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Lily Cdc42/Rac-interactive binding motif-containing protein, a Rop target, involves calcium influx and phosphoproteins during pollen germination and tube growth

机译:含有百合Cdc42 / Rac相互作用结合基序的蛋白质(一个Rop靶标)在花粉萌发和管生长过程中涉及钙内流和磷蛋白

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摘要

We report unique desiccation-associated ABA signaling transduction through which the Rop (Rho GTPase of plants) and its target LLP12-2 are regulated during the stage of pollen maturation and tube growth. Overexpression of LLP12-2 drastically inhibited pollen germination and tube growth. Studies on the germination inhibitors, Ca2+ influx blocking agents LaCl3 and EGTA and an actin-depolymerizing drug, latrunculin B (LatB), revealed that the LLP12-2-induced inhibition of germination and tube growth is significantly suppressed by LaCl3 and EGTA in the LLP12-2-overexpressing pollen but not by LatB. These results suggested that LLP12-2 is associated with Ca2+ influx in the cytoplasm and may be not with actin assembly. With the addition of LaCl3 and EGTA, LLP12-2-overexpressing pollen increased germination and tube growth compared with the one without addition, whereas pollen expressing GFP decreased germination and tube growth. Thus, an optimum level of [Ca2+]cyt influx is crucial for normal germination and tube growth. Studies on the inhibitors, staurosporine and okadaic acid in the LLP12-2-overexpressing pollen, showed no appreciable increase in germination when compared with the one without addition, suggesting that staurosporine-sensitive protein kinases and dephosphorylation of phosphoproteins may be not involved in the LLP12-2 mediated germination. However, the LLP12-2-induced inhibition of tube length was slightly but significantly suppressed by staurosporine, suggesting that staurosporine-sensitive protein kinases involve in the LLP12-2-induced inhibition of tube growth.
机译:我们报告独特的干燥相关的ABA信号转导,通过它在花粉成熟和管生长阶段调节Rop(植物的Rho GTPase)及其靶标LLP12-2。 LLP12-2的过表达极大地抑制了花粉的萌发和管的生长。对发芽抑制剂Ca2 +流入阻滞剂LaCl3和EGTA以及肌动蛋白解聚药物latrunculin B(LatB)的研究表明,LLP12-2对LLP12中的LaCl3和EGTA抑制了发芽和管生长的抑制作用。 -2-过表达花粉,但不是由LatB表达。这些结果表明,LLP12-2与细胞质中的Ca2 +内流有关,可能与肌动蛋白装配无关。与未添加LaCl3和EGTA相比,过表达LLP12-2的花粉与未添加花粉的植物相比,增加了发芽和管的生长,而表达GFP的花粉则降低了发芽和管的生长。因此,[Ca2 +] cyt流入量的最佳水平对于正常发芽和管生长至关重要。对过表达LLP12-2的花粉中的抑制剂,星形孢菌素和冈田酸的研究表明,与未添加花粉的抑制剂相比,发芽没有明显增加,这表明星形孢菌素敏感的蛋白激酶和磷蛋白的去磷酸化可能与LLP12不相关。 -2介导的发芽。但是,星形孢菌素对LLP12-2诱导的管长度的抑制作用被轻微但显着地抑制,这表明星形孢菌素敏感性蛋白激酶参与了LLP12-2诱导的管生长的抑制作用。

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