| 4011 References Angelovici R, Fait A, Fernie AR, Galili G. 2011. A seed high-lysine trait is negatively associated with the TCA cycle and slows down Arabidopsis seed germination. New Phytologist 189, 148–159. Dizigan MA, Kelly RA, Voyles DA, Luethy MH, Malvar TM, Malloy KP. 2007. High lysine maize compositions and event LY038 maize plants. United States Patent No. 7157281. Falco SC, Guida T, Locke M, Mauvais J, Sanders C, Ward RT, Webber P. 1995. Transgenic canola and soybean seeds with increased lysine. Bio-Technology 13, 577–582. Frizzi A, Huang S, Gilbertson LA, Armstrong TA, Luethy MH, Malvar TM. 2008. Modifying lysine biosynthesis and catabolism in corn with a single bifunctional expression/silencing transgene cassette. Plant Biotechnology Journal 6, 13–21. Galili G, Amir R. 2013. Fortifying plants with the essential amino acids lysine and methionine to improve nutritional quality. Plant Biotechnology Journal 11, 211–222. Galili G, Karchi H, Shaul O, Perl A, Cahana A, Tzchori IB, Zhu XZ, Galili S. 1994. Production of transgenic plants containing elevated levels of lysine and threonine. Biochemical Society Transactions 22, 921–925. Karchi H, Shaul O, Galili G. 1994. Lysine synthesis and catabolism are coordinately regulated during tobacco seed development. Proceedings of the National Academy of Sciences, USA 91, 2577–2581. Karchi H, Miron D, Benyaacov S, Galili G. 1995. The lysine-dependent stimulation of lysine catabolism in tobacco seed requires calcium and protein-phosphorylation. The Plant Cell 7, 1963–1970. Keeler SJ, Maloney CL, Webber PY, Patterson C, Hirata LT, Falco SC, Rice JA. 1997. Expression of de novo high-lysine alpha-helical coiled-coil
proteins may significantly increase the accumulated levels of lysine in mature seeds of transgenic tobacco plants. Plant Molecular Biology 34, 15–29. Kusano M, Yang Z, Okazaki Y, Nakabayashi R, Fukushima A, Saito K. 2015. Using metabolomic approaches to explore chemical diversity in rice. Molecular Plant 8, 58–67. Long X, Liu Q, Chan M, Wang Q, Sun SSM. 2013. Metabolic engineering and profiling of rice with increased lysine. Plant Biotechnology Journal 11, 490–501. Shaul O, Galili G. 1993. Concerted regulation of lysine and threonine synthesis in tobacco plants expressing bacterial feedback-insensitive aspartate kinase and dihydrodipicolinate synthase. Plant Molecular Biology 23, 759–768. Mertz ET, Bates LS, Nelson OE. 1964. Mutant gene that changes protein composition and increases lysine content of maize endosperm. Science 17, 279–280. Tzchori IBT, Perl A, Galili G. 1996. Lysine and threonine metabolism are subject to complex patterns of regulation in Arabidopsis. Plant Molecular Biology 32, 727–734. Wong HW, Liu Q, Sun SSM. 2015. Biofortification of rice with lysine using endogenous histones. Plant Molecular Biology 87, 235–248. Yang QQ, Zhang CQ, Chan MI, et al. 2016. Biofortification of rice with the essential amino acid lysine: molecular characterization, nutritional evaluation, and field performance. Journal of Experimental Botany 67, 4258–4296. Zhu XH, Galili G. 2003. Increased lysine synthesis coupled with a knockout of its catabolism synergistically boosts lysine content and also transregulates the metabolism of other amino acids in Arabidopsis seeds. The Plant Cell 15, 845–853. Zhu XH, Galili G. 2004. Lysine metabolism is concurrently regulated by synthesis and catabolism in both reproductive and vegetative tissues. Plant Physiology 135, 129–136.
Insight
Endogenous auxin biosynthesis and de novo root organogenesis Ya Lin Sang, Zhi Juan Cheng and Xian Sheng Zhang* State Key Laboratory of Crop Biology, College of Life Sciences, College of Forestry, Shandong Agricultural University, Taian, Shandong 271018, China * Correspondence: [email protected]
Induction of adventitious roots is essential for vegetative propagation of plants, and auxin has long been used as an exogenous root-inducing agent. In this issue of Journal of Experimental Botany, Chen et al. (pages 4273–4284) demonstrate that different members of the YUCCA family orchestrate the endogenous auxin biosynthesis that is required for the induction of adventitious roots.
Sun Wukong, also known as the Monkey King, is the main character in the classical Chinese novel Journey to the West. As a fabled deity, he was endowed with magical properties allowing each of his hairs to be transformed into clones of himself as needed. Plants also possess the remarkable ability of multiplication, with detached pieces of adult tissues capable of forming an entire plant body (Gordon et al., 2007; Birnbaum and Sánchez Alvarado, 2008; Sugimoto et al., 2010). This unique ability is mainly based on de novo organogenesis, in which adventitious
shoots or roots are generated from isolated tissues or organs (Duclercq et al., 2011; Cheng et al., 2013; Xu and Huang, 2014). De novo organogenesis can be induced under both natural and tissue culture conditions (Chen et al., 2014). Plant organs, such as stems and leaves, give rise to adventitious roots under natural growth conditions and this property has long been used for vegetative propagation of elite genotypes in agriculture, forestry and horticulture (De Klerk et al., 1999). Six decades ago, Skoog and Miller demonstrated that the entire plant could be regenerated by tissue culture (Skoog and Miller, 1957). They showed that culturing explants in medium containing high levels of cytokinin induced the formation of adventitious shoots, whereas medium with high levels of auxin triggered initiation of adventitious roots. This classic system laid the foundations for plant micropropagation and genetic transformation (Duclercq et al., 2011; Li et al., 2011). In both cases, a key step ensuring the success of plant regeneration is de novo root organogenesis,
© The Author 2016. Published by Oxford University Press on behalf of the Society for Experimental Biology. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
4012 | Box 1. Modulation of the dynamic expression pattern of YUC4 in response to wounding After detachment, leaf explants were cultured on B5 medium without exogenous hormone. At day 0, YUC4 is expressed in the hydathode. During the formation of adventitious roots, its expression is enhanced in mesophyll cells. After two days, strong expression signals are detected in the vascular tissues near the wound, where the adventitious roots initiate. DAC, days after culture.
which guarantees the water and nutrient supply for regeneration and survival of the new organism (Chen et al., 2014).
Cell fate transition The first cellular event of de novo organogenesis is cell fate transition (Duclercq et al., 2011; Chatfield et al., 2013). Evidence from different species has indicated that adventitious roots initiate from the procambium or cambium regions (Liu et al., 2014; Xu and Huang, 2014). To study the underlying mechanisms, Chen et al. have developed a simple system to mimic the formation of adventitious roots under natural conditions (Chen et al., 2014). By culturing Arabidopsis leaves on B5 medium without exogenous hormones for six to eight days, adventitious roots can be generated from the midvein near the wound (Liu et al., 2014). Using this system, Liu et al. revealed that the cell fate transition during the initiation of rooting contains two steps. In the first step, WUSCHELRELATED HOMEOBOX 11 (WOX11) and WOX12 act redundantly to regulate the transition from procambium cells to root founder cells. In the second step, root founder cells are further switched into root primordium cells, marked by WOX5 expression. Notably, endogenous auxin plays essential roles in the cell fate reprogramming process. Inhibiting polar auxin transport using naphthylphthalamic acid (NPA) abolishes rooting, an effect which can be rescued by exogenous indole-3-acetic acid. During adventitious root formation, the distribution of auxin response signals overlaps with the expression regions of WOX11. Mutations of the auxin response elements within the WOX11 promoter or NPA treatment disrupt the expression pattern of WOX11 (Liu et al., 2014). Moreover, the auxin response signals are progressively enhanced and distributed in the region of root initiation, suggesting that the wounding induces auxin accumulation in this area. However, the molecular events between explant detachment and adventitious root initiation remain to be elucidated.
YUCCA enzymes The research reported in this issue by Chen et al. (2016) describes the involvement of different members of the
YUCCA (YUC) family, which encode enzymes catalysing the rate-limiting step of auxin biosynthesis in de novo root organogenesis. Under natural growth conditions, some plant species can generate adventitious roots from detached organs spontaneously, but in most cases application of exogenous auxin is required (De Klerk et al., 1999), suggesting that the endogenous auxin biosynthesis varies among the different species. However, using culture methods to induce rooting using exogenous auxin could bypass the function of endogenous hormones. In the system used by Chen et al. (2016), no exogenous hormones were added. Thus, adventitious root generation depended on endogenous hormones, providing an opportunity to investigate the roles of endogenous auxin in de novo root organogenesis. Together with the previous findings from this lab (Chen et al., 2014; Liu et al., 2014), the results support a working model for de novo root organogenesis (see Chen et al., 2016, Fig. 9). The detachment of leaf explants leads to significant increases in the level of auxin. The elevated auxin content results from the function of YUC genes, which respond to wounding and act upstream of cell fate transition from competent cells (procambium and vascular parenchyma cells) to root founder cells. The YUC genes show division of labour and orchestrate auxin biosynthesis required for the formation of adventitious roots. Of them, YUC1, 2, 4 and 6 play major roles under both light and dark conditions. YUC1 and 4 function in a wounding-induced way, whereas YUC2 and 6 contribute to the basal auxin level (Box 1). In addition, YUC5, 8 and 9 mainly produce auxin in leaf margin and mesophyll cells in response to darkness.
More questions A critical open question is how wounding signals trigger the spatial expression of YUC1 and 4. The authors suggest that wounding-response factors could regulate YUC1 and 4 in cooperation with epigenetic factors. This is supported by the fact that up-regulation of YUC1 and 4 expression is accompanied by a reduced level of histone H3 lysine 27 trimethylation, a marker of transcriptional repression (Schatlowski et al., 2008; He et al., 2013). It would be interesting to investigate the relationship between wounding signals and epigenetic factors, as well as their regulatory role in de novo root organogenesis.
| 4013 Despite its importance to plant industries worldwide, adventitious root induction is still difficult in many species, hampering the development of forestry and horticulture (Rasmussen et al., 2012). The issue is mainly limited knowledge about the mechanisms controlling adventitious root formation, and therefore the findings presented here provide valuable new information. Genetic engineering approaches allowing the modification of endogenous auxin biosynthesis would now be powerful in enhancing our abilities.
cytokinin biosynthesis by AUXIN RESPONSE FACTOR3. Plant Physiology 161, 240–251.
Key words: Adventitious root, auxin biogenesis, de novo organogenesis, plant regeneration, YUCCA family.
He C, Huang H, Xu L. 2013. Mechanisms guiding Polycomb activities during gene silencing in Arabidopsis thaliana. Frontiers in Plant Science 4, 454.
Journal of Experimental Botany, Vol. 67 No. 14 pp. 4011–4013, 2016 doi:10.1093/jxb/erw250
References Birnbaum KD, Sanchez Alvarado A. 2008. Slicing across kingdoms: regeneration in plants and animals. Cell 132, 697–710. Chatfield SP, Capron R, Severino A, Penttila PA, Alfred S, Nahal H, Provart NJ. 2013. Incipient stem cell niche conversion in tissue culture: using a systems approach to probe early events in WUSCHEL-dependent conversion of lateral root primordia into shoot meristems. The Plant Journal 73, 798–813. Chen L, Tong J, Xiao L, Ruan Y, Liu J, Zeng M, Huang H, Wang J-W, Xu L. 2016. YUCCA-mediated auxin biogenesis is required for cell fate transition occurring during de novo root organogenesis in Arabidopsis. Journal of Experimental Botany 67, 4273–4284.
De Klerk G, VanDerKrieken W, DeJong J. 1999. The formation of adventitious roots: new concepts, new possibilities. In Vitro Cellular & Developmental Biology – Plant 35, 189–199. Duclercq J, Sangwan-Norreel B, Catterou M, Sangwan RS. 2011. De novo shoot organogenesis: from art to science. Trends in Plant Science 16, 597–606. Gordon SP, Heisler MG, Reddy GV, Ohno C, Das P, Meyerowitz EM. 2007. Pattern formation during de novo assembly of the Arabidopsis shoot meristem. Development 134, 3539–3548.
Li W, Liu H, Cheng ZJ, Su YH, Han HN, Zhang Y, Zhang XS. 2011. DNA methylation and histone modifications regulate de novo shoot regeneration in Arabidopsis by modulating WUSCHEL expression and auxin signaling. PLOS Genetics 7, e1002243. Liu J, Sheng L, Xu Y, Li J, Yang Z, Huang H, Xu L. 2014. WOX11 and 12 are involved in the first-step cell fate transition during de novo root organogenesis in Arabidopsis. The Plant Cell 26, 1081–1093. Rasmussen A, Mason MG, De Cuyper C, et al. 2012. Strigolactones suppress adventitious rooting in Arabidopsis and pea. Plant Physiology 158, 1976–1987. Schatlowski N, Creasey K, Goodrich J, Schubert D. 2008. Keeping plants in shape: polycomb-group genes and histone methylation. Seminars in Cell & Developmental Biology 19, 547–553. Skoog F, Miller CO. 1957. Chemical regulation of growth and organ formation in plant tissues cultured in vitro. Symposia of the Society for Experimental Biology 11, 118–130.
Chen X, Qu Y, Sheng L, Liu J, Huang H, Xu L. 2014. A simple method suitable to study de novo root organogenesis. Frontiers in Plant Science 5, 208.
Sugimoto K, Jiao Y, Meyerowitz EM. 2010. Arabidopsis regeneration from multiple tissues occurs via a root development pathway. Developmental Cell 18, 463–471.
Cheng ZJ, Wang L, Sun W, et al. 2013. Pattern of auxin and cytokinin responses for shoot meristem induction results from the regulation of
Xu L, Huang H. 2014. Genetic and epigenetic controls of plant regeneration. Current Topics in Developmental Biology 108, 1–33.
proteins may significantly increase the accumulated levels of lysine in mature seeds of transgenic tobacco plants. Plant Molecular Biology 34, 15–29. Kusano M, Yang Z, Okazaki Y, Nakabayashi R, Fukushima A, Saito K. 2015. Using metabolomic approaches to explore chemical diversity in rice. Molecular Plant 8, 58–67. Long X, Liu Q, Chan M, Wang Q, Sun SSM. 2013. Metabolic engineering and profiling of rice with increased lysine. Plant Biotechnology Journal 11, 490–501. Shaul O, Galili G. 1993. Concerted regulation of lysine and threonine synthesis in tobacco plants expressing bacterial feedback-insensitive aspartate kinase and dihydrodipicolinate synthase. Plant Molecular Biology 23, 759–768. Mertz ET, Bates LS, Nelson OE. 1964. Mutant gene that changes protein composition and increases lysine content of maize endosperm. Science 17, 279–280. Tzchori IBT, Perl A, Galili G. 1996. Lysine and threonine metabolism are subject to complex patterns of regulation in Arabidopsis. Plant Molecular Biology 32, 727–734. Wong HW, Liu Q, Sun SSM. 2015. Biofortification of rice with lysine using endogenous histones. Plant Molecular Biology 87, 235–248. Yang QQ, Zhang CQ, Chan MI, et al. 2016. Biofortification of rice with the essential amino acid lysine: molecular characterization, nutritional evaluation, and field performance. Journal of Experimental Botany 67, 4258–4296. Zhu XH, Galili G. 2003. Increased lysine synthesis coupled with a knockout of its catabolism synergistically boosts lysine content and also transregulates the metabolism of other amino acids in Arabidopsis seeds. The Plant Cell 15, 845–853. Zhu XH, Galili G. 2004. Lysine metabolism is concurrently regulated by synthesis and catabolism in both reproductive and vegetative tissues. Plant Physiology 135, 129–136.
Insight
Endogenous auxin biosynthesis and de novo root organogenesis Ya Lin Sang, Zhi Juan Cheng and Xian Sheng Zhang* State Key Laboratory of Crop Biology, College of Life Sciences, College of Forestry, Shandong Agricultural University, Taian, Shandong 271018, China * Correspondence: [email protected]
Induction of adventitious roots is essential for vegetative propagation of plants, and auxin has long been used as an exogenous root-inducing agent. In this issue of Journal of Experimental Botany, Chen et al. (pages 4273–4284) demonstrate that different members of the YUCCA family orchestrate the endogenous auxin biosynthesis that is required for the induction of adventitious roots.
Sun Wukong, also known as the Monkey King, is the main character in the classical Chinese novel Journey to the West. As a fabled deity, he was endowed with magical properties allowing each of his hairs to be transformed into clones of himself as needed. Plants also possess the remarkable ability of multiplication, with detached pieces of adult tissues capable of forming an entire plant body (Gordon et al., 2007; Birnbaum and Sánchez Alvarado, 2008; Sugimoto et al., 2010). This unique ability is mainly based on de novo organogenesis, in which adventitious
shoots or roots are generated from isolated tissues or organs (Duclercq et al., 2011; Cheng et al., 2013; Xu and Huang, 2014). De novo organogenesis can be induced under both natural and tissue culture conditions (Chen et al., 2014). Plant organs, such as stems and leaves, give rise to adventitious roots under natural growth conditions and this property has long been used for vegetative propagation of elite genotypes in agriculture, forestry and horticulture (De Klerk et al., 1999). Six decades ago, Skoog and Miller demonstrated that the entire plant could be regenerated by tissue culture (Skoog and Miller, 1957). They showed that culturing explants in medium containing high levels of cytokinin induced the formation of adventitious shoots, whereas medium with high levels of auxin triggered initiation of adventitious roots. This classic system laid the foundations for plant micropropagation and genetic transformation (Duclercq et al., 2011; Li et al., 2011). In both cases, a key step ensuring the success of plant regeneration is de novo root organogenesis,
© The Author 2016. Published by Oxford University Press on behalf of the Society for Experimental Biology. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
4012 | Box 1. Modulation of the dynamic expression pattern of YUC4 in response to wounding After detachment, leaf explants were cultured on B5 medium without exogenous hormone. At day 0, YUC4 is expressed in the hydathode. During the formation of adventitious roots, its expression is enhanced in mesophyll cells. After two days, strong expression signals are detected in the vascular tissues near the wound, where the adventitious roots initiate. DAC, days after culture.
which guarantees the water and nutrient supply for regeneration and survival of the new organism (Chen et al., 2014).
Cell fate transition The first cellular event of de novo organogenesis is cell fate transition (Duclercq et al., 2011; Chatfield et al., 2013). Evidence from different species has indicated that adventitious roots initiate from the procambium or cambium regions (Liu et al., 2014; Xu and Huang, 2014). To study the underlying mechanisms, Chen et al. have developed a simple system to mimic the formation of adventitious roots under natural conditions (Chen et al., 2014). By culturing Arabidopsis leaves on B5 medium without exogenous hormones for six to eight days, adventitious roots can be generated from the midvein near the wound (Liu et al., 2014). Using this system, Liu et al. revealed that the cell fate transition during the initiation of rooting contains two steps. In the first step, WUSCHELRELATED HOMEOBOX 11 (WOX11) and WOX12 act redundantly to regulate the transition from procambium cells to root founder cells. In the second step, root founder cells are further switched into root primordium cells, marked by WOX5 expression. Notably, endogenous auxin plays essential roles in the cell fate reprogramming process. Inhibiting polar auxin transport using naphthylphthalamic acid (NPA) abolishes rooting, an effect which can be rescued by exogenous indole-3-acetic acid. During adventitious root formation, the distribution of auxin response signals overlaps with the expression regions of WOX11. Mutations of the auxin response elements within the WOX11 promoter or NPA treatment disrupt the expression pattern of WOX11 (Liu et al., 2014). Moreover, the auxin response signals are progressively enhanced and distributed in the region of root initiation, suggesting that the wounding induces auxin accumulation in this area. However, the molecular events between explant detachment and adventitious root initiation remain to be elucidated.
YUCCA enzymes The research reported in this issue by Chen et al. (2016) describes the involvement of different members of the
YUCCA (YUC) family, which encode enzymes catalysing the rate-limiting step of auxin biosynthesis in de novo root organogenesis. Under natural growth conditions, some plant species can generate adventitious roots from detached organs spontaneously, but in most cases application of exogenous auxin is required (De Klerk et al., 1999), suggesting that the endogenous auxin biosynthesis varies among the different species. However, using culture methods to induce rooting using exogenous auxin could bypass the function of endogenous hormones. In the system used by Chen et al. (2016), no exogenous hormones were added. Thus, adventitious root generation depended on endogenous hormones, providing an opportunity to investigate the roles of endogenous auxin in de novo root organogenesis. Together with the previous findings from this lab (Chen et al., 2014; Liu et al., 2014), the results support a working model for de novo root organogenesis (see Chen et al., 2016, Fig. 9). The detachment of leaf explants leads to significant increases in the level of auxin. The elevated auxin content results from the function of YUC genes, which respond to wounding and act upstream of cell fate transition from competent cells (procambium and vascular parenchyma cells) to root founder cells. The YUC genes show division of labour and orchestrate auxin biosynthesis required for the formation of adventitious roots. Of them, YUC1, 2, 4 and 6 play major roles under both light and dark conditions. YUC1 and 4 function in a wounding-induced way, whereas YUC2 and 6 contribute to the basal auxin level (Box 1). In addition, YUC5, 8 and 9 mainly produce auxin in leaf margin and mesophyll cells in response to darkness.
More questions A critical open question is how wounding signals trigger the spatial expression of YUC1 and 4. The authors suggest that wounding-response factors could regulate YUC1 and 4 in cooperation with epigenetic factors. This is supported by the fact that up-regulation of YUC1 and 4 expression is accompanied by a reduced level of histone H3 lysine 27 trimethylation, a marker of transcriptional repression (Schatlowski et al., 2008; He et al., 2013). It would be interesting to investigate the relationship between wounding signals and epigenetic factors, as well as their regulatory role in de novo root organogenesis.
| 4013 Despite its importance to plant industries worldwide, adventitious root induction is still difficult in many species, hampering the development of forestry and horticulture (Rasmussen et al., 2012). The issue is mainly limited knowledge about the mechanisms controlling adventitious root formation, and therefore the findings presented here provide valuable new information. Genetic engineering approaches allowing the modification of endogenous auxin biosynthesis would now be powerful in enhancing our abilities.
cytokinin biosynthesis by AUXIN RESPONSE FACTOR3. Plant Physiology 161, 240–251.
Key words: Adventitious root, auxin biogenesis, de novo organogenesis, plant regeneration, YUCCA family.
He C, Huang H, Xu L. 2013. Mechanisms guiding Polycomb activities during gene silencing in Arabidopsis thaliana. Frontiers in Plant Science 4, 454.
Journal of Experimental Botany, Vol. 67 No. 14 pp. 4011–4013, 2016 doi:10.1093/jxb/erw250
References Birnbaum KD, Sanchez Alvarado A. 2008. Slicing across kingdoms: regeneration in plants and animals. Cell 132, 697–710. Chatfield SP, Capron R, Severino A, Penttila PA, Alfred S, Nahal H, Provart NJ. 2013. Incipient stem cell niche conversion in tissue culture: using a systems approach to probe early events in WUSCHEL-dependent conversion of lateral root primordia into shoot meristems. The Plant Journal 73, 798–813. Chen L, Tong J, Xiao L, Ruan Y, Liu J, Zeng M, Huang H, Wang J-W, Xu L. 2016. YUCCA-mediated auxin biogenesis is required for cell fate transition occurring during de novo root organogenesis in Arabidopsis. Journal of Experimental Botany 67, 4273–4284.
De Klerk G, VanDerKrieken W, DeJong J. 1999. The formation of adventitious roots: new concepts, new possibilities. In Vitro Cellular & Developmental Biology – Plant 35, 189–199. Duclercq J, Sangwan-Norreel B, Catterou M, Sangwan RS. 2011. De novo shoot organogenesis: from art to science. Trends in Plant Science 16, 597–606. Gordon SP, Heisler MG, Reddy GV, Ohno C, Das P, Meyerowitz EM. 2007. Pattern formation during de novo assembly of the Arabidopsis shoot meristem. Development 134, 3539–3548.
Li W, Liu H, Cheng ZJ, Su YH, Han HN, Zhang Y, Zhang XS. 2011. DNA methylation and histone modifications regulate de novo shoot regeneration in Arabidopsis by modulating WUSCHEL expression and auxin signaling. PLOS Genetics 7, e1002243. Liu J, Sheng L, Xu Y, Li J, Yang Z, Huang H, Xu L. 2014. WOX11 and 12 are involved in the first-step cell fate transition during de novo root organogenesis in Arabidopsis. The Plant Cell 26, 1081–1093. Rasmussen A, Mason MG, De Cuyper C, et al. 2012. Strigolactones suppress adventitious rooting in Arabidopsis and pea. Plant Physiology 158, 1976–1987. Schatlowski N, Creasey K, Goodrich J, Schubert D. 2008. Keeping plants in shape: polycomb-group genes and histone methylation. Seminars in Cell & Developmental Biology 19, 547–553. Skoog F, Miller CO. 1957. Chemical regulation of growth and organ formation in plant tissues cultured in vitro. Symposia of the Society for Experimental Biology 11, 118–130.
Chen X, Qu Y, Sheng L, Liu J, Huang H, Xu L. 2014. A simple method suitable to study de novo root organogenesis. Frontiers in Plant Science 5, 208.
Sugimoto K, Jiao Y, Meyerowitz EM. 2010. Arabidopsis regeneration from multiple tissues occurs via a root development pathway. Developmental Cell 18, 463–471.
Cheng ZJ, Wang L, Sun W, et al. 2013. Pattern of auxin and cytokinin responses for shoot meristem induction results from the regulation of
Xu L, Huang H. 2014. Genetic and epigenetic controls of plant regeneration. Current Topics in Developmental Biology 108, 1–33.
