Arabidopsis ECERIFERUM3 (CER3) Plays a Critical Role in Maintaining Hydration for Pollen-Stigma Recognition during Fertilization

Abstract

ABSTRACTPlants distinguish the pollen grains that land on their stigmas, only allowing compatible pollen to fertilize female gametes. To analyze the underlying mechanism, conditional male-sterile mutations with affected pollen coat and disrupted pollen-stigma recognition were isolated and described. The mutant pollen failed to germinate, but germinated in vitro, suggesting that they are viable. In mutants, stigma cells that contacted their own pollen generated callose, a carbohydrate produced in response to foreign pollen. High humidity restored pollen hydration and successful fertilization, indicating defective dehydration in pollen-stigma interaction. Further analysis results from mixed pollination experiments demonstrated that the mutant pollen specifically lacked a functional pollen-stigma recognition system. The sterile plants lacked stem waxes and displayed postgenital fusion between aerial floral organs. In addition, the mutant pollen was deficient in long-chain lipids and had excess tryphine. Transmission electron microscopy observation showed that mutant pollen had almost the same surface structure as the wild type at bicellular pollen stage. However, abnormal plastoglobuli were observed in the plastids of the mutant tapetum, which was indicative of altered lipid accumulation. CER3 transcript was found in anther tapetum and microspores at development stage 9 while CER3-GFP fusion protein was localized to the cell plasma membrane. Our data reveal that CER3 is required for biosynthesis of tryphine lipids which play a critical role in maintaining hydration for pollen-stigma recognition during fertilization.