Pu Rongsun, Robinson Kenneth R
Department of Biological Sciences, Purdue University, West Lafayette, IN 47907, USA.
Planta. 2003 Jul;217(3):407-16. doi: 10.1007/s00425-003-1012-9. Epub 2003 Mar 22.
Previous work has shown that distinct Ca(2+) 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 Ca(2+) gradients prior to germination and then germinate from the site of elevated Ca(2+). In no case did germination occur without a prior formation of a Ca(2+) gradient. Using the self-referencing Ca(2+)-selective probe, we measured highly localized influx of Ca(2+) during photopolarization, indicating that extracellular stores supply at least some of the Ca(2+) 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 Ca(2+) 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.
先前的研究表明,在褐藻扁浒苔(Silvetia compressa (J. Agardh) E. Serrão, T.O. Cho, S.M. Boo et Brawley)的合子中,独特的Ca(2+)梯度先于并预测了由单侧蓝光诱导极化后的萌发位点。我们在此表明,黑暗培养的扁浒苔合子在萌发前也会形成胞质Ca(2+)梯度,然后从Ca(2+)升高的位点萌发。在任何情况下,没有预先形成Ca(2+)梯度就不会发生萌发。使用自参考Ca(2+)选择性探针,我们测量了光极化过程中Ca(2+)的高度局部内流,表明细胞外储存至少提供了构建梯度所需的部分Ca(2+)。最后,我们发现,通过浴加钙/钙调蛋白依赖性激酶II(CaM激酶II)抑制剂KN-93(而非其无活性类似物KN-92)以及注射针对该激酶的抑制性肽,可抑制萌发。KN-93并不干扰合子的光极化,这与钙调蛋白不参与对光的初始反应的观点一致。KN-93的结果表明,在明显萌发前约2小时,萌发对活性CaM激酶II的需求结束。我们得出结论,部分由海水中局部钙内流产生的Ca(2+)梯度是这些细胞极性发育和表达过程的重要组成部分,无论引导轴取向的外部线索的性质如何。钙调蛋白和CaM激酶II参与解读(而非建立)钙梯度,使萌发能够在钙升高的位点发生,但CaM激酶II似乎不参与萌发的起始。