[Effects of G-protein regulators and stylar S-RNase on the growth and Ca2+ concentration of Pyrus pyrifolia pollen tube].

植物生理与分子生物学学报 Pub Date : 2007-10-01
Cai-Ping Zhao, Guo-Hua Xu, Shao-Ling Zhang, Zhu-Qin Liu, Chun-Lei Wang
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Abstract

The effects of G protein regulators and stylar S-RNase on the growth and [Ca(2+)](i) changes of the Pyrus pyrifolia pollen tube were investigated using Laser Confocal Scanning Microscope (LCSM). The results indicated that: (1) The growth of 'Housui' pollen tube could be inhibited by its stylar S-RNase and pertussis toxin (PTX), the inhibitor of heterotrimeric G protein. While 'Kousui' stylar S-RNase had little effect on the growth of 'Housui' pollen tube; cholera toxin (CTX), the activator of heterotrimeric G protein, could promote pollen tube growth and eliminate the suppression of stylar S-RNase on the growth of self-pollen tube, but the growth of 'Housui' pollen tube could be arrested under the co-action of PTX and S-RNase from 'Kousui' Fig.1). (2) Treatments with different stylar S-RNase and G protein regulators could have different effects on the change in [Ca(2+)](i) in the tip of pollen tube (Figs.2,3). The treatment with 'Housui' stylar S-RNase could induce the decrease of fluorescence gradient of [Ca(2+)](i) along the tip of self-pollen tube (Figs.2A, 3A), and the treatment with CTX could markedly elevate [Ca(2+)](i) in the tip of pollen tube showed (Fig.3C). The way of [Ca(2+)](i) changed in 'Housui' pollen tube under the co-action of CTX and its stylar S-RNase showed the compositive effect of the two respective treatment (Fig.3A, C, E), but the effect of the co-action of PTX and 'Kousui' stylar S-RNase showed increase in [Ca(2+)](i) in the pollen tube in 18 min after treatment, and then decrease between 18-36 min (Fig.3F). These results suggest that during self or cross pollination, the control of the growth of Pyrus pyrifolia pollen tube is by the synergistic effect of stylar S-RNase, G protein and [Ca(2+)](i) in the pollen tube.

g蛋白调控因子和花柱S-RNase对梨花粉管生长和Ca2+浓度的影响[j]。
利用激光共聚焦扫描显微镜(Laser Confocal Scanning Microscope, LCSM)研究了G蛋白调控因子和花柱S-RNase对梨花粉管生长和[Ca(2+)](i)变化的影响。结果表明:(1)“后穗”花柱S-RNase和异源三聚体G蛋白抑制剂百日咳毒素(PTX)可抑制花粉管的生长。而‘口穗’花柱S-RNase对‘后穗’花粉管生长影响不大;霍乱毒素(CTX)是异源三聚体G蛋白的激活剂,能促进花粉管生长,消除花柱S-RNase对自身花粉管生长的抑制作用,但在PTX和S-RNase的共同作用下,‘口穗’花粉管的生长受到抑制(图1)。(2)不同花柱S-RNase和G蛋白调节剂处理对花粉管尖端[Ca(2+)](i)的变化有不同的影响(图2、3)。‘后穗’花柱S-RNase处理可诱导自花粉管尖端[Ca(2+)](i)荧光梯度降低(图2a、3A), CTX处理可显著提高花粉管尖端[Ca(2+)](i)荧光梯度(图3c)。CTX及其花柱S-RNase共同作用下'后穗'花粉管中[Ca(2+)](i)的变化方式显示出两种处理的综合效应(图3a, C, E),但PTX与'口穗'花柱S-RNase共同作用的效果显示,处理后18 min花粉管中[Ca(2+)](i)增加,然后在18-36 min之间下降(图3f)。这些结果表明,在自花授粉或异花授粉过程中,花柱S-RNase、G蛋白和花粉管中[Ca(2+)](i)的协同作用对梨花粉管的生长起控制作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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