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Therefore, bulk segregation analysis (Michelmore et al. 1991) was performed on the outcrossed populations to determine associations between the seed composition phenotype and a chromosomal region.
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The seed composition (percentage of proteins and fatty acids) and the oil composition (percentage in oleic, linolenic, linoleic and erucic acids) was determined by NIRS method.
DeRocher and Nguyen [ 76] overexpressed Arabidopsis HD-Zip III gene REVOLUTA in soybean embryo, leading to seed yield increase with no change in the seed composition.
The altered seed composition of lec2 mutant plants closely resembles that of Pv, suggesting down regulation of LEC2 may affect seed composition.
There was no consistent pattern of inheritance at a population level between the E2 and E3 for seed composition traits.
We further interrogated the genetic architecture of seed composition using GWA scans.
Consequently, the genetic basis for soybean seed composition has been intensely studied using family-based mapping.
In the following study, we aim to explore the utility of GWA scans in soybean, to refine QTL for assorted seed composition traits, and to assess the relationship between population structure and genetic architecture with regard to these traits.
No phenotypic perturbation was observed as a result of modification of the seed oil composition.
The seed sequence composition was also reflected in the prediction rate, with the 8mer seed region providing the greatest predictive power for observed changes for each miRNA.
Final seed composition is influenced by both the genotype and environmental factors [ 2– 5].
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