Cloning and Characterization of the WAX2 Gene of Arabidopsis Involved in Cuticle Membrane and Wax Production
Open Access
- 10 April 2003
- journal article
- Published by Oxford University Press (OUP) in Plant Cell
- Vol. 15 (5) , 1170-1185
- https://doi.org/10.1105/tpc.010926
Abstract
Insertional mutagenesis of Arabidopsis ecotype C24 was used to identify a novel mutant, designated wax2, that had alterations in both cuticle membrane and cuticular waxes. Arabidopsis mutants with altered cuticle membrane have not been reported previously. Compared with the wild type, the cuticle membrane of wax2 stems weighed 20.2% less, and when viewed using electron microscopy, it was 36.4% thicker, less opaque, and structurally disorganized. The total wax amount on wax2 leaves and stems was reduced by >78% and showed proportional deficiencies in the aldehydes, alkanes, secondary alcohols, and ketones, with increased acids, primary alcohols, and esters. Besides altered cuticle membranes, wax2 displayed postgenital fusion between aerial organs (especially in flower buds), reduced fertility under low humidity, increased epidermal permeability, and a reduction in stomatal index on adaxial and abaxial leaf surfaces. Thus, wax2 reveals a potential role for the cuticle as a suppressor of postgenital fusion and epidermal diffusion and as a mediator of both fertility and the development of epidermal architecture (via effects on stomatal index). The cloned WAX2 gene (verified by three independent allelic insertion mutants with identical phenotypes) codes for a predicted 632–amino acid integral membrane protein with a molecular mass of 72.3 kD and a theoretical pI of 8.78. WAX2 has six transmembrane domains, a His-rich diiron binding region at the N-terminal region, and a large soluble C-terminal domain. The N-terminal portion of WAX2 is homologous with members of the sterol desaturase family, whereas the C terminus of WAX2 is most similar to members of the short-chain dehydrogenase/reductase family. WAX2 has 32% identity to CER1, a protein required for wax production but not for cuticle membrane production. Based on these analyses, we predict that WAX2 has a metabolic function associated with both cuticle membrane and wax synthesis. These studies provide new insight into the genetics and biochemistry of plant cuticle production and elucidate new associations between the cuticle and diverse aspects of plant development.Keywords
This publication has 47 references indexed in Scilit:
- The maize CR4 receptor-like kinase mediates a growth factor-like differentiation responseGenesis, 2000
- Transgenic Arabidopsis Plants Expressing a Fungal Cutinase Show Alterations in the Structure and Properties of the Cuticle and Postgenital Organ FusionsPlant Cell, 2000
- Activation Tagging in ArabidopsisPlant Physiology, 2000
- The glossy1 Locus of Maize and an Epidermis-Specific cDNA from Kleinia odora Define a Class of Receptor-Like Proteins Required for the Normal Accumulation of Cuticular WaxesPlant Physiology, 1997
- The CER3 gene of Arabidopsis thaliana is expressed in leaves, stems, roots, flowers and apical meristemsThe Plant Journal, 1996
- Molecular characterization of the CER1 gene of arabidopsis involved in epicuticular wax biosynthesis and pollen fertility.Plant Cell, 1995
- A Novel Cytochrome b5-like Domain Is Linked to the Carboxyl Terminus of the Saccharomyces cerevisiae Δ-9 Fatty Acid DesaturasePublished by Elsevier ,1995
- Eight Histidine Residues Are Catalytically Essential in a Membrane-Associated Iron Enzyme, Stearoyl-CoA Desaturase, and Are Conserved in Alkane Hydroxylase and Xylene MonooxygenaseBiochemistry, 1994
- A cobalt-porphyrin enzyme converts a fatty aldehyde to a hydrocarbon and CO.Proceedings of the National Academy of Sciences, 1992
- Sequence Alignment of the G-Protein Coupled Receptor SuperfamilyDNA and Cell Biology, 1992