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Abstract: The seed coat is a composite structure that serves as a conduit for nutrient acquisition for the developing embryo. Upon seed desiccation and maturation, the seed coat provides cover [...]

Dietary intake of isoflavones has been shown to reduce the risk of several major diseases in humans. Therefore, breeding soybean [Glycine max (L.) Merrill] seeds with desirable isoflavone content would be beneficial to the food and health industries, but the environmental sensitivity of the trait complicates phenotypic selection. The objective of this study was to identify quantitative trait loci (QTL) and epistatic interactions associated with isoflavone contents in soybean seeds. A population of 207 [F.sub.4:6] recombinant inbred lines (RILs) was produced from the cross 'AC756' x 'RCAT Angora'. The population was phenotyped at two locations in Ontario, Canada, and genotyped by means of 99 polymorphic SSR markers. A significant genotype x environment interaction was found. Seventeen QTLs were detected (P < 0.01) by single-factor ANOVA. Individual loci explained up to 10.5% (P < 0.0001) of the phenotypic variation. Interval mapping and composite interval mapping identified nine genomic regions (LGs A1, C2, D1a, F, G, H, J, K, and M) associated with isoflavone contents. Some QTL associated with agronomic or seed quality traits mapped to the same regions as those for individual isoflavone contents on LGs A1, C2, F, J, K, M, and N. Twenty-three epistatic interactions were detected for isoflavones. Multiple locus models explained up to 25.0% (P < 0.0001) of the phenotypic variation without epistasis and up to 35.8% (P < 0.0001) with it. The QTL identified in this study could be useful for developing soybean varieties with desirable isoflavone content in the seed through marker-assisted selection (MAS)., SOYBEAN has been mainly cultivated for the oil and protein content of the seed. In recent years, isoflavones have received considerable attention because of their high concentration in soybean seeds [...]

The interaction between soybean and the phytopathogenic oomycete Phytophthora sojae is controlled by host resistance (Rps) genes and pathogen avirulence (Avr) genes. We have mapped the Avr1a locus in [F.sub.2] populations derived from four different P. sojae races. Four RAPD and nine AFLP markers linked to Avr1a were initially identified. Nine markers were used to compare genetic linkage maps of the Avr1a locus in two distinct [F.sub.2] populations. Distorted segregation ratios favoring homozygous genotypes were noted in both crosses. Segregation analysis of all the markers in one [F.sub.2] population of 90 progeny generated a map of 113.2 cM encompassing Avr1a, with one marker cosegregating with the gene. The cosegregating DNA marker was used to isolate P. sojae BAC clones and construct a physical map covering 170 kb, from which additional DNA markers were developed. Three markers occurring within the BAC contig were mapped in an enlarged population of 486 [F.sub.2] progeny. Avr1a was localized to a 114-kb interval, and an average physical to genetic distance ratio of 391 kb/cM was calculated for this region. This work provides a basis for the positional cloning of Avr1a.

Abstract Ash dieback is a devastating fungal disease of ash trees that has swept across Europe and recently reached the UK. This emergent pathogen has received little study in the past and its effect threatens to overwhelm the ash population. In response to this we have produced some initial genomics datasets and taken the unusual step of releasing them to the scientific community for analysis without first performing our own. In this manner we hope to ‘crowdsource’ analyses and bring the expertise of the community to bear on this problem as quickly as possible. Our data has been released through our website at oadb.tsl.ac.uk and a public GitHub repository.

Abstract Background Hydrophobic protein from soybean (HPS) is an 8 kD cysteine-rich polypeptide that causes asthma in persons allergic to soybean dust. HPS is synthesized in the pod endocarp and deposited on the seed surface during development. Past evidence suggests that the protein may mediate the adherence or dehiscence of endocarp tissues during maturation and affect the lustre, or glossiness of the seed surface. Results A comparison of soybean germplasm by genomic DNA blot hybridization shows that the copy number and structure of the Hps locus is polymorphic among soybean cultivars and related species. Changes in Hps gene copy number were also detected by comparative genomic DNA hybridization using cDNA microarrays. The Hps copy number polymorphisms co-segregated with seed lustre phenotype and HPS surface protein in a cross between dull- and shiny-seeded soybeans. In soybean cultivar Harosoy 63, a minimum of 27 ± 5 copies of the Hps gene were estimated to be present in each haploid genome. The isolation and analysis of genomic clones indicates that the core Hps locus is comprised of a tandem array of reiterated units, with each 8.6 kb unit containing a single HPS open reading frame. Conclusion This study shows that polymorphisms at the Hps locus arise from changes in the gene copy number via gene amplification. We present a model whereby Hps copy number modulates protein expression levels and seed lustre, and we suggest that gene amplification may result from selection pressures imposed on crop plants.