Skip to main content


Front. Plant Sci., 14 November 2017
Sec. Plant Cell Biology
Volume 8 - 2017 |

The Kinase ERULUS Controls Pollen Tube Targeting and Growth in Arabidopsis thaliana

  • 1Integrated Molecular Plant Physiology Research, University of Antwerp, Antwerp, Belgium
  • 2Department of Biosciences, University of Milan, Milan, Italy
  • 3Institute of Biophysics, Consiglio Nazionale delle Ricerche, Milan, Italy
  • 4Plant Biochemistry and Biotechnology Lab, Technological Educational Institute of Crete: University of Applied Sciences, Crete, Greece

In this paper, we describe the role of the receptor-like kinase ERULUS (ERU) in PT growth of Arabidopsis thaliana. In silico analysis and transcriptional reporter lines revealed that ERU is only expressed in pollen and root hairs (RHs), making it a tip growth-specific kinase. Deviations from Mendelian inheritance were observed in the offspring of self-pollinated heterozygous eru plants. We found that in vivo eru PT targeting was disturbed, providing a possible explanation for the observed decrease in eru fertilization competitiveness. Extracellular calcium perception and intracellular calcium dynamics lie at the basis of in vivo pollen tube (PT) tip growth and guidance. In vitro, ERU loss-of-function lines displayed no obvious PT phenotype, unless grown on low extracellular calcium ([Ca2+]ext) medium. When grown at 12 the normal [Ca2+]ext, eru PTs grew 37% slower relative to WT PTs. Visualization of cytoplasmic [Ca2+]cyt oscillations using the Yellow Cameleon 3.6 (YC3.6) calcium sensor showed that, unlike in WT PTs, eru apical [Ca2+]cyt oscillations occur at a lower frequency when grown at lower [Ca2+]ext, consistent with the observed reduced growth velocity. Our results show that the tip growth-specific kinase ERULUS is involved in regulating Ca2+-dependent PT growth, and most importantly, fertilization efficiency through successful PT targeting to the ovules.


Pollen tube (PT) tip growth is a highly polarized form of cell elongation ultimately leading to the delivery of sperm cells at the embryo sac and subsequent double fertilization (Obermeyer and Feijó, 2017). The PT tip functions as the site of plasticity and extension, where vesicles filled with cell wall proteins and precursors fuse with the apical plasma membrane, providing extra membrane and cell wall material to the growing cell. Simultaneously, the PT apex provides the interface at which extracellular cues are perceived and translated toward changes in PT growth directionality.

During its penetration down the style and transmitting tract toward the ovule, many interactive signals are exchanged between the PT and its surrounding tissue (Qu et al., 2015; Obermeyer and Feijó, 2017). Upon reaching the female gametophyte, the PT encounters attracting signals that guide it to the synergids. These synergids, which flank the egg cell, secrete small cysteine-rich proteins (LUREs) that probably act as signaling ligands (Okuda et al., 2009; Takeuchi and Higashiyama, 2016). LUREs attract the incoming PT toward the target egg cell, a process that involves the membrane bound RLKs LIP1 and LIP2 (Liu et al., 2013). Subsequently, on the synergid cells, the receptor-like kinase (RLKs) FERONIA/SIRENE and the GPI-anchor protein LORELEI interact with an unknown signal, finally causing the cessation of PT growth (Miyazaki et al., 2009; Liu et al., 2016). ZmES4 signals to the PT tip and induces bursting, which involves activation of PT plasma membrane-localized KZM1, a K+ Shaker channel (Amien et al., 2010). Sperm cell discharge is controlled by RLKs ANXUR1/2 and the activity of a Ca2+ transporter, ACA9, that are all expressed in the PT (Schiott et al., 2004; Miyazaki et al., 2009).

The ability of PTs to perceive their extracellular environment and respond adequately by adjusting their growth regime seems to coincide with specific intracellular [Ca2+] signatures (Iwano et al., 2012; Damineli et al., 2017). More so, Ca2+-signatures seem embedded throughout the male–female tissue crosstalk pathway (Denninger et al., 2014; Hamamura et al., 2014). A number of highly dynamic cellular processes occur during PT growth (Obermeyer and Feijó, 2017), including the formation and maintenance of intra- and extracellular ion dynamics, apical endo-/exocytosis and the modification of the cytoskeleton, all of which depend on tight spatial and temporal control of cytosolic [Ca2+] oscillations at the tip (Schoenaers et al., 2017). Pharmacological interruption of the apical cytoplasmic Ca2+ gradient causes immediate growth cessation (Iwano et al., 2009), and local elevation of the [Ca2+]ext irreversibly steers tip growth directionality in vitro (Bibikova et al., 1997). In vivo alteration of the [Ca2+]ext might be an important factor in controling PT guidance. For instance, the [Ca2+]ext was found to increase in the Lily transmitting tract upon pollination (Zhao et al., 2004). More so, pollination induces transcription of the Ca2+ export system AUTOINHIBITED CALCIUM-ATPASE 13 (ACA13) in the Arabidopsis transmitting tract (Iwano et al., 2014). Most importantly, Ca2+ facilitates pectin cross-linking and ROS production in the cell wall (Rounds et al., 2011; Mangano et al., 2016). As such, Ca2+ ions have a pivotal role in controling cell wall flexibility, a sine qua non condition for (oscillatory) PT elongation.

Despite these findings, it remains poorly understood how small changes in the [Ca2+]cyt oscillatory regime are regulated, and how they can lead to alterations of PT growth. In addition, despite our improved understanding of the process of PT guidance and fertilization, the number of molecular players that are known to be involved is limited. With the characterization of FER and ANXUR1/2 and their role in Ca2+ mediated fertilization, members of the CrRLK1L family have gained attention to the study of polarized growth and its regulation. ERULUS (ERU), also a CrRLK1L protein, has been described as a core root hair (RH) regulator, involved in the establishment of a functional apical [Ca2+]cyt gradient (Bai et al., 2014a). ERU loss-of-function RHs are short and stunted and apparently have a perturbed tip [Ca2+]cyt accumulation. Here we describe a role for ERU during fertilization. We found that ERU is a PT-expressed kinase that is involved in Ca2+-dependent PT growth and the control of in vivo PT guidance and fertilization.

Materials and Methods

Plant Material and Growth Conditions of Arabidopsis

Arabidopsis thaliana ecotype Columbia-0 (Col-0) and mutant eru (SALK_083442C) seeds were obtained from the Nottingham Arabidopsis stock center. Plants homozygous for the eru T-DNA insert were selected by PCR using T-DNA and gene-specific primers (Supplementary Table 1), backcrossed to the Col-0 background twice and reselected for the eru T-DNA insert.

WT and eru plants were grown in soil (Tref substrate) and kept in a growth room at 21°C in a 16/8 h light period under a light intensity of 70–90 μmol m-2s-1.

Pollen from stage 13–15 flowers were germinated in the dark at 21–23°C in a closed Petri dish on a thin cellophane membrane overlaying solid pollen growth medium in accordance with Rodriguez-Enriquez et al. (2012). The medium was supplemented with 0.5, 1, or 2 mM CaCl2 or 1 mM (NH4)H2PO4 when appropriate. The solution was heated in a microwave for the agarose to dissolve and cooled down to 50–60°C for the pH to be readjusted. A 0.5 cm × 0.5 cm cellophane membrane (325P cellulose; AA Packaging Limited, Preston, United Kingdom) was placed on top of the medium, and pollen were applied directly onto the membrane.

In Silico Analysis

The putative 1500 bp promoter region of ERULUS was examined for cis-elements using Place1. Public transcriptomics data was consulted using the eFP browser (Winter et al., 2007) and Genevestigator (Hruz et al., 2008).

Molecular Cloning and Plant Transformation

Constructs were generated using the Gateway Cloning system2 (Life Technologies). Genomic DNA was extracted from WT seedlings using phenol extraction. For the promoter::reporter gene analysis a 619bp sequence upstream of the start codon of ERULUS was PCR amplified from Col-0 genomic DNA using Platinum high fidelity DNA polymerase (Life Technologies). The following primers were used: 5′-GGGGACAAGTTTGTACAAAAAAGCAGGCTTC-GCTTTGAGGTCATTTTT-3′ and 5′-GGGGACCACTTTGTACAAGAAAGCTGGGTAATATCCGGCGAGGTTTTG-A-3′. PCR products were subcloned into pDONR207 and the sequence was verified by DNA sequencing. The promoter region was subsequently fused to the β-glucuronidase reporter using the LR reaction and the pGWB3 destination vector (Nakagawa et al., 2007). The construct was electroporated into Agrobacterium tumefaciens C58. Plant transformation was done by the flower dip method (Clough and Bent, 1998). Seeds were selected on half strength MS medium containing 50 μg ml-1 Kanamycin or 25 μg ml-1 Hygromycin B. Homozygous T3 progeny was used for further analysis. Eight independent homozygous lines were examined for GUS expression.

GUS Staining

GUS activity staining was performed in WT plants homozygous for the proERU::GUS insert according to a modified protocol of Jefferson et al. (1987).

Pollen Germination and PT Growth Dynamics

To determine pollen germination, eru and Col-0 pollen from stage 15 flowers were grown on pollen medium and the percentage of germinated pollen was counted 16 and 24 h after pollination.

To quantify PT growth dynamics, eru and Col-0 pollen were grown on pollen medium and gently overlaid by a cover glass directly onto the medium. Time-lapse movies were collected for approximately 1 h with a framerate of 20 s using transmitted light on a Zeiss Axioplan microscope using a Zeiss Achroplan 100× (na 1.25) oil immersion Ph3 objective. The PT length gain was measured for each frame. The data for individual PTs was aligned based on their initial length, averaged, and plotted against time.

Fertilization Competitiveness

Siliques of the T3 progeny derived from three self-pollinated heterozygous eru T2 plants were investigated. Fifteen siliques from each plant were collected and cut in the middle to generate a top half and a bottom half as described previously (Schiefelbein et al., 1993). Due to the fact that the T-DNA-specific Kanamycin resistance gene was found to be silenced in the eru mutant and that this mutation is recessive, seeds were sown on solid RH medium and the percentage of mutants was calculated by visual screening of the obvious eru RH phenotype (Bai et al., 2014a; Haruta et al., 2014).

Aniline Blue Staining of in Vivo Grown PT

Stage 12 WT flowers were emasculated and stigma were hand-pollinated with WT or eru pollen from stage 13–15 flowers. Twenty-four hours after pollination, the pistils were fixed for 2 h in 1:3 acetic acid:ethanol solution, softened overnight in 8 M NaOH, cleared with distilled water and subsequently stained with decolorized aniline blue (0.1% filtered aniline blue in 0.1 M K2HPO4-KOH buffer, pH 11) for 2 h in the dark (Mori et al., 2006). PTs were subsequently visualized by exciting DAB-stained callose using UV lighting on a Zeiss Axioplan fluorescence microscope. More than 300 PTs originating from 10 (eru pollinated) or 13 (WT pollinated) ovaries were classified according to their targeting phenotype. The length of these PTs was quantified as the distance between the stigma’s surface and the tip of the PT.

Calcium Imaging

Agrobacterium GV3101 containing the NES-YC3.6 harboring pTKan vector with UBQ10 promoter (Krebs et al., 2012) was used to transform eru and WT plants by the floral dip method (Clough and Bent, 1998). Positive transformants were selected on MS plates containing 50 mg L-1 Kanamycin and transferred to soil. Their progeny was screened for fluorescence using a Nikon AZ100 macroscope coupled to a fluorescence unit, and seeds were collected from plants showing a clear cpVenus-based fluorescence. Note that throughout the text, for simplicity, we will use YFP when referring to cpVenus.

Pollen from plants grown in long day cycles were used for subsequent in vitro germination and calcium imaging. A setup was devised to visualize growing PTs on an inverted Nikon Eclipse Ti-E. A small cover glass was covered by a thin film of pollen growth medium (prepared fresh each day), which was overlaid with a 0.5 cm × 0.5 cm square of cellophane membrane. Agarose was chosen as a gelling agent for its lack of ‘contaminating’ calcium compared to other gelling agents, and the fact that it does not rely on the presence of bivalent cations for matrix establishment. In addition, this specific solid medium was used to more closely resemble Arabidopsis dry stigma conditions and it was confirmed that its use leads to in vivo-like pollen germination and PT growth (Rodriguez-Enriquez et al., 2012). Finally, the use of solid medium prevented sample drifting during prolonged imaging. Pollen were applied on the membrane and the cover glass was flipped on another cover glass that was attached to an opening at the bottom of a small Petri dish. Water was applied on the inner sides of the Petri dish to maintain high humidity and the Petri dish was closed using parafilm. The pollen grains were germinated in a climate controlled room at 23°C, in the dark, and visualized approximately 2 h after pollination.

YC3.6 positive PTs were visualized at the tip using a 60× oil immersion objective and excited using the Prior Lumen 200 PRO fluorescent lamp (Prior Scientific) at 440 nm (436/20 nm). Images were collected with a Hamamatsu Dual CCD Camera ORCA-D2. CFP (465–500 nm) and FRET-induced YFP (520–570 nm) emission were detected simultaneously every 5 s with an exposure time of 300–400 ms using a beam splitter (A11400-03 optical block; 483/32 nm for CFP; 542/27 nm for YFP) and Hamamatsu dichroic 510 nm mirror. Images were collected simultaneously for each channel using binning 4 × 4.

Image analysis was performed in Fiji ImageJ (Schneider et al., 2012). For both channels, all frames were aligned with respect to the PT tip using the stackreg plugin and the rigid body detection algorithm. The YFP and CFP fluorescence intensities were extracted from the very tip of the growing PT, as well as the background signal intensity. The background intensity value was subtracted independently from both YFP and CFP gray values before YFP/CFP ratio calculation. The change in the ratio (ΔR) was normalized to the average ratio of the series (<R>) and plotted versus time (ΔR/<R>). The Ratio Plus Plugin for Fiji was used to visualize the calcium oscillations. Oscillograms were analyzed by Fourier transformation, in order to isolate the main oscillation frequency.


Statistics were performed using the R statistics platform (R Core Team, 2008). Significance (α = 0.05) was assessed by two-way analysis of variance (ANOVA; parametric) using linear mixed-effects models followed by a TukeyHSD (for pairwise statistical analysis), or Kruskal–Wallis tests (non-parametric).


ERULUS Is Transcribed in Mature Pollen Grains and PTs

Recent data showed that ERULUS, a RLK from the Arabidopsis thaliana subfamily of Catharanthus roseus RECEPTOR-LIKE KINASE 1-LIKE proteins (CrRLK1Ls), is expressed in trichoblast cells and that it controls tip growth of RHs in Arabidopsis (Bai et al., 2014a; Haruta et al., 2014). In higher plants, tip growth is restricted to RHs and PTs. Publicly available micro-array data indicated that ERULUS is transcribed in pollen too (Figure 1A). We performed an in silico analysis of the 1500 bp upstream promoter region and found that the ERU promoter contains two auxin response elements (AuxREs; TGTCTC), putative binding sites for auxin response factors (ARFs) which regulate auxin-induced transcription (Ulmasov et al., 1997), and (in addition to two RH-specific cis-elements), six pollen-specific cis-elements (Supplementary Table 1).


FIGURE 1. Characterization of tissue specific ERU transcription. (A) Tissue specific expression of ERU based on publicly available transcriptomics datasets (Genevestigator). (B) GUS-staining of WT × promERU::GUS flowers, pollen, pollen tubes (PTs), and ovules. Scale bars = 10 μm.

We visualized ERU expression by GUS staining in stably transformed WT x proERU::GUS plants and found that, in the areal parts, ERU transcription is restricted to mature pollen grains and in vitro growing PTs (Figure 1B). GUS staining was not detected in any other flower part, even after prolonged staining.

Standard Growth Conditions Do Not Affect eru Pollen Development

Given the apparent tip growth phenotype of eru RHs and the possibility of a similar defect in growing PTs, we performed an in vitro phenotyping of eru pollen and PTs. We compared pollen viability by Alexander staining and found no difference in viability between WT and eru mature pollen grains (Supplementary Figure 1A). Next, we germinated mutant pollen under standard growth conditions. Both WT and eru pollen germinated and produced normal looking PTs (Supplementary Figure 1B). No significant difference between eru and WT was detected with respect to both pollen germination (Supplementary Figure 1C) and PT length (Supplementary Figure 1D). In addition, callose plug formation, a prerequisite for normal sperm migration in the PT (Qin et al., 2012), was unaffected in eru PTs (Supplementary Figure 1E). Bai et al. (2014a) suggested that ERULUS plays a role in ammonium homeostasis in RHs. We therefore investigated the effect of ammonium supplementation on in vitro eru and WT pollen germination and PT growth. NH4+ was supplemented to the medium and the pollen germination percentage (Supplementary Figures 2A,B) and PT length (Supplementary Figures 2A,C) were quantified 2.5 h after pollen application, when PTs are still in the process of growing. We observed no significant difference between WT and eru pollen in both control and NH4+ supplemented conditions, implying that excess NH4+ does not affect pollen germination (Supplementary Figure 2B), PT length (Supplementary Figure 2C), and PT morphology (Supplementary Figure 2A).

eru PT Growth Is Altered When Grown under Low [Ca2+]ext

Given the importance of calcium signaling in PT growth and the role of ERU in establishing a functional calcium gradient during RH tip growth (Bai et al., 2014a), we grew mutant pollen on solid medium containing 1 mM (control), 0.5 mM (low) or 2 mM CaCl2 (high). In agreement with our previous observations (Supplementary Figure 1) we observed no significant differences with respect to average eru and WT PT growth velocities when grown under standard conditions (Figure 2A). Strikingly though, in response to 0.5 mM CaCl2 WT PTs grew faster than in the control condition (Figure 2B; 0.70 ± 0.04 vs. 0.57 ± 0.02 μm min-1) whereas eru PTs grew slower on lower [Ca2+]ext (0.44 ± 0.03 vs. 0.70 ± 0.04 μm min-1). As a result, eru PTs grew 37% slower compared to WT PTs at low [Ca2+]ext conditions. When grown on medium with increased [Ca2+]ext (2 mM CaCl2), both WT and eru PTs grew faster than in control conditions but no relative difference in average growth rate was seen (Figure 2C). Twenty minutes tracking of individual PT growth confirmed a consistently lower growth rate throughout the acquisition time (Figures 2D,E). Together, these findings indicate that ERU has a role in regulating PT growth velocity in response to [Ca2+]ext.


FIGURE 2. Wild type and eru PT growth rates differ in low [Ca2+]ext conditions. (A) WT and eru PT growth rate on standard (1 mM CaCl2), (B) low calcium (0.5 mM CaCl2), and (C) high calcium (2 mM CaCl2) growth medium. (D) PT growth dynamics of WT and eru PTs grown in low calcium (0.5 mM CaCl2) conditions. Individual traces are represented by black (WT) and orange (eru) lines. (E) Average of the PT growth dynamics presented in (D). Error bars represent SE. Different letters reflect a pairwise significant difference (α ≤ 0.05).

ERU Loss-Of-Function Alters Tip-Focused Calcium Oscillations in Growing PTs in Response to [Ca2+]ext

To further dissect ERU-mediated signal transduction in response to [Ca2+]ext, we visualized the tip-focused [Ca2+]cyt gradient in growing eru and WT PTs. The cytosol-targeted Yellow Cameleon 3.6 (NES-YC3.6) calcium sensor was introduced in eru and WT plants by Agrobacterium-mediated transformation and [Ca2+]cyt oscillations were visualized in in vitro growing PTs under low (0.5 mM), normal (1 mM), and high (2 mM) [Ca2+]ext (Figure 3). Kymograms of the recorded cytoplasmic calcium dynamics indicated that in all conditions oscillating tip-focused calcium gradients were present (Figure 3A). Fourier analysis of the acquired oscillograms revealed that WT and eru PTs showed similar oscillation frequencies (0.042 ± 0.002 and 0.039 ± 0.002 Hz, respectively) and amplitude (5.05 ± 0.12 and 4.96 ± 0.10, respectively) under control conditions (Figures 3B–E). In the presence of high [Ca2+]ext (2 mM CaCl2), oscillations occurred so rapidly that image acquisition every 5 sec could not resolve separate peaks (Figure 3A at the bottom). However, the average amplitude (5.48 ± 0.10 for WT PTs and 5.46 ± 0.10 for eru PTs) remained unaffected (Figure 3E). Strikingly, however, WT PTs responded to low [Ca2+]ext (0.5 mM CaCl2) by increasing their main oscillation frequency from 0.042 ± 0.002 to 0.048 ± 0.003 Hz (Figures 3B–D). Contrastingly, and in direct agreement with the average growth speed response, the main oscillation frequency in eru PTs decreased to 0.033 ± 0.002 Hz when subjected to low [Ca2+]ext (Figures 3B–D). Together, these results show that ERU is involved in regulating apical [Ca2+]cyt oscillations in response to [Ca2+]ext.


FIGURE 3. Analysis of [Ca2+]cyt oscillations at the tip of growing WT and eru PTs at different [Ca2+]ext. (A) Kymograph of 420 sec acquisitions showing regular [Ca2+]cyt oscillations at the tip of growing WT and mutant PTs when grown on medium containing 0.5 mM or 1 mM CaCl2. (B) Representative Fourier transform series of apical calcium dynamics in WT and eru PTs. Distinct main frequency peaks were observed at 0.5 and 1 mM, but not at 2 mM CaCl2. (C) Graphs showing the average of all acquired Fourier transform series. Curves were smoothed using a floating average with a period of 0.004 Hz. (D) Bar plot showing the main frequency of oscillation. Main Fourier frequency peaks were isolated from individual Fourier traces and averaged. Fourier analysis did not detect frequency peaks in PTs grown on 2 mM CaCl2. (E) Average [Ca2+]cyt signal amplitude. Error bars represent SE. Different letters reflect a pairwise significant difference (α ≤ 0.05).

The eru Loss-Of-Function Mutation Leads to Aberrant PT Targeting and Decreased Fertilization Competitiveness

Given the role of calcium-mediated cross-talk during the PTs journey through the transmitting tract toward the ovule, we investigated in vivo PT targeting of WT and eru pollen. We emasculated non-pollinated WT flowers, hand-pollinated them with WT or eru pollen and visualized in vivo grown PTs using aniline blue staining. ERU loss-of-function PTs grew through the WT transmitting tract in a WT-like manner. However, compared to WT PTs, eru PTs were more likely to show aberrant ovule targeting (Figures 4A,B). More specifically, proportionally more mutant PTs grew around the funiculus or made multiple turns before targeting the micropyle (Figure 4A). Defective targeting was independent of the PT length (Figure 4C). Hence, aberrant targeting was not skewed toward ovules that were either situated at the top or bottom of the ovary.


FIGURE 4. In Vivo PT targeting and fertilization efficiency of WT and eru pollen. (A) Classification of in vivo grown pollen tubes using aniline blue staining. More than 300 PTs originating from 10 (eru pollinated) or 13 (WT pollinated) ovaries were classified. PTs either grow straight toward the micropyle (M) or show abnormal targeting: turning around the funiculus (marked by ) or curling. Scale bars = 30 μm. (B) Quantification of the PT targeting phenotype. (C) Quantification of in vivo PT length for normal and abnormal targeted WT and eru PTs. (D) Result of heterozygous eru-plant self-pollination. Homozygous offspring was scored in the top and bottom half of the resulting siliques for three plants. Significance codes p-value: p = 0.05; ∗∗p = 0.01; ∗∗∗p < 0.001.

To understand the biological relevance of this phenotype, we quantified the transmission efficiency of the eru mutant allele versus that of the WT ERU allele. Plants that were heterozygous for the eru T-DNA insertion were allowed to self-pollinate and their progeny was screened toward the presence of the eru short RH phenotype. In addition, to gain insight into the distribution of mutant seeds along the silique, each silique was cut in half and both parts were examined separately. A smaller proportion of eru homozygotes in the bottom part of a silique would indicate slower growth of mutant PTs in vivo (Schiefelbein et al., 1993). We observed a strong deviation from the expected Mendelian inheritance ratio (25% eruHOM, 50% eruHET, and 25% WT) and found consistently more seedlings with a normal RH phenotype (86.1 ± 1.4% eruHET+ WT), and thus less homozygous eru progeny (13.9 ± 1.4% eruHOM) in both silique halves (Figure 4D), illustrating decreased fertilization efficiency of eru pollen. We observed no difference in inheritance ratio between the top and bottom silique parts. Given the complete lack of ovular ERU transcription (shown by public transcriptomics data and proERU::GUS expression), the altered eru transmission efficiency is ought to be specifically due to a PT defect (Figures 1A,B).

Together, these data show that ERU regulates PT targeting in vivo and is an important component of the fertilization pathway in Arabidopsis thaliana.


The PT and RH tip growth pathways likely share multiple regulatory components (Schiefelbein et al., 1993; Procissi et al., 2003; Becker et al., 2014; Schoenaers et al., 2017). The CrRLK1L family protein ERULUS was shown to have a crucial role in regulating RH morphogenesis in Arabidopsis thaliana (Bai et al., 2014a; Haruta et al., 2014). In agreement with public transcriptomics data (Figure 1A; Pina et al., 2005; Wang et al., 2008) we now found that ERU is also transcribed in mature pollen grains and growing PTs (Figure 1B). The ERU promoter contains several pollen-specific cis-elements (Supplementary Table 1) and, by GUS-staining of stably transformed WT x proERU::GUS lines, we showed that the promoter is highly active throughout PT development (Figure 1B). ERU transcription was not detected in any other flower tissues. Taken together, these data suggest that ERU functions specifically in tip growing cells.

Our promoter analysis also identified two canonical auxin response elements (AuxREs), which suggests auxin-regulated ERU transcription (Supplementary Table 1). Auxins are known to play a determining role in pollen development and PT growth (Pina et al., 2005; Cheng et al., 2006; Wu et al., 2008; Dal Bosco et al., 2012; Yang et al., 2013). Auxin regulates transcription through the action of ARF transcription factors. The latter bind directly to the consensus auxin response element TGTCTC (Ulmasov et al., 1997). Several ARFs are expressed in dry and germinated pollen (Supplementary Figure 3), suggesting that ERU transcription in pollen could be regulated by auxin through present ARFs binding to its promoter.

In RHs, loss of ERU function results in early growth cessation and RH bulging. As such, ERU was shown to be involved in regulating the tip growth stage of RH development. Our data now shows that ERU is also involved in regulating PT tip growth in response to the [Ca2+]ext. When grown on low [Ca2+]ext, eru PTs grew slower than WT PTs, but displayed a normal morphology. In addition, in vivo PT growth occurred normally regarding morphology up to the ovule targeting stage (see further). This relatively subtle growth phenotype stands in stark contrast to the eru RH phenotype. However, despite that fact that we do not know what is causing the eru PT growth defect, and the similarities between PT and RH tip growth, important differences between both apical growth regimes exist and could relate to the observed phenotypic difference (Schoenaers et al., 2017). To better understand the mechanism(s) related to affected eru PT growth we studied [Ca2+]cyt dynamics under different [Ca2+]ext.

At the apex of growing PTs, hyperpolarization activated calcium channels import calcium from the extracellular region (Véry and Davies, 2000; Qu et al., 2007) leading to a steep calcium gradient at the growing tip. Similar to RHs, the existence of such an oscillating tip-focused calcium gradient is essential to regulate PT growth speed and growth directionality (Bibikova et al., 1997; Holdaway-Clarke et al., 1997; Michard et al., 2011). Our results now show that both lower and higher than control [Ca2+]ext stimulated WT PT growth, whereas a different response was observed for eru PTs. Importantly, we found that the eru mutation affects the [Ca2+]cyt oscillations in response to [Ca2+]ext (Figure 3). When grown on low [Ca2+] medium, eru pollen grew slower than WT pollen (Figure 2) and exhibited regular yet lower frequency [Ca2+]cyt oscillations (Figure 3). The link between [Ca2+]ext, [Ca2+]cyt and PT growth is far from fully understood and as such we cannot provide a causal explanation for the observed differences. Whether ERU is directly or indirectly involved in the regulation of [Ca2+]cyt oscillations in growing PTs remains to be investigated. ERU loss-of-function roots grow short and stunted RHs which fail to accumulate apical cytoplasmic Ca2+. The latter is presumed to be a secondary defect due to a misbalance in ammonium transport across the tonoplast (Bai et al., 2014a). It’s important to consider that Ca2+-ions intersect with the tip growth pathway at several levels (Schoenaers et al., 2017). For instance, amongst a myriad of other responses, Ca2+ regulates cell wall plasticity through apoplastic pectin cross-linking and cytoplasmic activation of apoplastic ROS production (Rounds et al., 2011; Kaya et al., 2014). ERU has been suggested to regulate ROS production in RHs and members of the CrRLK1L family were suggested before to have a role in cell wall sensing (Lindner et al., 2012; Bai et al., 2014b; Nissen et al., 2016). As such, it would be interesting to investigate the effect of the [Ca2+]ext on ROS production and the cell wall in eru PTs.

Nevertheless, earlier findings suggested that [Ca2+]ext might be an important factor controling in vivo PT growth. Apoplastic Ca2+ levels (in Lily) and ACA13 transcription (coding for an Arabidopsis plasma membrane localized Ca2+-ATPase which exports Ca2+ into the apoplast) both increase in the transmitting tract upon pollination (Zhao et al., 2004; Iwano et al., 2014). Moreover, Ca2+-signaling/crosstalk is of central importance for PT guidance toward the ovule and the steps preceding successful fertilization (Iwano et al., 2012; Ngo et al., 2014). Given the role of ERU in PT tip growth, its involvement in regulating the response to extracellular calcium, and the importance of controlled PT growth in plant fertilization, we investigated whether eru PTs targeted the ovules and fertilized the eggs with an efficiency similar to that of WT PTs. Fertility strongly depends on successful directional tip growth and directional cues provided by the female tissue (Higashiyama and Takeuchi, 2015). Therefore PTs possess highly conserved and specific mechanisms to sense and integrate responses to their extracellular environment (Higashiyama and Takeuchi, 2015). Our results show that, in vivo, eru pollen are less competitive than WT pollen in terms of plant fertilization efficiency (Figure 4D). More so, we found that eru PTs grown through WT tissue show aberrant ovule targeting (Figures 4A,B). Hence, proportionally more mutant PTs grew around the funiculus or made multiple turns before targeting the micropyle (Figure 4A). The eru PT targeting and fertilization phenotypes are strikingly similar to what has been observed for the double lip1 lip2 mutant, which is defective in two PT plasma membrane localized RLKs (Liu et al., 2013). LIP1 and LIP2 are thought to be crucial components of the receptor complex regulating PT guidance in response to the micropyle-secreted AtLURE1 signaling peptide. Since both proteins are cytoplasmic, the LURE receptor remains to be identified. It is tempting to hypothesize that ERU could function as this receptor, and as such could regulate PT targeting in a complex with LIP1 and LIP2.

In the female synergids, a similar mechanism seems to exist. FER and LRE regulate PT attraction and PT/synergid crosstalk by perception of a yet to identify PT-derived ligand (Ngo et al., 2014; Liu et al., 2016). FER is thought to be the receptor for this ligand, whereas the cytoplasm localized, membrane-anchored EF-hand containing LRE has been hypothesized to form a complex with FER and regulate ligand-induced Ca2+ crosstalk between the PT and synergids.

Contrastingly, PTs targeted to fer (-/-) and lre (-/-) ovules show PT overgrowth inside the female tissue due to failed PT rupture rather than mistargeting prior to physical male-female contact (Huck et al., 2003; Liu et al., 2016). The latter suggests that FER- and ERU-mediated guidance are spatiotemporally separated events. As to investigate this presumption, it would be crucial to investigate PT targeting in double eru/fer mutant lines. This could lead to a better understanding of the different stages of PT/ovule cross-talk, and provide excellent knowledge on the signal pathways involved.

We identified ERU as an important component of the fertilization process in Arabidopsis. How ERU regulates in vivo PT targeting remains to be investigated. However, based on the common role of ERU in regulating [Ca2+]cyt dynamics in both RHs and PTs, the ubiquity of calcium signaling throughout the PT growth and fertilization pathway, and the Ca2+-associated role of other CrRLK1Ls during PT development, it is sensible to hypothesize that altered Ca2+ signaling in eru PTs could be an important aspect relating to the observed in vivo phenotype. Nevertheless, characterization of the direct mechanistic involvement of ERU in the PT targeting process is a key element to be addressed.

Author Contributions

SS and DB identified and phenotyped the mutant. SS and DB performed microscopy and gene expression studies. SS and AC performed calcium measurements. SS and DB analyzed the data and KV wrote the article with contribution from SS, DB, and AC. SS, DB, AC, and KV conceived the project and KV supervised the research.


This work was supported by University of Antwerp (UA) research grants to SS and DB, by the Research Foundation Flanders (FWO-Vlaanderen) and by Università degli Studi di Milano, Piano di Sviluppo di Ateneo 2015 and 2016 to AC, Fonds Wetenschappelijk Onderzoek (G.0656.13N, G.0.602.11.N.10, and, and Universiteit Antwerpen (DOCPRO4 and BOF/NOI/LP/DOCPRO). The research leading to these results has received funding from LASERLAB-EUROPE (grant agreement no. 654148, European Union’s Horizon 2020 research and innovation programme).

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

The reviewer MH and handling Editor declared their shared affiliation.

Supplementary Material

The Supplementary Material for this article can be found online at:


  1. ^
  2. ^


Amien, S., Kliwer, I., Márton, M. L., Debener, T., Geiger, D., Becker, D., et al. (2010). Defensin-like ZmES4 mediates pollen tube burst in maize via opening of the potassium channel KZM1. PLOS Biol. 8:e1000388. doi: 10.1371/journal.pbio.1000388

PubMed Abstract | CrossRef Full Text | Google Scholar

Bai, L., Ma, X., Zhang, G., Song, S., Zhou, Y., Gao, L., et al. (2014a). A receptor-like kinase mediates ammonium homeostasis and is important for the polar growth of root hairs in Arabidopsis. Plant Cell 26, 1497–1511. doi: 10.1105/tpc.114.124586

PubMed Abstract | CrossRef Full Text | Google Scholar

Bai, L., Zhou, Y., Ma, X., Gao, L., and Song, C. P. (2014b). Arabidopsis CAP1-mediated ammonium sensing required reactive oxygen species in plant cell growth. Plant Signal. Behav. 9:e29582. doi: 10.4161/psb.29582

PubMed Abstract | CrossRef Full Text | Google Scholar

Becker, J. D., Takeda, S., Borges, F., Dolan, L., and Feijó, J. A. (2014). Transcriptional profiling of Arabidopsis root hairs and pollen defines an apical cell growth signature. BMC Plant Biol. 14:197. doi: 10.1186/s12870-014-0197-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Bibikova, T. N., Zhigilei, A., and Gilroy, S. (1997). Root hair growth in Arabidopsis thaliana is directed by calcium and an endogenous polarity. Planta 203, 495–505. doi: 10.1007/s004250050219

PubMed Abstract | CrossRef Full Text | Google Scholar

Cheng, Y., Dai, X., and Zhao, Y. (2006). Auxin biosynthesis by the YUCCA flavin monooxygenases controls the formation of floral organs and vascular tissues in Arabidopsis. Genes Dev. 20, 1790–1799. doi: 10.1101/gad.1415106

PubMed Abstract | CrossRef Full Text | Google Scholar

Clough, S. J., and Bent, A. F. (1998). Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana. Plant J. 16, 735–743. doi: 10.1046/j.1365-313x.1998.00343.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Dal Bosco, C., Dovzhenko, A., Liu, X., Woerner, N., Rensch, T., Eismann, M., et al. (2012). The endoplasmic reticulum localized PIN8 is a pollen-specific auxin carrier involved in intracellular auxin homeostasis. Plant J. 71, 860–870. doi: 10.1111/j.1365-313X.2012.05037.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Damineli, D. S. C., Portes, M. T., and Feijó, J. A. (2017). Oscillatory signatures underlie growth regimes in Arabidopsis pollen tubes: computational methods to estimate tip location, periodicity, and synchronization in growing cells. J. Exp. Bot. 68, 3267–3281. doi: 10.1093/jxb/erx032

PubMed Abstract | CrossRef Full Text | Google Scholar

Denninger, P., Bleckmann, A., Lausser, A., Vogler, F., Ott, T., Ehrhardt, D. W., et al. (2014). Male-female communication triggers calcium signatures during fertilization in Arabidopsis. Nat. Commun. 5:4645. doi: 10.1038/ncomms5645

PubMed Abstract | CrossRef Full Text | Google Scholar

Hamamura, Y., Nishimaki, M., Takeuchi, H., Geitmann, A., Kurihara, D., and Higashiyama, T. (2014). Live imaging of calcium spikes during double fertilization in Arabidopsis. Nat. Commun. 5:4722. doi: 10.1038/ncomms5722

PubMed Abstract | CrossRef Full Text | Google Scholar

Haruta, M., Sabat, G., Stecker, K., Minkoff, B. B., and Sussman, M. R. (2014). A peptide hormone and its receptor protein kinase regulate plant cell expansion. Science 343, 408–411. doi: 10.1126/science.1244454

PubMed Abstract | CrossRef Full Text | Google Scholar

Higashiyama, T., and Takeuchi, H. (2015). The mechanism and key molecules involved in pollen tube guidance. Annu. Rev. Plant Biol. 66, 393–413. doi: 10.1146/annurev-arplant-043014-115635

PubMed Abstract | CrossRef Full Text | Google Scholar

Holdaway-Clarke, T. L., Feijo, J. A., Hackett, G. R., Kunkel, J. G., and Hepler, P. K. (1997). Pollen tube growth and the intracellular cytosolic calcium gradient oscillate in phase while extracellular calcium influx is delayed. Plant Cell 9, 1999–2010. doi: 10.1105/tpc.9.11.1999

PubMed Abstract | CrossRef Full Text | Google Scholar

Hruz, T., Laule, O., Szabo, G., Wessendorp, F., Bleuler, S., Oertle, L., et al. (2008). Genevestigator V3: a reference expression database for the meta-analysis of transcriptomes. Adv. Bioinformatics 2008:420747. doi: 10.1155/2008/420747

PubMed Abstract | CrossRef Full Text | Google Scholar

Huck, N., Moore, J. M., Federer, M., and Grossniklaus, U. (2003). The Arabidopsis mutant feronia disrupts the female gametophytic control of pollen tube reception. Development 130, 2149–2159. doi: 10.1242/dev.00458

PubMed Abstract | CrossRef Full Text | Google Scholar

Iwano, M., Entani, T., Shiba, H., Kakita, M., Nagai, T., Mizuno, H., et al. (2009). Fine-tuning of the cytoplasmic Ca2+ concentration is essential for pollen tube growth. Plant Physiol. 150, 1322–1334. doi: 10.1104/pp.109.139329

PubMed Abstract | CrossRef Full Text | Google Scholar

Iwano, M., Igarashi, M., Tarutani, Y., Kaothien-Nakayama, P., Nakayama, H., Moriyama, H., et al. (2014). A pollen coat-inducible autoinhibited Ca2+-ATPase expressed in stigmatic papilla cells is required for compatible pollination in the Brassicaceae. Plant Cell 26, 636–649. doi: 10.1105/tpc.113.121350

PubMed Abstract | CrossRef Full Text | Google Scholar

Iwano, M., Ngo, Q. A., Entani, T., Shiba, H., Nagai, T., Miyawaki, A., et al. (2012). Cytoplasmic Ca2+ changes dynamically during the interaction of the pollen tube with synergid cells. Development 139, 4202–4209. doi: 10.1242/dev.081208

PubMed Abstract | CrossRef Full Text | Google Scholar

Jefferson, R. A., Kavanagh, T. A., and Bevan, M. W. (1987). GUS fusions: beta-glucuronidase as a sensitive and versatile gene fusion marker in higher plants. EMBO J. 6, 3901–3907.

PubMed Abstract | Google Scholar

Kaya, H., Nakajima, R., Iwano, M., Kanaoka, M. M., Kimura, S., Takeda, S., et al. (2014). Ca2+-activated reactive oxygen species production by Arabidopsis RbohH and RbohJ is essential for proper pollen tube tip growth. Plant Cell 26, 1069–1080. doi: 10.1105/tpc.113.120642

PubMed Abstract | CrossRef Full Text | Google Scholar

Krebs, M., Held, K., Binder, A., Hashimoto, K., Den Herder, G., Parniske, M., et al. (2012). FRET-based genetically encoded sensors allow high-resolution live cell imaging of Ca2+ dynamics. Plant J. 69, 181–192. doi: 10.1111/j.1365-313X.2011.04780.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Lindner, H., Müller, L. M., Boisson-Dernier, A., and Grossniklaus, U. (2012). CrRLK1L receptor-like kinases: not just another brick in the wall. Curr. Opin. Plant Biol. 15, 659–669. doi: 10.1016/j.pbi.2012.07.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, J., Zhong, S., Guo, X., Hao, L., Wei, X., Huang, Q., et al. (2013). Membrane-bound RLCKs LIP1 and LIP2 are essential male factors controlling male-female attraction in Arabidopsis. Curr. Biol. 23, 993–998. doi: 10.1016/j.cub.2013.04.043

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, X., Castro, C. A., Wang, Y., Noble, J. A., Ponvert, N. D., Bundy, M. G. R., et al. (2016). The role of LORELEI in pollen tube reception at the interface of the synergid cell and pollen tube requires the modified eight-cysteine motif and the receptor-like kinase FERONIA. Plant Cell 28, 1035–1052. doi: 10.1105/tpc.15.00703

PubMed Abstract | CrossRef Full Text | Google Scholar

Mangano, S., Juarez, S. P. D., and Estevez, J. M. (2016). ROS regulation of polar-growth in plant cells. Plant Physiol. 171, 1593–1605. doi: 10.1104/pp.16.00191

PubMed Abstract | CrossRef Full Text | Google Scholar

Michard, E., Lima, P. T., Borges, F., Silva, A. C., Portes, M. T., Carvalho, J. E., et al. (2011). Glutamate receptor-like genes form Ca2+ channels in pollen tubes and are regulated by pistil D-serine. Science 332, 434–437. doi: 10.1126/science.1201101

PubMed Abstract | CrossRef Full Text | Google Scholar

Miyazaki, S., Murata, T., Sakurai-Ozato, N., Kubo, M., Demura, T., Fukuda, H., et al. (2009). ANXUR1 and 2, sister genes to FERONIA/SIRENE, are male factors for coordinated fertilization. Curr. Biol. 19, 1327–1331. doi: 10.1016/j.cub.2009.06.064

PubMed Abstract | CrossRef Full Text | Google Scholar

Mori, T., Kuroiwa, H., Higashiyama, T., and Kuroiwa, T. (2006). Generative Cell Specific 1 is essential for angiosperm fertilization. Nat. Cell Biol. 8, 64–71. doi: 10.1038/ncb1345

PubMed Abstract | CrossRef Full Text | Google Scholar

Nakagawa, T., Kurose, T., Hino, T., Tanaka, K., Kawamukai, M., Niwa, Y., et al. (2007). Development of series of gateway binary vectors, pGWBs, for realizing efficient construction of fusion genes for plant transformation. J. Biosci. Bioeng. 104, 34–41. doi: 10.1263/jbb.104.34

PubMed Abstract | CrossRef Full Text | Google Scholar

Ngo, Q. A., Vogler, H., Lituiev, D. S., Nestorova, A., and Grossniklaus, U. (2014). A calcium dialog mediated by the FERONIA signal transduction pathway controls plant sperm delivery. Dev. Cell 29, 491–500. doi: 10.1016/j.devcel.2014.04.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Nissen, K. S., Willats, W. G. T., and Malinovsky, F. G. (2016). Understanding CrRLK1L function: cell walls and growth control. Trends Plant Sci. 21, 516–527. doi: 10.1016/j.tplants.2015.12.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Obermeyer, G., and Feijó, J. (2017). Pollen Tip Growth: From Biophysical Aspects to Systems Biology. Berlin: Springer.

Google Scholar

Okuda, S., Tsutsui, H., Shiina, K., Sprunck, S., Takeuchi, H., Yui, R., et al. (2009). Defensin-like polypeptide LUREs are pollen tube attractants secreted from synergid cells. Nature 458, 357–361. doi: 10.1038/nature07882

PubMed Abstract | CrossRef Full Text | Google Scholar

Pina, C., Pinto, F., Feijó, J. A., and Becker, J. D. (2005). Gene family analysis of the Arabidopsis pollen transcriptome reveals biological implications for cell growth, division control, and gene expression regulation. Plant Physiol. 138, 744–756. doi: 10.1104/pp.104.057935

PubMed Abstract | CrossRef Full Text | Google Scholar

Procissi, A., Guyon, A., Pierson, E. S., Giritch, A., Knuiman, B., Grandjean, O., et al. (2003). Kinky Pollen encodes a Sabre-like protein required for tip growth in Arabidopsis and conserved among eukaryotes. Plant J. 36, 894–904. doi: 10.1046/j.1365-313X.2003.01933.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Qin, P., Ting, D., Shieh, A., and McCormick, S. (2012). Callose plug deposition patterns vary in pollen tubes of Arabidopsis thaliana ecotypes and tomato species. BMC Plant Biol. 12:178. doi: 10.1186/1471-2229-12-178

PubMed Abstract | CrossRef Full Text | Google Scholar

Qu, H. Y., Shang, Z. L., Zhang, S. L., Liu, L. M., and Wu, J. Y. (2007). Identification of hyperpolarization-activated calcium channels in apical pollen tubes of Pyrus pyrifolia. New Phytol. 174, 524–536. doi: 10.1111/j.1469-8137.2007.02069.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Qu, L.-J., Li, L., Lan, Z., and Dresselhaus, T. (2015). Peptide signalling during the pollen tube journey and double fertilization. J. Exp. Bot. 66, 5139–5150. doi: 10.1093/jxb/erv275

PubMed Abstract | CrossRef Full Text | Google Scholar

R Core Team (2008). R: A Language and Environment for Statistical Computing. Vienna: R Foundation for Statistical Computing.

Google Scholar

Rodriguez-Enriquez, M., Mehdi, S., Dickinson, H., and Grant-Downtown, R. (2012). A novel method for efficient in vitro germination and tube growth of Arabidopsis thaliana pollen. New Phytol. 197, 668–679. doi: 10.1111/nph.12037

PubMed Abstract | CrossRef Full Text | Google Scholar

Rounds, C. M., Lubeck, E., Hepler, P. K., and Winship, L. J. (2011). Propidium iodide competes with Ca2+ to label pectin in pollen tubes and Arabidopsis root hairs. Plant Physiol. 157, 175–187. doi: 10.1104/pp.111.182196

PubMed Abstract | CrossRef Full Text | Google Scholar

Schiefelbein, J., Galway, M., Masucci, J., and Ford, S. (1993). Pollen tube and root-hair tip growth is disrupted in a mutant of Arabidopsis thaliana. Plant Physiol. 103, 979–985. doi: 10.1104/pp.103.3.979

PubMed Abstract | CrossRef Full Text | Google Scholar

Schiott, M., Romanowsky, S. M., Baekgaard, L., Jakobsen, M. K., Palmgren, M. G., and Harper, J. F. (2004). A plant plasma membrane Ca2+ pump is required for normal pollen tube growth and fertilization. Proc. Natl. Acad. Sci. U.S.A. 101, 9502–9507. doi: 10.1073/pnas.0401542101/r0401542101

CrossRef Full Text | Google Scholar

Schneider, C. A., Rasband, W. S., and Eliceiri, K. W. (2012). NIH Image to ImageJ: 25 years of image analysis. Nat. Methods 9, 671–675.

Google Scholar

Schoenaers, S., Balcerowicz, D., and Vissenberg, K. (2017). “Molecular mechanisms regulating root hair tip growth: a comparison with pollen tubes,” in Pollen Tip Growth: From Biophysical Aspects to Systems Biology, eds G. Obermeyer and J. Feijo (Berlin: Springer), 167–243.

Google Scholar

Takeuchi, H., and Higashiyama, T. (2016). Tip-localized receptors control pollen tube growth and LURE sensing in Arabidopsis. Nature 531, 245–248. doi: 10.1038/nature17413

PubMed Abstract | CrossRef Full Text | Google Scholar

Ulmasov, T., Hagen, G., and Guilfoyle, T. J. (1997). ARF1, a transcription factor that binds to auxin response elements. Science 276, 1865–1868. doi: 10.1126/science.276.5320.1865

PubMed Abstract | CrossRef Full Text | Google Scholar

Véry, A. A., and Davies, J. M. (2000). Hyperpolarization-activated calcium channels at the tip of Arabidopsis root hairs. Proc. Natl. Acad. Sci. U.S.A. 97, 9801–9806. doi: 10.1073/pnas.160250397

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, Y., Zhang, W.-Z., Song, L.-F., Zou, J.-J., Su, Z., and Wu, W.-H. (2008). Transcriptome analyses show changes in gene expression to accompany pollen germination and tube growth in Arabidopsis. Plant Physiol. 148, 1201–1211. doi: 10.1104/pp.108.126375

PubMed Abstract | CrossRef Full Text | Google Scholar

Winter, D., Vinegar, B., Nahal, H., Ammar, R., Wilson, G., and Provart, N. (2007). An “electronic fluorescent pictograph” browser for exploring and analyzing large-scale biological data sets. PLOS ONE 2:e718. doi: 10.1371/journal.pone.0000718

PubMed Abstract | CrossRef Full Text | Google Scholar

Wu, J.-Z., Lin, Y., Zhang, X.-L., Pang, D.-W., and Zhao, J. (2008). IAA stimulates pollen tube growth and mediates the modification of its wall composition and structure in Torenia fournieri. J. Exp. Bot. 59, 2529–2543. doi: 10.1093/jxb/ern119

PubMed Abstract | CrossRef Full Text | Google Scholar

Yang, J., Tian, L., Sun, M.-X., Huang, X.-Y., Zhu, J., Guan, Y.-F., et al. (2013). AUXIN RESPONSE FACTOR17 is essential for pollen wall pattern formation in Arabidopsis. Plant Physiol. 162, 720–731. doi: 10.1104/pp.113.214940

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhao, J., Yang, H. Y., and Lord, E. M. (2004). Calcium levels increase in the lily stylar transmitting tract after pollination. Sex. Plant Reprod. 16, 259–263. doi: 10.1007/s00497-003-0193-5

CrossRef Full Text | Google Scholar

Keywords: ERULUS, calcium, fertilization, kinase, pollen tube, tip growth

Citation: Schoenaers S, Balcerowicz D, Costa A and Vissenberg K (2017) The Kinase ERULUS Controls Pollen Tube Targeting and Growth in Arabidopsis thaliana. Front. Plant Sci. 8:1942. doi: 10.3389/fpls.2017.01942

Received: 01 September 2017; Accepted: 27 October 2017;
Published: 14 November 2017.

Edited by:

Simon Gilroy, University of Wisconsin–Madison, United States

Reviewed by:

Miyoshi Haruta, University of Wisconsin-Madison, United States
Viktor Zarsky, Charles University, Czechia

Copyright © 2017 Schoenaers, Balcerowicz, Costa and Vissenberg. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Kris Vissenberg,