly. First, they provide anchor points to genetic maps facilitating functional genomic studies. Second, they reduce the overlap required for BAC contig assembly from 80 to 50 percent. Finally, they validate assemblies based solely on BAC fingerprints. We employed a six-dimensional BAC pooling strategy in combination with a high-throughput PCR-based screening method to anchor the maize genetic and physical maps.
A total of 110,592 maize BAC clones (approximately 6x haploid genome equivalents) were pooled into six different matrices, each containing 48 pools of BAC DNA. The quality of the BAC DNA pools and their utility for identifying BACs containing target genomic sequences was tested using 254 PCR-based STS markers. Five types of PCR-based STS markers were screened to assess potential uses for the BAC pools. An average of 4.68 BAC clones were identified per marker analyzed. These results were integrated with BAC fingerprint data generated by the Arizona Genomics Institute (AGI) and the Arizona Genomics Computational Laboratory (AGCoL) to assemble the BAC contigs using the FingerPrinted Contigs (FPC) software and contribute to the construction and anchoring of the physical map. A total of 234 markers (92.5%) anchored BAC contigs to their genetic map positions. The results can be viewed on the integrated map of maize 12.
This BAC pooling strategy is a rapid, cost effective method for genome assembly and anchoring. The requirement for six replicate positive amplifications makes this a robust method for use in large genomes with high amounts of repetitive DNA such as maize. This strategy can be used to physically map duplicate loci, provide order information for loci in a small genetic interval or with no genetic recombination, and loci with conflicting hybridization-based information.
分子标记在物理图谱构建中发挥着三个重要作用。首先,它们为遗传图谱提供锚定位点,便于进行功能基因组学研究。其次,它们将BAC重叠群组装所需的重叠率从80%降低到50%。最后,它们仅基于BAC指纹图谱来验证组装结果。我们采用了一种六维BAC混合策略,并结合基于高通量PCR的筛选方法来锚定玉米遗传图谱和物理图谱。
总共110,592个玉米BAC克隆(约6倍单倍体基因组当量)被混合到六个不同的矩阵中,每个矩阵包含48个BAC DNA池。使用254个基于PCR的STS标记测试了BAC DNA池的质量及其用于鉴定含有目标基因组序列的BAC的效用。筛选了五种基于PCR的STS标记以评估BAC池的潜在用途。每个分析的标记平均鉴定出4.68个BAC克隆。这些结果与亚利桑那基因组学研究所(AGI)和亚利桑那基因组学计算实验室(AGCoL)生成的BAC指纹数据相结合,使用指纹重叠群(FPC)软件组装BAC重叠群,并为物理图谱的构建和锚定做出贡献。共有234个标记(92.5%)将BAC重叠群锚定到它们在遗传图谱上的位置。结果可在玉米12的整合图谱上查看。
这种BAC混合策略是一种用于基因组组装和锚定的快速、经济有效的方法。需要进行六次重复阳性扩增使得这成为一种适用于具有大量重复DNA的大基因组(如玉米)的稳健方法。该策略可用于对重复位点进行物理定位,为小遗传区间内或无遗传重组的位点以及基于杂交的信息相互冲突的位点提供排序信息。