bioRxivPlant BiologyPreprint
Large seed size accompanying GmSDP1 suppression is linked to cellular remodeling and phytohormone regulation
Thiya MukherjeeiD, Sophia Crowley, Maneesh LingwaniD, Kevin Chu, Katherine M MurphyiD, Katia Gutierrez, Anastasiya Klebanovych, Russell Williams, Anuradha Dhingra, Kirk J CzymmekiD, Ben Mansfeld, Timothy P Durrett, Douglas AlleniD
Abstract
Soybean (Glycine max) seeds contain approximately 20% oil and 40% protein and are important for food, feed, and biofuel. Improving soybean productivity and seed quality requires optimizing carbon partitioning during seed development. Previously, seed-specific suppression of the lipase-encoding gene Sugar-Dependent 1 (SDP1) increased seed oil content by approximately 5% while slightly reducing raffinose family oligosaccharides without compromising protein content. Seed-specific SDP1 suppression also increased seed size by 18-25% without affecting seed number, resulting in greater seed biomass per plant. To determine the developmental basis of the increased seed size, we investigated the cellular and molecular mechanisms underlying this phenotype. Microscopy and biochemical analyses showed that larger seeds were associated with increased seed cell size and enhanced lignocellulosic cell wall accumulation. Temporal biochemical and transcriptomic analyses further revealed coordinated changes in hormone homeostasis, including altered levels of abscisic acid, 12-oxo-phytodienoic acid, and jasmonoyl-isoleucine, together with differential expression of F-box and RING/U-box family genes. The results indicate that the enhanced seed size resulting from SDP1 suppression is associated with coordinated changes in cellular development, cell wall accumulation, hormone homeostasis, and regulation of gene expression during seed development. Developmental and metabolic changes associated with the increased seed size phenotype support SDP1 manipulation as a potential strategy for improving soybean seed yield and quality.
- organism: plant (other)
- assay: proteomics
- assay: metabolomics
- assay: bulk RNA-seq
- research focus: cell type annotation
- research focus: differential expression
- research focus: development & morphogenesis
- approach: experimental assay
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