ROS and calcium oscillations are required for polarized root hair growth

References

• Grierson C, Nielsen E, Ketelaarc T, Schiefelbein J. Root hairs. Arabidopsis Book/American Soc Plant Bio. 2014;12:e0172. doi:10.1199/tab.0172.
   PubMedGoogle Scholar
• Cormack RGH. Investigations on the development of root hairs. New Phytol. 1935;34(1):30–6. doi:10.1111/j.1469-8137.1935.tb06826.x.
   Google Scholar
• Bünning E. Über die Differenzierungsvorgänge in der Cruciferenwurzel. Planta. 1951;39(2):126–153. doi:10.1007/BF01910114.
   Web of Science ®Google Scholar
• Dolan L, Duckett CM, Grierson CS, Linstead PJ, Roberts K, Dean C, Poethig S, Roberts K. Clonal relationships and cell patterning in the root epidermis of Arabidopsis. Development. 1994;120(9):2465–2474. doi:10.1101/gad.8.18.2241.
   Web of Science ®Google Scholar
• Galway ME, Masucci JD, Lloyd AM, Walbot V, Davis RW, Schiefelbein JW. The TTG gene is required to specify epidermal cell fate and cell patterning in the Arabidopsis root. Dev Biol. 1994;166(2):740–754. doi:10.1006/dbio.1994.1352.
   PubMed Web of Science ®Google Scholar
• Pacheco JM, Ranocha P, Kasulin L, Fusari CM, Servi L, Aptekmann AA, Gabarain VB, Peralta JM, Borassi C, Marzol E, et al. Apoplastic class III peroxidases PRX62 and PRX69 promote Arabidopsis root hair growth at low temperature. Nat Commun. 2022;13(1):1–14. doi:10.1038/s41467-022-28833-4.
   PubMed Web of Science ®Google Scholar
• Mangano S, Denita-Juarez SP, Choi H-S, Estevez JM, Hwang Y, Ranocha P, Velasquez SM, Borassi C, Barberini ML, Aptekmann AA. Molecular link between auxin and ROS-mediated polar growth. Proc Natl Acad Sci USA. 2017;114(20):5289–5294. doi:10.1073/pnas.1701536114.
   PubMed Web of Science ®Google Scholar
• Mangano S, Juárez SPD, Estevez JM. ROS regulation of polar growth in plant cells. Plant Physiol. 2016;171(3):1593–1605. doi:10.1104/pp.16.00191.
   PubMed Web of Science ®Google Scholar
• Tian W, Wang C, Gao Q, Li L, Luan S. Calcium spikes, waves and oscillations in plant development and biotic interactions. Nat Plants. 2020;6(7):750–759. doi:10.1038/s41477-020-0667-6.
   PubMed Web of Science ®Google Scholar
• Zhang X, Köster P, Schlücking K, Balcerowicz D, Hashimoto K, Kuchitsu K, Vissenberg K, Kudla J. CBL1-CIPK26-mediated phosphorylation enhances activity of the NADPH oxidase RBOHC, but is dispensable for root hair growth. FEBS Lett. 2018;592(15):2582–2593. doi:10.1002/1873-3468.13187.
   PubMed Web of Science ®Google Scholar
• Dolan L, Janmaat K, Willemsen V, Linstead P, Poethig S, Roberts K, Scheres B. Cellular organisation of the Arabidopsis thaliana root. Development. 1993;119(1):71–84. doi:10.1242/dev.119.1.71.
   PubMed Web of Science ®Google Scholar
• Wada T, Kurata T, Tominaga R, Koshino-Kimura Y, Tachibana T, Goto K, Marks DM, Shimura Y, Okada K. Role of a positive regulator of root hair development, CAPRICE, in Arabidopsis root epidermal cell differentiation. Development. 2002;129(23):5409–5419. doi:10.1242/dev.00111.
   PubMed Web of Science ®Google Scholar
• Wada T, Tachibana T, Shimura Y, Okada K. Epidermal cell differentiation in Arabidopsis determined by a Myb homolog. CPC Sci. 1997;277(5329):1113–1116. doi:10.1126/science.277.5329.1113.
   PubMed Web of Science ®Google Scholar
• Masucci JD, Schiefelbein JW. The rhd6 mutation of Arabidopsis thaliana alters root-hair initiation through an auxin- and ethylene-associated process. Plant Physiol. 1994;106(4):1335–1346. doi:10.1104/pp.106.4.1335.
   PubMed Web of Science ®Google Scholar
• Masucci JD, Rerie WG, Foreman DR, Zhang M, Galway ME, Marks MD, Schiefelbein JW. The homeobox gene GLABRA2 is required for position-dependent cell differentiation in the root epidermis of Arabidopsis thaliana. Development. 1996;122(4):1253–1260. doi:10.1242/dev.1224.1253.
   PubMed Web of Science ®Google Scholar
• Di Cristina M, Sessa G, Dolan L, Linstead P, Baima S, Ruberti I, Morelli G. The Arabidopsis Athb-10 (GLABRA2) is an HD-Zip protein required for regulation of root hair development. Plant J. 1996;10(3):393–402. doi:10.1046/j.1365-313X.1996.10030393.x.
   PubMed Web of Science ®Google Scholar
• Lin Q, Ohashi Y, Kato M, Tsuge T, Gu H, Qu L-J, Aoyama T. GLABRA2 directly suppresses basic helix-loop-helix transcription factor genes with diverse functions in root hair development. Plant Cell. 2015;27(10):2894–2906. doi:10.1105/tpc.15.00607.
   PubMed Web of Science ®Google Scholar
• Menand B, Yi K, Jouannic S, Hoffmann L, Ryan E, Linstead P, Schaefer DG, Dolan L. An ancient mechanism controls the development of cells with a rooting function in land plants. Science. 2007;316(5803):1477–1480. doi:10.1126/science.1142618.
   PubMedGoogle Scholar
• Yi K, Menand B, Bell E, Dolan L. A basic helix-loop-helix transcription factor controls cell growth and size in root hairs. Nat Genet. 2010;42(3):264–267. doi:10.1038/ng.529.
   PubMed Web of Science ®Google Scholar
• Molendijk AJ, Bischoff F, Rajendrakumar CSV, Friml J, Braun M, Gilroy S, Palme K. Arabidopsis thaliana Rop GTPases are localized to tips of root hairs and control polar growth. EMBO J. 2001;20(11):2779–2788. doi:10.1093/emboj/20.11.2779.
   PubMed Web of Science ®Google Scholar
• Jones MA, Shen -J-J, Fu Y, Li H, Yang Z, Grierson CS. The Arabidopsis ROP2 GTPase is a positive regulator of both root hair initiation and tip growth. Plant Cell. 2002;14(4):763–776. doi:10.1105/tpc.010359.
   PubMed Web of Science ®Google Scholar
• Gendre D, Baral A, Dang X, Esnay N, Boutté Y, Stanislas T, Vain T, Claverol S, Gustavsson A, Lin D, et al. Rho-of-plant activated root hair formation requires Arabidopsis YIP4a/b gene function. Development. 2019;146(5):dev168559. doi:10.1242/dev.168559.
   PubMed Web of Science ®Google Scholar
• Li C, Yeh F-L, Cheung AY, Duan Q, Kita D, Liu M-C, Maman J, Luu EJ, Wu BW, Gates L. Glycosylphosphatidylinositol-anchored proteins as chaperones and co-receptors for FERONIA receptor kinase signaling in Arabidopsis. eLife. 2015;4:e06587. doi:10.7554/eLife.06587.
   PubMed Web of Science ®Google Scholar
• Liao H, Tang R, Zhang X, Luan S, Yu F. FERONIA receptor kinase at the crossroads of hormone signaling and stress responses. Plant Cell Physiol. 2017;58(7):1143–1150. https://doi.org/10.1093/pcp/pcx048.
   PubMed Web of Science ®Google Scholar
• Franck CM, Westermann J, Boisson-Dernier A. Plant malectin-like receptor kinases: from cell wall integrity to immunity and beyond. Annu Rev Plant Biol. 2018;69:301–328. doi:10.1146/annurev-arplant-042817-040557.
   PubMed Web of Science ®Google Scholar
• Li C, Wu H-M, Cheung AY. FERONIA and her pals: functions and mechanisms. Plant Physiol. 2016;171(4):2379–2392. doi:10.1104/pp.16.00667.
   PubMed Web of Science ®Google Scholar
• Zhu S, Martínez Pacheco J, Estevez JM, Yu F. Autocrine regulation of root hair size by the RALF-FERONIA-RSL4 signaling pathway. New Phytol. 2020;227(1):45–49. doi:10.1111/nph.16497.
   PubMed Web of Science ®Google Scholar
• Zhu S, Estévez JM, Liao H, Zhu Y, Yang T, Li C, Wang Y, Li L, Liu XM, Pacheco JM, et al. The RALF1–FERONIA complex phosphorylates eIF4E1 to promote protein synthesis and polar root hair growth. Mol Plant. 2020;13(5):698–716. doi:10.1016/j.molp.2019.12.014.
   PubMed Web of Science ®Google Scholar
• Akkerman M, Franssen‐verheijen M, Immerzeel P, Hollander L, Schel J, Emons AMC. Texture of cellulose microfibrils of root hair cell walls of Arabidopsis thaliana. Medicago Truncatula Vicia Sativa J Microsc. 2012;247(1):60–67. doi:10.1111/j.1365-2818.2012.03611.x.
   Google Scholar
• Velasquez SM, Ricardi MM, Dorosz JG, Fernandez PV, Nadra AD, Pol-Fachin L, Egelund J, Gille S, Harholt J, Clancia M, et al. O-glycosylated cell wall proteins are essential in root hair growth. Science. 2011;332(6036):1401–1403. doi:10.1126/science.1206657.
   PubMed Web of Science ®Google Scholar
• Nielsen E. Plant cell wall biogenesis during tip growth in root hair cells. : Springer, Berlin; 2008. doi:10.1007/978-3-540-79405-9_11.
   Google Scholar
• Hocq L, Pelloux J, Lefebvre V. Connecting homogalacturonan-type pectin remodeling to acid growth. Trends Plant Sci. 2017;22(1):20–29. doi:10.1016/j.tplants.2016.10.009.
   PubMed Web of Science ®Google Scholar
• Mittler R. ROS are good. Trends Plant Sci. 2017;22(1):11–19. doi:10.1016/j.tplants.2016.08.002.
   PubMed Web of Science ®Google Scholar
• Monshausen GB, Bibikova TN, Messerli MA, Shi C, Gilroy S. Oscillations in extracellular pH and reactive oxygen species modulate tip growth of Arabidopsis root hairs. Proc Natl Acad Sci USA. 2007;104(52):20996–21001. doi:10.1073/pnas.0708586104.
   PubMed Web of Science ®Google Scholar
• Passardi F, Penel C, Dunand C. Performing the paradoxical: how plant peroxidases modify the cell wall. Trends Plant Sci. 2004;9(11):534–540. doi:10.1016/j.tplants.2004.09.002.
   PubMed Web of Science ®Google Scholar
• Dunand C, Crèvecoeur M, Penel C. Distribution of superoxide and hydrogen peroxide in Arabidopsis root and their influence on root development: possible interaction with peroxidases. New Phytol. 2007;174(2):332–341. doi:10.1111/j.1469-8137.2007.01995.x.
   PubMed Web of Science ®Google Scholar
• Fry SC. Oxidative scission of plant cell wall polysaccharides by ascorbate-induced hydroxyl radicals. Biochem J. 1998;332(2):507–515. doi:10.1042/bj3320507.
   PubMedGoogle Scholar
• Schopfer P. Hydroxyl radical‐induced cell‐wall loosening in vitro and in vivo: implications for the control of elongation growth. Plant J. 2001;28(6):679–688. doi:10.1046/j.1365-313x.2001.01187.x.
   PubMed Web of Science ®Google Scholar
• Carol RJ, Takeda S, Linstead P, Durrant MC, Kakesova H, Derbyshire P, Drea S, Zarsky V, Dolan L. A RhoGDP dissociation inhibitor spatially regulates growth in root hair cells. Nature. 2005;438(7010):1013–1106. doi:10.1038/nature04198.
   PubMedGoogle Scholar
• Foreman J, Demidchik V, Bothwell JHF, Mylona P, Miedema H, Torres MA, Linstead P, Costa S, Brownlee C, Jones JDG, et al. Reactive oxygen species produced by NADPH oxidase regulate plant cell growth. Nature. 2003;422(6930):442–446. doi:10.1038/nature01485.
   PubMed Web of Science ®Google Scholar
• Cosio C, Dunand C. Specific functions of individual class III peroxidase genes. J Exp Bot. 2009;60(2):391–408. doi:10.1093/jxb/ern318.
   PubMed Web of Science ®Google Scholar
• Kimura S, Kaya H, Kawarazaki T, Hiraoka G, Senzaki E, Michikawa M, Kuchitsu K. Protein phosphorylation is a prerequisite for the Ca2+-dependent activation of Arabidopsis NADPH oxidases and may function as a trigger for the positive feedback regulation of Ca2+ and reactive oxygen species. Biochim Biophys Acta. 2012;1823(2):398–405. doi:10.1016/j.bbamcr.2011.09.011.
   PubMed Web of Science ®Google Scholar
• Marino D, Dunand C, Puppo A, Pauly N. A burst of plant NADPH oxidases. Trends Plant Sci. 2012;17(1):9–15. doi:10.1016/j.tplants.2011.10.001.
   PubMed Web of Science ®Google Scholar
• Suzuki N, Miller G, Morales J, Shulaev V, Torres MA, Mittler R. Respiratory burst oxidases: the engines of ROS signaling. Curr Opin Plant Biol. 2011;14(6):691–699. doi:10.1016/j.pbi.2011.07.014.
   PubMed Web of Science ®Google Scholar
• Schiefelbein JW, Somerville C. Genetic control of root hair development in Arabidopsis thaliana. Plant Cell. 1990;2(3):235–243. doi:10.1105/tpc.2.3.235.
   PubMed Web of Science ®Google Scholar
• Wymer CL, Bibikova TN, Gilroy S. Cytoplasmic free calcium distributions during the development of root hairs of Arabidopsis thaliana. Plant J. 1997;12(2):427–439. doi:10.1046/j.1365-313X.1997.12020427.x.
   PubMed Web of Science ®Google Scholar
• Oda T, Hashimoto H, Kuwabara N, Akashi S, Hayashi K, Kojima C, Wong HL, Kawasaki T, Shimamoto K, and Sato M, et al. Structure of the N-terminal regulatory domain of a plant NADPH oxidase and its functional implications. J Biol Chem. 2010;285(2):1435–1445. doi:10.1074/jbc.M109.058909.
   PubMed Web of Science ®Google Scholar
• Torres MA, Dangl JL. Functions of the respiratory burst oxidase in biotic interactions, abiotic stress and development. Curr Opin Plant Biol. 2005;8(4):397–403. doi:10.1016/j.pbi.2005.05.014.
   PubMed Web of Science ®Google Scholar
• Torres MA, Onouchi H, Hamada S, Machida C, Hammond-Kosack KE, Jones JDG. Six Arabidopsis thaliana homologues of the human respiratory burst oxidase (gp91phox). Plant J. 1998;14(3):365–370. doi:10.1046/j.1365-313X.1998.00136.x.
   PubMed Web of Science ®Google Scholar
• Ogasawara Y, Kaya H, Hiraoka G, Yumoto F, Kimura S, Kadota Y, Hishinuma H, Senzaki E, Yamagoe S, Nagata K, et al. Synergistic activation of the Arabidopsis NADPH oxidase AtrbohD by Ca2+ and phosphorylation. J Biol Chem. 2008;283(14):8885–8892. doi:10.1074/jbc.M708106200.
   PubMed Web of Science ®Google Scholar
• Takeda S, Gapper C, Kaya H, Bell E, Kuchitsu K, Dolan L. Local positive feedback regulation determines cell shape in root hair cells. Science. 2008;319(5867):1241–1244. doi:10.1126/science.1152505.
   PubMed Web of Science ®Google Scholar
• Nestler J, Liu S, Wen T-J, Paschold A, Marcon C, Tang HM, Li D, Li L, Meeley RB, and Sakai H, et al. Roothairless5, which functions in maize (Zea mays L.) root hair initiation and elongation encodes a monocot-specific NADPH oxidase. Plant J. 2014;79(5):729–740. doi:10.1111/tpj.12578.
   PubMed Web of Science ®Google Scholar
• Carol RJ, Dolan L. The role of reactive oxygen species in cell growth: lessons from root hairs. J Exp Bot. 2006;57(8):1829–1834. doi:10.1093/jxb/erj201.
   PubMed Web of Science ®Google Scholar
• Parker JS, Cavell AC, Dolan L, Roberts K, Grierson CS. Genetic interactions during root hair morphogenesis in Arabidopsis. Plant Cell. 2000;12(10):1961–1974. doi:10.1105/tpc.12.10.1961.
   PubMed Web of Science ®Google Scholar
• Xu J, Scheres B. Dissection of Arabidopsis ADP-RIBOSYLATION FACTOR 1 function in epidermal cell polarity. Plant Cell. 2005;17(2):525–536. doi:10.1105/tpc.104.028449.
   PubMed Web of Science ®Google Scholar
• Francoz E, Ranocha P, Nguyen-Kim H, Jamet E, Burlat V, Dunand C. Roles of cell wall peroxidases in plant development. Phytochemistry. 2015;112:15–21. doi:10.1016/j.phytochem.2014.07.020.
   PubMed Web of Science ®Google Scholar
• Plieth C, Vollbehr S. Calcium promotes activity and confers heat stability on plant peroxidases. Plant Signal Behav. 2012;7(6):650–660. doi:10.4161/psb.20065.
   PubMedGoogle Scholar
• Passardi F, Tognolli M, De Meyer M, Penel C, Dunand C. Two cell wall associated peroxidases from Arabidopsis influence root elongation. Planta. 2006;223(5):965–974. doi:10.1007/s00425-005-0153-4.
   PubMed Web of Science ®Google Scholar
• Schopfer P, Liszkay A, Bechtold M, Frahry G, Wagner A. Evidence that hydroxyl radicals mediate auxin-induced extension growth. Planta. 2002;214(6):821–828. doi:10.1007/s00425-001-0699-8.
   PubMed Web of Science ®Google Scholar
• Kwon T, Sparks JA, Nakashima J, Allen SN, Tang Y, Blancaflor EB. Transcriptional response of Arabidopsis seedlings during spaceflight reveals peroxidase and cell wall remodeling genes associated with root hair development. Am J Bot. 2015;102(1):21–35. doi:10.3732/ajb.1400458.
   PubMed Web of Science ®Google Scholar
• Marzol E, Borassi C, Carignani Sardoy M, Ranocha P, Aptekmann AA, Bringas M, Pennington J, Paez-Valencia J, Peralta JM, Fleming M, et al. Class III peroxidases PRX01, PRX44, and PRX73 control root hair growth in Arabidopsis thaliana. Int J Mol Sci. 2022;23(10):5375. doi:10.3390/ijms23105375.
   PubMed Web of Science ®Google Scholar
• Bibikova TN, Zhigilei A, and Gilroy S. Root hair growth in Arabidopsis thaliana is directed by calcium and an endogenous polarity. Planta. 1997;203(4):495–505. doi:10.1007/s004250050219.
   PubMed Web of Science ®Google Scholar
• Ketelaar T. The actin cytoskeleton in root hairs: all is fine at the tip. Curr Opin Plant Biol. 2013;16(6):749–756. doi:10.1016/j.pbi.2013.10.003.
   PubMed Web of Science ®Google Scholar
• Sanders D, Pelloux J, Brownlee C, Harper JF. Calcium at the crossroads of signaling. Plant Cell. 2002;14:S401–S417. doi:10.1105/tpc.002899.
   PubMed Web of Science ®Google Scholar
• Carroll AD, Moyen C, Van Kesteren P, Tooke F, Battey NH, Brownlee C. Ca2+, annexins, and GTP modulate exocytosis from maize root cap protoplasts. Plant Cell. 1998;10(8):1267–1276. doi:10.1105/tpc.10.8.1267.
   PubMed Web of Science ®Google Scholar
• Cramer GR, Jones RL. Osmotic stress and abscisic acid reduce cytosolic calcium activities in roots of Arabidopsis thaliana. Plant Cell Environ. 1996;19(11):1291–1298. doi:10.1111/j.1365-3040.1996.tb00007.
   Web of Science ®Google Scholar
• Clapham DE. Calcium signaling. Cell. 2007;131(6):1047–1058. doi:10.1016/j.cell.2007.11.028.
   PubMed Web of Science ®Google Scholar
• Zhang S, Pan Y, Tian W, Dong M, Zhu H, Luan S, Li L. Arabidopsis CNGC14 mediates calcium influx required for tip growth in root hairs. Mol Plant. 2017;10(7):1004–1006. doi:10.1016/j.molp.2017.02.007.
   PubMed Web of Science ®Google Scholar
• Zeb Q, Wang X, Hou C, Zhang X, Dong M, Zhang S, Zhang Q, Ren ZJ, Tian W, Zhu HF, et al. The interaction of CaM7 and CNGC14 regulates root hair growth in Arabidopsis. J Integr Plant Biol. 2020;62(7):887–896. doi:10.1111/jipb.12890.
   PubMed Web of Science ®Google Scholar
• Brost C, Studtrucker T, Reimann R, Denninger P, Czekalla J, Krebs M, Fabry B, Schumacher K, Grossmann G, Dietrich P. Multiple cyclic nucleotide-gated channels coordinate calcium oscillations and polar growth of root hairs. Plant J. 2019;99(5):910–923. doi:10.1111/tpj.14371.
   PubMed Web of Science ®Google Scholar
• Tan Y-Q, Yang Y, Zhang A, Fei C-F, L-L G, Sun S-J, Xu W, Wang LL, Liu HT, Wang YF. Three CNGC family members, CNGC5, CNGC6, and CNGC9, are required for constitutive growth of Arabidopsis root hairs as Ca2+-permeable channels. Plant Commun. 2020;1(1):100001. doi:10.1016/j.xplc.2019.100001.
   PubMedGoogle Scholar
• Maciver SK, Hussey PJ. The ADF/cofilin family: actin-remodeling proteins. Genome Biol. 2002;3(5):reviews3007. doi:10.1186/gb-2002-3-5-reviews3007.
   PubMed Web of Science ®Google Scholar
• Monshausen GB, Messerli MA, Gilroy S. Imaging of the yellow cameleon 3.6 indicator reveals that elevations in cytosolic Ca2+ follow oscillating increases in growth in root hairs of Arabidopsis. Plant Physiol. 2008;147(4):1690–1698. doi:10.1104/pp.108.123638.
   PubMed Web of Science ®Google Scholar
• Gilroy S, Suzuki N, Miller G, Choi WG, Toyota M, Devireddy AR, Mitter R. A tidal wave of signals: calcium and ROS at the forefront of rapid systemic signaling. Trends Plant Sci. 2014;19(10):623–630. doi:10.1016/j.tplants.2014.06.013.
   PubMed Web of Science ®Google Scholar
• Drerup MM, Schlücking K, Hashimoto K, Manishankar P, Steinhorst L, Kuchitsu K, Kudla J. The calcineurin B-like calcium sensors CBL1 and CBL9 together with their interacting protein kinase CIPK26 regulate the Arabidopsis NADPH oxidase RBOHF. Mol Plant. 2013;6(2):559–569. doi:10.1093/mp/sst009.
   PubMed Web of Science ®Google Scholar
• Jones MA, Raymond MJ, Yang Z, Smirnoff N. NADPH oxidase-dependent reactive oxygen species formation required for root hair growth depends on ROP GTPase. J Exp Bot. 2007;58(6):1261–1270. doi:10.1093/jxb/erl279.
   PubMed Web of Science ®Google Scholar
• Miedema H, Demidchik V, Véry -A-A, Bothwell JHF, Brownlee C, Davies JM. Two voltage-dependent calcium channels co-exist in the apical plasma membrane of Arabidopsis thaliana root hairs. New Phytol. 2008;179(2):378–385. doi:10.1111/j.1469-8137.2008.02465.x.
   PubMed Web of Science ®Google Scholar
• Cosgrove DJ. Characterization of long-term extension of isolated cell walls from growing cucumber hypocotyls. Planta. 1989;177(1):121–130. doi:10.1007/BF00392162.
   Web of Science ®Google Scholar
• McQueen-Mason S, Durachko DM, Cosgrove DJ. Two endogenous proteins that induce cell wall extension in plants. Plant Cell. 1992;4(11):1425–1433. doi:10.1105/tpc.4.11.1425.
   PubMed Web of Science ®Google Scholar
• Rayle DL, Cleland R. Enhancement of wall loosening and elongation by acid solutions. Plant Physiol. 1970;46(2):250–253. doi:10.1104/pp.46.2.250.
   PubMed Web of Science ®Google Scholar
• Eklöf JM, Brumer H. The XTH gene family: an update on enzyme structure, function, and phylogeny in xyloglucan remodeling. Plant Physiol. 2010;153(2):456–466. doi:10.1104/pp.110.156844.
   PubMed Web of Science ®Google Scholar
• Rayle DL, Cleland RE. The acid growth theory of auxin-induced cell elongation is alive and well. Plant Physiol. 1992;99(4):1271–1274. doi:10.1104/pp.99.4.1271.
   PubMed Web of Science ®Google Scholar
• Cosgrove DJ. Loosening of plant cell walls by expansins. Nature. 2000;407(6802):321–326. doi:10.1038/35030000.
   PubMed Web of Science ®Google Scholar
• Altartouri B, Geitmann A. Understanding plant cell morphogenesis requires real-time monitoring of cell wall polymers. Curr Opin Plant Biol. 2014 11;2015(23):76–82. doi:10.1016/j.pbi.
   Google Scholar
• Hoffmann RD, Olsen LI, Ezike CV, Pedersen JT, Manstretta R, López-Marqués RL, and Palmgren M. Roles of plasma membrane proton ATPases AHA2 and AHA7 in normal growth of roots and root hairs in Arabidopsis thaliana. Physiol Plant. 2019; 166(3): 848–861. doi:10.1111/ppl.12842
   PubMed Web of Science ®Google Scholar
• Haruta M, Sabat G, Stecker K, Minkoff BB, Sussman MR. A peptide hormone and its receptor protein kinase regulate plant cell expansion. Science. 2014;343(6169):408–411. doi:10.1126/science.1244454.
   PubMed Web of Science ®Google Scholar
• Mangano S, Martínez Pacheco J, Marino-Buslje C, Estevez JM. How does pH fit in with oscillating polar growth? Trends Plant Sci. 2018;23(6):479–489. doi:10.1016/j.tplants.2018.02.008.
   PubMed Web of Science ®Google Scholar
• Feijó JA. The pollen tube oscillator: towards a molecular mechanism of tip growth? Fertilization in higher plants. : Springer, Berlin; 1999. 317–336. doi:10.1007/978-3-642-59969-9_22.
   Google Scholar