Department of Plant and Microbial Biology, University of Zurich, Zurich, Switzerland.
Institute of Experimental Botany, Centre of the Region Haná for Biotechnological and Agricultural Research, Olomouc, Czech Republic.
Nat Biotechnol. 2017 Aug;35(8):793-796. doi: 10.1038/nbt.3877. Epub 2017 May 15.
Cereal crops such as wheat and maize have large repeat-rich genomes that make cloning of individual genes challenging. Moreover, gene order and gene sequences often differ substantially between cultivars of the same crop species. A major bottleneck for gene cloning in cereals is the generation of high-quality sequence information from a cultivar of interest. In order to accelerate gene cloning from any cropping line, we report 'targeted chromosome-based cloning via long-range assembly' (TACCA). TACCA combines lossless genome-complexity reduction via chromosome flow sorting with Chicago long-range linkage to assemble complex genomes. We applied TACCA to produce a high-quality (N50 of 9.76 Mb) de novo chromosome assembly of the wheat line CH Campala Lr22a in only 4 months. Using this assembly we cloned the broad-spectrum Lr22a leaf-rust resistance gene, using molecular marker information and ethyl methanesulfonate (EMS) mutants, and found that Lr22a encodes an intracellular immune receptor homologous to the Arabidopsis thaliana RPM1 protein.
谷物作物(如小麦和玉米)的基因组含有大量重复序列,使得单个基因的克隆变得具有挑战性。此外,同一作物品种的基因顺序和基因序列通常存在很大差异。谷物基因克隆的主要瓶颈是从感兴趣的品种中生成高质量的序列信息。为了加速任何作物品系的基因克隆,我们报告了“基于目标染色体的长程组装克隆”(TACCA)。TACCA 结合了染色体流式分选的无损基因组复杂度降低与芝加哥长程连锁,以组装复杂的基因组。我们应用 TACCA 在短短 4 个月内生成了小麦品系 CH Campala Lr22a 的高质量(N50 为 9.76 Mb)从头染色体组装。使用这个组装,我们使用分子标记信息和乙基甲磺酸(EMS)突变体克隆了广谱 Lr22a 叶锈病抗性基因,并发现 Lr22a 编码一种类似于拟南芥 RPM1 蛋白的细胞内免疫受体。