Agrobacterium-mediated transient expression via root absorption in flowering Chinese cabbage
© The Author(s) 2016
Received: 30 May 2016
Accepted: 11 October 2016
Published: 21 October 2016
Because most transient transformation techniques are inadequate for functional genomics research in roots, we aimed to develop a simple and efficient Agrobacterium-mediated transient transformation system that utilized root absorption for research in flowering Chinese cabbage.
Both semi-quantitative and fluorescent quantitative RT-PCR confirmed that the target gene BcAMT1;3 was more highly expressed in plants that were infected with the transformed Agrobacterium strain (EHA105-p35S-BcAMT1;3) than in control plants that were infected with the control strain (EHA105-p35S). Furthermore, GUS staining analysis conformed the availability of this transient transformation system. In addition, we found that the highest transformation efficiency was achieved using an Agrobacterium cell density of OD600 = 0.3 for 3–6 h, without hyperosmotic pretreatment, and under these conditions, the peak transformation efficiency was observed at 2 and 4 d after infection.
The transformation method developed by the present study is simple and convenient, since no special equipment is required, and since the method causes no damage, the plants can be used for subsequent experiments.
Functional genomics research often involves transgenic approaches that overexpress or silence genes, and among those approaches, both stable and transient transformation methods are valid for studying the functions and regulatory mechanisms of genes (Parinov and Sundresan 2000; Wroblewski et al. 2005). Compared to stable transformation, transient transformation is a more attractive alternative that allows transgenes to be assayed more rapidly and easily (Janssen and Gardner 1989; Kapila et al. 1997), so transient transformation has become the main strategy in functional genomics research and has been increasingly employed for research in various species (Ben-Amar et al. 2013; Bhaskar et al. 2009; Wu et al. 2014; Yang et al. 2008).
Various transient transformation methods have been developed. However, both polyethylene glycol-mediated transformation (Wilson et al. 1989; Yoo et al. 2007) and particle bombardment (Oard et al. 1990; Schenk et al. 1998) are complex and costly, since they require special devices, and virus-based methods (Fischer et al. 2013; Ratcliff et al. 2001) are limited to use in only a few plant species. As a result, Agrobacterium-mediated methods are used most widely and have facilitated research in various areas, including gene–gene interactions, gene silencing, gene regulation and expression (Gurlebeck et al. 2009; Ji et al. 2014; Johansen and Carrington 2001; Kim et al. 2007), and protein production (Barta et al. 1986; Benchabane et al. 2009). For Agrobacterium-mediated transient expression, leaf infiltration is the most common and efficient strategy used for Agrobacterium-mediated transient expression (Bhaskar et al. 2009; Voinnet et al. 2003). However, the method has limited applications for research involving roots, since the effects are mainly observed in leaves and because the method is incapable of investigating root-specific genes.
Flowering Chinese cabbage (Brassica campestris L. ssp. chinensis var. Utilis Tsen et Lee), whose edible organ is crisp flower stalk, is a subspecies variant of pak choi (Brassica campestris L. ssp. chinensis Makino var. communis Tsen et Lee), and one of the most widely cultivated vegetables in south China, and has the largest grown area and yield in local area (Song et al. 2012). Although both belong to a same species, there is great difference in morphology between flowering Chinese cabbage and pak choi, as the former is non-heading, and has flat green leaves and bolting flower stem. In addition, few transient transformation methods of flowering Chinese cabbage were reported, which seriously hindered its genetic research. Therefore, we aimed to develop a simple and efficient Agrobacterium-mediated transient transformation system that utilized root absorption for research in flowering Chinese cabbage and to optimize the key factors of transformation efficiency, including Agrobacterium cell density, transformation time, and hyperosmotic pretreatment conditions. As a result, a root-specific expression gene, ammonium transporter 1;3 of flowering Chinese cabbage (BcAMT1;3) was successfully overexpressed in root.
The experiments were conducted in the Horticultural Science greenhouse (25–30 °C, with natural sunshine) at South China Agricultural University. Seeds of flowering Chinese cabbage (B. campestris L. ssp. chinensis var. utilis Tsen et Lee) were sown in plug trays with perlite as a substrate, and after 3 weeks, the seedlings were transferred to hydroponic cultures in plastic pots. Each pot contained 12 plants and 24 L normal nutrient solution (4.0 mM NaNO3, 1.0 mM KH2PO4, 2.0 mM KCl, 1.0 mM MgSO4, 0.5 mM CaCl2, 0.1 mM Fe-EDTA, 50 μM H3BO3, 12 μM MnSO4, 1 μM ZnC12, 1 μM CuSO4, and 0.2 μM Na2MoO4; pH 6.0, adjusted with 1 M NaOH or 10 % HCl), and 10 mg L−1 ampicillin was added to the nutrient solution to inhibit microbial activity. In addition, the growth solution was changed every 4 d.
The 1515 bp CDS of the BcAMT1;3 gene, including its stop codon, was amplified from the DNA of flowering Chinese cabbage roots using the following primers 5′-CACGGGGGACTCTAGAATGTCAGGACCTCTAACTTG-3′ (forward) and 5′-TCCTTTACCCATCCCGGGTTAAACGCGAGGAGGAGTAA-3′ (reverse). The sequence-verified amplicon was then cloned into the XbaI and SmaI sites of pBI121-35S vector using the In-Fusion HD Cloning Kit (TaKaRa Bio, Inc., Kusatsu, Japan), and the resulting constructs (pBI121-35S-BcAMT1;3) were verified by sequencing.
Preparation of Agrobacterium suspension
The vectors pBI121-35S-BcAMT1;3 and pBI121-35S were introduced into Agrobacterium tumefaciens strain EHA105 using the freeze–thaw method (Holsters et al. 1978). Single colonies of the A. tumefaciens strain EHA105-p35S-BcAMT1;3 and EHA105-p35S were then grown in YEP medium (containing 30 mg kanamycin L−1 and 30 mg rifampicin L−1) at 28 °C with shaking. After overnight incubation, 1 mL of each culture was separately transferred to 50 mL of fresh YEP medium and incubated at 28 °C with shaking. When the culture density reached an OD600 of about 1.0, the cells were harvested by centrifugation at 5000 rpm for 10 min, and then adjusted to an OD600 of 0.6 in transformation solution (pH 6.0) that included the normal nutrient solution described above, 100 μM acetosyringone (AS), and 0.01 % (w/v) Tween20.
Infection by root absorption
The root absorption infection procedure was modified from the method described by Ji et al. (2014). Briefly, the roots of plant seedlings were soaked in a hyperosmotic pretreatment solution of 20 % (w/v) sucrose (pH 6.0), and after 2 h, the roots were incubated in the transformation solution at 28 °C for 6 h with shaking at 120 rpm. Subsequently, the transformed seedling roots were washed with distilled water, transferred to normal nutrient solution containing 150 μM AS, and then sampled after 2 d for RT-PCR analysis.
Optimization of the conditions of the transformation system
To optimize the transformation system, we also manipulated some of the transformation conditions, including the Agrobacterium cell density, length of transformation, sucrose concentration of hypertonic solution, length of pretreatment, and the use of both shaking and AS. The optimization experiments for each condition were performed independently, with each of the other conditions were described above. Then, under the optimized conditions, we sampled the transformed roots after 0, 2, 4, 6, and 8 d to determine the post-infection interval at which the target gene was most highly expressed.
Total RNA was extracted using RNAiso Reagent (TaKaRa, Bio, Inc). To reduce the effect of plant-to-plant variability, a total of 24 plants were sampled from each treatment, and every eight plants were pooled together as one biological replicate. Subsequently, cDNA was synthesized from 1 μg aliquots of total RNA, using the PrimeScript RT Reagent Kit with gDNA Eraser (TaKaRa, Bio, Inc) in a reaction volume of 20 μL, and the synthesized cDNA was diluted 20 times with sterile water for use as the RT-PCR template. To determine the expression level of BcAMT1;3, semi-quantitative RT-PCR was performed using TaKaRa Ex Taq (TaKaRa, Japan), and fluorescent quantitative PCR was performed using a LightCycler 480 Real-Time PCR system (Roche, Basel, Switzerland) with SYBR Premix Ex Taq (TaKaRa, Bio, Inc). The primers 5′-TCGGAGAAGGATGAGATGG-3′ (forward) and 5′-CGAGGAGGAGTAACAGAACG-3′ (reverse) were used for amplification, and relative expression was calculated using the expression levels of two housekeeper genes, ACTIN and GAPDH, and the 2−ΔΔCt method.
Histochemical GUS Analysis
Reporter gene GUS was cloned into the pBI121-35S vector, and introduced into Agrobacterium tumefaciens strain EHA105, then the EHA105-p35S-GUS was transformed into flowering Chinese cabbage roots using the transformation system described above. GUS staining was carried out as previously described (Dong et al. 2001), and images of GUS-stained plants were obtained using a stereo light microscope (Leica, Germany).
15NH4 + uptake analysis
Ammonium (NH4 +) influx assay was performed with flowering Chinese cabbage plants infected by EHA105-p35S-BcAMT1;3 and EHA105-p35S, respectively. NH4 + influx measurements in Arabidopsis roots were conducted after rinsing the roots of hydroponically grown plants in 1 mM CaSO4 solution for 1 min, then to nutrient solution containing 0.2 mM 15N-labeled NH4 + (99 atom% 15N) for 5 min, and finally washed in 1 mM CaSO4 for 1 min. The influx solution was the same as used for plant growth except that 4.0 mM NaNO3 was replaced by 0.1 mM (15NH4)2SO4. Roots were separated from shoots and dried for 24 h at 65 °C. Samples were ground and approximately 1.0 mg of powder was used for 15N determination using isotope mass spectrometry (Thermo-Finnigan, Bremen, Germany).
Statistical and graphical analyses
All data were statistically analyzed using one-way analysis of variance (ANOVA) and Duncan post hoc tests in SPSS 12.0 program (SPSS, Inc., Chicago, IL, USA). Graphs were produced using SigmaPlot 11.1.0 (Systat Software, Inc., Chicago, IL, USA), and all graphs and images were arranged using Adobe Photoshop 7.0.
In the present study, we developed an Agrobacterium-mediated transient transformation system that utilized root absorption for research in flowering Chinese cabbage, and both semi-quantitative and fluorescent quantitative RT-PCR showed that plants transiently transformed with p35S-BcAMT1;3 exhibited significantly higher expression of BcAMT1;3 in roots (Figs. 1, 2). In addition, reporter gene GUS was transformed into flowering Chinese cabbage roots, and GUS staining activity detected in roots infected by EHA105-p35S-GUS further conformed the availability of this transient transformation system (Fig. 6). The method is both simple and convenient, because no special equipment was required, and moreover, since no damage is inflicted on the plants by vacuum infiltration or injection, the plants can be retained and used for subsequent experiments. We successfully examined the effects of BcAMT1;3 overexpression of transient transformation plants on NH4 + absorption rate (Fig. 7). And in the case of Ji et al. (2014), for example, the method was used to detect the stress tolerance of transformed plants.
In the present study, we also optimized several key factors of transformation efficiency in flowering Chinese cabbage and found that infection with an Agrobacterium cell density of OD600 = 0.3 for 3–6 h, without hyperosmotic pretreatment, yielded the highest transformation efficiency. In the tobacco (Nicotiana benthamiana) root-absorption transient system used by Yang et al. (2008), the highest transformation efficiency was attained using an Agrobacterium cell density of OD600 = 1.23, which is more than four times greater than the optimum cell density for flowering Chinese cabbage, and in the Tamarix hispida root-absorption transient system, an Agrobacterium cell density of OD600 = 0.9 was used in all experiments (Ji et al. 2014). In the present study, higher Agrobacterium cell densities and longer infection times may have failed to yield better results, possibly because the roots of flowering Chinese cabbage are more tender than those of N. benthamiana and T. hispida, and young tissue composed of newly expanded cells from vigorously growing plants often exhibited higher levels of transient expression (Wroblewski et al. 2005). This could also explain why hyperosmotic pretreatment and shaking were not required either. In fact, we found that the leaves of transformed plants wilted after hyperosmotic pretreatment, which suggested that the hyperosmotic pretreatment might damage flowering Chinese cabbage roots.
Root-absorption transient transformation systems have been developed in various species, including N. benthamiana, A. thaliana, T. hispida, Betula platyphylla (Ji et al. 2014; Yang et al. 2008), and, now, flowering Chinese cabbage; however, the conditions for transforming different species may differ. The transformation method developed by the present study is simple and convenient, since no special equipment is required, and since the method causes no damage, the plants can be used for subsequent experiments.
SS and RC conceived and designed the experiments. LZ and YZ performed the experiment, LZ also analyzed the data, contributed reagents/materials/analysis tools, and wrote the paper. HL and GS provided comments and suggestions for both experiments and manuscript. All authors have read and approved the final manuscript.
We would like to thank Editage (www.editage.cn) for English language editing.
The authors declare that they have no competing interests.
Research funding was provided by the National Natural Science Foundation of China (31401855; http://www.nsfc.gov.cn/), scientific research support of “Excellent Young College Teachers” in Guangdong China (Yq2013030), Pearl River Science and Technology Nova Program of Guangzhou, China (2013J2200089), and China Agriculture Research System (CARS-25-C-04; http://22.214.171.124/).
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