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The involvement of Ca2+ gradients, Ca2+ fluxes, and CaM kinase II in polarization and germination of Silvetia compressa zygotes

机译:Ca2 + 梯度,Ca2 + 通量和CaM激酶II与Silvetia compressa zygotes的极化和萌发有关

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Previous work has shown that distinct Ca2+ gradients precede and predict the loci of germination of the zygotes of the brown alga, Silvetia compressa (J. Agardh) E. Serrão, T.O. Cho, S.M. Boo et Brawley, that are polarized by unilateral blue light. We show here that dark-grown S. compressa zygotes also form cytosolic Ca2+ gradients prior to germination and then germinate from the site of elevated Ca2+. In no case did germination occur without a prior formation of a Ca2+ gradient. Using the self-referencing Ca2+-selective probe, we measured highly localized influx of Ca2+ during photopolarization, indicating that extracellular stores supply at least some of the Ca2+ needed to construct a gradient. Finally, we find that germination was inhibited by a bath-applied inhibitor of calcium/calmodulin-dependent kinase II (CaM kinase II), KN-93 (but not by its inactive analog, KN-92), and by an injected inhibitory peptide for the kinase. KN-93 did not interfere with the photopolarization of the zygotes, consistent with the view that calmodulin is not involved in the initial response to light. The KN-93 results indicate that the requirement for active CaM kinase II for germination ends about 2 h before overt germination. We conclude that Ca2+ gradients, generated in part by localized calcium entry from the seawater, are an essential part of the process of polarity development and expression in these cells, regardless of the nature of the external cue that directs the orientation of the axis. Calmodulin and CaM kinase II are involved in interpreting (but not in establishing) the calcium gradient, allowing germination to occur at the site of elevated calcium, but CaM kinase II appears not to be involved in the initiation of germination.
机译:先前的工作表明,不同的Ca2 + 梯度先于并预测了褐藻合子Silvetia compressa(J. Agardh)E.Serrão,T.O.的合子萌发的位点。 Cho,S.M. Boo et Brawley,它们被单边蓝光偏振。我们在这里表明,深色的S. compressa zygotes在发芽之前也形成了胞质Ca2 + 梯度,然后从升高的Ca2 + 部位发芽。在没有事先形成Ca2 + 梯度的情况下,都不会发生发芽。使用自参考Ca2 + 选择性探针,我们测量了光极化过程中Ca2 + 的高度局部流入,这表明细胞外存储区至少提供了一些构建梯度所需的Ca2 + 。最后,我们发现钙/钙调蛋白依赖性激酶II(CaM激酶II),KN-93(但不受其非活性类似物KN-92抑制)和注射的抑制性肽抑制了浴的萌发对于激酶。 KN-93不会干扰合子的光极化,这与钙调蛋白不参与对光的初始反应的观点一致。 KN-93结果表明,在发芽前约2小时,对萌发的活性CaM激酶II的需求就结束了。我们得出的结论是,Ca2 + 梯度(部分由海水中的局部钙进入而产生)是这些细胞中极性发育和表达过程的重要组成部分,而与指导细胞定向的外部线索的性质无关。轴。钙调蛋白和CaM激酶II参与解释(但不建立)钙梯度,使发芽发生在钙含量升高的部位,但CaM激酶II似乎不参与发芽的开始。

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