2019
DOI: 10.1534/g3.118.200866
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Using Maize Chromosome Segment Substitution Line Populations for the Identification of Loci Associated with Multiple Disease Resistance

Abstract: Southern Leaf Blight (SLB), Northern Leaf Blight (NLB), and Gray Leaf Spot (GLS) caused by Cochliobolus heterostrophus, Setosphaeria turcica, and Cercospora zeae-maydis respectively, are among the most important diseases of corn worldwide. Previously, moderately high and significantly positive genetic correlations between resistance levels to each of these diseases were identified in a panel of 253 diverse maize inbred lines. The goal of this study was to identify loci underlying disease resistance in some of … Show more

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Cited by 49 publications
(108 citation statements)
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“…10% per NIL, compared with the expected 6.25% based on the breeding design; alleles from Ki3 were also more homozygous than expected (92% compared with the expected 78%) (Supporting Information Fig. S1; Lopez‐Zuniga et al ., ). Within each set of NILs there was little overlap between introgressed regions, and cumulatively they carried c .…”
Section: Methodsmentioning
confidence: 97%
“…10% per NIL, compared with the expected 6.25% based on the breeding design; alleles from Ki3 were also more homozygous than expected (92% compared with the expected 78%) (Supporting Information Fig. S1; Lopez‐Zuniga et al ., ). Within each set of NILs there was little overlap between introgressed regions, and cumulatively they carried c .…”
Section: Methodsmentioning
confidence: 97%
“…Additionally, DRIL78, a CSSL population, was evaluated. The parents of the population are NC344, an MDR line, and Oh7B, a multiple disease susceptible line (Lopez‐Zuniga et al., 2019; Wisser et al., 2011). The nomenclature for the population is as follows: disease resistance introgression line (DRIL) 7 (code for NC344), 8 (code for Oh7B).…”
Section: Methodsmentioning
confidence: 99%
“…Similarly, we examined the correlations between BLS, NCLB, SCLB, and GLS phenotypes in the DRIL78 population using data reported in Lopez‐Zuniga et al. (2019). Only lines with phenotypes for all the diseases were included in the analysis.…”
Section: Methodsmentioning
confidence: 99%
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