Hirotomo Takatsuka*
Masaki Ito- School of Biological Science and Technology, College of Science and Engineering, Kanazawa University, Kanazawa, Japan
Introduction
Polarity is at the core of plant development, as well as that of other multicellular organisms since polarization acts as a driving force to generate a variety of specialized cells. Therefore, unraveling how cells establish polarity is the most fundamental issue toward understanding the principles of plant morphogenesis.
Cell polarity coordinated within the plane of a single tissue layer is particularly termed “planar polarity (also termed planar cell polarity),” which offers an experimentally accessible model system. Therefore, planar polarity is studied in various multicellular organisms. In the animal kingdom, polarized arrangement of ommatidia and bristles in Drosophila melanogaster and the orientation of hair follicles in mammalian skin are well-known examples of planar polarity.
Root Hair Positioning as a Model System for Planar Polarity
Root hairs possess crucial roles in nutrient and water uptake from the soil, as well as in providing anchorage for plants (Gilroy and Jones, 2000). In Arabidopsis thaliana, root hair emergence is restricted to close to the basal ends (rootward ends) of specialized cells aligned within a single file, namely the hair-forming cell lineage (trichoblasts), thus manifesting typical planar polarity (Figure 1A) (Masucci and Schiefelbein, 1994; Fischer et al., 2007). The site of root hair emergence intriguingly appears to be evolutionarily conserved across plant species (Salazar-Henao et al., 2016; Dolan, 2017) and is easily observable under laboratory conditions without any special equipment; root hair positioning provides an excellent model to elucidate the mechanisms behind establishing polarity in plants, which indeed has been studied extensively.
Figure 1 (A) Root hair positioning of wild-type, mutants with altered cytoskeleton or Rho-of-plants (ROP) level, and plants treated with reagents related to auxin and ethylene. (B) Cytoskeletal control of root hair positioning. Black solid lines represent direct protein interactions. Black solid and black broken arrows represent direct or indirect action on the target, respectively.
Rho-of-Plants, an Early Marker for Root Hair Positioning
The members of the Rho-of-plant (ROP) small GTPase protein family are implicated in establishing root hair planar polarity. Among the 11 members of the ROP family in Arabidopsis, ROP2, ROP4, and ROP6 localize to the hair initiation site (Figure 1B) (Molendijk et al., 2001; Jones et al., 2002). Severe defects in root hair growth were observed in the rop2/4/6 triple mutant (Gendre et al., 2019). More importantly, increased ROP activities from either overexpression of ROP2 or defects in ROP-GDP dissociation inhibitor lead to root hair formation at multiple sites in one cell (Figure 1A) (Jones et al., 2002; Carol et al., 2005), indicating that an adequate ROP protein level needs to be placed at the adequate site to establish planar polarity during root hair development. ROP proteins begin accumulating at the future hair initiation site prior to the actual onset of hair formation (Figure 1B) (Molendijk et al., 2001), providing an early marker for the established root hair planar polarity; thus, clarifying the mechanism behind ROP placement at the future initiation site is key toward understanding planar polarity establishment during root hair development.
Auxin and Ethylene Provide a Cue for Root Hair Positioning
Among phytohormones, auxin and ethylene have been reported to provide a cue for root hair positioning (Masucci and Schiefelbein, 1994; Vicente-Agullo et al., 2004). Exogenous application of either auxin or 1-aminocyclopropane-1-carboxylic acid (ACC), an ethylene precursor, causes a basal shift of root hair positioning. Root hairs in plants with either a reduced level of auxin signaling or ethylene perception emerge from more apical sites compared with those in wild-type plants (Figure 1A) (Masucci and Schiefelbein, 1994; Ikeda et al., 2009). Ikeda et al. (2009) reported that the auxin applied locally at the very tip of roots was actively transported to hair-forming cells, eventually generating a basal shift of root hair positioning. Contrastingly, auxin transport inhibition from the root tip to hair-forming cells results in an apical shift (Figure 1A). These findings suggest that auxin redistribution involving both local synthesis and polar transport is required for properly establishing root hair planar polarity. Ethylene potentially acts upstream of auxin to control planar polarity by regulating local auxin synthesis (Figure 1B) (Ikeda et al., 2009). Recent studies have shed light on the role of the cytoskeleton in mediating hormonal control of root hair positioning,
Cytoskeletal Control of the ROP Placement in Root Hair Initiation
Eukaryotic cells possess three types of cytoskeleton, namely, actin microfilaments (MFs), microtubules (MTs), and intermediate filaments; the presence of intermediate filaments in plants is albeit still unresolved (Kost and Chua, 2002; Ivakov and Persson, 2013). In this review, we describe recent advances in actin- and MT-mediated establishment of root hair planar polarity.
Actin
The involvement of the actin cytoskeleton in root hair positioning has long been recognized, according to the finding that a mutation in the ACTIN2 (ACT2) gene encoding globular actin (G-actin) causes an apical shift of root hair positioning in Arabidopsis (Figure 1A) (Ringli et al., 2002). Moreover, the knockout mutant for ACT7, another member of the ACT gene family in Arabidopsis, exhibits more severe defects in root hair positioning than act2; both apical and basal shifts of root hair positioning are frequently observed in act7 (Figure 1A) (Kiefer et al., 2015). Filamentous actin (F-actin) formed through polymerization of G-actin encoded by ACT genes is highly accumulated at the future initiation site before polar root hair emergence takes place; hence, actin filaments containing G-actin produced from ACT7 and/or ACT2 are possibly required for establishing planar polarity in root hair development (Figure 1B) (Kiefer et al., 2015). Recent studies identified key regulators that modulate ROP placement and eventual root hair positioning by influencing actin dynamics.
Kiefer et al. (2015) found that ACT7 and ACT2 modulate planar polarity along with their direct interactor, ACTIN-INTERACTING PROTEIN1-2 (AIP1-2) (Figure 1B). The aip1-2 knockout mutant displays a basal shift of the ROP placement and resultant root hair positioning as in act mutants (Figure 1A). Moreover, analyses of the genetic interaction between ACT7 and AIP1-2 revealed that AIP1-2 acts upstream of ACT7 (Figure 1B) (Kiefer et al., 2015). AIP1-2 affects actin-filament organization by physically interacting with ACT7, thereby determining ROP placement (Figure 1B). Ethylene and auxin signaling possibly converges on the AIP1-2-ACT7 module to control root hair planar polarity (Figure 1B), since expression of ACT7 and AIP1-2 is upregulated by auxin and ethylene in an auxin-dependent manner, respectively (Kandasamy et al., 2001; Kiefer et al., 2015). However, whether the AIP1-2-ACT7 module precisely determines the ROP placement site is still unclear.
TWISTED DWARF1 (TWD1) is another actin-related key regulator for root hair planar polarity (Figure 1B) (Zhu et al., 2016). TWD1 is an FK506-binding protein originally identified as a direct interactor of N-1-naphthylphthalamic acid (NPA), an auxin-transport inhibitor (Figure 1B) (Geisler et al., 2003; Bailly et al., 2008), and twd1 mutant showed an apical shift of root hair positioning, resembling NPA treatment of wild-type roots (Figure 1A) (Zhu et al., 2016). TWD1 interacts with ACT7, albeit indirectly, to remodel actin organization (Figure 1B) (Zhu et al., 2016). The TWD1-mediated control of actin organization has been shown to influence auxin redistribution in roots by modulating the subcellular localization of both ABCB- and PIN-type auxin transporters (Zhu et al., 2016). Therefore, the TWD1-ACT7 module possibly mediates root hair planar polarity by controlling auxin transport (Figure 1B). However, in the absence of clear evidence, it still remains possible that abnormally organized actin filaments in twd1 are responsible for root hair misplacement, independent of the perturbed auxin transport.
Myosin, a motor protein involved in vesicle trafficking by interacting with actin filaments, is required for tip growth of root hair, based on the finding that the lack of a member of the myosin family results in a shorter root hair phenotype (Park and Nebenführ, 2013). However, whether actin-myosin interaction is required for ROP placement and root hair positioning remains elusive.
Microtubule
Microtubules (MTs), which consist of α-tubulin and β-tubulin, play an essential role in determining plant cell shape, including that of root hair (Hashimoto, 2015). Impaired MT organization induced by MT-depolymerizing drugs, such as oryzalin, gives rise to shorter and wavy root hairs (Bibikova et al., 1999). In comparison, the knowledge concerning their role in root hair positioning is limited; however, accumulated evidence indicates their involvement in establishing root hair planar polarity. Firstly, MTs are dynamically reorganized at the future hair initiation site; transversely aligned cortical MTs are rearranged into unique radial patterns (Figure 1B) (Pietra et al., 2013). Furthermore, Bao et al. (2001) demonstrated that a reduction in α-tubulin leads to multiple root hair formation from one cell, reminiscent of ROP overexpressors (Figure 1A), implying the role of MTs in proper ROP placement. Lastly, the engagement of the MT-associated protein CLIP170-ASSOCIATED PROTEIN (CLASP) and its genetic interactor SABRE (SAB) in establishing root hair planar polarity has been recently reported (Figure 1B) (Pietra et al., 2013). CLASP, known as a central regulator of cell-division plane orientation, is required for properly determining ROP placement; clasp mutant exhibits a basal shift of ROP foci (Figure 1A). SAB, with an unknown molecular function, localizes to the plasma membrane and regulates cortical MT dynamics (Pietra et al., 2013). Unlike clasp, root hair positioning shifts either apically or basally in sab (Figure 1A). Moreover, sab clasp double mutant is indistinguishable from sab, suggesting that sab is epistatic to clasp in controlling planar root hair polarity (Pietra et al., 2013). CLASP has been notably reported to regulate the abundance of PIN2 protein, which is a central auxin transporter in root epidermis, by regulating MT dynamics, thereby playing an important role in auxin gradient formation (Figure 1B) (Ambrose et al., 2013). It is still unclear whether CLASP-SAB-guided MT reorganization directly sets ROP proteins at the proper site or indirectly influences ROP placement by controlling auxin transport (Figure 1B).
Kinesins are motor proteins that assist cells with transport of molecules along microtubules. The armadillo domain-containing putative kinesin MRH2 has been reported to control root hair morphology by altering MT organization (Yang et al., 2007), but kinesin involvement in root hair positioning is still unclear.
Summary and Future Perspectives
Root hair positioning provides an excellent model for planar polarity, but some important questions and points are still open as follows: 1) how does the cytoskeleton place ROPs at the future initiation site? The cytoskeleton possibly acts as a scaffold of ROP proteins, constraining ROP subcellular localization at the initiation site. To support this view, in some cases, the cytoskeleton affects polarity establishment by functioning as a scaffold-like structure required for polarization of key molecules (Inagaki and Katsuno, 2017; Liu et al., 2018; Raman et al., 2018). For example, in leaf epidermal cells, actin filaments are implicated in PIN protein recycling to the plasma membrane, enabling polarized PIN localization (Xu et al., 2010). Recently, Denninger et al. (2019) found that the accumulation of ROPGEF3, which tethers and activates ROPs at the plasma membrane, at the future hair initiation site precedes that of ROPs; therefore, it is possible that the cytoskeleton places ROPGEF3 at the future hair site and thereby determines the ROP position. 2) The direct link between auxin signaling and the cytoskeleton is still missing. Despite extensive studies on the target genes of auxin response factors (ARFs), a transcription factor family acting downstream of auxin signaling, there is still no evidence showing that ARF directly regulates cytoskeleton-related genes involved in root hair planar polarity (Okushima et al., 2005; Schlereth et al., 2010; Boer et al., 2014). Note that it remains possible that auxin affects cytoskeletal organization through non-transcriptional responses, as is the case of leaf cells wherein auxin alters cytoskeletal dynamics in a manner that does not require ARF-dependent transcriptional responses, thereby forming zigzag-shaped pavement cells (Xu et al., 2010). 3) In many tissues, actin filaments and MTs cooperatively regulate many aspects of plant morphogenesis, including root hair elongation (Takeuchi et al., 2017). However, their cooperative actions have not been elucidated in terms of root hair planar polarity. 4) Small GTPases other than ROPs might participate in establishing root hair polarity. Indeed, a recent study demonstrated that ARF-GAP that localizes to the hair initiation is required for root hair positioning (Yoo et al., 2018). However, whether and how the cytoskeleton is engaged in the placement of other small GTPases is still unknown. The answers to these important questions will help to better understand more general principle of how polarity is established in plant cells.
Author Contributions
All authors listed have made a substantial and direct contribution to the work, and approved it for publication.
Funding
This work was supported by JSPS KAKENHI Grant Number 19K05951 and the 2017 Inamori Research Grant Program to HT.
Conflict of Interest
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.
References
Ambrose, C., Ruan, Y., Gardiner, J., Tamblyn, L. M., Catching, A., Kirik, V., et al. (2013). CLASP Interacts with Sorting Nexin 1 to Link Microtubules and Auxin Transport via PIN2 Recycling in Arabidopsis thaliana. Dev. Cell 24, 649–659. doi: 10.1016/j.devcel.2013.02.007
Bailly, A., Sovero, V., Vincenzetti, V., Santelia, D., Bartnik, D., Koenig, B. W., et al. (2008). Modulation of P-glycoproteins by auxin transport inhibitors is mediated by interaction with immunophilins. J. Biol. Chem. 283, 21817–21826. doi: 10.1074/jbc.M709655200
Bao, Y., Kost, B., Chua, N. H. (2001). Reduced expression of α-tubulin genes in Arabidopsis thaliana specifically affects root growth and morphology, root hair development and root gravitropism. Plant J. 28, 145–157. doi: 10.1046/j.1365-313X.2001.01142.x
Bibikova, T. N., Blancaflor, E. B., Gilroy, S. (1999). Microtubules regulate tip growth and orientation in root hairs of Arabidopsis thaliana. Plant J. 17, 657–665. doi: 10.1046/j.1365-313X.1999.00415.x
Boer, D. R., Freire-Rios, A., Van Den Berg, W. A. M., Saaki, T., Manfield, I. W., Kepinski, S., et al. (2014). Structural basis for DNA binding specificity by the auxin-dependent ARF transcription factors. Cell 156, 577–589. doi: 10.1016/j.cell.2013.12.027
Carol, R. J., Takeda, S., Linstead, P., Durrant, M. C., Kakesova, H., Derbyshire, P., et al. (2005). A RhoGDP dissociation inhibitor spatially regulates growth in root hair cells. Nature 438, 1013–1016. doi: 10.1038/nature04198
Denninger, P., Reichelt, A., Schmidt, V. A. F., Mehlhorn, D. G., Asseck, L. Y., Stanley, C. E., et al. (2019). Distinct RopGEFs Successively Drive Polarization and Outgrowth of Root Hairs. Curr. Biol. 29, 1854–1865.e5. doi: 10.1016/j.cub.2019.04.059
Dolan, L. (2017). Root hair development in grasses and cereals (Poaceae). Curr. Opin. Genet. Dev. 45, 76–81. doi: 10.1016/j.gde.2017.03.009
Fischer, U., Ikeda, Y., Grebe, M. (2007). Planar polarity of root hair positioning in Arabidopsis. Biochem. Soc. Trans. 35, 149–151. doi: 10.1042/BST0350149
Geisler, M., Kolukisaoglu, H.Ü., Bouchard, R., Billion, K., Berger, J., Saal, B., et al. (2003). TWISTED DWARF1, a unique plasma membrane-anchored immunophilin-like protein, interacts with Arabidopsis multidrug resistance-like transporters AtPGP1 and AtPGP19. Mol. Biol. Cell 14, 4238–4249. doi: 10.1091/mbc.E02-10-0698
Gendre, D., Baral, A., Dang, X., Esnay, N., Boutte, Y., Stanislas, T., et al. (2019). Rho-of-plant activated root hair formation requires arabidopsis YIP4a/b gene function. Development. 146, 1–7. doi: 10.1242/dev.168559
Gilroy, S., Jones, D. L. (2000). Through form to function: Root hair development and nutrient uptake. Trends Plant Sci. 5, 56–60. doi: 10.1016/S1360-1385(99)01551-4
Ikeda, Y., Men, S., Fischer, U., Stepanova, A. N., Alonso, J. M., Ljung, K., et al. (2009). Local auxin biosynthesis modulates gradient-directed planar polarity in Arabidopsis. Nat. Cell Biol. 11, 731–738. doi: 10.1038/ncb1879
Inagaki, N., Katsuno, H. (2017). Actin Waves: Origin of Cell Polarization and Migration? Trends Cell Biol. 27, 515–526. doi: 10.1016/j.tcb.2017.02.003
Ivakov, A., Persson, S. (2013). Plant cell shape: Modulators and measurements. Front. Plant Sci. 4, 439. doi: 10.3389/fpls.2013.00439
Jones, M. A., Shen, J. J., Fu, Y., Li, H., Yang, Z., Grierson, C. S. (2002). The arabidopsis Rop2 GTPase is a positive regulator of both root hair initiation and tip growth. Plant Cell 14, 763–776. doi: 10.1105/tpc.010359
Kandasamy, M. K., Gilliland, L. U., McKinney, E. C., Meagher, R. B. (2001). One Plant Actin Isovariant, ACT7, Is Induced by Auxin and Required for Normal Callus Formation. Plant Cell 13, 1541–1554. doi: 10.1105/tpc.010026
Kiefer, C. S., Claes, A. R., Nzayisenga, J. C., Pietra, S., Stanislas, T., Hüser, A., et al. (2015). Arabidopsis AIP1-2 restricted by WER-mediated patterning modulates planar polarity. Development 142, 151–161. doi: 10.1242/dev.111013
Kost, B., Chua, N. H. (2002). The Plant Cytoskeleton: Vacuoles and Cell Walls Make the Difference. Cell 108, 9–12. doi: 10.1016/S0092-8674(01)00634-1
Liu, C., Zhang, Y., Ren, H. (2018). Actin Polymerization Mediated by AtFH5 Directs the Polarity Establishment and Vesicle Trafficking for Pollen Germination in Arabidopsis. Mol. Plant 11, 1389–1399. doi: 10.1016/j.molp.2018.09.004
Masucci, J. D., Schiefelbein, J. W. (1994). The rhd6 mutation of Arabidopsis thaliana alters root-hair initiation through an auxin- and ethylene-associated process. Plant Physiol. 106, 1335–1346. doi: 10.1104/pp.106.4.1335
Molendijk, A. J., Bischoff, F., Rajendrakumar, C. S. V., Friml, J., Braun, M., Gilroy, S., et al. (2001). Arabidopsis thaliana Rop GTPases are localized to tips of root hairs and control polar growth. EMBO J. 20, 2779–2788. doi: 10.1093/emboj/20.11.2779
Okushima, Y., Overvoorde, P. J., Arima, K., Alonso, J. M., Chan, A., Chang, C., et al. (2005). Functional genomic analysis of the AUXIN RESPONSE FACTOR gene family members in Arabidopsis thaliana: Unique and overlapping functions of ARF7 and ARF19. Plant Cell 17, 444–463. doi: 10.1105/tpc.104.028316
Park, E., Nebenführ, A. (2013). Myosin XIK of Arabidopsis thaliana Accumulates at the Root Hair Tip and Is Required for Fast Root Hair Growth. PloS One 8, 1–18. doi: 10.1371/journal.pone.0076745
Pietra, S., Gustavsson, A., Kiefer, C., Kalmbach, L., Hörstedt, P., Ikeda, Y., et al. (2013). Arabidopsis SABRE and CLASP interact to stabilize cell division plane orientation and planar polarity. Nat. Commun. 4, 1–15. doi: 10.1038/ncomms3779
Raman, R., Pinto, C. S., Sonawane, M. (2018). Polarized Organization of the Cytoskeleton: Regulation by Cell Polarity Proteins. J. Mol. Biol. 430, 3565–3584. doi: 10.1016/j.jmb.2018.06.028
Ringli, C., Baumberger, N., Diet, A., Frey, B., Keller, B. (2002). ACTIN2 is essential for bulge site selection and tip growth during root hair development of arabidopsis. Plant Physiol. 129, 1464–1472. doi: 10.1104/pp.005777
Salazar-Henao, J. E., Vélez-Bermúdez, I. C., Schmidt, W. (2016). The regulation and plasticity of root hair patterning and morphogenesis. Development 143, 1848–1858. doi: 10.1242/dev.132845
Schlereth, A., Möller, B., Liu, W., Kientz, M., Flipse, J., Rademacher, E. H., et al. (2010). MONOPTEROS controls embryonic root initiation by regulating a mobile transcription factor. Nature 464, 913–916. doi: 10.1038/nature08836
Takeuchi, M., Staehelin, L. A., Mineyuki, Y. (2017). “Actin-Microtubule Interaction in Plants,” in Cytoskeleton - Structure, Dynamics, Function and Disease. (IntechOpen). doi: 10.5772/66930
Vicente-Agullo, F., Rigas, S., Desbrosses, G., Dolan, L., Hatzopoulos, P., Grabov, A. (2004). Potassium carrier TRH1 is required for auxin transport in Arabidopsis roots. Plant J. 40, 523–535. doi: 10.1111/j.1365-313X.2004.02230.x
Xu, T., Wen, M., Nagawa, S., Fu, Y., Chen, J. G., Wu, M. J., et al. (2010). Cell surface- and Rho GTPase-based auxin signaling controls cellular interdigitation in Arabidopsis. Cell 143, 99–110. doi: 10.1016/j.cell.2010.09.003
Yang, G., Gao, P., Zhang, H., Huang, S., Zheng, Z. L. (2007). A mutation in MRH2 kinesin enhances the root hair tip growth defect caused by constitutively activated ROP2 small GTPase in Arabidopsis. PloS One 2, 1–12. doi: 10.1371/journal.pone.0001074
Yoo, C. M., Naramoto, S., Alan Sparks, J., Khan, B. R., Nakashima, J., Fukuda, H., et al. (2018). Deletion analysis of AGD1 reveals domains crucial for plasma membrane recruitment and function in root hair polarity. J. Cell Sci. 131, 1–13. doi: 10.1242/jcs.203828
Keywords: root hair, planar polarity, cytoskeleton, actin, microtubule, Rho-of-plant, Arabidopsis thaliana
Citation: Takatsuka H and Ito M (2020) Cytoskeletal Control of Planar Polarity in Root Hair Development. Front. Plant Sci. 11:580935. doi: 10.3389/fpls.2020.580935
Received: 07 July 2020; Accepted: 19 August 2020;
Published: 04 September 2020.
Edited by:
Satoshi Naramoto, Hokkaido University, JapanReviewed by:
Elison B. Blancaflor, Noble Research Institute, LLC, United StatesOoi-kock Teh, Hokkaido University, Japan
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*Correspondence: Hirotomo Takatsuka, aC10YWthdHN1a2FAc2Uua2FuYXphd2EtdS5hYy5qcA==