Faculty of Engineering and Natural Sciences, Sabanci University, Tuzla, Istanbul, Turkey.
PLoS One. 2013 Apr 16;8(4):e59542. doi: 10.1371/journal.pone.0059542. Print 2013.
Bread wheat (Triticum aestivum L.) is one of the most important crops worldwide and its production faces pressing challenges, the solution of which demands genome information. However, the large, highly repetitive hexaploid wheat genome has been considered intractable to standard sequencing approaches. Therefore the International Wheat Genome Sequencing Consortium (IWGSC) proposes to map and sequence the genome on a chromosome-by-chromosome basis.
METHODOLOGY/PRINCIPAL FINDINGS: We have constructed a physical map of the long arm of bread wheat chromosome 1A using chromosome-specific BAC libraries by High Information Content Fingerprinting (HICF). Two alternative methods (FPC and LTC) were used to assemble the fingerprints into a high-resolution physical map of the chromosome arm. A total of 365 molecular markers were added to the map, in addition to 1122 putative unique transcripts that were identified by microarray hybridization. The final map consists of 1180 FPC-based or 583 LTC-based contigs.
CONCLUSIONS/SIGNIFICANCE: The physical map presented here marks an important step forward in mapping of hexaploid bread wheat. The map is orders of magnitude more detailed than previously available maps of this chromosome, and the assignment of over a thousand putative expressed gene sequences to specific map locations will greatly assist future functional studies. This map will be an essential tool for future sequencing of and positional cloning within chromosome 1A.
小麦(Triticum aestivum L.)是全球最重要的作物之一,其生产面临着紧迫的挑战,解决这些挑战需要基因组信息。然而,庞大且高度重复的六倍体小麦基因组被认为难以通过标准测序方法解决。因此,国际小麦基因组测序联盟(IWGSC)提议在染色体基础上对基因组进行作图和测序。
方法/主要发现: 我们使用染色体特异性 BAC 文库通过高信息量指纹图谱(HICF)构建了面包小麦 1A 染色体长臂的物理图谱。两种替代方法(FPC 和 LTC)被用于将指纹图谱组装成染色体臂的高分辨率物理图谱。除了通过微阵列杂交鉴定的 1122 个假定的独特转录本外,该图谱还添加了 365 个分子标记。最终图谱由 1180 个基于 FPC 的或 583 个基于 LTC 的图谱组成。
结论/意义: 本文呈现的物理图谱标志着六倍体面包小麦作图的重要进展。该图谱比以前该染色体的图谱详细了几个数量级,并且将一千多个假定的表达基因序列分配到特定的图谱位置将极大地有助于未来的功能研究。该图谱将是未来在 1A 染色体上进行测序和定位克隆的重要工具。