Chen Christine Y-h, Cheung Alice Y, Wu Hen-ming
Molecular and Cell Biology Program, University of Massachusetts, Amherst, Massachusetts 01003, USA.
Plant Cell. 2003 Jan;15(1):237-49. doi: 10.1105/tpc.007153.
Pollen tube elongation is a rapid tip growth process that is driven by a dynamic actin cytoskeleton. A ubiquitous family of actin binding proteins, actin-depolymerizing factors (ADFs)/cofilins, bind to actin filaments, induce severing, enhance depolymerization from their slow-growing end, and are important for maintaining actin dynamics in vivo. ADFs/cofilins are regulated by multiple mechanisms, among which Rho small GTPase-activated phosphorylation at a terminal region Ser residue plays an important role in regulating their actin binding and depolymerizing activity, affecting actin reorganization. We have shown previously that a tobacco pollen-specific ADF, NtADF1, is important for maintaining normal pollen tube actin cytoskeleton organization and growth. Here, we show that tobacco pollen grains accumulate phosphorylated and nonphosphorylated forms of ADFs, suggesting that phosphorylation could be a regulatory mechanism for their activity. In plants, Rho-related Rac/Rop GTPases have been shown to be important regulators for pollen tube growth. Overexpression of Rac/Rop GTPases converts polar growth into isotropic growth, resulting in pollen tubes with ballooned tips and a disrupted actin cytoskeleton. Using the Rac/Rop GTPase-induced defective pollen tube phenotype as a functional assay, we show that overexpression of NtADF1 suppresses the ability of NtRac1, a tobacco Rac/Rop GTPase, to convert pollen tube tip growth to isotropic growth. This finding suggests that NtADF1 acts in a common pathway with NtRac1 to regulate pollen tube growth. A mutant form of NtADF1 with a nonphosphorylatable Ala substitution at its Ser-6 position [NtADF1(S6A)] shows increased activity, whereas the mutant NtADF1(S6D), which has a phospho-mimicking Asp substitution at the same position, shows reduced ability to counteract the effect of NtRac1. These observations suggest that phosphorylation at Ser-6 of NtADF1 could be important for its integration into the NtRac1 signaling pathway. Moreover, overexpression of NtRac1 diminishes the actin binding activity of green fluorescent protein (GFP)-NtADF1 but has little effect on the association of GFP-NtADF1(S6A) with actin cables in pollen tubes. Together, these observations suggest that NtRac1-activated activity regulates the actin binding and depolymerizing activity of NtADF1, probably via phosphorylation at Ser-6. This notion is further supported by the observation that overexpressing a constitutively active NtRac1 in transformed pollen grains significantly increases the ratio of phosphorylated to nonphosphorylated ADFs. Together, the observations reported here strongly support the idea that NtRac1 modulates NtADF1 activity through phosphorylation at Ser-6 to regulate actin dynamics.
花粉管伸长是一个由动态肌动蛋白细胞骨架驱动的快速顶端生长过程。肌动蛋白解聚因子(ADFs)/切丝蛋白是一类普遍存在的肌动蛋白结合蛋白家族,它们与肌动蛋白丝结合,诱导切断,增强其缓慢生长末端的解聚,并且对于维持体内肌动蛋白动力学很重要。ADFs/切丝蛋白受多种机制调控,其中Rho小GTP酶激活的末端区域丝氨酸残基磷酸化在调节其肌动蛋白结合和解聚活性、影响肌动蛋白重组方面起着重要作用。我们之前已经表明,烟草花粉特异性ADF,NtADF1,对于维持正常的花粉管肌动蛋白细胞骨架组织和生长很重要。在这里,我们表明烟草花粉粒积累了ADFs的磷酸化和非磷酸化形式,这表明磷酸化可能是其活性的一种调节机制。在植物中,Rho相关的Rac/Rop GTP酶已被证明是花粉管生长的重要调节因子。Rac/Rop GTP酶的过表达将极性生长转变为各向同性生长,导致花粉管顶端呈气球状且肌动蛋白细胞骨架被破坏。利用Rac/Rop GTP酶诱导的有缺陷的花粉管表型作为功能检测,我们表明NtADF1的过表达抑制了烟草Rac/Rop GTP酶NtRac1将花粉管顶端生长转变为各向同性生长的能力。这一发现表明NtADF1与NtRac1在一条共同途径中起作用来调节花粉管生长。一种在其丝氨酸-6位置具有不可磷酸化丙氨酸替代的NtADF1突变形式[NtADF1(S6A)]显示出活性增加,而在相同位置具有模拟磷酸化天冬氨酸替代的突变体NtADF1(S6D)显示出抵消NtRac1作用的能力降低。这些观察结果表明,NtADF1丝氨酸-6位点的磷酸化对于其整合到NtRac1信号通路中可能很重要。此外,NtRac1的过表达降低了绿色荧光蛋白(GFP)-NtADF1的肌动蛋白结合活性,但对GFP-NtADF1(S6A)与花粉管中肌动蛋白束的结合影响很小。总之,这些观察结果表明NtRac1激活的活性可能通过丝氨酸-6位点的磷酸化来调节NtADF1的肌动蛋白结合和解聚活性。在转化的花粉粒中过表达组成型激活的NtRac1会显著增加磷酸化ADFs与非磷酸化ADFs的比例,这一观察结果进一步支持了这一观点。总之,这里报道的观察结果有力地支持了NtRac1通过丝氨酸-6位点的磷酸化调节NtADF1活性以调控肌动蛋白动力学的观点。