The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
Joint linkage–linkage disequilibrium mapping is a powerful approach to detecting quantitative trait loci underlying drought tolerance in maize
Open accessAbstract
This paper describes two joint linkage–linkage disequilibrium (LD) mapping approaches: parallel mapping (independent linkage and LD analysis) and integrated mapping (datasets analyzed in combination). These approaches were achieved using 2,052 single nucleotide polymorphism (SNP) markers, including 659 SNPs developed from drought-response candidate genes, screened across three recombinant inbred line (RIL) populations and 305 diverse inbred lines, with anthesis-silking interval (ASI), an important trait for maize drought tolerance, as the target trait. Mapping efficiency was improved significantly due to increased population size and allele diversity and balanced allele frequencies. Integrated mapping identified 18 additional quantitative trait loci (QTL) not detected by parallel mapping. The use of haplotypes improved mapping efficiency, with the sum of phenotypic variation explained (PVE) increasing from 5.4% to 23.3% for single SNP-based analysis. Integrated mapping with haplotype further improved the mapping efficiency, and the most significant QTL had a PVE of up to 34.7%. Normal allele frequencies for 113 of 277 (40.8%) SNPs with minor allele frequency (<5%) in 305 lines were recovered in three RIL populations, three of which were significantly associated with ASI. The candidate genes identified by two significant haplotype loci included one for a SET domain protein involved in the control of flowering time and the other encoding aldo/keto reductase associated with detoxification pathways that contribute to cellular damage due to environmental stress. Joint linkage–LD mapping is a powerful approach for detecting QTL underlying complex traits, including drought tolerance.
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Cites
Genomic Control for Association Studies
Devlin, B., & Roeder, K. (1999) · Biometrics · doi:10.1111/j.0006-341x.1999.00997.x · Cited by 3,162 · cited 1×
“Excluding these effects from the LD analysis (6, 7) can be commonly achieved using the STRUCTURE program (8, 9), principal component analysis (10), or random molecular markers to estimate pairwise relatedness among all individuals via a mixed linear model (5).”
MethodPersonal genomes: The case of the missing heritability
Maher, B. (2008) · Nature · doi:10.1038/456018a · Cited by 1,737
QTL analysis in plants; where are we now?
Kearsey, M. J., & Farquhar, A. G. L. (1998) · Heredity · doi:10.1046/j.1365-2540.1998.00500.x · Cited by 492
Welcker, C., Boussuge, B., Bencivenni, C., Ribaut, J.-M., & Tardieu, F. (2006) · Journal of Experimental Botany · doi:10.1093/jxb/erl227 · Cited by 174 · cited 2×
“We compared our mapping results with those from previous reports using the same RIL populations but tested in multiple seasons (33, 34).”
BackgroundResultSelf-citation
Cited by
Genetic variation in ZmVPP1 contributes to drought tolerance in maize seedlings
Wang, X., Wang, H., Liu, S., Ferjani, A., Li, J., Yan, J., Yang, X., & Qin, F. (2016) · Nature Genetics · doi:10.1038/ng.3636 · Cited by 614
Phenotyping for drought tolerance of crops in the genomics era
Tuberosa, R. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00347 · Cited by 558
A transposable element in a NAC gene is associated with drought tolerance in maize seedlings
Mao, H., Wang, H., Liu, S., Li, Z., Yang, X., Yan, J., Li, J., Tran, L.-S. P., & Qin, F. (2015) · Nature Communications · doi:10.1038/ncomms9326 · Cited by 542
Integrated genomics, physiology and breeding approaches for improving drought tolerance in crops
Mir, R. R., Zaman-Allah, M., Sreenivasulu, N., Trethowan, R., & Varshney, R. K. (2012) · Theoretical and Applied Genetics · doi:10.1007/s00122-012-1904-9 · Cited by 477
Metadata
- Authors
- Lu, Y., Zhang, S., Shah, T., Xie, C., Hao, Z., Li, X., Farkhari, M., Ribaut, J.-M., Cao, M., Rong, T., & Xu, Y.
- Venue
- Proceedings of the National Academy of Sciences
- Published
- 2010-10-25
- Volume
- 107
- Issue
- 45
- Pages
- 19585-19590
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- OpenAlex
- W2005734688
- Cited by
- 228
- References
- 4
- FWCI
- 7.54
- Type
- journal article
- Language
- en
- Open access
- green
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- Lu, Y., Zhang, S., Shah, T., Xie, C., Hao, Z., Li, X., Farkhari, M., Ribaut, J.-M., Cao, M., Rong, T., & Xu, Y. (2010). Joint linkage–linkage disequilibrium mapping is a powerful approach to detecting quantitative trait loci underlying drought tolerance in maize. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.1006105107
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