A calcium-dependent protein kinase interacts with and activates a calcium channel to regulate pollen tube growth.

A calcium-dependent protein kinase interacts with and activates a calcium channel to regulate pollen tube growth.
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DOI:
10.1093/mp/sst125
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发表时间:
2014-02
期刊:
影响因子:
27.5
通讯作者:
Liming Zhou;Wenzhi Lan;Yuan-Qing Jiang;Wei-Ling Fang;S. Luan
Liming Zhou;Wenzhi Lan;Yuan-Qing Jiang;Wei-Ling Fang;S. Luan
中科院分区:
生物学1区
文献类型:
--
作者:
Liming Zhou;Wenzhi Lan;Yuan-Qing Jiang;Wei-Ling Fang;S. Luan

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钙作为一种普遍存在的第二信使,在动物神经元、植物花粉管和根毛等尖端生长细胞中起着重要作用。然而,关于植物中编码和解码Ca(2+)信号的调节机制却知之甚少。这里提出的证据表明,钙依赖性蛋白激酶,CPK32,控制极性生长的花粉管。CPK 32的过表达破坏了极性生长沿着的生长,并导致顶端Ca(2+)的过度积累。对CPK32的下游效应分子的搜索导致鉴定了环核苷酸门控通道CNGC 18作为CPK32的相互作用伴侣。CPK32和CNGC 18的共表达导致爪蟾卵母细胞中CNGC 18的活化,其中单独表达CNGC 18没有表现出显著的钙通道活性。CNGC 18的过表达产生了一种生长停滞表型,并伴随着尖端钙的积累,类似于CPK 32过表达所诱导的。CPK32和CNGC 18的共表达具有协同效应,导致更严重的花粉管生长的去极化。这些结果提供了一种潜在的前馈机制,其中钙激活的CPK 32激活CNGC 18,进一步促进在花粉管极性生长中Ca(2+)振荡的升高阶段的钙进入。
Calcium, as a ubiquitous second messenger, plays essential roles in tip-growing cells, such as animal neurons, plant pollen tubes, and root hairs. However, little is known concerning the regulatory mechanisms that code and decode Ca(2+) signals in plants. The evidence presented here indicates that a calcium-dependent protein kinase, CPK32, controls polar growth of pollen tubes. Overexpression of CPK32 disrupted the polar growth along with excessive Ca(2+) accumulation in the tip. A search of downstream effector molecules for CPK32 led to identification of a cyclic nucleotide-gated channel, CNGC18, as an interacting partner for CPK32. Co-expression of CPK32 and CNGC18 resulted in activation of CNGC18 in Xenopus oocytes where expression of CNGC18 alone did not exhibit significant calcium channel activity. Overexpression of CNGC18 produced a growth arrest phenotype coupled with accumulation of calcium in the tip, similar to that induced by CPK32 overexpression. Co-expression of CPK32 and CNGC18 had a synergistic effect leading to more severe depolarization of pollen tube growth. These results provide a potential feed-forward mechanism in which calcium-activated CPK32 activates CNGC18, further promoting calcium entry during the elevation phase of Ca(2+) oscillations in the polar growth of pollen tubes.