Development in multicellular organisms depends on the ability of individual cells to coordinate their behavior by means of small signaling molecules to form correctly patterned tissues. In plants, a unique mechanism of directional transport of the signaling molecule auxin between cells connects cell polarity and tissue patterning and thus is required for many aspects of plant development. Direction of auxin flow is determined by polar subcellular localization of PIN auxin efflux transporters. Dynamic PIN polar localization results from the constitutive endocytic cycling to and from the plasma membrane, but it is not well understood how this mechanism connects to regulators of cell polarity. The Rho family small GTPases ROPs/RACs are master regulators of cell polarity, however their role in regulating polar protein trafficking and polar auxin transport has not been established. Here, by analysis of mutants and transgenic plants, we show that the ROP interactor and polarity regulator scaffold protein ICR1 is required for recruitment of PIN proteins to the polar domains at the plasma membrane. icr1 mutant embryos and plants display an a array of severe developmental aberrations that are caused by compromised differential auxin distribution. ICR1 functions at the plasma membrane where it is required for exocytosis but does not recycle together with PINs. ICR1 expression is quickly induced by auxin but is suppressed at the positions of stable auxin maxima in the hypophysis and later in the embryonic and mature root meristems. Our results imply that ICR1 is part of an auxin regulated positive feedback loop realized by a unique integration of auxin-dependent transcriptional regulation into ROP-mediated modulation of cell polarity. Thus, ICR1 forms an auxin-modulated link between cell polarity, exocytosis, and auxin transport-dependent tissue patterning.
The coordination of different cells during pattern formation is a fundamental process in the development of multicellular organisms. In plants, a unique mechanism of directional transport of the signaling molecule auxin between cells demonstrates the importance of cell polarity for tissue patterning. The direction of auxin flow is determined by polar subcellular localization of auxin transport proteins called PINs, which facilitate auxin efflux. At the same time, an auxin-mediated positive feedback mechanism reinforces the polar distribution of PINs. However, the molecular mechanisms that underlie polar PIN localization are not well understood. In eukaryotic cells, the Rho family of small GTPases function as central regulators of cell polarity. We show that a Rho-interacting protein from plants, called ICR1, is required for recruitment via the secretory system of PIN proteins to polar domains in the cell membrane. As a result, ICR1 is required for directional auxin transport and distribution and thereby for proper pattern formation. In addition, both the expression and subcellular localization of ICR1 are regulated by auxin, suggesting that ICR1 could function in a positive feedback loop that reinforces auxin distribution. Thus, ICR1 forms an auxin-modulated link between cell polarity, protein secretion, and auxin-dependent tissue patterning.
Citation: Hazak O, Bloch D, Poraty L, Sternberg H, Zhang J, et al. (2010) A Rho Scaffold Integrates the Secretory System with Feedback Mechanisms in Regulation of Auxin Distribution. PLoS Biol 8(1): e1000282. doi:10.1371/journal.pbio.1000282
Academic Editor: Ottoline Leyser, University of York, United Kingdom
Received: June 2, 2009; Accepted: December 9, 2009; Published: January 19, 2010
Copyright: © 2010 Hazak et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by Israel Science Foundation (ISF-312/07) (http://www.isf.org.il/), US-Israel Binational Research and Development fund (BARD-IS-4032-07) (http://www.bard-isus.com/), and the Deutschland-Israel Program (DIP-H.3.1) to SY. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Abbreviations: ARF, ADP ribosylation factor; BFA, brefeldin A; bp, base pair; CA, Constitutive Active; CLSM, Confocal Laser Scanning Microscope; Col-0, Columbia-0; DAG, days after germination; DIC, Differential Interference Contrast; FRAP, Fluorescence Recovery After Photobleaching; GEF, Guanine Nucleotide Exchange Factor; GFP, Green Fluorescent Protein; GUS, βGlucoronidase; HLR, HALTEDROOT; ICR1, Interactor of Constitutive active ROP 1; MS, Murashige & Skoog; MT, microtubules; NAA, Naphthalene Acetic Acid; NPA, 1-N-naphthylphthalamic acid; PI, Propidium Iodide; PID, PINOID; PIN, PINFORMED; PtdIns P-K, phosphatidylinositol monophosphate kinase; QC, quiescent center; q-PCR, Quantitative Real-Time RT-PCR; RIP1, ROP Interacting Protein 1; ROP, Rho of Plants; ROS, Reactive Oxygen Species; SCR, SCARECRAW; SHR, SHORTROOT; UTR, Untranslated Region; WOX5, WUSCHEL related homeobox 5; WT, wild type
ROP (Rho of Plants), also known as RAC GTPases, have been implicated as master regulators of cell polarity ,. In their GTP-bound, active state, ROPs interact with downstream effector proteins to regulate organization of actin and microtubules (MT), vesicle trafficking, production of phosphoinositides, and gradients of reactive oxygen species (ROS) and Ca2+ –. ROPs function at the plasma membrane to which they attach by virtue of posttranslational lipid modifications prenylation and S-acylation ,–. The ability of ROPs to interact with membranes allows these proteins to regulate actin polymerization and vesicle trafficking at discrete sites of the plasma membrane and of internal membranes, which is essential for their role in the control of cell polarity . ROPs are polarly localized and expression of activated dominant ROP mutants that cannot hydrolyze GTP compromises cell polarization – and inhibits endocytic vesicle recycling . Due to their essential role in generation of cell polarity, it was plausible that ROPs also regulate distribution of polar cargos including PIN auxin efflux transporters .
We have previously identified a ROP interacting coiled coil domain scaffold protein Interactor of Constitutive active ROP 1 (ICR1) and demonstrated that it affects cell polarity . Recently, ICR1/RIP1 has been implicated as a regulator of polar pollen tube growth . The primary root meristem of icr1 mutant and RNAi silenced plants collapses soon after germination, resembling mutants affected in basal localization of PIN proteins and multiple pin loss-of-function mutants . These results suggested that ICR1 might form a link between Rho-regulated cell polarity and polar auxin transport.
Auxin is the major signal for tissue polarity and patterning in plants. Polar auxin transport and resulting asymmetric auxin distribution within tissues (auxin maxima and gradients) are essential for proper development of the embryo, the root, and the shoot, differentiation and regeneration of vascular tissues, and for tropic responses –. Directionality of auxin transport depends on polar subcellular distribution of PINFORMED (PIN) family of efflux transporters ,,. Dynamic PIN polarity is a result of constitutive endocytic recycling. Recycling to the membrane requires the function of the brefeldin A (BFA)-sensitive ADP ribosylation factor GDP/GTP Exchange Factors (ARF GEFs) ,. The endocytic step is clathrin dependent and requires function of endosomal Rab5/Ara7 ,. However, little is known on how PIN recycling is directed to result in their polar distribution.
In this work we show that ICR1 is an essential component of the auxin transport machinery functioning in exocytosis and as a part of an auxin modulated feedback loop. Thus, ICR1 links between Rho-regulated cell polarity and auxin associated pattern formation.
Auxin Distribution in icr1 Roots
To address the potential function of ICR1 in auxin transport, we examined auxin distribution in wild type (WT) Col-0 and icr1 mutant plants using the auxin sensitive reporters DR5::GUS and DR5rev::GFP ,. The formation of the DR5-visualized auxin maximum in the quiescent center (QC) and proximal columella cells is required for root meristem maintenance and correct tissue patterning . In young 2 days after germination (DAG) icr1 roots the auxin maximum was displaced towards the distal tier of root cap and was reduced (Figure 1A and B). Concomitant with the reduction of the auxin maximum at the root tip, it started to accumulate in the vascular bundle (Figure 1A). In older (14 DAG) roots auxin accumulated in the vascular bundle but did not reach the tip (Figure 1A). These results suggested that the collapse of the root meristem in icr1 plants resulted from compromised auxin transport and in-turn gradual disappearance of the auxin maximum at the root tip.
(A) DR5::GUS in WT and 2 and 14-d-old icr1 seedlings. (B) DR5rev::ER-GFP in WT and 2-d-old icr1 seedlings. Note the displacement of the auxin maximum toward the root cup in icr1 (B) and the accumulation of auxin signal in the stele (A). In 14-d-old plants auxin did not reach the meristem and accumulated in the stele (A brackets). Bars correspond to 50 µm.
Columella Specification in icr1
The specification of the columella at the root tip is closely associated with the formation of a stable auxin maximum . Columella cells contain starch granules that can be easily identified by staining of roots with Lugol staining (IKI). No starch granules were detected in the collapsed primary roots of icr1 , indicating that columella identity was lost. Because the stable auxin maximum was displaced in icr1 embryos and roots, it was plausible that columella cells may be specified in young roots but would later disappear, concomitant with the proximal shift of the auxin maximum. To examine the specification of the columella cells, the existence of starch granules was examined in WT and icr1 roots at 2, 4, and 6 DAG (Figure 2). In 2 DAG seedlings, starch granules were detected in two cell tiers, in both WT and icr1 root tips. At 4 DAG, starch granules were detected in 3 cell tiers of WT plants but remained confined to 2 cell tiers in the icr1 roots. Furthermore, the columella initials could not be detected in icr1. At 6 DAG, WT roots had 4 columella cell tiers, while starch granules were barely detected or absent in the icr1 roots (Figure 2). These results indicate that columella identity is initially specified in icr1 root tip cells and then gradually disappears, concomitant with the diminishing local auxin maximum.
Lugol's (IKI) staining was used for detection of starch granules in 2, 4, and 6 DAG WT and icr1 seedlings. In WT roots, the number of columella tiers containing starch granules increase with the age of seedlings (arrows). In icr1 roots, at 2 DAG, two tiers of cells containing starch granules could be detected (arrows), whereas at older stages starch granules staining decreased and almost completely disappears at 6 DAG (arrowhead). The bar corresponds to 50 µM for all images.
Development of icr1 Embryos
In plants, the polar shoot to root axis and the primary shoot and root meristems develop during embryogenesis. These developmental processes are associated with stereotypical series of cell divisions and gene expression and depend on auxin distribution . Development of WT and icr1 mutant embryos was analyzed to further establish the role of ICR1 in auxin distribution and embryo development. About 10% (27/273) of the icr1 embryos showed defects in stereotypic cell divisions of the basal embryo pole at the globular stage as well as abnormal divisions in the suspensor, including the uppermost cell, which forms hypophysis (Figure 3A and Figure S1). The majority (90%, 246/273) of the mutant embryos developed normally through the globular stage (Figure S2 and Table S1). From the triangular stage and onward, abnormal divisions of the suspensor, QC and columella cells were detected. Moreover, abnormal division planes were observed in the protoderm at the position of future cotyledons (Figure 3A, Figure S2, and Table S1). The variable penetrance of the icr1 mutation also resulted in reduced developmental synchronization of embryos within single siliques. Whereas in WT siliques the embryos were found in two to three developmental stages, in icr1 siliques the embryos were spread between four and five stages (Figure S3), indicating that developmental delay in icr1 occurs at different stages. The data suggested that the loss of ICR1 function results in a gradient of phenotypic defects primarily at the places of auxin maxima and in processes requiring differential auxin distribution.
(A) Early and late patterning defects in icr1, as revealed by Nomarsky DIC of cleared embryos. Approximately 10% of icr1 embryos showed early developmental defects at the globular stage. Arrows denote abnormal cell divisions in the suspensor and hypophysis. The majority (90%) of the embryos developed normally up to the triangular stage. At the heart stage, abnormal cell divisions in the embryonic root meristem are seen (arrows). Note the non-steriotipic divisions of the protoderm in the cotyledons (arrowheads). (B) Auxin distribution in icr1 embryos revealed by the DR5rev::ER-GFP marker. Arrow indicates shift in auxin maxima toward the low columella layers. Arrowheads point to the strong auxin signals at the tip of the cotyledons. Insets are single confocal scans throughout the middle of the embryonic root meristem showing the reduced auxin accumulation in QC and upper columella layers. (C) Expression of the QC marker pWOX5::ER-GFP. Arrowheads denote altered accumulation in heart and mature icr1 embryos. (D) Expression of the endodermis marker pSCR::YFP-H2b. Arrowheads indicate spreading of the marker to adjacent cell layers in icr1. Bars correspond to 10 µm (A), 20 µm (B), and 50 µm (C and D). For additional information and high resolution images, see Figures S1, S2, S3, S4, S5, S6.
Auxin Distribution in icr1 Embryos
Next we examined the auxin distribution in embryos to determine its association with the icr1 phenotype (Figure 3B and Figure S4). In comparison to WT, in the icr1 embryos the auxin response maximum was shifted distally from the QC to the lower tier of the future columella cells (Figure 3B, arrow). Furthermore, ectopically strong DR5 activity was detected at the tip of the cotyledons (Figure 3B, arrowheads, and Figure S4). The abnormal auxin distribution coincided with the non-stereotypic divisions of the future root meristem, further suggesting that the developmental abnormalities in icr1 result from compromised auxin distribution.
Patterning of icr1 Embryos and Roots
Root and embryo patterning and QC maintenance depend on highly specific expression pattern and subcellular localization of transcriptional regulators, including WOX5 (WUSCHEL related homeobox 5) and SCR (SCARECRAW), that define the stem cell niche –. In roots, formation of a stable auxin maximum is required for correct expression pattern of WOX5, SCR, and an additional marker SHORTROOT (SHR) ,. To verify that ICR1 is indeed involved in regulation of auxin distribution rather than this gene network, the expression of WOX5 and SCR in embryos was examined (Figure 3C and 3D and Figures S5 and S6). Both WOX5 and SCR were expressed in the icr1 mutant embryos, but their expression pattern was altered, reflecting changes in cell identity and disruption of the embryo polar axis. The embryo development and auxin response further suggested that the alterations in icr1 mutant plants are related to defects in auxin distribution.
To further establish that the altered patterning in icr1 mutants resulted from compromised auxin transport rather than the genetic framework that regulates root development, we compared the expression of WOX5, SCR, and SHR in WT and icr1 roots. This analysis showed that like in embryos, all the three markers were expressed in the icr1 roots (Figure 4). Similar to laser ablation experiments of the root meristem , expression of WOX5, SCR, and SHR appeared at more proximal locations in older, 14-d-old, icr1 roots and was associated with a formation of a new auxin maximum (Figure 4A–C and Figure 1). The abnormal expression pattern of WOX5, SCR, and SHR in roots further suggested that the compromised root development of icr1 is associated with altered auxin distribution.
In icr1 roots, expression of the QC and stem cells markers pWOX5::ER-GFP (A), pSHR::YFP-SHR (B), and pSCR::YFP-H2b (C) spread to the neighboring cells in 2- to 4-d-old seedlings and was diminished in old (14-d-old) roots meristems and coincidently appeared at more apical locations at the sites of auxin accumulation (brackets). Note the expression and cytoplasmic localization of SHR in epidermis (arrowheads). (D) Expression pattern of pPIN1::GFP-PIN1 in WT and icr1 roots. Note the abnormal expression pattern of GFP-PIN1 in the epidermis and root hairs in icr1 roots (arrowheads). (E) Irregular spacing (right inset) and arrested growth of lateral roots soon after emergence seen in an icr1 mutant plant. Note the abnormal expression pattern of WOX5 in the icr1 lateral root primordia (insets). Bars correspond to 50 µm.
To further examine the function of ICR1 in root patterning, we examined the expression pattern of PIN1 in icr1 roots. In the root, PIN1 is expressed mainly in the vascular cylinder. In icr1 mutant roots, however, pPIN1-driven PIN1-GFP expression was detected also in the epidermis and root hairs where it formed intracellular aggregates (Figure 4D). The mis-expression of PIN1 was a further indication that the altered auxin distribution in icr1 mutant plants resulted from compromised auxin transport and is not an indirect effect of perturbations in auxin-independent patterning mechanisms.
Lateral Root Development in icr1
The initiation and growth of lateral roots are separable events that depend on local auxin accumulation and polar transport ,. Given the function of ICR1 in primary root development, it was plausible that it would affect development of lateral roots. The primary root of icr1 mutant plants collapses before formation of lateral roots. However, the mutant plants develop adventitious roots that grow for some time and then collapse . The formation of these adventitious roots is preceded by formation of local auxin maxima (unpublished data). Lateral roots were initiated on these adventitious roots, but their growth was arrested after emergence (Figure 4E). Often, multiple initiations of lateral roots were observed (Figure 4E, inset), indicating that the onset as well as growth of lateral roots was perturbed in icr1. In the icr1 arrested lateral roots, WOX5 was mis-expressed (Figure 4E, compare left and right panels), indicating that the new root meristem was not properly setup. Taken together, these results indicate that in icr1 mutant plants the basic genetic framework that regulates root development is present and that the root meristem collapse, the altered organ development, and changes in cell identities can be attributed primarily to the compromised auxin distribution.
The function of roots as an auxin sink has long been postulated to play a major role in vascular differentiation . The “canalization hypothesis,” which became a hallmark for explaining auxin-dependent patterning, postulates that differentiation and regeneration of vascular tissues depend on an auxin-regulated positive feedback loop ,,. That is, auxin induces a process that enhances its own transport from cells while inhibiting its transport in neighboring cells. This process eventually leads to the formation of auxin transporting cell files that differentiate into vascular tissues. Given the involvement of ICR1 in auxin transport, we suspected that the vascular tissues in icr1 mutant plants would be abnormal. Transverse sections through rosette leaves were prepared to compare the vascular tissues in WT and icr mutant plants. Analysis of these sections showed that the leaf veins in icr1 mutant plants are much reduced compared to WT (Figure S7). The reduced vascular tissues in icr1 mutants further suggested the involvement of ICR1 protein in auxin transport and that it could be part of an auxin modulated feedback loop.
In summary, the detailed phenotype analyses using markers for the auxin response and major regulators of patterning in multiple auxin-regulated processes revealed pronounced defects in icr1 mutant plants that presumably result from the defects in auxin distribution.
Localization of PIN1 and PIN2 in icr1
To examine a possible mechanism by which ICR1 mediates auxin distribution, we examined the localization and expression of PIN1 and PIN2 auxin transporters in WT and icr1 roots and embryos (Figure 5 and Figures S8, S9, S10, S11, S12). Immunolocalization analysis showed a defect in polar localization of PIN proteins, in more pronounced cases resulting in basal-to-apical shift of PIN1 in the stele and of PIN2 in the cortex of icr1 roots (Figure 5A, see arrowheads, and Figure S8). Consistently, in approximately 90% of the cells, reduced association of PIN1-GFP with the plasma membrane and basal to apical shift of PIN2-GFP of the cells in the cortex were observed (Figures S9 and S10A). In the epidermis, PIN2 is primarily localized at the apical side of the cells and is resistant to BFA at this location ,. PIN2 remained associated with the apical side of the icr1 root epidermis cells (Figures 5A and S10A), suggesting that ICR1 primarily interacts with a BFA sensitive PIN delivery pathway. In globular icr1 embryos showing early developmental defects, GFP-PIN1 was not expressed at the basal pole, accumulated in large aggregates inside the cells, and was largely absent from the plasma membrane (Figure 5B, arrow, and Figure S11). In embryos with late developmental aberrations, obvious changes in PIN1-GFP localization started to appear at the early heart stage and were associated with intracellular PIN1-GFP aggregations and overall loss of polar membrane localization (Figure 5B and Figure S11). The differences between the immunolocalizations and the PIN1-GFP possibly reflect differences between embryo and root cells or higher stability GFP-PIN1. Alternatively, the changes in auxin distribution affect pPIN1-driven PIN1-GFP expression such that it accumulates at higher levels in certain cells. Importantly, localization of the plasma membrane marker LTi-GFP was not affected in icr1 mutants (Figure 5C), suggesting that ICR1 does not regulate targeting of membrane proteins in general. The model in Figure S12 summarizes the effects of ICR1 on embryo patterning, PIN1 localization, and auxin distribution. The reduced polarity and membrane association of PIN1 in icr1 embryos likely leads to defective polar auxin transport and thus to defects in formation of auxin maxima in embryonic root and cotyledons. The reduction in auxin levels is associated with inhibition of PIN1 expression in the provascular tissue. This leads, in turn, to failure of the auxin maximum formation causing a collapse of the root meristem.
(A) Indirect immunofluorescence of roots with α-PIN1/PIN2 antibodies. Arrowheads denote the direction of PIN polarity. Note the changes in polarity of PIN1 in provascular tissue and of PIN2 in the cortex (arrow). (B) Localization and expression pattern of pPIN1::GFP-PIN1 in embryos. Projection of multiple confocal sections shows that the PIN1 polarity in provascular tissue and protoderm in heart-stage icr1 embryos is altered. Arrow indicates no expression at the basal side of the icr1 embryo with early patterning defects. Insets are single confocal scans throughout the region of future cotyledons. Note the reduced PIN1 polarity and large intracellular aggregations in heart stage icr1 embryo and almost complete loss of PIN1 membrane localization in embryo with early patterning defects. (C) Localization of the plasma membrane marker LTi-GFP is similar in roots of WT and icr1 seedlings. Bars correspond to 20 µm. For additional information and high resolution images, see Figures S8, S9, S10, S11.
ICR1 Expression Pattern
An auxin response element (GTGCTC), which is located 254 base pairs (bp) upstream of the initiation AUG codon of ICR1 (Figure S13), indicated that ICR1 could be part of an auxin-induced positive feedback loop that influences polarity of auxin transport. It further suggested that ICR1 might integrate nuclear auxin signaling  and ROP-regulated cell polarity. To examine these hypotheses, we studied the ICR1 expression pattern and subcellular localization using a genomic clone of ICR1 fused to GFP (Figure 6 and Figure S13). In globular and torpedo stage embryos, GFP-ICR1 expression was observed throughout the embryo proper but interestingly not in the hypophysis and QC where a stable auxin maximum is formed (Figure 6A). Similarly in roots, ICR1 was absent from the QC and the stem cells, positions of stable auxin maxima (Figure 6A and 6B and Video S1). The absence of ICR1 expression at the position of the auxin maxima correlated with non-polar PIN4 localization in the hypophesis, QC, and columella initials .
(A) ICR1 expression in embryos and roots. In globular and torpedo stage embryos, GFP-ICR1 expression is absent from the hypophysis and QC, respectively. A projection stack of multiple confocal scans through mature roots shows GFP-ICR1 expression in the root cup and epidermis, but a partial projection stack through the inner layers only reveals that GFP-ICR1 is absent from the QC and neighboring cells (arrowheads). (B) Regulation of ICR1 expression involves the ICR gene and/or protein. pICR1 driven GFP-rop6CA but not GFP-ICR1 was expressed in the QC and stem cells (arrowhead). (C) ICR1 expression in lateral roots. GFP-ICR1 expression is detected in lateral root (LR) founder cells and throughout LR development. Note the polarized localization of the GFP-ICR1 (arrowheads). (D) Subcellular localization of GFP-ICR1. Plasma membrane and polarized GFP-ICR1 localization in globular embryos GFP-ICR1 is detected in basal and periclinal membranes (arrowheads). In roots, GFP-ICR1 becomes progressively polarized as cells in the stele mature. (E) ICR1 expression is induced by auxin. Bar graph Q-PCR analysis showing induction of ICR1 expression within 30 min of incubation with auxin (10 µM NAA). Strong induction of pICR1-driven GFP-ICR1 expression detected 24 h after local auxin induction with 1 mm2 solid-medium particles with or without 10 µM NAA that were put 5 mm above the root tip. pICR1-driven GFP-ICR1 expression was suppressed by treatment with the auxin transport inhibitor NPA. Bars correspond to 10 µm for globular embryos (A and D) and 50 µm in all the other images. For additional information and high resolution images, see Figures S13, S14, S15, S16.
Several experiments were carried out to examine whether ICR1 expression is influenced by auxin. Expression analysis by quantitative real-time RT-PCR (q-PCR) showed that ICR1 expression is quickly induced following 30 min of incubation in auxin (NAA) (Figure 6E). The expression of pICR≫GFP-ICR1 and pICR1≫GUS reporters following growth of seedling on medium containing the polar auxin transport inhibitor NPA (1-N-naphthylphthalamic acid) and followed by addition of auxin (NAA) to the growth medium were studied. Confirming the prediction, ICR1 expression was lower when seedlings were grown on NPA and was induced as early as 4–6 h following treatment with NAA (Figure 6E and Figure S14). As shown above, lateral root development is compromised in icr1 (Figure 4E). The initiation of lateral roots is induced by auxin and occurs at places of transient local auxin maxima ,. Consistently, GFP-ICR1 expression was observed at positions of lateral root initiation (Figure 6C), further indicating that ICR1 expression is induced by auxin.
The absence of ICR1 in the QC and stem cells, where the stable auxin maximum is formed, was in apparent discrepancy to the induction of its expression by auxin and suggested that it might be suppressed by a different mechanism. To examine whether a stable auxin maximum could suppress ICR1 expression directly, auxin was applied locally to pICR1≫GFP-ICR1 roots, using small, 1 mm2, agar particles that contained 10 µM NAA. Strong local GFP-ICR1 expression was observed in the auxin treated roots, while no increase was observed in control roots that were treated with agar particles without auxin (Figure 6E). These results reconfirmed that ICR1 expression is induced by auxin and further suggested that stable auxin maxima, likely, do not suppress ICR1 expression directly. The site of the stable auxin maximum at the root tip was shown to express a specific group of genes ,,. Thus, possibly, the suppression of ICR1 expression is associated with specific cellular processes taking place at and around the site of the stable auxin maxima.
To obtain further insight into regulation of ICR1 expression, we examined whether the suppression of its expression may be associated with the ICR1 gene or protein. To this end, a GFP-rop6CA reporter (Poraty and Yalovsky, unpublished data) was expressed under regulation of the ICR1 promoter. To reduce the possibility of differences in expression due to position effects, expression was carried out using the LhG4/pOp transcription/transactivation system ,, using the same pICR1 promoter activator lines to express GFP-rop6CA, GUS, or GFP-ICR1 (Figure S13). In contrast to GFP-ICR1, the GFP-rop6CA was observed in the QC and stem cells (Figure 6B), indicating that indeed the suppression of ICR1 expression in the root meristem could be regulated by a mechanism associated with the ICR1 gene or protein. To summarize these data, while auxin induced transcription of ICR1 is part of a positive feedback loop that facilitates auxin transport, the suppression of ICR1 expression in the root meristem is associated with a cell-specific mechanism/s, presumably leading to inhibition of directional auxin transport, and contributes to the formation of a stable auxin maximum.
Subcellular Localization of ICR1
Next, we examined whether the subcellular localization of GFP-ICR1 reflects ICR1 function in polar localization of PIN proteins. GFP-ICR1 complemented root growth in icr1 mutant plants (Figure S15). Furthermore, in pollen tubes, overexpression of either GFP-ICR1 or non-fused recombinant ICR1 had the same phenotypic effects . It thus appears that localization of the GFP-ICR1 fusion protein reflected that of the native ICR1 protein. Importantly, GFP-ICR1 localization was not sensitive to BFA (Figure 7D), consistent with earlier studies showing that recruitment of ICR1 to the plasma membrane is not ARFGEF- but ROP-dependent ,. GFP-ICR1 was localized both at the plasma membrane and intracellularly. Plasma membrane localization was confirmed by plasmolysis, which induces detachment of membrane from the cell wall (Figure S16). In lateral root founder cells and embryos, GFP-ICR1 had polarized localization (Figure 6C and 6D, arrowheads). In the primary root, the localization of GFP-ICR1 became progressively polarized away from the auxin maximum (Figure 6D, arrowheads). The non-polarized ICR localization around the auxin maximum could contribute to the reduction of auxin transport leading to the formation of stable auxin maximum.
(A, B) BFA treatments of embryos and roots stained with FM4-64, respectively. Arrowheads mark BFA compartments. Note that in icr1 BFA compartments are formed in all root tissues examined. (C) pPIN1::GFP-PIN1 co-localizes with FM4-64 in BFA compartments of WT and icr1 (arrowheads) root cells. (D) pICR1 driven GFP-ICR1 does not accumulate in FM4-64-labelled BFA bodies and its membrane localization is not affected by BFA treatments. Bars correspond to 10 µm (A) and 20 µm (B to D). For additional information, see Figure S10B.
ICR1 and Constitutive Endocytic Recycling
The reduced polarity and association with the plasma membrane of PIN1 and PIN2 in the icr1 plants suggested that ICR1 is required for recruitment of the PIN proteins to the plasma membrane rather than their Rab5-regulated endocytic recycling . Indeed, internalization of endocytosis tracer FM4-64 into BFA bodies occurred normally in icr1 mutant roots and embryos (Figure 7A and 7B). Furthermore, similar to WT roots, PIN1-GFP and PIN2-GFP were internalized into the BFA bodies in icr1 roots (Figures 7C and S10B). These data confirmed that endocytosis of FM4-64-labeled plasma membrane derived vesicles in general and of PIN1 and PIN2 in particular were not affected in icr1 mutant plants.
The effects of BFA on endocytic recycling are reversible. When BFA is washed from the medium, the BFA bodies disappear and PIN proteins regain their localization in the plasma membrane ,. BFA washout experiments were carried out to examine whether PIN dynamics is compromised in icr1. Following incubation of GFP-PIN2 and GFP-PIN2 icr1 plants in BFA, the GFP-PIN2-containing BFA bodies appeared in 80% to 90% of the cells and no significant differences were found between WT and icr1 (Figure 8A, 8C, and 8E). However, following a 2-h incubation in medium without BFA, 20%–27% of the cells in the icr1 roots still contained BFA bodies compared to only 2%–5% of the cells in WT plants (Figure 8B, 8D, and 8E). The differences between WT and icr1 roots in the percentage of BFA bodies containing cells were statistically significant (p≤0.001; Student's t test). These results reconfirmed that ICR1 is likely not involved in the Rab5-mediated endocytosis accumulation of PIN proteins following BFA treatments and indicated that ICR1 affects the recycling of PIN proteins back to the plasma membrane.
PIN2-GFP labeled BFA compartments in PIN2-GFP (A) and PIN2-GFP icr1 (C) epidermal and cortical layers treated with 50 µM BFA for 1 h PIN2-GFP (B) and PIN2-GFP icr1 (D) after 2 h BFA washout. (E) Percentage of epidermal cells with BFA bodies before and after BFA washout in PIN2-GFP and PIN2-GFP icr1. Error bars indicate SE; *** p≤0.001; Student's t test. Arrowheads mark BFA bodies. The scale bar corresponds to 10 µm for all images.
Function of ICR1 in Exocytosis
Previously, we showed that ICR1 interacts with AtSEC3A exocyst complex subunit and that ROPs can recruit ICR1-SEC3 complexes to the plasma membrane . This suggested that ICR1 could be involved in regulation of polarized exocytosis. To test this hypothesis, comparison of the distribution of a protein secretion marker, secGFP, in WT and icr1 mutant plants was carried out. SecGFP is a secreted form of GFP that is fused to the chitinase signal peptide at its N-terminus and to HDEL, ER-retention signal, at its C-terminus and has been used in analysis of protein trafficking ,. Secretion of secGFP to the apoplast results in weak signal due to the relatively acidic pH of this compartment. Perturbation of secretion results in fluorescence of intracellular accumulating protein. Thus, the effect of a given mutant or treatment on secretion can be evaluated by monitoring the differences in fluorescence. Transgenic plants expressing secGFP , were crossed into the icr1 background. Qualitative and quantitative fluorescence imaging analyses showed that the GFP fluorescence in icr1 roots was significantly stronger (p≤0.001; Student's t test) than in WT roots (Figure 9A and B). Fluorescence of secreted GFP can be recovered when seedlings are grown at a pH value higher than 8.1 . To validate that the differences in GFP fluorescence between WT and icr1 roots were associated with protein secretion rather than an unrelated mechanism, seedlings were transferred from low (pH 5.5) to high (pH 8.5) pH medium. Quantitative analysis showed significant (p≤0.01; Student's t test) increase in GFP fluorescence of WT roots, while no increase was observed in icr1 roots (Figure S17). These data confirmed that the secGFP secretion was compromised in icr1. High magnification fluorescent confocal images showed that in icr1 plants secGFP accumulated in punctuate structures (Figure 9C). The internalized secGFP was not co-localized with FM4-64-labeled intracellular vesicles (Figure 9D) and did not accumulate in BFA compartment (Figure 9E).
(A) Representative secGFP fluorescence images (two bottom panels) of WT and icr1 roots at 4 DAG imaged under identical conditions. White dotted lines on the DIC images (two upper panels) mark an area of 500 µm in length from the root tip that was used for quantification of the mean fluorescence shown in (B). (B) Mean fluorescence in WT and icr1 roots at 4 and 7 DAG. The mean fluorescence in icr1 roots was ~1.5-fold stronger at 4 DAG and ~2-fold stronger at 7 DAG. afu, arbitrary fluorescence units. Error bars correspond to SE; n≥20; *** fluorescence intensity was significantly different between WT and icr1 roots (p≤0.001; Student's t test). (C) Localization of secGFP in icr1 roots at 4 DAG. Note the accumulation of secGFP in punctuate structures (arrowheads). (D) secGFP (green) punctuate structures in icr1 were not co-localized with early/recycling endosomes marked with FM4-64 (red) (arrowheads). (E) secGFP (green) is not internalized into the BFA compartments marked by FM4-64 (red, arrowheads). Bars correspond to 100 µm in (A) and 10 µm in (C to E).
Our results show that ICR1 regulates directionality of polar auxin transport and is thus required for the formation of a stable auxin maximum and tip localized auxin gradient during embryogenesis, organogenesis, and meristem activity. Earlier work on auxin related patterning enforced the notion that patterns do not reflect a rigid program but rather the inherent developmental potential of each cell . Results presented in this work imply that ICR1 is part of an auxin regulated positive feedback loop, integrating auxin-dependent transcriptional regulation with Rho family GTPases-mediated modulation of cell polarity. Thus, ICR1 forms an auxin-modulated link between cell polarity and auxin transport-dependent tissue patterning.
Dynamic PIN polarity is achieved by (1) integration of a previously described constitutive endocytic recycling that involves clathrin-dependent endocytosis , and BFA-sensitive ARF GEFs-mediated recycling , and (2) a ROP-ICR1-regulated, BFA-insensitive exocytosis (this work). ROP-ICR1 complexes were detected in the plasma membrane ,. Furthermore, following plasmolysis a substantial fraction of pICR1 driven GFP-ICR1 remained associated with the plasma membrane (Figure S16). Thus, it is likely that ICR1 functions in conjunction with ROPs to recruit PIN proteins to specific sites in the membrane. Future analysis of PINs dynamics, using techniques such as Fluorescence Recovery After Photobleaching (FRAP) , would be required to elucidate the interactions between ICR1-associated exocytosis and the BFA-sensitive PIN endocytic recycling.
The exocytosis defects in icr1 are consistent with a previous finding that ICR1 can interact with both ROPs and AtSEC3A exocyst subunit at the plasma membrane . Plants have an evolutionarily conserved exocyst complex  that based on mutational analysis was implicated in regulation of polarized secretion, cell morphogenesis, and patterning –. The reduced association of PINs with the membrane, their accumulation inside the cells in the icr1 mutant background (Figure 5 and Figures S8, S9, S10, S11), and the slower recruitment of PIN2 to the plasma membrane following BFA washout (Figure 8) indicate that ICR1 and possibly exocyst-dependent exocytosis acting at or close to the plasma membrane is required for proper PIN localization. Thus, in the absence of ICR1, due to endocytic recycling, the PIN proteins are degraded or accumulate in the cells. Basal to apical shift of PIN1 and PIN2 have been associated with function of PINOID (PID) protein kinase as well as a BFA-insensitive pathway ,. The basal to apical shift of PIN1 and PIN2 that were observed in icr1 suggests that ICR1 has either reduced or no effect on this BFA insensitive pathway.
ROPs are recruited to the plasma membrane by virtue of the posttranslational lipid modifications prenylation or S-acylation that take place on conserved C-terminal cysteine residues ,,,,. In addition, at least some ROPs also undergo activation-dependent transient S-acylation and consequent partitioning into detergent resistant membranes that could be lipid rafts . Association with the inner leaflet of the plasma membrane also requires a polybasic domain proximal to the lipid modified cysteines . It has been shown that the polybasic domain in Rho proteins associates with phosphatidylinositol 4,5-bisphosphate (PtdIns-P2) and phosphatidylinositol 3,4,5-trisphosphate (PtdIns-P3) . Consistently, in pollen tubes tip, ROP/RAC proteins were shown to physically associate with a phosphatidylinositol monophosphate kinase (PtdIns P-K) activity , and PtdIns-P2, the product of PtdIns P-K, had similar distribution ,. When expressed in pollen tubes, ICR1/RIP1 and ROP1 stabilized the membrane localization of each other at the growing tip, suggesting that ICR1 may interact with other components in the membrane in addition to ROPs . It appears therefore that determination of ROP-ICR1 subcellular localization involves multiple mechanisms, including different protein lipid modifications, partitioning into discrete membrane microdomains, and association with phosphatidylphosphoinositides and possibly with yet unidentified components.
At the root tip, localization of GFP-ICR1 became progressively associated with the plasma membrane and polarized in cells that were more distantly located away from the stable auxin maximum (Figure 6D). This suggests that membrane localization and polarization of ICR1 are locally regulated, possibly by a local auxin gradient associated mechanism.
Auxin modulates its polar efflux from cells by inhibiting PIN endocytosis  and possibly by regulating the expression of ICR1 (this work). Thus, ICR1 may be part of an auxin modulated positive feedback loop that facilitates auxin efflux. ICR1 expression in the root (Figure 6) coincides with pattern of auxin flux and with non-polar localization of PIN4 in the sites of the auxin maxima in the hypophesis, QC, and columella initials ,. In most regions of the primary root, the expression of ICR1 is limited to the stele (Figure 6). The expression pattern changes in two regions: (1) lateral root founder cells and initials and (2) around the root tip where expression is detected in epidermis, cortex, endodermis, and the root cap. The stable auxin maximum and local gradient at the root tip are associated with expression of specific genes. The expression level of some of these genes has been shown to correlate with auxin levels ,,. It is likely that the repression of ICR1 expression in the QC and the meristematic stem cells is associated with one or some of these auxin maximum-specific genes. The quick induction of ICR1 expression by auxin and the strong expression of pICR1-driven GFP-ICR1 by local application of auxin further suggest that suppression of ICR1 expression at the site of auxin maxima is indirectly regulated by auxin. Interestingly, mutants in the HALTEDROOT (HLR) gene, which encodes an RPT2a 26S proteasome subunit, share a similar phenotype with icr1. Like icr1, the root meristem of hlr collapses, the QC is lost, and expression pattern of several markers including SCR and SHR is altered . In contrast to icr1, however, additional tiers of columella cells, compared to WT, were observed in 6-d-old hlr seedling, while in icr1 plants, of similar age, the specification of the columella is significantly reduced (Figure 2). No differences in the icr1 expression pattern were observed when pICR1≫GFP-ICR1 plants were treated with a proteasome inhibitor (unpublished data). Thus, it is currently unclear whether the proteasome is involved in regulation of ICR1 expression.
Based on computational modeling, it has been proposed that the PIN-mediated auxin fluxes in the root are sufficient for maintaining a stable auxin maximum . Results of this work (Figure 6) implicate the repression of ICR1 expression and possibly also regulation of its subcellular localization in the formation of the stable auxin maximum. The stable auxin maximum may facilitate a positive feedback loop that maintains the repression of ICR1 expression and its distribution in the immediate proximal and subtending cells.
Constitutive active ROP-induced cell deformation has been associated with reorganization of actin and MT cytoskeleton, as well as compromised vesicle uptake at the plasma membrane ,. Ectopic expression of ICR1 induced deformation of leaf epidermis pavement cells and root hairs  as well as pollen tubes , resembling the effect of activated ROP mutants. Thus, ICR1 may act as a scaffold that facilitates compartmentalization of ROPs and other proteins such as the exocyst complex at specific membrane domains . This also suggests that ICR1 could be involved in regulation of various processes.
ROPs orchestrate cell polarization by regulating cytoskeleton organization through proteins that include RIC1 (ROP Interacting CRIB containing 1), RIC3 and RIC4 ,, ADF/Cofilin , and the WAVE and Arp2/3 complexes ,. As shown in this work and based on previous findings , the ROP-ICR1-associated cell polarization machinery is required for plasma membrane recruitment and polar localization of PIN proteins, consequently directing auxin transport.
Materials and Methods
The ICR1 promoter was cloned by amplifying a 2,050 bp fragment upstream of the initiation ATG codon from genomic DNA with the oligonucleotide primers SYP1502 (CCGGTACCTTTGATTTCGTGTTGAGG) and SYP1503 (CGTGTCGACCCTCCTACAGAAGGTTGG) and cloned into pGEM (Promega). The resulting plasmid (pSY1500) was digested with Kpn1 and Sal1, and the resulting fragment was subcloned into pLhG4-Bj36 upstream of the synthetic transcriptional factor gene LhG4 , to yield pSY1501. pSY1501 was digested with Not1, and the pICR1-LhG4 fragment was subcloned into the plant binary vector pART27 to yield pSY1502.
A 2,339 bp genomic fragment of ICR1, including the entire 5′-UTR of the gene, exons, introns, and the 3′-UTR, was cloned into the plant binary vector pMLBART as follows: the ICR1 5′-UTR was amplified from genomic DNA by PCR using oligonucleotide primers SYP321 (CAGCCATGGGACGTCGACATTTGATCAGC) and SYP322 (ATTATATCCTCAACACGAAATCAAACCATGGCTG), digested with NcoI and subcloned upstream of GFP in pGFP-MRC  to yield pSY350. The genomic ICR1 gene starting from the initiating ATG codon was amplified by PCR from genomic DNA using primers SYP323 (CTAGAGCTCATGCCAAGACCAAGGTTACG) and SYP324 (GCAGGTACCGTTTAACGGGTTTCTCCATTTACGA), digested with SacI and KpnI and subcloned into pSY350 downstream of GFP to yield pSY351. pSY351 was in turn digested with SalI and KpnI, and the resulting fragment containing pICR1-5′UTR′-GFP-ICR1genomic-ICR1-3′UTR was subcloned into pOPTATABJ36 to yield pSY352. pSY352 was in turn digested with NotI, and the resulting fragment was subcloned into the plant binary vector pMLBART to yield pSY353.
The pSY812 plasmid containing His6-GFP-rop6CA was prepared as previously described . pSY812 was digested with XhoI. The resulting fragment containing His6-GFP-rop6CA was subcloned into p10Op-Bj36  to obtain pSY819. In turn, pSY819 was digested with NotI, and the resulting fragment containing 10Op-His6-GFP-rop6CA-OCS terminator was subcloned into the plant binary vector pMLBART , to obtain pSY818. Expression in the transcription-transactivation system , was achieved by crossing the promoter::LhG4 activator lines with the respective pOp::reporter lines.
Total RNA was isolated with “SV Total RNA isolation” according to the manufacturer's instructions (Promega, Madison). cDNA first strand synthesis was carried out using Super ScriptII reverse transcriptase (Invitrogen Carlsbad, USA). Quantification with the oligonucleotide primer set SY1582: TCAAAATGCCAAGACCAAGA and SY1583: TTGGAATGATTGGAATCAGAAG was carried out by q-PCR using an ABI Prism 7700 StepOnePlus™ Instrument (Applied Biosystems, Weiterstadt, Germany). Study samples were run in triplicate on 8-well optical PCR strips (Applied Biosystems) in a final volume of 10 µl. Primers were designed using Roche Universal Probe Library (https://www.roche-applied-science.com/sis/rtpcr/upl/index.jsp). The PCR cycles were run as follows: 10 min initial denaturation at 95°C, followed by 40 subsequent cycles of 15 s denaturation at 95°C, and 1 min annealing and elongation at 60°C. The specificity of the unique amplification product was determined by a melting curve analysis according to the manufacturer's instructions (Applied Biosystems, Weiterstadt, Germany). Relative quantities of RNA were calculated by the ddCt method (Applied Biosystems Incorporated (2001), User Bulletin #2: ABI PRISM 7700 Sequence Detection System, http://www.appliedbiosystems.com). cDNA dilution series were prepared to calculate amplification efficiency coefficient. The relative levels of RNA were calculated according to the amplification efficiency coefficient and normalized against an UBQ21 gene standard , whose level was taken as 1. The stability of the standard in each experiment was verified with the geNorm analysis tool (http://medgen.ugent.be/jvdesomp/genorm/) and was calculated as M≤0.7. The analysis was repeated with three independent biological replicates.
Plant Growth Conditions
Seeds of WT Columbia-0 (Col-0) and mutant Arabidopsis plants were sown on soil (Universal potting soil, Tuff Moram Golan, Israel) and left for 2 d at 4°C. Then, plants were transferred to a growth chamber and were grown under long-day conditions (16 h light/8 h dark cycles) at 22°C. The light intensity was 100 µE m−2 s−1. For seedling analysis, seeds were surface sterilized and sown on plates containing 0.5× Murashige & Skoog (0.5× MS) salt mixture (Duchefa) titrated to pH 5.5 with MES and KOH, 1% sucrose, and 0.8% plant agar (Duchefa) and left for 2 d at 4°C. Then plates were transferred to the growth chamber and grown under long-day conditions (16 h light/8 h dark cycles) at 22°C for an indicated period. The light intensity was 100 µE·m−2·s−1. For auxin induction experiments, seedlings were germinated on plates (as above) for 5 d, then transferred to liquid medium (0.5× MS), and grown for 2 additional days before application of either NPA (10 µM) or NAA (10 µM).
Drug and Dye Treatments and Plasmolysis
BFA (Fluka) treatments.
Two to 3-d-old seedlings were submerged in 25, 50, or 90 µM BFA (prepared from a 100 mM stock solution in DMSO) and 4 µM FM4-64 (prepared from a 1 mM stock solution in DMSO) diluted in 0.5× MS liquid medium for 1–2 h at room temperature. For control treatments, seedlings were submerged in 0.09% DMSO solution containing 4 µM FM4-64. For BFA treatments of embryos, heart and torpedo stage embryos were dissected from ovules under stereo-microscope and immediately transferred into 0.5× MS liquid media supplemented with 1% sucrose. Dissected embryos were treated with 50 µM BFA and 5 µM FM4-64 on glass slides for 1–2 h in dark and observed with a 63× water-dipping (cover slide-free) objective using the Confocal Laser Scanning Microscope (CLSM).
Propidiumiodide (PI) staining.
Seedlings were in 50 µg/ml PI in water solution submerged on microscope slides.
Plasmolysis was carried out by incubating detached leaves in 0.8 M NaCl for 5 min .
β-Glucoronidase (GUS) staining was carried out as previously described , except that seedling were submerged in the staining solution for 2 h and then clarified in either chloralhydrate/glycerol/water (8:1:2) or 70% ethanol.
Clearing of Arabidopsis Embryos
Clearing of Arabidopsis embryos was performed as previously described . In short, growing siliques were harvested from soil-grown plants and dissected under a stereo-microscope. Ovules from individual siliques were collected and fixed for 1–4 h in ethanol/acetic acid (6:1) at room temperature. Then, ovules were washed three times for 5 min in 100% ethanol and one time in 70% ethanol. In turn, the ovules were incubated in a clearing solution (chloralhydrate/glycerol/water 8:1:2 v/v) for 24 h, mounted on slide with 30% glycerol, and observed by Nomarsky Differential Interference Contrast (DIC) optics.
Seedlings of indicated age were transferred into Lugol (IKI—0.2% w/v iodine and 2% potassium iodine) and incubated for 3 min. The Lugol-stained seedlings were then briefly washed with water and mounted on the slide with a clearing solution (chloral hydrate in 30% glycerol).
Local Auxin Induction
Small solid medium (0.5× MS, 1% sucrose, neutral red, 0.8% plant agar) particles, approximately 1 mm2 in diameter, with or without 10 µM NAA were applied onto roots of vertically grown 7-d-old pICR1≫GFP-ICR1genomic seedlings 5 mm above the root-tip. GFP-ICR1 expression was observed 24 h after the treatment.
Light and Confocal Laser Scanning Microscopy
Nomarsky/DIC imaging was performed with an Axioplan-2 Imaging microscope (Carl Zeiss, Jena, Germany) equipped with an Axio-Cam, cooled charge-coupled device (CCD) camera by using either 40× or 100× oil immersion objectives with numerical aperture (NA) values of 1.3 or a 63× water immersion objective with NA value of 1.2. Low magnification imaging was carried out with Olympus MVX10 fluorescence stereomicroscope. CLSM imaging was performed with Leica TCS-SL CLSM with 20× multi-immersion, 63× water, and 63× water dipping (cover slide-free) objectives with NAs of 0.7, 1.2, and 0.9, respectively.
Visualization of fluorescent markers.
GFP was visualized by excitation with an argon laser at 488 nm. Emission was detected with a spectral detector set between 505 and 530 nm. YFP was visualized by excitation with an Argon laser at 514 nm and spectral detector set between 525 and 560 nm for detection of emission. FM4-64 was visualized by excitation with an argon laser at 514 nm. Emission was detected with a spectral detector set between 530 and 560 nm. PI was visualized by excitation at 514 nm. The emission was detected with the spectral detector set between 600 and 650 nm.
BFA Washout Assays
Four-day-old GFP-PIN2 and GFP-PIN2 icr1 seedlings were treated with 50 µM BFA for 1 h and then washed with 0.5× MS medium for 2 h. For calculation of epidermal cells with BFA bodies, at least 15 roots were used for each line and treatment. The experiment was repeated three times. Statistical analysis was performed with Student's t test.
Analysis of secretion was performed as previously described ,. Transgenic Arabidopsis homozygous line expressing 35S::secGFP in the Col-0 background was crossed to icr1. T2 progeny homozygous for both icr1 and secGFP were selected. Seedlings were grown on 0.5× MS plates (pH 5.5) supplemented with 1% sucrose for the indicated time. Images of WT and icr1 root tips were taken with Leica LCS LSCM under identical conditions using a 10× objective, fully opened pinhole (600 µm) and emission/excitations of GFP as described above. The mean signal intensity was measured on an area spanning up to 500 µm from the root tip, using Image-J. DIC images of the same root were used for the adjustment of the measured area. At least 20 seedlings of each line were used in each experimental repeat. Statistical analysis was performed with Student's t test.
Effect of external pH on secGFP fluorescence.
For comparison of secGFP fluorescence at external pH values of 5.5 and 8.5, seedlings were grown for 5 d on 0.5× MS plates pH 5.5, supplemented with 1% sucrose, and in turn transferred for 3 h to 0.5× MS liquid medium titrated to pH 5.5 or 8.5 with MES or KOH and supplemented with 1% sucrose.
Abnormal development of early icr1 embryos. (A–F) Col-0, (G–L) 90% of icr1 progeny with normal development at early embryo development, (M–P) 10% of icr1 progeny with early basal defects. (A and G) 1-cell stage, (B and H) 4-cell stage, (C, I, and M) 8-cell stage, (D, J, and N) 16-cell stage, (E, K, and O) early globular stage, and (F, L, and P) late globular. h, hypophysis; lc, lens-shaped cell; llc, large lower cell. Arrowheads in (M and N) mark abnormal division in hypophysis and suspensor; vertical brackets in (O and P) mark unshaped basal region. Bars correspond to 10 µm for all images.
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Abnormal development of late icr1 embryos. (A–D) Triangular stage, (A) Col-0, and (B–D) icr1. Arrowheads in (B) indicate abnormal divisions in suspensor and columella initials; arrowhead in (C and D) marks abnormal division in protoderm. (D) Enlargement of the arrow-highlighted section in (C). (E–K) Early/mid-heart stage, (E and J) Col-0, (F–I and K) icr1. Arrowheads in (G–I) mark abnormal divisions in protoderm. Arrowhead in (J) indicates a normal periclinal division in a WT columella. Arrowheads in (K) point to abnormal division planes in columella initials of icr1 embryos. (L–S) A bent cotyledon stage, (L, N, P, and R) Col-0, and (M, O, Q, and S) icr1. (N and O) Enlargement of the root meristem (RM). The arrowhead in (O) marks abnormal division in columella. Vertical bars in (L and M) indicate enlarged region shown in (P and Q). pd, protoderm; pc, procambium; col, columella initials; QC, quiescent center; v, vascular tissue; ep, epidermis; c, cortex; en, endodermis. Bars correspond to 20 µm (A–M), 10 µm (N–Q), and 50 µm (R and S).
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icr1 siliques display greater developmental variability. Stacked-bar charts show the developmental stages of embryos collected from 12 representative siliques. (A) Col-0 and (B) icr1 siliques of various ages. Each color marks a single silique. The high mixing of colors in icr1 mutant indicates that the synchronization of embryo development within a single silique is compromised. Note that the embryo-lethal icr1 embryos were excluded.
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Abnormal DR5 response in icr1 embryos. DR5rev::ER-GFP expression in WT and icr1 embryos. (A–E and L) Col-0, (F–K) icr1. (A and F) Early globular stage, (B and G) triangular, (C and H) early/mid-heart, and (D, E, and I–L) late heart stage. Panels (K) and (L) are enlargements of the RM of (D) and (I), respectively. Arrows mark the auxin accumulation foci in developing cotyledons. Arrowheads in (C, D, H, I, K, and L) indicate position of QC. Arrowheads in (E and J) point to the downward movement of auxin through provascular tissue. (A–J) Maximum projection Z-stack of multiple confocal sections; (K and L) single confocal scans throughout the center of RM. (A–D, F–I, K, and L) are fluorescence/DIC overlay images. (E) and (J) are fluorescent images. GFP fluorescence is shown in green. Bars correspond to 20 µm.
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Abnormal expression pattern of pWOX5::ER-GFP in icr1 embryos. WOX5 expression was first detected in globular stage embryos. In WT embryos expression is seen in the lens shape and the upper suspensor cells. In icr1 globular and heart stage embryos expression is spread to cell neighboring the lens-shape cell (arrowhead). In adult icr1 embryos strong WOX5 expression is seen in the lower part of the hypocotyl (arrowhead) and in the cotyledons. In contrast in adult WT embryo WOX5 expression is detected in the QC and the cotyledons. However, the expression in the cotyledon is weak and its detection required using high detector sensitivity. Bars correspond to 10 µm globular embryos, 20 µm heart stage embryos, and 50 µm adult embryos.
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The expression pattern of SCR is altered in icr1 embryos. Expression pattern of SCR was determined with pSCR::YFP-His2b reporter seen as yellow nuclei. In WT globular embryos SCR is expressed in the hypophysis, ground meristem, and provascular cells. The inset is a projection stack of multiple confocal scans. At the heart stage expression expanded to the QC cells. In adult embryos expression was detected in the QC and future endodermis of the embryonic roots and in the hypocotyls. Note the clear differences in the expression pattern between the hypocotyl and the embryonic root (noted by the rectangular and curved brackets). In bent cotyledon embryos the expression was confined to the QC and endodermis/cortex stem cells of the embryonic root. Low levels of expression were detected in the cotyledons. Abnormal expression pattern of SCR was seen in globular stage icr1 embryos with early developmental aberrations (arrowhead). In heart stage icr1 embryos expression was spread to additional cells (arrowheads). Similar to WT, in mature icr1 embryos SCR expression was detected in the embryonic root and hypocotyls. However, unlike WT embryos no clear distinction in expression pattern could be made between the embryonic root and the hypocotyls. In bent cotyledons icr1 embryos SCR expression was confined to the embryonic root but was more spread compared to WT embryos (arrowhead). Bars correspond to 10 µm globular embryos, 20 µm heart stage embryos, and 50 µm adult embryos.
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The differentiation of vascular tissues in leaves of icr1 is compromised. Cross-sections across a rosette leave's central vascular strand. The reduced sized of the vascular strand in icr1 is apparent. Note also the altered mesophyll cell shape and large air spaces in the icr1 leaf. Bars correspond to 20 µm.
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High-resolution images demonstrating the altered localization of PIN1 and PIN2 in icr1 roots. Arrowheads denote the orientation of PIN localization in cells. Bars are 20 µm.
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pPIN1-driven GFP-PIN1 localization in WT and icr1 roots. GFP-PIN1 expression in 3 DAG primary root of Col-0 (A to C) and icr1 (D to F). (A and D) Overlay between DIC and GFP fluorescence, (B and E) GFP, and (C and F) PIN1-GFP expressing roots stained with 5 µM FM4-64. Insets in (C and F) are close-up views of the RM. (G–I) pPIN1::GFP-PIN1 expression in root hairs and epidermis. (G) Col-0 (H and I) icr1. Arrowheads in (H) indicate ectopic expression in epidermis and root hairs. Arrowhead in (I) marks accumulation of GFP-PIN1 in internal bodies. (A, B, D, and E) Maximum projection Z-stack of multiple confocal sections. (C, F, and G–I) single confocal scans. (A, D, G, and H) are fluorescence/DIC overlay images. (B, C, E, F, and I) are fluorescent images. (C and F) are GFP/FM4-64 overlay images. GFP fluorescence is shown in green and FM4-64 in red. Bars correspond to 20 µm (A to F) and 50 µm (G to I).
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Localization of pPIN2-driven GFP-PIN2 in icr1 roots. (A) WT and icr1 roots expressing pPIN2::GFP-PIN2 and stained with FM4-64 at 4 DAG. White boxes indicate the enlarged regions shown on the right panels. Arrows in WT mark apical localization of GFP-PIN2 in the epidermis and basal in the cortex. Note apicalization of GFP-PIN2 in both epidermis and cortex in icr1 roots (arrows). (B) BFA treatments of WT and icr1 seedlings resulted in co-localization of FM4-64 and GFP-PIN2 in BFA compartments (arrowheads). Bars correspond to 20 µm.
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The altered pPIN1-driven GFP-PIN1 localization in icr1 embryos. (A–D, I, and J) Col-0, (E–H, K, and L) icr1 embryos showing mild basal defects, (M and N) icr1 embryos with strong basal defects. (A, B, E, and F) mid-globular stage, (C, D, G, H, M, and N) triangular stage, (I–L) heart stage. Arrowheads in (B, D, F, H, J, and L) indicate the orientation of GFP-PIN1 localization, basal in procambial cells, and apical in protoderm. Arrows in (M and N) indicate the loss of PIN1-GFP expression in the basal region of icr1 embryos with strong basal defects. Insets in (I and K) are enlargements of a developing cotyledon. (A, C, E, G, I, K, and M) Maximum projection Z-stack of multiple confocal sections. (B, D, F, H, J, and N) Single confocal scans throughout the center of embryo. (A, C, E, G, I, M, and K) are fluorescence/DIC overlay images. (B, D, F, H, J, L, N, and insert in I and K) are fluorescent images. GFP fluorescence is shown in green. Bars correspond to 20 µm.
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A model summarizing PIN1 localization, auxin distribution, and patterning in WT and icr1 embryos. Cell outlines of WT (A) and icr1 embryos (B and C). (A) Polar membrane localization of PIN1 mediates directional auxin flux and appearance of auxin maxima in embryonic root meristem and future cotyledon tips during the development. (B) Reduced PIN1 polarity results in weak auxin flux and gradually disrupts formation of auxin maxima in icr1 embryos with late patterning defects. (C) In icr1 embryos with early patterning defects PIN1 membrane localization and polarity are strongly affected, likely leading to non-polar auxin distribution (crossed arrows).
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The pICR1::LhG4 and the pOp::ICR15′-UTR-GFP-ICR1genomic constructs. (A) The pICR1 driven effector/reporter lines. The LhG4/pOp system allows expression of different reporters from the same effector, thereby reducing positional effects on gene expression ,. In this work, GFP-ICR1, GFP-rop6CA, and GUS were expressed using the same pICR1 effector lines. (B) Schematic representations of the pICR1 promoter. (C) The GFP-ICRgenomic construct.
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ICR1 expression is induced by auxin. pICR1≫GUS expression following growth on NPA or induction by NAA for 6 h. Arrows denote GUS expression in pericycle cells following NAA treatments. Bars correspond to 50 µm.
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Complementation of root growth in icr1 mutants by GFP-ICR1. Expression of GFP-ICR1 was driven by the ICR1 promoter using transcription/transactivation system (see Figure S12). Bars correspond to 100 µm.
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Plasma membrane localization of GFP-ICR1 detected following plasmolysis. PI-stained GFP-ICR1 expressing leaf epidermis pavement cells before and after plasmolysis. The bottom large panel is a magnification of the overlay panel after plasmolysis. Red arrowheads denote the cell wall and the white arrowheads denote the detached plasma membrane. The fluorescent green patches detected after plasmolysis indicate that some of the GFP-ICR1 was not attached to the plasma membrane. Bars correspond to 20 µm.
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Effect of the apoplastic pH on secGFP fluorescence and its localization in WT and icr1 roots. (A) Mean fluorescence of WT and icr1 roots at 5 DAG that were transferred and incubated for 3 h in liquid MS medium titrated to either pH 5.5 or pH 8.5. Error bars correspond to SE, n≥20, ** significant differences in fluorescence of WT roots were detected between pH 8.5 and 5.5 (p≤0.01; Student's t test). Fluorescence differences in icr1 between pH 8.5 and 5.5 were insignificant (p≥0.72). (B) A WT root incubated in MS medium titrated to pH 8.5 stained with PI (red). Arrows denote the apoplastic localization of secGFP. (C) An icr1 root incubated in MS medium tittered to pH 8.5 and stained with PI (red). Note that the GFP fluorescence remained intracellular. Bars correspond to 10 µm.
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The frequency of icr1−/− embryos exhibiting patterning defects at indicated developmental stages. * Embryos with strong basal defects were excluded from analysis. 1 Embryos were analyzed at 1-cell, 2-cell, 4-cell, 8-cell (octant), and 16-cell (dermatogen) stages.
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Expression of pICR1≫GFP-ICR1 at the root tip. The movie highlights the absence of ICR1 expression at and around the QC.
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We thank Ben Scheres, Viktor Zarski, Yuval Eshed, and the Arabidopsis Biological Research Center, University of Ohio, for materials and the Manna Center in The Department of Plant Sciences at Tel Aviv University for equipment support.
The author(s) have made the following declarations about their contributions: Conceived and designed the experiments: OH DB JF SY. Performed the experiments: OH DB LP HS JZ. Analyzed the data: OH DB JF SY. Wrote the paper: JF SY.
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