Two Membrane-Anchored Aspartic Proteases Contribute to Pollen and Ovule Development

• Published in: Plant physiology (Bethesda) 2017-01, Vol.173 (1), p.219-239
• Main Authors: Gao, Hui, Zhang, Yinghui, Wang, Wanlei, Zhao, Keke, Liu, Chunmei, Bai, Lin, Li, Rui, Guo, Yi
• Format: Article
• Language: English
• Subjects: Apoptosis; Arabidopsis - enzymology; Arabidopsis - growth & development; Arabidopsis Proteins - metabolism; Aspartic Acid Proteases - metabolism; Cell Membrane - enzymology; Chromosome Segregation; Crosses, Genetic; FOCUS ON FLOWERING AND REPRODUCTION; Genetic Complementation Test; Germination; Glucans - metabolism; Green Fluorescent Proteins - metabolism; Mutation - genetics; Ovule - enzymology; Ovule - growth & development; Pectins - metabolism; Phenotype; Pollen - cytology; Pollen - enzymology; Pollen - growth & development; Pollen - ultrastructure; Pollen Tube - growth & development; Pollination; Proteolysis; Seeds - metabolism; Subcellular Fractions - enzymology; Xylans - metabolism
• ISSN: 0032-0889; 1532-2548
• DOI: 10.1104/pp.16.01719

Aspartic proteases are a class of proteolytic enzymes with conserved aspartate residues, which are implicated in protein processing, maturation, and degradation. Compared with yeast and animals, plants possess a larger aspartic protease family. However, little is known about most of these enzymes. Here, we characterized two Arabidopsis (Arabidopsis thaliana) putative glycosylphosphatidylinositol (GPI)-anchored aspartic protease genes, A36 and A39, which are highly expressed in pollen and pollen tubes. a36 and a36 a39 mutants display significantly reduced pollen activity. Transmission electron microscopy and terminal-deoxynucleotidyl transferase-mediated nick end labeling assays further revealed that the unviable pollen in a36 a39 may undergo unanticipated apoptosis-like programmed cell death. The degeneration of female gametes also occurred in a36 a39. Aniline Blue staining, scanning electron microscopy, and semi in vitro guidance assays indicated that the micropylar guidance of pollen tubes is significantly compromised in a36 a39. A36 and A39 that were fused with green fluorescent protein are localized to the plasmamembrane and display punctate cytosolic localization and colocalize with the GPI-anchored protein COBRA-LIKE10. Furthermore, in a36 a39, the abundance of highly methylesterified homogalacturonans and xyloglucans was increased significantly in the apical pollen tube wall. These results indicate that A36 and A39, two putative GPI-anchored aspartic proteases, play important roles in plant reproduction in Arabidopsis.