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 |
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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
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,
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
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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. |
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ISSN: | 1087-0156 1546-1696 |
DOI: | 10.1038/nbt.3877 |