Arabidopsis Reversibly Glycosylated Polypeptides 1 and 2 Are Essential for Pollen Development

• Published in: Plant physiology (Bethesda) 2006-12, Vol.142 (4), p.1480-1492
• Main Authors: Drakakaki, Georgia, Zabotina, Olga, Delgado, Ivan, Robert, Stéphanie, Keegstra, Kenneth, Raikhel, Natasha
• Format: Article
• Language: English
• Subjects: Agronomy. Soil science and plant productions; Anthers; Arabidopsis - growth & development; Arabidopsis - metabolism; Arabidopsis Proteins - chemistry; Arabidopsis Proteins - genetics; Arabidopsis Proteins - physiology; Arabidopsis thaliana; Biological and medical sciences; Biosynthesis; Cell Biology and Signal Transduction; Cell walls; Crosses, Genetic; Cytoplasm - metabolism; Developmental biology; Economic plant physiology; Flowering, floral biology, reproduction patterns; Fundamental and applied biological sciences. Psychology; Gametophytes; Glucosyltransferases - chemistry; Glucosyltransferases - genetics; Glucosyltransferases - physiology; Glycoproteins - chemistry; Glycoproteins - genetics; Glycoproteins - physiology; Golgi Apparatus - metabolism; Growth and development; Microspores; Mitosis - genetics; Mitosis - physiology; Multigene Family; Phylogeny; Plant cells; Plants; Pollen; Pollen - anatomy & histology; Pollen - growth & development; Pollen - metabolism; Pollen tubes; Recombinant Fusion Proteins - analysis
• ISSN: 0032-0889; 1532-2548; 1532-2548
• DOI: 10.1104/pp.106.086363

Reversibly glycosylated polypeptides (RGPs) have been implicated in polysaccharide biosynthesis. To date, to our knowledge, no direct evidence exists for the involvement of RGPs in a particular biochemical process. The Arabidopsis (Arabidopsis thaliana) genome contains five RGP genes out of which RGP1 and RGP2 share the highest sequence identity. We characterized the native expression pattern of Arabidopsis RGP1 and RGP2 and used reverse genetics to investigate their respective functions. Although both genes are ubiquitously expressed, the highest levels are observed in actively growing tissues and in mature pollen, in particular. RGPs showed cytoplasmic and transient association with Golgi. In addition, both proteins colocalized in the same compartments and coimmunoprecipitated from plant cell extracts. Single-gene disruptions did not show any obvious morphological defects under greenhouse conditions, whereas the double-insertion mutant could not be recovered. We present evidence that the double mutant is lethal and demonstrate the critical role of RGPs, particularly in pollen development. Detailed analysis demonstrated that mutant pollen development is associated with abnormally enlarged vacuoles and a poorly defined inner cell wall layer, which consequently results in disintegration of the pollen structure during pollen mitosis I. Taken together, our results indicate that RGP1 and RGP2 are required during microspore development and pollen mitosis, either affecting cell division and/or vacuolar integrity.