Joint International Research Laboratory of Metabolic & Developmental Sciences, State Key Laboratory of Hybrid Rice, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai 200240, China.
Department of Life Science and Environmental Biochemistry, Pusan National University, Miryang 50463, Republic of Korea.
Plant Cell. 2020 Dec;32(12):3961-3977. doi: 10.1105/tpc.20.00551. Epub 2020 Oct 22.
The highly variable and species-specific pollen surface patterns are formed by sporopollenin accumulation. The template for sporopollenin deposition and polymerization is the primexine that appears on the tetrad surface, but the mechanism(s) by which primexine guides exine patterning remain elusive. Here, we report that the Poaceae-specific (), which encodes a nonspecific lipid transfer protein, is required for primexine integrity and pollen exine patterning in rice (). Disruption of leads to abnormal exine pattern and complete male sterility, although sporopollenin biosynthesis is unaffected. is specifically expressed in male meiocytes, indicating that reproductive cells exert genetic control over exine patterning. EPAD1 possesses an N-terminal signal peptide and three redundant glycosylphosphatidylinositol (GPI)-anchor sites at its C terminus, segments required for its function and localization to the microspore plasma membrane. In vitro assays indicate that EPAD1 can bind phospholipids. We propose that plasma membrane lipids bound by EPAD1 may be involved in recruiting and arranging regulatory proteins in the primexine to drive correct exine deposition. Our results demonstrate that EPAD1 is a meiocyte-derived determinant that controls primexine patterning in rice, and its orthologs may play a conserved role in the formation of grass-specific exine pattern elements.
高度可变且具有物种特异性的花粉表面图案是由花粉外壁物质积累形成的。花粉外壁物质沉积和聚合的模板是在四分体表面出现的原外壁,但是原外壁指导外壁模式形成的机制仍不清楚。在这里,我们报告说,禾本科特异性的 (),其编码一种非特异性脂转移蛋白,对于水稻中原外壁的完整性和花粉外壁模式形成是必需的。 ()的破坏导致异常的外壁模式和完全的雄性不育,尽管花粉外壁物质生物合成不受影响。在雄性减数分裂细胞中特异性表达,表明生殖细胞对外壁模式形成具有遗传控制。 EPAD1 在其 N 端具有信号肽,在 C 端具有三个冗余的糖基磷脂酰肌醇(GPI)锚定位点,这些片段对于其功能和定位到小孢子质膜是必需的。体外测定表明 EPAD1 可以结合磷脂。我们提出,由 EPAD1 结合的质膜脂质可能参与募集和排列原外壁中的调节蛋白,以驱动正确的外壁沉积。我们的结果表明,EPAD1 是一种减数分裂细胞衍生的决定因素,控制着水稻中原外壁的模式形成,其同源物可能在形成草类特异性外壁模式元素中发挥保守作用。