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Genomic selection to resistance to Stenocarpella maydis in maize lines using DArTseq markers
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Springer
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Abstract
Background: The identification of lines resistant to ear diseases is of great importance in maize breeding because
such diseases directly interfere with kernel quality and yield. Among these diseases, ear rot disease is widely
relevant due to significant decrease in grain yield. Ear rot may be caused by the fungus Stenocarpella maydi;
however, little information about genetic resistance to this pathogen is available in maize, mainly related to
candidate genes in genome. In order to exploit this genome information we used 23.154 Dart-seq markers in 238
lines and apply genome-wide selection to select resistance genotypes. We divide the lines into clusters to identify
groups related to resistance to Stenocarpella maydi and use Bayesian stochastic search variable approach and
rr-BLUP methods to comparate their selection results.
Results: Through a principal component analysis (PCA) and hierarchical clustering, it was observed that the three
main genetic groups (Stiff Stalk Synthetic, Non-Stiff Stalk Synthetic and Tropical) were clustered in a consistent
manner, and information on the resistance sources could be obtained according to the line of origin where
populations derived from genetic subgroup Suwan presenting higher levels of resistance. The ridge regression best
linear unbiased prediction (rr-BLUP) and Bayesian stochastic search variable (BSSV) models presented equivalent
abilities regarding predictive processes.
Conclusion: Our work showed that is possible to select maize lines presenting a high resistance to Stenocarpella
maydis. This claim is based on the acceptable level of predictive accuracy obtained by Genome-wide Selection
(GWS) using different models. Furthermore, the lines related to background Suwan present a higher level of resistance
than lines related to other groups.
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SANTOS, J. P. R. dos et al. Genomic selection to resistance to Stenocarpella maydis in maize lines using DArTseq markers. BMC Genetics, [S.l.], v. 17, 2016.
