Abstract

For fertilization to occur in plants, the pollen tube must be guided to enter the ovule via the micropyle. Previous reports have implicated actin filaments, actin binding proteins, and the tip-focused calcium gradient as key contributors to polar growth of pollen tubes; however, the regulation of directional pollen tube growth is largely unknown. We reported previously that Arabidopsis thaliana MICROTUBULE-ASSOCIATED PROTEIN18 (MAP18) contributes to directional cell growth and cortical microtubule organization. The preferential expression of MAP18 in pollen and in pollen tubes suggests that MAP18 also may function in pollen tube growth. In this study, we demonstrate that MAP18 functions in pollen tubes by influencing actin organization, rather than microtubule assembly. In vitro biochemical results indicate that MAP18 exhibits Ca(2+)-dependent filamentous (F)-actin-severing activity. Abnormal expression of MAP18 in map18 and MAP18 OX plants was associated with disorganization of the actin cytoskeleton in the tube apex, resulting in aberrant pollen tube growth patterns and morphologies, inaccurate micropyle targeting, and fewer fertilization events. Experiments with MAP18 mutants created by site-directed mutagenesis suggest that F-actin-severing activity is essential to the effects of MAP18 on pollen tube growth direction. Our study demonstrates that in Arabidopsis, MAP18 guides the direction of pollen tube growth by modulating actin filaments.

Highlights

  • Pollen tube growth is a rapid and polarized process that occurs exclusively at the tube tip and involves the elongation of pollen tubes within the female reproductive tissues to deliver sperm cells to ovules for fertilization

  • MICROTUBULE-ASSOCIATED PROTEIN18 (MAP18) Is Required for Normal Pollen Tube Growth in Vitro

  • The Arabidopsis pollen GeneChip indicates that MAP18 is elevated in growing pollen tubes compared with germinating or hydrated pollens (Wang et al, 2008)

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Summary

Introduction

Pollen tube growth is a rapid and polarized process that occurs exclusively at the tube tip and involves the elongation of pollen tubes within the female reproductive tissues to deliver sperm cells to ovules for fertilization. The pollen tube is comprised of the shank, the subapex, and the apex, which each exhibit distinctly organized filamentous (F)-actin (Geitmann and Emons, 2000; Vidali and Hepler, 2001). These actin structures may perform diverse functions. Organelles and secretory vesicles are trafficked along longitudinal actin cables throughout the shank of elongating pollen tubes (Hepler et al, 2001; Cheung et al, 2002).

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