Centro de Investigaciones en Química Biológica de Córdoba (CIQUIBIC-CONICET), Departamento de Química Biológica, Universidad Nacional de Córdoba, Córdoba, Argentina.
Ann Bot. 2012 Sep;110(4):787-95. doi: 10.1093/aob/mcs153. Epub 2012 Jul 9.
The integrity of actin filaments (F-actin) is essential for pollen-tube growth. In S-RNase-based self-incompatibility (SI), incompatible pollen tubes are inhibited in the style. Consequently, research efforts have focused on the alterations of pollen F-actin cytoskeleton during the SI response. However, so far, these studies were carried out in in vitro-grown pollen tubes. This study aimed to assess the timing of in vivo changes of pollen F-actin cytoskeleton taking place after compatible and incompatible pollinations in Nicotiana alata. To our knowledge, this is the first report of the in vivo F-actin alterations occurring during pollen rejection in the S-RNase-based SI system.
The F-actin cytoskeleton and the vacuolar endomembrane system were fluorescently labelled in compatibly and incompatibly pollinated pistils at different times after pollination. The alterations induced by the SI reaction in pollen tubes were visualized by confocal laser scanning microscopy.
Early after pollination, about 70 % of both compatible and incompatible pollen tubes showed an organized pattern of F-actin cables along the main axis of the cell. While in compatible pollinations this percentage was unchanged until pollen tubes reached the ovary, pollen tubes of incompatible pollinations underwent gradual and progressive F-actin disorganization. Colocalization of the F-actin cytoskeleton and the vacuolar endomembrane system, where S-RNases are compartmentalized, revealed that by day 6 after incompatible pollination, when the pollen-tube growth was already arrested, about 80 % of pollen tubes showed disrupted F-actin but a similar percentage had intact vacuolar compartments.
The results indicate that during the SI response in Nicotiana, disruption of the F-actin cytoskeleton precedes vacuolar membrane breakdown. Thus, incompatible pollen tubes undergo a sequential disorganization process of major subcellular structures. Results also suggest that the large pool of S-RNases released from vacuoles acts late in pollen rejection, after significant subcellular changes in incompatible pollen tubes.
肌动蛋白丝(F-actin)的完整性对于花粉管的生长至关重要。在 S-RNase 介导的自交不亲和(SI)中,不亲和的花粉管在花柱中受到抑制。因此,研究工作集中在 SI 反应过程中花粉 F-actin 细胞骨架的改变上。然而,到目前为止,这些研究都是在体外培养的花粉管中进行的。本研究旨在评估在 Nicotiana alata 中进行亲和和不亲和授粉后,花粉 F-actin 细胞骨架的体内变化时间。据我们所知,这是 S-RNase 介导的 SI 系统中花粉排斥过程中发生的体内 F-actin 改变的首次报道。
在授粉后不同时间,用荧光标记亲和和不亲和授粉的柱头中的 F-actin 细胞骨架和液泡内膜系统。通过共聚焦激光扫描显微镜观察 SI 反应诱导的花粉管中的变化。
授粉后早期,约 70%的亲和和不亲和花粉管都显示出沿着细胞主轴排列的 F-actin 纤维的有序模式。而在亲和授粉中,这一比例在花粉管到达子房之前保持不变,但不亲和授粉的花粉管则逐渐发生 F-actin 解聚。F-actin 细胞骨架和液泡内膜系统(其中 S-RNases 被分隔)的共定位显示,在不亲和授粉后第 6 天,当花粉管生长已经停止时,约 80%的花粉管显示出破坏的 F-actin,但仍有类似比例的花粉管具有完整的液泡隔室。
结果表明,在 Nicotiana 中的 SI 反应过程中,F-actin 细胞骨架的破坏先于液泡膜的破裂。因此,不亲和花粉管经历了主要亚细胞结构的顺序解聚过程。结果还表明,从液泡中释放的大量 S-RNases 在后在不亲和花粉管中发生显著的亚细胞变化后,在花粉排斥中起作用。