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Resequencing of 145 Landmark Cultivars Reveals Asymmetric Sub-genome Selection and Strong Founder Genotype Effects on Wheat Breeding in China
Open accessAbstract
Controlled pedigrees and multi-decade timescale of national crop plant breeding programs offer a unique experimental context for examining how selection affects plant genomes. More than 3,000 wheat cultivars have been registered, released and documented since 1949 in China. Here, a set of 145 elite cultivars from the historical series of wheat breeding in China were re-sequenced. A total of 43.75 Tb of sequence data was generated with an average read depth of 17.94× for each cultivar, and more than 60.92 million SNPs and 2.54 million InDels were captured, based on the Chinese Spring RefSeq v1.0. Seventy years of breeder driven selection led to dramatic changes in grain yield and related phenotypes, with distinct genomic regions and phenotypes targeted by different breeders across the decades. There are very clear instances of how the introduced Italian and other foreign germplasm was integrated into Chinese wheat programs and reshaped the genome landscape of local modern cultivars. Importantly, the resequencing data also highlighted significant asymmetric breeding selection amongst the three sub-genomes: this was evident in both the collinear blocks for homeologous chromosomes and among sets of three homeologous genes. Accumulation of more newly assembled genes in newer cultivars implied potential values of these genes in breeding. Conserved and extended sharing of LD-blocks were highlighted among pedigree-related cultivars, in which fewer haplotypes differences were detected. Fixation or replacement of haplotypes from founder genotypes after generations of breeding was related to their breeding value. Based on the haplotype frequency changes in LD-blocks of pedigree-related cultivars, we propose a strategy for evaluating the breeding value of any given line on the basis of the accumulation (pyramiding) of beneficial haplotypes. This research also demonstrates the impact of "founder genotypes" on the output of breeding efforts over multiple decades, and suggests "founder genotype" perspectives are in fact more dynamic when applied in the context of modern genomics-informed breeding.
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Cites
The Sequence Alignment/Map format and SAMtools
Li, H., Handsaker, B., Wysoker, A., Fennell, T., Ruan, J., Homer, N., Marth, G., Abecasis, G., Durbin, R., & 1000 Genome Project Data Processing Subgroup (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp352 · Cited by 62,041
Fast and accurate short read alignment with Burrows-Wheeler transform
Li, H., & Durbin, R. (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp324 · Cited by 58,607
PLINK: a tool set for whole-genome association and population-based linkage analyses.
Purcell, S., Neale, B., Todd-Brown, K., Thomas, L., Ferreira, M. A. R., Bender, D., Maller, J., Sklar, P., de Bakker, P. I. W., Daly, M. J., et al. (2007) · The American Journal of Human Genetics · doi:10.1086/519795 · Cited by 34,089
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
McKenna, A., Hanna, M., Banks, E., Sivachenko, A., Cibulskis, K., Kernytsky, A., Garimella, K., Altshuler, D., Gabriel, S., Daly, M., et al. (2010) · Genome Research · doi:10.1101/gr.107524.110 · Cited by 27,895
The variant call format and VCFtools
Danecek, P., Auton, A., Abecasis, G., Albers, C. A., Banks, E., DePristo, M. A., Handsaker, R. E., Lunter, G., Marth, G. T., Sherry, S. T., et al. (2011) · Bioinformatics · doi:10.1093/bioinformatics/btr330 · Cited by 16,200
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
Wang, K., Li, M., & Hakonarson, H. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq603 · Cited by 14,621
Fast model-based estimation of ancestry in unrelated individuals
Alexander, D. H., Novembre, J., & Lange, K. (2009) · Genome Research · doi:10.1101/gr.094052.109 · Cited by 9,898
GCTA: a tool for genome-wide complex trait analysis
Yang, J., Lee, S. H., Goddard, M. E., & Visscher, P. M. (2011) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2010.11.011 · Cited by 8,279
circlize implements and enhances circular visualization in R
Gu, Z., Gu, L., Eils, R., Schlesner, M., & Brors, B. (2014) · Bioinformatics · doi:10.1093/bioinformatics/btu393 · Cited by 4,246
Mao, X., Cai, T., Olyarchuk, J. G., & Wei, L. (2005) · Bioinformatics · doi:10.1093/bioinformatics/bti430 · Cited by 3,828
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Snowdon, R. J., Wittkop, B., Chen, T.-W., & Stahl, A. (2021) · Theoretical and Applied Genetics · doi:10.1007/s00122-020-03729-3 · Cited by 172
Metadata
- Authors
- Hao, C., Jiao, C., Hou, J., Li, T., Liu, H., Wang, Y., Zheng, J., Liu, H., Bi, Z., Xu, F., Zhao, J., Ma, L., Wang, Y., Majeed, U., Liu, X., Appels, R., Maccaferri, M., Tuberosa, R., Lu, H., & Zhang, X.
- Venue
- Molecular Plant
- Publisher
- Elsevier BV
- Published
- 2020-12
- Volume
- 13
- Issue
- 12
- Pages
- 1733-1751
- ISSN
- 1674-2052 (ISSN-L)
- OpenAlex
- W3083462409
- Cited by
- 267
- References
- 73
- FWCI
- 21.10
- Type
- journal article
- Language
- en
- Open access
- bronze
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- Hao, C., Jiao, C., Hou, J., Li, T., Liu, H., Wang, Y., Zheng, J., Liu, H., Bi, Z., Xu, F., Zhao, J., Ma, L., Wang, Y., Majeed, U., Liu, X., Appels, R., Maccaferri, M., Tuberosa, R., Lu, H., & Zhang, X. (2020). Resequencing of 145 Landmark Cultivars Reveals Asymmetric Sub-genome Selection and Strong Founder Genotype Effects on Wheat Breeding in China. Molecular Plant. https://doi.org/10.1016/j.molp.2020.09.001
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