Abstract
Woody cutting is customarily utilized as a material in research on grape adventitious root formation (ARF). However, phenotypic heterogeneity caused by the complex background influenced its use for molecular mechanism research of ARF of grape. The present study tested various types of explants from grape tissue culture plantlets and found that the whole leaf: blade with the petiole (LP) was the simplest unit that can easily form adventitious roots (ARs). LP explants which can be easily obtained, directly generate ARs via de novo organogenesis from the base of the petiole. Plantlet age, node position, blade size, the health condition of leaves, and light intensity have been demonstrated to affect the homogeneity of the ARF phenotype in LP. By controlling these parameters, selected LPs cultured on a medium with 6 g·L-1 agar and 10 g·L-1 sucrose under dark conditions started rooting at 6–7 days after culture (DAC) and reached 100% rooting rate within 13–14 DAC. Using this system, the core role of auxin on ARF was verified by exogenous application of indole butyric acid (IBA) and N-1-naphthylphthalamic acid (NPA). Strikingly, we found that light promoted ARF in the absence of sucrose, but inhibited ARF in the presence of sucrose (10 g·L-1), while a low concentration of 0.34 µM NPA partially relieved the inhibition. Finally, this study confirmed that exogenous plant growth regulators (PGRs), including 6-benzyl aminopurine (6-BA), gibberellic acid 3 (GA3), and 2,4-epibrassinolide (EBR), significantly inhibited ARF. This simple, rapid, quantifiable ARF research system provides a new approach to studying the factors influencing the formation and development of grape adventitious roots and establishes a framework for investigating the mechanism of grape adventitious root induction and initiation.
Similar content being viewed by others
References
Ahkami AH, Melzer M, Ghaffari MR, Pollmann S, Ghorbani Javid M, Shahinnia F, Hajirezaei MR, Druege U (2013) Distribution of indole-3-acetic acid in Petunia hybrida shoot tip cuttings and relationship between auxin transport, carbohydrate metabolism and adventitious root formation. Planta 238(3):499–517. doi:https://doi.org/10.1007/s00425-013-1907-z
Bai Z, Zhang J, Ning X, Guo H, Xu X, Huang X, Wang Y, Hu Z, Lu C, Zhang L, Chi W (2020) A kinase-phosphatase-transcription factor module regulates adventitious root emergence in Arabidopsis root-hypocotyl junctions. Mol Plant 13(8):1162–1177. doi:https://doi.org/10.1016/j.molp.2020.06.002
Bannoud F, Bellini C (2021) Adventitious rooting in populus species: Update and perspectives. Front Plant Sci 12:668837. doi:https://doi.org/10.3389/fpls.2021.668837
Bellini C, Pacurar DI, Perrone I (2014) Adventitious roots and lateral roots: similarities and differences. Annu Rev Plant Biol 65:639–666. doi:https://doi.org/10.1146/annurev-arplant-050213-035645
Bustillo-Avendano E, Ibanez S, Sanz O, Sousa Barros JA, Gude I, Perianez-Rodriguez J, Micol JL, Del Pozo JC, Moreno-Risueno MA, Perez-Perez JM (2018) Regulation of hormonal control, cell reprogramming, and patterning during de novo root organogenesis. Plant Physiol 176(2):1709–1727. doi:https://doi.org/10.1104/pp.17.00980
Castro PRC, Melotto E, Soares FC, Passos IRS, Pommer CV (1994) Rooting stimulation in muscadine grape cuttings. Sci Agr 51(3):436–445. doi:https://doi.org/10.1590/s0103-90161994000300009
Chen X, Qu Y, Sheng L, Liu J, Huang H, Xu L (2014) A simple method suitable to study de novo root organogenesis. Front Plant Sci 5:208. doi:https://doi.org/10.3389/fpls.2014.00208
da Costa CT, de Almeida MR, Ruedell CM, Schwambach J, Maraschin FS, Fett-Neto AG (2013) When stress and development go hand in hand: main hormonal controls of adventitious rooting in cuttings. Front Plant Sci 4:133. doi:https://doi.org/10.3389/fpls.2013.00133
Di Battista F, Maccario D, Beruto M, Grauso L, Lanzotti V, Paolo Curir P, Monroy F (2019) Metabolic changes associated to the unblocking of adventitious root formation in aged, rooting-recalcitrant cuttings of Eucalyptus gunnii Hook. Plant Growth Regul 89:73–82. doi:https://doi.org/10.1007/s10725-019-00515-0. Myrtaceae
Druege U, Hilo A, Perez-Perez JM, Klopotek Y, Acosta M, Shahinnia F, Zerche S, Franken P, Hajirezaei MR (2019) Molecular and physiological control of adventitious rooting in cuttings: phytohormone action meets resource allocation. Ann Bot 123(6):929–949. doi:https://doi.org/10.1093/aob/mcy234
Ford YY, Taylor JM, Blake PS, Marks TR (2002) Gibberellin A3 stimulates adventitious rooting of cuttings from cherry (Prunus avium). Plant Growth Regul 37:127–133. doi:https://doi.org/10.1023/A:1020584627919
Garcia-Gonzalez J, Lacek J, Retzer K (2021) Dissecting hierarchies between light, sugar and auxin action underpinning root and root hair growth. Plants (Basel) 10(1):111. doi:https://doi.org/10.3390/plants10010111
Gonin M, Bergougnoux V, Nguyen TD, Gantet P, Champion A (2019) What makes adventitious roots? Plants (Basel) 8(7):240. doi:https://doi.org/10.3390/plants8070240
Halliday KJ, Martinez-Garcia JF, Josse EM (2009) Integration of light and auxin signaling. Cold Spring Harb Perspect Biol 1(6):a001586. doi:https://doi.org/10.1101/cshperspect.a001586
Jaleta A (2019) A Review on the effect of rooting media on rooting and growth of cutting propagated grape (Vitis vinifera L). World J Agric Soil Sci 3(4):1–8. doi:https://doi.org/10.33552/wjass.2019.03.000567
Joshi M, Ginzberg I (2021) Adventitious root formation in crops-potato as an example. Physiol Plant 172(1):124–133. doi:https://doi.org/10.1111/ppl.13305
Kaur S, Cheema SS, Chhabra BR, Talwar KK (2002) Chemical induction of physiological changes during adventitious root formation and bud break in grapevine cuttings. Plant Growth Regul 37:63–68. doi:https://doi.org/10.1023/A:1020355505105
Keeley K, Preece JE, Taylor BH, Dami IE (2004) Effects of high auxin concentrations, cold storage, and cane position on improved rooting of Vitis aestivalis Michx. Norton cuttings. Am J Enol Viticult 55(3):265–268. doi:https://doi.org/10.1021/bk-2004-0887.ch012
Kracke H, Cristoferi G, Marangoni B (1981) Hormonal changes during the rooting of hardwood cuttings of grapevine rootstocks. Am J Enol Viticult 32(2):135–137. doi:https://doi.org/10.1016/S0065-2628(08)60296-7
Li SW (2021) Molecular bases for the regulation of adventitious root generation in plants. Front Plant Sci 12:614072. doi:https://doi.org/10.3389/fpls.2021.614072
Mauriat M, Petterle A, Bellini C, Moritz T (2014) Gibberellins inhibit adventitious rooting in hybrid aspen and Arabidopsis by affecting auxin transport. Plant J 78(3):372–384. doi:https://doi.org/10.1111/tpj.12478
Mensuali-Sodi A, Panizza M, Tognoni F (1995) Endogenous ethylene requirement for adventitious root induction and growth in tomato cotyledons and lavandin microcuttings in vitro. Plant Growth Regul 17:205–212. doi:https://doi.org/10.1007/BF00024727
Niu SH, Li ZX, Yuan HW, Fang P, Chen XY, Li W (2013) Proper gibberellin localization in vascular tissue is required to regulate adventitious root development in tobacco. J Exp Bot 64(11):3411–3424. doi:https://doi.org/10.1093/jxb/ert186
Omoarelojie LO, Kulkarni MG, Finnie JF, van Staden J (2021) Strigolactone inhibits hydrogen peroxide and plasma membrane H+-ATPase activities to downregulate adventitious root formation in mung bean hypocotyls. Plant Growth Regul 94:11–21. doi:https://doi.org/10.1007/s10725-021-00691-y
Rolland F, Baena-Gonzalez E, Sheen J (2006) Sugar sensing and signaling in plants: conserved and novel mechanisms. Annu Rev Plant Biol 57(1):675–709
Sairanen I, Novak O, Pencik A, Ikeda Y, Jones B, Sandberg G, Ljung K (2012) Soluble carbohydrates regulate auxin biosynthesis via PIF proteins in Arabidopsis. Plant Cell 24(12):4907–4916. doi:https://doi.org/10.1105/tpc.112.104794
Sharma M, Singh D, Saksena HB, Sharma M, Tiwari A, Awasthi P, Botta HK, Shukla BN, Laxmi A (2021) Understanding the intricate web of phytohormone signalling in modulating root system architecture. Int J Mol Sci 22(11):5508. doi:https://doi.org/10.3390/ijms22115508
Shiozaki S, Makibuchi M, Ogata T (2013) Indole-3-acetic acid, polyamines, and phenols in hardwood cuttings of recalcitrant-to-root wild grapes native to east asia: Vitis davidii and Vitis kiusiana. J Bot 2013:1–9. doi:https://doi.org/10.1155/2013/819531
Smart DR, Kocsis L, Andrew Walker M, Stockert C (2003) Dormant buds and adventitious root formation by vitis and other woody plants. J Plant Growth Regul 21(4):296–314. doi:https://doi.org/10.1007/s00344-003-0001-3
Steffens B, Rasmussen A (2016) The physiology of adventitious roots. Plant Physiol 170(2):603–617. doi:https://doi.org/10.1104/pp.15.01360
Thomas P, Lee MM, Schiefelbein J (2003) Molecular identification of proline-rich protein genes induced during root formation in grape (Vitis vinifera L.) stem cuttings. Plant Cell Environ 26:1497–1504. doi:https://doi.org/10.1046/j.1365-3040.2003.01071.x
Thomas P, Schiefelbein JW (2004) Roles of leaf in regulation of root and shoot growth from single node softwood cuttings of grape (Vitis vinifera). Ann Appl Biol 144(1):27–37. doi:https://doi.org/10.1111/j.1744-7348.2004.tb00313.x
Wei K, Ruan L, Wang L, Cheng H (2019) Auxin-induced adventitious root formation in nodal cuttings of Camellia sinensis. Int J Mol Sci 20(19):4817
Xu L (2018) De novo root regeneration from leaf explants: wounding, auxin, and cell fate transition. Curr Opin Plant Biol 41:39–45. doi:https://doi.org/10.1016/j.pbi.2017.08.004
Zhou Q, Gao B, Li WF, Mao J, Yang SJ, Li W, Ma ZH, Zhao X, Chen BH (2020) Effects of exogenous growth regulators and bud picking on grafting of grapevine hard branches. Sci Hort 264:109186. doi:https://doi.org/10.1016/j.scienta.2020.109186
Acknowledgements
This work was supported by the National Key Research and Development Program of China (No. 2021YFD1200200), Natural Science Foundation of Hunan Province, China (No. 2021JJ30310), and Research Foundation of Education Department of Hunan Province, China (No. 19B278).
Author information
Authors and Affiliations
Contributions
All authors contributed to the study’s conception and design. Material preparation and data collection were performed by XYC, KZ, YZY, PYN, JM, HL, and SYG. Data analysis was performed by XYC and MB. The first draft of the manuscript was written by GSY and MB and all authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.
Corresponding author
Additional information
Communicated by Vaclav Motyka.
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
XinYu Chang, Kai Zhang and Yunzhang Yuan have contributed equally to this work.
Electronic supplementary material
Below is the link to the electronic supplementary material.
Rights and permissions
About this article
Cite this article
Chang, X.Y., Zhang, K., Yuan, Y. et al. A simple, rapid, and quantifiable system for studying adventitious root formation in grapevine. Plant Growth Regul 98, 117–126 (2022). https://doi.org/10.1007/s10725-022-00838-5
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10725-022-00838-5