Song Beng-Kah, Nadarajah Kalaivani, Romanov Michael N, Ratnam Wickneswari
School of Environmental and Natural Resource Sciences, Faculty of Science and Technology, Kebangsaan University Malaysia, 43600 Bangi, Selangor, Malaysia.
Cell Mol Biol Lett. 2005;10(3):425-37.
The construction of BAC-contig physical maps is an important step towards a partial or ultimate genome sequence analysis. Here, we describe our initial efforts to apply an overgo approach to screen a BAC library of the Malaysian wild rice species, Oryza rufipogon. Overgo design is based on repetitive element masking and sequence uniqueness, and uses short probes (approximately 40 bp), making this method highly efficient and specific. Pairs of 24-bp oligos that contain an 8-bp overlap were developed from the publicly available genomic sequences of the cultivated rice, O. sativa, to generate 20 overgo probes for a 1-Mb region that encompasses a yield enhancement QTL yld1.1 in O. rufipogon. The advantages of a high similarity in melting temperature, hybridization kinetics and specific activities of overgos further enabled a pooling strategy for library screening by filter hybridization. Two pools of ten overgos each were hybridized to high-density filters representing the O. rufipogon genomic BAC library. These screening tests succeeded in providing 69 PCR-verified positive hits from a total of 23,040 BAC clones of the entire O. rufipogon library. A minimal tilling path of clones was generated to contribute to a fully covered BAC-contig map of the targeted 1-Mb region. The developed protocol for overgo design based on O. sativa sequences as a comparative genomic framework, and the pooled overgo hybridization screening technique are suitable means for high-resolution physical mapping and the identification of BAC candidates for sequencing.
细菌人工染色体(BAC)重叠群物理图谱的构建是朝着部分或最终基因组序列分析迈出的重要一步。在此,我们描述了我们初步尝试应用重叠延伸法来筛选马来西亚野生稻种——普通野生稻(Oryza rufipogon)的BAC文库。重叠延伸设计基于重复元件屏蔽和序列独特性,并使用短探针(约40个碱基对),使得该方法高效且特异。从栽培稻——亚洲栽培稻(O. sativa)的公开基因组序列中开发出包含8个碱基对重叠的24个碱基对寡核苷酸对,以生成20个重叠延伸探针,用于一个1兆碱基区域,该区域包含普通野生稻中的一个产量增强数量性状位点yld1.1。重叠延伸片段在解链温度、杂交动力学和比活性方面具有高度相似性的优点,进一步使得通过滤膜杂交进行文库筛选的混合策略成为可能。将两个各包含10个重叠延伸片段的池与代表普通野生稻基因组BAC文库的高密度滤膜杂交。这些筛选测试成功地从普通野生稻文库总共23,040个BAC克隆中获得了69个经PCR验证的阳性克隆。生成了一个最小克隆路径,以构建目标1兆碱基区域的完全覆盖的BAC重叠群图谱。基于亚洲栽培稻序列作为比较基因组框架开发的重叠延伸设计方案以及混合重叠延伸杂交筛选技术,是用于高分辨率物理图谱构建和鉴定用于测序的BAC候选克隆的合适方法。