- freely available
Int. J. Mol. Sci. 2013, 14(2), 2515-2528; doi:10.3390/ijms14022515
Abstract: Poplar is a model organism for high in vitro regeneration in woody plants. We have chosen a hybrid poplar Populus davidiana Dode × Populus bollena Lauche. By optimizing the Murashige and Skoog medium with (0.3 mg/L) 6-benzylaminopurine and (0.08 mg/L) naphthaleneacetic acid, we have achieved the highest frequency (90%) for shoot regeneration from poplar leaves. It was also important to improve the transformation efficiency of poplar for genetic breeding and other applications. In this study, we found a significant improvement of the transformation frequency by controlling the leaf age. Transformation efficiency was enhanced by optimizing the Agrobacterium concentration (OD600 = 0.8–1.0) and an infection time (20–30 min). According to transmission electron microscopy observations, there were more Agrobacterium invasions in the 30-day-old leaf explants than in 60-day-old and 90-day-old explants. Using the green fluorescent protein (GFP) marker, the expression of MD–GFP fusion proteins in the leaf, shoot, and root of hybrid poplar P. davidiana Dode × P. bollena Lauche was visualized for confirmation of transgene integration. Southern and Northern blot analysis also showed the integration of T-DNA into the genome and gene expression of transgenic plants. Our results suggest that younger leaves had higher transformation efficiency (~30%) than older leaves (10%).
Poplar has several exceptional qualities, such as a high capacity for vegetative propagation and a fast growth rate. It has been extensively used for the pulp and paper industry, reforestation of lowlands, and phytoremediation of contaminated soils. The micro-vegetative propagation and regeneration of poplar has been reported in recent decades. Different poplar genotypes have been used to perform regeneration experiments [1–10]. Growth and differentiation response is not only controlled by the cultural environment, but is also dependent upon the genotype . In vitro regeneration has been attempted in several poplar species using different explants such as leaves [8,11–14], petioles , internodes [8,14], stems [5,16], roots [8,11], and shoot tips . The leaf disc transformation method  has been widely used in plant genetic engineering.
Parsons et al.  first reported the genetic transformation of poplar. This technology has been applied to various Populus species to improve their transformation efficiency [20–28]. Several factors were systematically analyzed to improve transformation efficiency, including poplar genotype, Agrobacterium tumefaciens strain for transformation, bacterial concentration, acetosyringone (AS) [20,29–32], and different explants including leaf discs and stems [23,33].
It is important to improve the transformation efficiency of poplar for genetic breeding and other applications. For example, the improvement of the transformation efficiency is crucial to build the full-length (fl) cDNA overexpression (FOX) hunting system and T-DNA mutant system. FOX requires large numbers of dominant mutations that enable the comprehensive characterization of mutant phenotypes and the identification of functional genes. 15,000 transgenic lines were used for expressing Arabidopsis full-length (fl) cDNAs , and >23,000 independent Arabidopsis transgenic lines for expressing rice fl-cDNAs ; Nakamura et al.  generated approximately 12,000 FOX-rice lines. Busov et al.  also reported that from the 627 independent activation-tagged poplar lines, nine exhibited an obvious morphological phenotype that had never been seen among the thousands of transgenic poplars produced.
We have chosen a hybrid poplar Populus davidiana Dode × P. bollena Lauche to improve the transformation efficiency. Populus was planted in northeast China and has a well-characterized morphology with cold resistance features. We have optimized the Murashige and Skoog  medium with supplementary 6-Benzylaminopurine and Naphthaleneacetic acid to achieve a high regeneration efficiency of Populus. Subsequently, we attempted to maximize the transformation efficiency. Although several factors effecting transformation efficiency have been studied, there were no attention to explant age. In order to improve the transformation efficiency in this work, we optimized the conditions of the leaf explants age, as well as Agrobacterium concentration.
2. Results and Discussion
2.1. Optimization of Poplar Shoot Regeneration
Leaf explants of a hybrid poplar Populus davidiana Dode × P. bollena Lauche were cultured in media with 0.1~0.5 mg/L BA and 0.01~0.1 mg/L NAA. There were no explants regenerated for 0.1 mg/L BA and 0.01–0.03 mg/L NAA (Table 1). Low regeneration frequencies were induced using BA (0.1 mg/L) and NAA (0.05, 0.08, or 0.1 mg/L) and BA (0.5 mg/L) with NAA (0.01, 0.03, 0.05, 0.08, or 0.1 mg/L). Ninety percent of the explants regeneration shoots when BA (0.3 mg/L) and NAA (0.08 mg/L) were used. Regenerated shoots from leaf explants were shown in Figure 1a. Confalonieri et al.  reported the positive effect of BA and NAA on shoot regeneration in Populus nigra. To obtain shoot regeneration, leaf discs were cultivated in Petri dishes on MS medium with 0.5 mg/L BA and 0.2 mg/L NAA.
The rooting experiments showed that new root formation and growth were promoted by NAA at any concentration, and root regeneration was 100%. However, NAA at 0.25 mg/L was the optimal rooting concentration because the growth status of roots was long and polyrhizal (Figure 1b). After the hardening process, 90% of the poplar plantlets survived acclimatization.
Previously, various media were used to different genotypes and explants for shoot regeneration and rooting. IBA was used to induce roots for leaf of aspen and zeatin was used for shoot regeneration . Adventitious shoots regenerated in a woody plant medium (WPM) supplemented with TDZ (Thidiazuron) from aspen stem explants . Ferreira et al.  reported that adventitious shoot regeneration of P. euphratica from organogenic nodules of leaf explants was achieved within a range of concentrations of a-naphtalenacetic acid and 6-benzylaminopurine, at a fixed 2:1 ratio. Shoots of Populus ciliata Wall were regenerated at high frequencies from explants grown on Murashige and Skoog (MS) medium supplemented with 0.5 mg/L kinetin and 0.2 mg/L indole-3-acetic acid (IAA). Regenerated shoots developed roots in MS medium supplemented with 0.1 mg/L IAA .
2.2. Improvement of Genetic Transformation of Poplar
The effect of Agrobacterium concentration on transformation frequency was shown in Figure 2. At OD600 = 0.6, a lower transformation frequency was observed. As OD600 ranging from 0.8 to 1.0, a higher transformation frequency was observed with little contamination. At OD600 = 1.2, the transformation frequency was also reduced because of a higher contamination frequency. At OD600 ranging from 0.8 to 1.0, the suitable incubation time of the explants in the bacterial suspension ranged from 20 min to 30 min (Figure 2). Previous study by Confalonieri et al.  optimized the production of transgenic plantlets from different P. nigra clones, Agrobacterium concentration (7 × 108; 1.2 × 109 cells/mL) were used. The results show that the optimal procedure involved dipping of leaf discs into a bacterial suspension (7 × 108 cells/mL) for 20 min. Previous research has shown that the transformation efficiency increases in the presence of AS in the co-cultivation medium [32,39]. However, in the current experiment, the presence of AS during co-cultivation did not increase further the transformation efficiency (data not shown).
In addition to Agrobacterium concentration, and infection time, the transformation frequency was also influenced by leaf age. We selected three different leaf age groups, 30-, 60-, and 90-day-old (Figure 3). The transformation frequency of the 30-day-old leaves was more than that of the 60-day-old and 90-day-old leaves (Figure 4). As the age of the sample leaf increased, the transformation frequency decreased (Figure 4d). The transformation frequency was 10% for the 90-day-old samples, while ~30% for the 30-day-old samples. Although several factors affecting transformation efficiency have been studied, there was no focus on explant age. A previous study by Smith and McCown  reported that juvenile sources of explant tissues have superior growth and regeneration potential compared with other sources. Civinova and Sladky  reported that juvenile explants have superior regeneration capacity and they are less lignified. Han et al.  reported that incompletely lignified explant sections of hybrid cottonwoods have also been efficiently transformed with Agrobacterium.
Different genotypes may respond differently to the optimal treatment conditions, and genetic transformation efficiency would be changed. According to published works, transformation frequency appeared to be different: 4%–6% for Populus trichocarpa, genotype Nisqually-1 , 16% for Populus tremuloides , and 20% for Populus nigra var. italica . To improve its utility for functional genomics research, mutant library construction using the FOX hunting system was necessary for an efficient means for transformation and regeneration. Using hybrid poplar Populus davidiana Dode × P. bollena Lauche for transformation, the transformation frequency exceeded 30% by controlling the age of the leaf.
In order to understand the higher transformation ability in the younger leaf explants, the Agrobacterium invasion of various leaves were analyzed to confirm that leaf age was an important factor in Agrobacterium-mediated transformation. Figure 5a,b showed the magnified TEM image of the intercellular spaces with no Agrobacterium invasion. For 30-day-old leaf explants, some bacteria were scattered throughout the intercellular space (Figure 5c,d). For the 60-day-old leaf explants, the bacteria decreased slightly in number, and some of the intercellular space appeared empty (Figure 5e,f). For the 90-day-old leaf explants, almost all the intercellular space appeared clean and just a few bacteria were observed in the intercellular space (Figure 5g,h). These results demonstrated that there were Agrobacterium-mediated transgenic activities in the leaf explants, as well as the 30-day-old leaf explants contained more Agrobacterium than the 60-day-old and 90-day-old explants. The highest transformation efficiency was generated by the 30-day-old leaf explants (Figure 4d). The transformation frequencies were influenced by the amount of invasive bacteria.
Younger leaf explants may have a higher capability of shoot regeneration. However, in our TEM observations, the younger leaf explants had higher Agrobacterium infection. The invasion behavior of Agrobacterium in plant cells and their effects on genetic transformation is interesting. Agrobacterium invasion into plant cells can be affected by plant tissue age . Younger poplar leaves were more susceptible to Agrobacterium-mediated transformation. As leaf age increased, the susceptibility to genetic transformation by Agrobacterium invasion decreased. A possible reason for the observed differential response of Agrobacterium invasion in different tissues was because of changes in the cell wall composition at different physiologic and developmental stages. As the plant cells mature, their cell wall composition changes so that Agrobacterium-binding sites were gradually lost .
2.3. Observations of Genetic Transformation
We observed the genetic transformation further using a GFP label and Southern and Northern blot analysis. A plant transformation vector designed to express the MD–GFP fusion protein was used to detect the GFP signals in transgenic poplar. There were no GFP signals in the non-transgenic plants, shoots (Figure 6c,d), or roots (Figure 6g,h). However, the GFP signals from the shoots (Figure 6a,b), roots (Figure 6e,f), and leaf epidermis (Figure 6i,j) of the transgenic plants were detected. These results demonstrated that the pBI121-MD-GFP plasmid was introduced into hybrid poplar P. davidiana Dode × P. bollena Lauche.
Genomic DNA from seven of the different independent transgenic lines was subjected to Southern blot analysis. In line 1, non-specific DNA bands appeared as a result of the continuous distribution (line 1, Figure 7a), but all other lines contained the distinct bands. The banded MD–GFP gene was associated with high molecular weight invaded transgenic DNA(T-DNA), and produced the diverse copies as shown in line 2~8 (Figure 7a). The T-DNA appeared to be randomly integrated into the poplar genome.
For Northern blot analysis, all transgenic lines displayed a distinct band consistent with the predicted MD–GFP mRNA (lines 2~8, Figure 7b), whereas no hybridization signal was detected from the non-transgenic wild-type plant (line 1, Figure 7b). These results indicated that the MD–GFP gene was successfully integrated and expressed in the seven transgenic poplar lines 2~8 (Figure 7b).
3. Experimental Section
3.1. Plant Material, Agrobacterium Strain, Probe, and Plasmid
Populus davidiana Dode × P. bollena Lauche leaf explants were obtained randomly from in vitro shoot cultures and then used for regeneration and transformation. Populus davidiana Dode × P. bollena Lauche was hybrid by Xinjiang poplar as the male parent and aspen as female parent. The plasmid pBI121-MD-GFP and DIG-labeled MD gene probe were kindly provided by Prof. Che (Northeast Agricultural University) and used as a marker for plant transformation in our laboratory. The plasmid pBI121-MD-GFP with the CaMV 35S promoter was transferred into Agrobacterium tumefaciens EHA105 using electroporation method (Bio-Rad, Micropluser, Hercules, CA, USA).
3.2. Establishment of Regeneration System for Poplar
Murashige and Skoog (MS) medium  was supplemented with 6-benzylaminopurine (BA) at 0.1 mg/L to 0.5 mg/L and naphthaleneacetic acid (NAA) at 0.01 mg/L to 0.1 mg/L (Table 1). The leaves were cut into 1 cm × 1 cm blades and were cultured adaxial. The leaves were transferred to fresh regeneration medium at 10-day intervals. The regenerated shoots (3 cm to 5 cm in length) were excised and rooted on MS medium containing NAA at 0.1, 0.2, 0.25, 0.3, or 0.4 mg/L. All media included 3% (w/v) sucrose and 0.8% (w/v) agar. The pH of the media was adjusted to 5.8 after adding the plant growth regulation, and then autoclaved at 121 °C for 20 min.
After 1 to 2 months, the root formation was lignified, and the well-developed plantlets were removed from the media. The plantlets were gently washed under running tap water to remove the adhering media. For the hardening process, the plantlets were transferred into plastic cups containing a mixture of sterile compost. The regeneration experiments were designed with 10 Petri dishes for shoot regeneration and 10 triangular flasks for rooting per treatment, and each dish contained at least six leaf explants per treatment for shoot regeneration analysis, and each flask contained three shoots per treatment for rooting frequency analysis. Experiments were done in triplicate. The cultures were incubated at 25 °C ± 2 °C under a 16 h photoperiod (45 μmol m−2 s−1).
3.3. Plant Transformation
3.3.1. Sample Cultivation
Leaves were cut into 0.5 cm × 0.5 cm blades, immersed in the bacterial suspension in Petri dishes, and inoculated for different durations. Leaf explants were then dried on sterile filter paper and cultured on the shoot regeneration medium without Kanamycin sulfate (Kan) and cefotaxime sodium (Cef) in the dark. After 48 h of co-cultivation, leaf explants were washed five to six times (20 min to 30 min each) in liquid co-cultivation medium containing 200 mg/L Cef, and then blotted dry on sterile filter paper. The explants were then transferred to shoot regeneration medium containing Kan and Cef for selection, and cultured at 25 °C ± 2 °C under a 16-h photoperiod (45 μmol m−2 s−1) for 4 to 6 weeks. The cultures were transferred to fresh selection medium at 15-day intervals until shoot differentiation. The shoots were then transferred to rooting medium containing Kan and Cef after regeneration selection. Approximately 100 leaf explants were used for each transformation experiment and replicated thrice. The transformation frequencies were calculated by dividing the number of Kan-resistant regenerated shoots with the number of infected explants.
3.3.2. Effects of Agrobacterium Concentration and Infection Time
A single Agrobacterium colony was inoculated into 3 mL of liquid YEP (Yeast extract 10 g/L; Tryptone 10 g/L; NaCl 5 g/L) medium with 100 mg/L rifampicin (Rif) and 50 mg/L Kan, and then incubated at 28 °C for 24 h with constant agitation (175 rpm). An additional 30 mL of YEP was added and cultured overnight in the same culture conditions until OD600 = 1.2. After centrifuging at 5000 rpm for 5 min, the pellet was diluted to OD600 = 0.6, 0.8, 1.0, or 1.2 for transformation. The leaf explants were incubated in the bacterial suspension at 10, 20, 30, or 40 min. The experiment was repeated thrice with around 100~130 leaf explants per Agrobacterium treatment.
3.3.3. Effects of Leaf Ages
Leaf explant age (leaf age) was timed since it was 5mm in length. The interval durations were 30-day-old leaf, 60-day-old leaf, or 90-day-old leaf (Figure 3). The experiment was repeated thrice with around 100 leaf explants per treatment. The leaf explants used for transformation were also examined under transmission electron microscopy (TEM).
3.4. Visualization of Genetic Transformation
3.4.1. TEM Observations of Agrobacterium Infection
The leaf explants used for transformation were washed five times for 15 s in 0.2 M phosphate buffer (pH = 6.8) containing 0.9% (w/v) NaCl to remove the Agrobacterium that were not firmly attached after co-cultivation. The leaf explants were then sampled for TEM (H-7650, Hitachi, Kyushu, Japan). The method was carried out following the reference of Williams et al. .
3.4.2. Green Fluorescent Protein Fluorescence Observations in Transgenic Poplar
The leaves, shoots, and roots were removed from the transgenic poplar and observed under the fluorescent microscope (Olympus, Nagano-ken, Japan) and using a laser-scanning confocal imaging system (Olympus Fluoview, FV500, Nagano-ken, Japan). The GFP fluorescent signals were detected at an emitting wavelength of 480 nm.
3.4.3. Southern and Northern Blot Analysis
DNA and RNA were extracted from leaf samples of the non-transgenic poplar and 7 different independent transgenic lines poplar. Poplar genomic DNA was extracted using the procedure of Porebski et al. . Total RNA were extracted using the RNeasy Mini Kit (Qiagen) according to the manufacturer’s instructions. For Southern analysis, a total of 20 μg genomic DNA was digested with restriction enzyme BamHI at 37 °C in a water bath overnight. The digested DNA fragments were then electrophoresed in 0.8% agarose gel. For Northern analysis, 10 μg total RNA was electrophoresed on a 1% formaldehyde agarose gel. DNA and RNA samples were hybridized with DIG-labeled MD gene probe, and samples blotted onto a Hybond N+- membrane (Amersham Pharmacia, Piscataway, NJ, USA). The membrane was hybridized and washed according to Sambrook et al. . The signals were detected with CDP-Star detection reagent using a LAS-4000 plus image analyzer (Fuji Film, Tokyo, Japan).
A hybrid poplar Populus davidiana Dode × Populus bollena Lauche planted in northeast China with cold tolerance has been optimized for high regeneration efficiency (90%). Genetic transformation was improved in terms of the age of the leaf explants (30-day-old leaf), Agrobacterium concentration (OD600 = 0.8–1.0), and infection time (20–30 min). The transmission electron microscopy observations of Agrobacterium invasions in the leaf explants, the visualization of the green fluorescent protein marker, and Southern and Northern blot analyses supported that there was successful integration of T-DNA into the genome and gene expression of transgenic plants.
This work was supported by the State Forestry Administration 948 Program of China (No.2008429) and Heilongjiang Provincial Program for Distinguished Young Scholars (JC200609) to S. Liu. We thank Daidi Che (Northeast Agricultural University) for kindly providing the plasmid pBI121-MD-GFP and DIG-labeled MD gene probe.
Green fluorescent protein
Murashige and Skoog
Transmission electron microscopy
Full-length cDNA overexpression
Conflict of Interest
The authors declare no conflict of interest.
- Christie, C.B. Rapid propagation of aspens and silver poplars using tissue culture techniques. Proc. Int. Plant Prop. Soc 1978, 28, 255–260. [Google Scholar]
- De Block, M. Factors influencing the tissue culture and the Agrobacterium tumefaciens-mediated transformation of hybrid aspen and Poplar clones. Plant Physiol 1990, 93, 1110–1116. [Google Scholar]
- Son, S.H.; Hall, R.B. Multiple shoot regeneration from root organ cultures of Populus alba × P. grandidentata. Plant Cell Tiss. Organ. Cult 1990, 20, 53–57. [Google Scholar]
- Tsai, C.J.; Podila, G.K.; Chiang, V.L. Agrobacterium-mediated transformation of quaking aspen (Populus tremuloides) and regeneration of transgenic plants. Plant Cell Rep 1994, 14, 94–97. [Google Scholar]
- Gozukirmizi, N.; Bajrovic, K.; Ipekqi, Z. Genotype differencies in direct plant regeneration from stem explants of Populus tremula in Turkey. J. For. Res 1998, 3, 123–126. [Google Scholar]
- Noel, N.; Leple, J.C.; Pilate, G. Optimization of in vitro micropropagation and regeneration for Populus × interamericana and Populus × euramericana hybrids (P. deltoides, P. trichocarpa, and P. nigra). Plant Cell Rep 2002, 20, 1150–1155. [Google Scholar]
- Thakur, D.K.; Srivastava, D.K. High-efficiency plant regeneration from leaf explants of male Himalayan poplar (Populus ciliata Wall). In Vitro Cell Dev. Biol. Plant 2006, 42, 144–147. [Google Scholar]
- Yadav, R.; Arora, P.; Kumar, D.; Katyal, D.; Dilbaghi, N.; Chaudhury, A. High frequency direct plant regeneration from leaf, internode, and root segments of Eastern Cottonwood (Populus deltoides). Plant Biotechnol. Rep 2009, 3, 175–182. [Google Scholar]
- Huang, D.Q.; Dai, W.H. Direct regeneration from in vitro leaf and petiole tissues of Populus tremula ‘Erecta’. Plant Cell Tiss. Organ. Cult 2011, 107, 169–174. [Google Scholar]
- Harry, I.S.; Thrope, T.A. In vitro Culture of Forest Trees. In Plant Cell and Tissue Culture; Vasil, I.K., Thrope, T.A., Eds.; Kluwer Academic: Dordrecht, The Netherlands, 1994; pp. 539–560. [Google Scholar]
- Ahuja, M.R. Somatic cell differentiation and rapid clonal propagation of aspen. Silvae Genet 1983, 32, 131–135. [Google Scholar]
- Fillatti, J.J.; Sellmer, J.; McCown, B.; Haissig, B.; Comai, L. Agrobacterium mediated transformation and regeneration of Populus. Mol. Gen. Genet. 1987, 206, 192–199. [Google Scholar]
- Dai, W.H.; Cheng, Z.M.; Sargent, W. Plant regeneration and Agrobacterium-mediated transformation of two elite aspen hybrid clones from in vitro leaf tissues. In Vitro Cell Dev. Biol. Plant 2003, 39, 6–11. [Google Scholar]
- Ferreira, S.; Batista, D.; Serrazina, S.; Pais, M.S. Morphogenesis induction and organogenic nodule differentiation in Populus euphratica Oliv. leaf explants. Plant Cell Tiss. Organ. Cult 2009, 96, 35–43. [Google Scholar]
- Thakur, A.K.; Sarita, S.; Srivastava, D.K. Plant regeneration and genetic transformation studies in petiole tissue of Himalayan poplar (Populus ciliata Wall). Curr. Sci 2005, 89, 664–668. [Google Scholar]
- Tzfira, T.; Jensen, C.S.; Vainstein, A.; Altman, A. Transformation and regeneration of transgenic aspen plants via shoot formation from stem explants. Physiol. Plant 1997b, 99, 554–561. [Google Scholar]
- Kang, B.; Osburn, L.; Kopsell, D.; Tuskan, G.A.; Cheng, Z.M. Micropropagation of Populus trichocarpa ‘Nisqually-1’: The genotype deriving the Populus reference genome. Plant Cell Tiss. Organ. Cult 2009, 99, 251–257. [Google Scholar]
- Horsch, R.B.; Fry, J.E.; Hoffmann, N.L.; Eichholtz, D.; Rogers, S.G.; Fraley, R.T. A simple and general method for transferring genes into plants. Science 1985, 227, 1229–1231. [Google Scholar]
- Parsons, T.J.; Sinkar, V.P.; Stettler, R.F.; Nester, E.W.; Gordon, M.P. Transformation of poplar by Agrobacterium tumefaciens. Nat. Biotech 1986, 4, 533–536. [Google Scholar]
- Confalonieri, M.; Balestrazzi, A.; Bisoffi, S. Genetic transformation of Populus nigra by Agrobacterium tumefaciens. Plant Cell Rep 1994, 13, 256–261. [Google Scholar]
- Tzfira, T.; Jensen, C.S.; Wang, W.X.; Zuker, A.; Vinocur, B.; Altman, A.; Vainstein, A. Transgenic Populus tremula: A step-by-step protocol for its Agrobacterium-mediated transformation. Plant Mol. Biol. Rep 1997a, 15, 219–235. [Google Scholar]
- Han, K.H.; Gordon, M.P.; Strauss, S.H. High-frequency transformation of cottonwoods (genus Populus) by Agrobacterium rhizogenes. Can. J. For. Res 1997, 27, 464–470. [Google Scholar]
- Han, K.H.; Meilan, R.; Ma, C.; Strauss, S.H. An Agrobacterium tumefaciens transformation protocol effective on a variety of cottonwood hybrids (genus Populus). Plant Cell Rep 2000, 19, 315–320. [Google Scholar]
- Zhan, X.C.; Kawai, S.; Katayama, Y.; Morohoshi, N. A new approach based on the leaf disc method for Agrobacterium mediated transformation and regeneration of aspen. Plant Sci 1997, 123, 105–112. [Google Scholar]
- Okumura, S.; Sawada, M.; Park, Y.W.; Takahisa, H.Y.S.; Shimamura, H.; Takase, H.; Tomizawa, K.I. Transformation of poplar (Populus alba) plastids and expression of foreign proteins in tree chloroplasts. Transgenic Res 2006, 15, 637–646. [Google Scholar]
- Nishiguchi, M.; Yoshida, K.; Mohri, T.; Igasaki, T.; Shinohara, K. An improved transformation system for Lombardy poplar (Populus nigra var. italica). J. For. Res 2006, 11, 175–180. [Google Scholar]
- Cseke, L.J.; Cseke, S.B.; Podila, G.K. High efficiency poplar transformation. Plant Cell Rep 2007, 26, 1529–1538. [Google Scholar]
- Yevtushenko, D.P.; Santosh, M. Efficient Agrobacterium-mediated transformation of commercial hybrid poplar Populus nigra L. × P. maximowiczii A. Henry. Plant Cell Rep 2010, 29, 211–221. [Google Scholar]
- Meilan, R.; Ma, C. Protocols, 2nd ed; Wang, K., Ed.; Humana Press: Totowa, NJ, USA, 2006; Volume 344, pp. 143–151. [Google Scholar]
- Confalonieri, M.; Balestrazzi, A.; Bisoffi, S.; Cella, R. Factors affecting Agrobacterium tumefaciens-mediated transformation in several black poplar clones. Plant Cell Tiss. Organ. Cult 1995, 43, 215–222. [Google Scholar]
- Confalonieri, M.; Balestrazzi, A.; Cella, R. Genetic transformation of Populus deltoides and P.x euramericana clones using Agrobacterium tumefaciens. Plant Cell Tiss. Organ. Cult 1997, 48, 53–61. [Google Scholar]
- Li, X.Y.; Huang, F.H.; Gbur, E.E. Factors affecting transformation efficiency of poplar hybrid line NC5331 by Agrobacterium tumefaciens. J. Arkansas Acad. Sci 1997, 51, 116–120. [Google Scholar]
- Ma, C.P.; Strauss, S.H.; Meilan, R. Agrobacterium-mediated transformation of the genome sequenced poplar clone, Nisqually-1(Populus trichocarpa). Plant Mol. Biol. Rep 2004, 22, 1–9. [Google Scholar]
- Ichikawa, T.; Nakazawa, M.; Kawashima, M. The FOX hunting system: An alternative gain-of-function gene hunting technique. Plant J 2006, 45, 974–985. [Google Scholar]
- Kondou, Y.; Higuchi, M.; Takahashi, S. Systematic approaches to using the FOX hunting system to identify useful rice genes. Plant J 2009, 57, 883–894. [Google Scholar]
- Nakamura, H.; Hakata, M.; Amano, K.; Miyao, A. A genome-wide gain-of-function analysis of rice genes using the FOX-Hunting system. Plant Mol. Biol 2007, 65, 357–371. [Google Scholar]
- Busov, V.B.; Meilan, R.; Pearce, D.W.; Ma, C.; Rood, S.B.; Strauss, S.H. Activation tagging of a dominant gibberellin catabolism gene (GA 2-oxidase) from poplar that regulates tree stature. Plant Physiol 2003, 132, 1283–1291. [Google Scholar]
- Murashige, T.; Skoog, F. A revised medium for rapid growth and bioassays with tobacco tissue culture. Physiol. Plant 1962, 15, 473–497. [Google Scholar]
- Godwin, I.; Todd, G.; Brian, F.L.; Newbury, H.J. The effects of acetosyringone and pH on Agrobacterium-mediated transformation vary according to plant species. Plant Cell Rep 1991, 9, 671–675. [Google Scholar]
- Smith, M.A.L.; McCown, B.H. A comparison of source tissue for protoplast isolation from three woody plant species. Plant Sci. Lett 1983, 28, 149–156. [Google Scholar]
- Civinova, B.; Sladky, Z. Stimulation of the regeneration capacity of tree shoot segment explants in vitro. Biol. Plant 1990, 32, 407–413. [Google Scholar]
- Graves, A.E.; Goldman, S.L.; Banks, S.W.; Graves, A.C.F. Scanning electron microscope studies of Agrobacterium tumefaciens attachment to Zea mays, Gladiolus sp., and Triticum aestivum. J. Bactriol 1988, 170, 2395–2400. [Google Scholar]
- Verma, A.; Nain, V.; Kumari, C.; Singh, S.K.; Lakshmi, N.M.; Ananda, K.P. Tissue specific response of Agrobacterium tumefaciens attachment to Sorghum bicolor (L) Moench. Physiol. Mol. Biol. Plants 2008, 14, 307–313. [Google Scholar]
- Willians, D.; Carter, C.B. Transmission Electron Microscopy; Plenum Press: New York, NY, USA, 1996. [Google Scholar]
- Porebski, L.; Bailey, L.; Baum, B. Modification of a CTAB DNA extraction protocol for plants containing high polysaccharide and polyphenol components. Plant Mol. Biol. Rep 1997, 15, 8–15. [Google Scholar]
- Sambrook, J.; Fritsch, E.F.; Maniatis, T. Molecular Cloning: A Laboratory Manual, 2nd ed; Cold Spring Harbor Laboratory Press: New York, NY, USA, 1989. [Google Scholar]
|Medium||BA (mg/L)||NAA (mg/L)||Mean No. shoots formed per explant||Explant regeneration (%)|
|3||0.1||0.05||0.18 ± 0.51||14.4 ± 1.93|
|4||0.1||0.08||0.08 ± 0.02||5.56 ± 1.93|
|5||0.1||0.1||0.02 ± 0.02||2.22 ± 1.92|
|6||0.3||0.01||3.61 ± 0.27||76.7 ± 6.65|
|7||0.3||0.03||1.82 ± 0.27||60.0 ± 10.0|
|8||0.3||0.05||0.42 ± 0.15||17.8 ± 5.09|
|9||0.3||0.08||5.87 ± 0.49||90.0 ± 8.81|
|10||0.3||0.1||2.08 ± 0.34||55.6 ± 5.09|
|11||0.5||0.01||0.59 ± 0.17||14.4 ± 3.85|
|12||0.5||0.03||1.54 ± 0.68||16.7 ± 5.77|
|13||0.5||0.05||0.78 ± 0.31||40.0 ± 10.0|
|14||0.5||0.08||0.03 ± 0.03||3.33 ± 3.34|
|15||0.5||0.1||0.53 ± 0.12||5.56 ± 3.85|
© 2013 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).