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A calcium-dependent protein kinase, ZmCPK32, specifically expressed in maize pollen to regulate pollen tube growth

机译:钙依赖性蛋白激酶,ZMCPK32,在玉米花粉中特异性表达,以调节花粉管生长

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摘要

Calcium-dependent protein kinases (CPKs) play an essential role in the regulation of pollen tube growth. Although CPK genes have been identified in maize, and some have been functionally characterized, the molecular function of ZmCPKs associated with pollen tube development remains less well studied. Here, we report that a pollen-specific CPK, ZmCPK32, is involved in the regulation of pollen germination and tube extension. ZmCPK32 exhibited CPK activity and was localized on the plasma membrane and punctate internal membrane compartments via N-terminal acylation. In situ hybridization and real-time PCR revealed that ZmCPK32 transcripts accumulated in pollen and expression was dramatically upregulated during shedding. To elucidate the function of this gene, we transiently expressed a ZmCPK32-GFP fusion protein in tobacco pollen using microparticle bombardment. ZmCPK32 accumulation inhibited pollen germination and reduced pollen tube growth, but this effect was abolished when the kinase-inactive variant was expressed, indicating that kinase activity is critical for its regulatory function. In addition, the plasma membrane localization of ZmCPK32 is essential for regulating polar growth, as pollen expressing the cytosol-localized kinase displayed reduced tube length but germinated well. Moreover, the constitutively active form of ZmCPK32 enhanced the reduction in the germination rate, indicating that the specific activation of ZmCPK32 via calcium ions at the cortical growth point is essential for regulating appropriate germination. The results suggest that ZmCPK32 is functionally associated with pollen tube growth, and could represent a potential target for breeding male-sterile maize.
机译:钙依赖蛋白激酶(CPKs)起到花粉管生长的调节中起重要作用。虽然CPK基因在玉米中被识别,以及一些在功能上表征,与花粉管发展相关ZmCPKs的分子功能保持较少很好的研究。在这里,我们报告说,花粉特异性CPK,ZmCPK32,参与花粉萌发和花粉管延伸的调节。 ZmCPK32表现出CPK活性和是局部经由N-末端酰化的质膜和点状内部膜隔室。在原位杂交和实时PCR结果显示,在花粉和表达积累ZmCPK32成绩单下降时急剧上调。为了阐明这个基因的功能,我们瞬时表达在烟草花粉微粒使用轰击ZmCPK32-GFP融合蛋白。 ZmCPK32积累抑制花粉萌发和降低的花粉管生长,但这种影响表达的激酶失活变体时被废除,这表明激酶活性是其调节功能是至关重要的。此外,ZmCPK32的质膜定位是用于调节极性生长,如花粉表达胞质溶胶定位的激酶显示的缩小管的长度,但发芽以及必不可少的。此外,ZmCPK32的组成型活性形式增强了发芽率的降低,这表明通过钙离子ZmCPK32的特异性活化在皮质增长点是用于调节适当发芽必不可少的。结果表明,ZmCPK32在功能上与花粉管生长相关联,且可以代表一个潜在目标繁殖雄性不育玉米。

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