Updated January 24, 2021:
March 15, 2020 Report
This project has the following four objectives. A brief summary of the project status for the current quarter is given under each objective. The objectives form a coordinated, comprehensive program with both basic and applied research objectives to address these challenges and achieve our goals.
1) Use PI accessions from the USDA Soybean Germplasm Collection that have never before been used in US soybean breeding programs for yield improvement to develop and release soybean lines with significantly increased genetic diversity, greater productivity, higher seed protein concentration, and improved nutrition bundle compared with current high-yield cultivars. This activity is tightly linked with our industry partners for wide-area cooperative evaluation throughout the major soybean production region in the US in Maturity Groups 0, I, II, III, IV, and V.
We conducted the 2019 Diversity Cooperative Tests with USDA, university and industry partners evaluating MG 0, I, II, III, IV and V soybean lines with improved yield and seed protein. The 2019 Diversity Coop Tests have more than 340 entries in 12 tests being grown in 20 locations in 7 states. The 2019 Diversity Coop Test report and summary was shared with cooperators in January 2020 and results were presented at the Soybean Breeders Workshop and USB Composition Workshop in St. Louis in March.
We expect results from the soluble carbohydrate and amino acid composition tests at the end of March. Those results will be added to the summary report and redistributed to all cooperators so they can use the information for selection of parent lines for 2020 crossing.
2) Identify and characterize candidate genes for the large-effect QTLs on Chr 15 and Chr 20, including the development and evaluation of transgenic lines to evaluate effects of gene candidates in different genetic backgrounds in greenhouse and field environments. This objective also includes the analysis of the genetically diverse germplasm developed by all cooperators for allele status at the Chr 15 and Chr 20 QTLs.
- The most likely gene candidate for the QTL is Glyma.20G085100 based on consistency of the allelic state in populations that the QTL was mapped.
- A hair-pin element was transformed into soybean to knock down the expression the candidate gene.
- Preliminary results show slightly higher protein and lower oil concentration for two T2 plants, no difference for two others.
- The plants and lines of these and additional transformation events will be grown in the field in 2020 in Nebraska for evaluation of seed composition and other traits.
3) Characterize protein composition, amino acid profiles, and soluble carbohydrate composition of seeds from our developed high-protein, high-yield lines from diverse G. max accessions and of selected experimental extreme high-protein lines from long-term selection programs.
Awaiting analysis results for amino acids and soluble carbohydrate composition for the high-yield experimental lines and the unltra-high protein lines. We expect results for both at the end of March.
4) Increase genetic diversity, seed composition, and seed quality in the early-planting soybean production system (ESPS) in southern US production areas.
The improved lines DS31-243 and DS1260-260 that we reported on in the last quarter, have improved seed quality scores that result in lower dockage for producers at the elevator. Both lines also produce a soybean meal with 48% or more protein and virtually zero dollar loss (discount) due to seed damage, compared to a high of more than $3,000 per 100 acres loss for one of the commercial checks.
Updated January 24, 2021:
September 15, 2020 Report
This project has four main objectives that form a coordinated, comprehensive program with both basic and applied research objectives to address these challenges and achieve our goals. For the previous three quarterly reports, we have itemized accomplishments as deliverables and KPIs by objective. For this fourth quarter report, we provide a general summary of the current status of the field plots including the Diversity Cooperative Test with our industry partners, and general status. There is not too much to specifically report regarding new results until after harvest and analysis of the 2020 data. We will plan to provide some of those preliminary results for the December 2020 quarterly report.
Programs initiated more than 200 new populations for genetically diverse, high-yielding lines with improved balance of seed protein and oil.
Diversity Coop Tests are going well, with the exception of some Dicamba damage at some locations, and loss of plots due to that damage plus severe hail or other environmental conditions. But overall, the mult-location cooperative tests with university, USDA, and industry programs is doing well and we look forward to good data after harvest for our yield, agronomic, and compositional quality analyses.
Initiated transformation for mutation of genes that underlie the QTL regions on Chr 10 and Chr 20. Field plots planted with the soybean events that carry the RNAi element targeting down-regulation of the gene call that underlies the protein QTL on chromosome 20 are maturing. Harvest is expected by the second week of October. Data will be ascertained on various agronomics, 100 seed weight, plot weight along with total protein and oil, and amino acid profile.
Research focused on fine mapping a gene on chromosome 15 that is important for increasing seed protein concentration progressed during the past quarter. For this work, we used results from previous field testing of 415 experimental lines from nine populations. Each population was derived from a plant that had a cross over event in a different position across the 450,000 base pair (450 kb) interval the protein gene was previously mapped. Attempts to use this field data previously to fine map the gene failed because we had poor quality marker data. To fix this problem, DNA was re-isolated from the lines and marker tests were completed using the new DNA. The new marker data were excellent and was used to position the protein gene relative to the cross over event in each population. These tests allowed us to position the gene to a 72.7 kb interval with a high degree of certainty and likely to a 50.9 kb interval. Within the 72.7 kb interval, there are 11 gene models in the soybean genome assembly 2. Among these genes, three have putative functions suggesting that they could be the protein gene. One of the three is listed as a late embryogenesis abundant protein and two as nodulin MtN21/EamA-like transporter family proteins. Further research is needed to identify which of these genes is the primary gene candidate for this important protein gene.
A draft of our research publication entitled “Biochemical characterization of UP2Y lines generated from a long-term breeding program using exotic soybean germplasm reveal that it is possible to increase the concentration of protein without lowering the quality” is currently being reviewed by coauthors.
We have conducted transcriptome analysis of two high protein lines (UP2PC7(S3)-0115 and UP2PC7(S3)-0230), two founder lines (PI404177 and MD83-2048) along with a standard soybean cultivar (Maverick). The RNAseq data will be analyzed during the next quarter.
Evaluation of seed quality for several 2020 Diversity Coop Test entries in MG 2 and 3 will begin at the MS location in the next week or two after exposure of mature soybean plants to hot humid conditions in Mississippi.