Skip to main content
Log in

Effects of Yariv phenylglycoside on cell wall assembly in the lily pollen tube

  • Article
  • Published:
Planta Aims and scope Submit manuscript

Abstract.

Arabinogalactan-proteins (AGPs) are proteoglycans with a high level of galactose and arabinose. Their current functions in plant development remain speculative. In this study, (β-D-glucosyl)3 Yariv phenylglycoside [(β-D-Glc)3] was used to perturb AGPs at the plasmalemma-cell wall interface in order to understand their functional significance in cell wall assembly during pollen tube growth. Lily (Lilium longiflorum Thunb.) pollen tubes, in which AGPs are deposited at the tip, were used as a model. Yariv phenylglycoside destabilizes the normal intercalation of new cell wall subunits, while exocytosis of the secretory vesicles still occurs. The accumulated components at the tip are segregated between fibrillar areas of homogalacturonans and translucent domains containing callose and AGPs. We propose that the formation of AGP/(β-D-Glc)3 complexes is responsible for the lack of proper cell wall assembly. Pectin accumulation and callose synthesis at the tip may also change the molecular architecture of the cell wall and explain the lack of proper cell wall assembly. The data confirm the importance of AGPs in pollen tube growth and emphasize their role in the deposition of cell wall subunits within the previously synthesized cell wall.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Author information

Authors and Affiliations

Authors

Additional information

Received: 14 August 1997 / Accepted: 9 September 1997

Rights and permissions

Reprints and permissions

About this article

Cite this article

Roy, S., Jauh, G., Hepler, P. et al. Effects of Yariv phenylglycoside on cell wall assembly in the lily pollen tube. Planta 204, 450–458 (1998). https://doi.org/10.1007/s004250050279

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/s004250050279

Navigation