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Guerault, A.

Publications and source records attributed to Guerault, A..

2 recordsLinked to original sources

GPAT2 plays a role in the root cap cuticle formation of Arabidopsis that is not redundant to GPAT4 and GPAT8

During the first days after germination, the root cap protects the seeding with its cuticle, which persists until the embryonic outer root cap cell layer is shed. The polyester constituting the delicate Arabidopsis root cap cuticle of the primary root has an atypical composition, containing unsubstituted very-long-chain fatty acids in addition to the oxygenated fatty acids typically found in cutin. The sn2-glycerol-3-phosphate acyltransferases GPAT4 and GPAT8, which possess an active phosphatase domain, synthesize monoacylglycerols and are crucial for incorporating oxygenated fatty acids into the root cap cutin. Here, we show that the incorporation of very-long-chain fatty acids into cutin requires the glycerol-3-phosphate acyltransferase GPAT2, which lacks an active phosphatase domain and produces lysophosphatidic acids. The GPAT2 knockout alters the properties of the root cap leading to increased mucilage deposition but lower barrier properties. Furthermore, we demonstrate that the long-chain CoA synthetase LACS2 is required solely for the incorporation of oxygenated fatty acids into cutin, similar to GPAT4 and GPAT8. Consequently, two largely non-redundant pathways contribute to root cap cuticle formation in the primary root: both the LACS2/GPAT4/GPAT8- and the GPAT2-dependent pathways contribute non-redundantly to its barrier and surface properties. LACS2 also plays an important role in the formation of the root cap cuticle in emerging lateral roots, whereas GPAT2 has a minor function in this process. These findings underscore the diverse mechanisms by which cuticle synthesis is fine-tuned across plant organs and developmental stages to achieve specialized barrier and surface properties.

plant biology↗

Spatiotemporal variation in cutin polymerization and remodeling mediated by GDSL-hydrolase enzymes during tomato fruit development

Land plants produce a cuticle, an extracellular hydrophobic layer that covers aerial organs and is involved in many critical protective roles, most notably in preventing desiccation. The predominant component of the cuticle is the lipidic polyester, cutin, which is deposited in the epidermal primary cell wall. Most of cutin of tomato fruit, a model for cuticle research, is polymerized by the extracellular GDSL-hydrolase enzyme CUTIN SYNTHASE-LIKE 1 (CUS1). However, other enzymes involved in cutin assembly remain to be identified and characterized. In this current study, we investigated whether other GDSL-hydrolases that are highly expressed in fruit epidermis might also contribute to cutin polymerization and restructuring. Candidates include homologs of Arabidopsis thaliana CUTICLE DESTRUCTIVE FACTOR 1 (CDEF1), which has been reported to catalyze cutin hydrolysis, as well as other phylogenetically diverse and distantly related GDSL-hydrolases. We determined that members of the CUS and CDEF families can catalyze the transesterification of cutin precursors in vitro, and can modify tomato fruit cutin structure in semi-in vivo assays. Tomato mutant knockout lines of CUS and CDEF genes generated by CRISPR/Cas9 and cross mutations with cus1 (previously cd1) were found to exhibit different fruit and flower phenotypes related to cutin assembly, including an effect on cutin monomer esterification, composition and content, cutin nanoridge formation in flowers, fruit cuticle permeability and permeance. Characterization of the mutant phenotypes, in combination with the enzyme analysis and bioassays, revealed distinct differences in the contribution of CUS and CDEF enzymes to cutin biosynthesis and remodeling. Our analysis also revealed unexpected spatiotemporal variation in cutin polymerization and structure coordinated by distinct GDSL-hydrolase enzymes over the fruit surface, which further suggests great complexity in cutin deposition and cuticle functions during organ development. HighlightsO_LICutin polymerization in tomato is catalyzed by coordinating the spatiotemporal expression of CUTIN SYNTHASE enzymes in different organs, including during fruit development. C_LIO_LIExtracellular cutin polymerization is not a function limited to the canonical CUTIN SYNTHASE family members but can be also be catalyzed by other GDSL-hydrolase enzymes, as suggested by evidence in vitro. C_LIO_LITomato CDEF enzymes, a clade within the GDSL-hydrolase superfamily, are involved in remodeling cutin structure during fruit development. C_LIO_LIThe biosynthesis and remodeling of cutin over the tomato fruit surface is spatially heterogeneous. C_LI

plant biology↗