Search

Drought is a major constraint on maize (Zea mays L.) production and productivity in Sub-Saharan Africa (SSA). The increase in frequency and severity of drought, driven by climate change, is expected to worsen in the future. These occurrences are likely to adversely affect maize production and productivity, threatening the economic and social stability of millions of smallholder farmers. Understanding the genetics of hybrid performance under drought stress is crucial for designing breeding strategies to develop high-yielding hybrids. This study aimed to (i) evaluate the performance of three-way cross hybrids developed from elite inbred lines, including several drought-tolerant lines, using a line-by-tester mating design, and (ii) estimate the general combining ability (GCA) and specific combining ability (SCA) effects of the tropical maize inbred lines under managed drought and optimum conditions. A total of 265 maize inbred lines from the CIMMYT global maize breeding program were used as parents and crossed to six single cross testers to generate 795 testcross hybrids. These hybrids, along with six commercial hybrids as a check, were evaluated under managed drought and optimum conditions. Significant (p < 0.001) variations were observed among genotypes and genotypes-by-environment interactions (GEIs) for grain yield and other traits. There was a preponderance of GCA variance (lines and tester) over SCA variance, indicating that additive effects were more important in determining grain yield and other key traits under both managed drought and optimum conditions. Ten inbred lines (S2_8, S10_1, S6_4, S10_14, S2_14, S10_15, S8_7, S2_3, S8_15, and S13_5) with desirable GCA effects for grain yield and other traits were identified. Fourteen testcross hybrids were identified with high grain yield and desirable agronomic traits under both drought and optimum conditions. The identified lines and hybrids are useful sources to be used in breeding and deploying as stress-tolerant hybrids. High correlations observed between observed and GCA-predicted hybrid performance suggest the possibility to evaluate more hybrids with fixed resources. The study demonstrates that it is feasible to obtain high-yielding and drought-tolerant lines and hybrids. These testcross hybrids should undergo rigorous on-farm trials to ensure consistent performance before commercialization and release. Deploying these hybrids could help in mitigating the effects of drought stress in SSA and contribute to improved maize productivity in the region. [ABSTRACT FROM AUTHOR]

Background: Rp1 is a complex locus of maize, which carries a set of genes controlling race-specific resistance to the common rust fungus, Puccinia sorghi. The resistance response includes the "Hypersensitive response" (HR), a rapid response triggered by a pathogen recognition event that includes localized cell death at the point of pathogen penetration and the induction of pathogenesis associated genes. The Rp1-D21gene is an autoactive allelic variant at the Rp1 locus, causing spontaneous activation of the HR response, in the absence of pathogenesis. Previously we have shown that the severity of the phenotype conferred by Rp1-D21 is highly dependent on genetic background. Results: In this study we show that the phenotype conferred by Rp1-D21 is highly dependent on temperature, with lower temperatures favoring the expression of the HR lesion phenotype. This temperature effect was observed in all the 14 genetic backgrounds tested. Significant interactions between the temperature effects and genetic background were observed. When plants were grown at temperatures above 30°C, the spontaneous HR phenotype conferred by Rp1-D21 was entirely suppressed. Furthermore, this phenotype could be restored or suppressed by alternately reducing and increasing the temperature appropriately. Light was also required for the expression of this phenotype. By examining the expression of genes associated with the defense response we showed that, at temperatures above 30°C, the Rp1-D21 phenotype was suppressed at both the phenotypic and molecular level. Conclusions: We have shown that the lesion phenotype conferred by maize autoactive resistance gene Rp1-D21 is temperature sensitive in a reversible manner, that the temperature-sensitivity phenotype interacts with genetic background and that the phenotype is light sensitive. This is the first detailed demonstration of this phenomenon in monocots and also the first demonstration of the interaction of this effect with genetic background. The use of temperature shifts to induce a massive and synchronous HR in plants carrying the Rp1-D21 genes will be valuable in identifying components of the defense response pathway. [ABSTRACT FROM AUTHOR]

In vivo haploid induction (HI) triggered by pollination with special intraspecific genotypes, called inducers, is unique to Zea mays L. within the plant kingdom and has revolutionized maize breeding during the last decade. However, the molecular mechanisms underlying HI in maize are still unclear. To investigate the genetic basis of HI, we developed a new approach for genome-wide association studies (GWAS), termed conditional haplotype extension (CHE) test that allows detection of selective sweeps even under almost perfect confounding of population structure and trait expression. Here, we applied this test to identify genomic regions required for HI expression and dissected the combined support interval (50.34 Mb) of the QTL qhir1, detected in a previous study, into two closely linked genomic segments relevant for HI expression. The first, termed qhir11 (0.54 Mb), comprises an already fine-mapped region but was not diagnostic for differentiating inducers and noninducers. The second segment, termed qhir12 (3.97 Mb), had a haplotype allele common to all 53 inducer lines but not found in any of the 1482 noninducers. By comparing resequencing data of one inducer with 14 noninducers, we detected in the qhir12 region three candidate genes involved in DNA or amino acid binding, however, none for qhir11. We propose that the CHE test can be utilized in introgression breeding and different fields of genetics to detect selective sweeps in heterogeneous genetic backgrounds. [ABSTRACT FROM AUTHOR]

In order to leverage novel sequencing techniques for cloning genes in eukaryotic organisms with complex genomes, the false positive rate of variant discovery must be controlled for by experimental design and informatics. We sequenced five lines from three pedigrees of ethyl methanesulfonate (EMS)-mutagenized Sorghum bicolor , including a pedigree segregating a recessive dwarf mutant. Comparing the sequences of the lines, we were able to identify and eliminate error-prone positions. One genomic region contained EMS mutant alleles in dwarfs that were homozygous reference sequences in wild-type siblings and heterozygous in segregating families. This region contained a single nonsynonymous change that cosegregated with dwarfism in a validation population and caused a premature stop codon in the Sorghum ortholog encoding the gibberellic acid (GA) biosynthetic enzyme ent -kaurene oxidase. Application of exogenous GA rescued the mutant phenotype. Our method for mapping did not require outcrossing and introduced no segregation variance. This enables work when line crossing is complicated by life history, permitting gene discovery outside of genetic models. This inverts the historical approach of first using recombination to define a locus and then sequencing genes. Our formally identical approach first sequences all the genes and then seeks cosegregation with the trait. Mutagenized lines lacking obvious phenotypic alterations are available for an extension of this approach: mapping with a known marker set in a line that is phenotypically identical to starting material for EMS mutant generation., (Copyright © 2017 Addo-Quaye et al.)