Rapid cloning of genes in hexaploid wheat using cultivar-specific long-range chromosome assembly

Rapid cloning of genes from any crop plant species (or cultivar) whose chromosomes can be flow sorted is enabled by a combination of short-read sequencing and proximity ligation. Cereal crops such as wheat and maize have large repeat-rich genomes that make cloning of individual genes challenging. Mo...

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Veröffentlicht in:Nature biotechnology 2017-08, Vol.35 (8), p.793-796
Hauptverfasser: Thind, Anupriya Kaur, Wicker, Thomas, Šimková, Hana, Fossati, Dario, Moullet, Odile, Brabant, Cécile, Vrána, Jan, Doležel, Jaroslav, Krattinger, Simon G
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Sprache:eng
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Zusammenfassung:Rapid cloning of genes from any crop plant species (or cultivar) whose chromosomes can be flow sorted is enabled by a combination of short-read sequencing and proximity ligation. 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 1 , 2 , 3 , 4 . 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 5 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.
ISSN:1087-0156
1546-1696
DOI:10.1038/nbt.3877