Unregulated Sphingolipid Biosynthesis in Gene-Edited Arabidopsis ORM Mutants Results in Nonviable Seeds with Strongly Reduced Oil Content. Issue 8 (11th June 2020)

• Record Type: Journal Article
• Authors: Gonzalez-Solis, Ariadna; Han, Gongshe; Gan, Lu; Li, Yunfeng; Markham, Jonathan E.; Cahoon, Rebecca E.; Dunn, Teresa M.; Cahoon, Edgar B.
• Is Part Of: The Plant Cell. Volume 32:Issue 8(2020)
• Page Start: 2474
• Page End: 2490
• Publication Date: 2020-06-11
• DOI: 10.1105/tpc.20.00015
• Languages: English
• ISSNs: 1040-4651

Abstract

Abstract : Removing the regulation of sphingolipid biosynthesis by completely knocking out Orosomucoid-like protein (ORM) genes results in ceramide hyperaccumulation and nonviable seeds with strongly reduced oil content. Abstract: Orosomucoid-like proteins (ORMs) interact with serine palmitoyltransferase (SPT) to negatively regulate sphingolipid biosynthesis, a reversible process critical for balancing the intracellular sphingolipid levels needed for growth and programmed cell death. Here, we show that ORM1 and ORM2 are essential for life cycle completion in Arabidopsis ( Arabidopsis thaliana ). Seeds from orm1 − / − orm2 − / − mutants, generated by crossing CRISPR/Cas9 knockout mutants for each gene, accumulated high levels of ceramide, indicative of unregulated sphingolipid biosynthesis. orm1 − / − orm2 − / − seeds were nonviable, displayed aberrant embryo development, and had >80% reduced oil content versus wild-type seeds. This phenotype was mimicked in Arabidopsis seeds expressing the SPT subunit LCB1 lacking its first transmembrane domain, which is critical for ORM-mediated regulation of SPT. We identified a mutant for ORM1 lacking one amino acid (Met-51) near its second transmembrane domain that retained its membrane topology. Expressing this allele in the orm2 background yielded plants that did not advance beyond the seedling stage, hyperaccumulated ceramides, and showed altered organellar structures and increased senescence- and pathogenesis-related gene expression. These seedlings also showed upregulated expression of genes for sphingolipid catabolic enzymes, pointing to additional mechanisms for maintaining sphingolipid homeostasis. ORM1 lacking Met-51 had strongly impaired interactions with LCB1 in a yeast ( Saccharomyces cerevisiae ) model, providing structural clues about regulatory interactions between ORM and SPT.