Patent Application
20180346922
The present application claims priority to Chinese Patent Application No. 201510858859.0, filed on Dec. 1, 2015, the disclosure of which is incorporated herein by reference in its entirety.
The invention belongs to the field of plant genetic engineering, and specifically, relates to the use of tobacco gene NtTCTP for resisting potato virus Y in plants.
Translationally controlled tumor protein (TCTP), also called p21 or p23, is a protein commonly expressed and distributed in eukaryotes. It was first discovered in mammalian tumor cells and regulated at the post-transcriptional level.
Based on a large number of studies in various organisms, it has been found that TCTP is involved in various cytological processes such as promotion of histamine release, apoptosis, microtubule assembly, ion balance, etc., and interacts with a series of proteins such as Polo kinase, tubulin, actin and sodium Potassium ATPase. In animals, TCTP participates in cell growth and differentiation, malignant transformation, stress resistance, and apoptosis and the like. Mice with TCTP gene knocked out showed embryonic lethality due to the lack of cell differentiation and excessive apoptosis. In drosophila, when the expression of TCTP in a specific organ is disrupted, the number of cells in the organ is decreased and defects in cell growth occur, eventually leading to decrease in size of the organ. TCTP mRNA expression in plants is closely related to mitosis, and darkness can induce TCTP mRNA accumulation in morning glory. In addition, TCTP proteins play an important role in regulating the long-distance transport of phloem proteins and the growth of pollen tubes. It has been found from recent studies that TCTP, as a positive regulatory factor of mitotic growth, can specifically regulate the cell cycle time in Arabidopsis. TCTP regulates cell differentiation through the TOR (Target of rapamycin) growth regulatory pathway. From the studies on cabbage, it has been found that TCTP regulates growth and development, and meanwhile is induced by the external environment. These existing studies have shown that, TCTP not only can regulate the growth and development of organisms, but also has exclusive functions in plants. Therefore, the study on this class of genes is of great significance in the study on resistance to PVY.
It is a key in plant antiviral breeding to dig into the gene against potato virus Y (PVY) in the plant genome.
The object of the present invention is to provide the use of tobacco gene NtTCTP for resisting potato virus Y in plants.
In order to achieve the purpose of the present invention, the tobacco gene NtTCTP according to the present invention, whose activity is closely related to the PVY-resistance of tobacco, has a gene sequence of:
i) a nucleotide sequence represented by SEQ ID NO: 1; or
ii) a nucleotide sequence represented by SEQ ID NO: 1 with one or more nucleotides substituted, deleted, and/or added therein, which expresses the same functional protein; or
iii) a nucleotide sequence that hybridizes to the sequence represented by SEQ ID NO: 1 under stringent conditions and expresses the same functional protein, the stringent conditions are given as follows: hybridizing in 0.1×SSPE with 0.1% SDS or 0.1×SSC solution with 0.1% SDS at 65° C., and washing the membrane with the solution; or
iv) a nucleotide sequence having 90% or more homology with the nucleotide sequence of i), ii) or iii) and expressing the same functional protein.
The present invention also provides a protein encoded by the gene NtTCTP, and its amino acid sequence is represented by SEQ ID NO: 2.
The present invention also provides the use of the gene NtTCTP for resisting potato virus Y (PVY) in tobacco. That is, the tobacco gene NtTCTP is used to regulate the PVY-resistance of tobacco. The potato virus Y includes a PVY necrosis strain (N strain).
The use is utilizing RNAi technology to silence the gene NtTCTP in tobacco. For example, a nucleotide sequence represented by SEQ ID NO: 3 can be cloned into a plant expression vector, and then the recombinant expression vector is transformed into tobacco via Agrobacterium-mediated transformation, and screening is performed to obtain transgenic tobacco plants. Preferably the plant expression vector is pBin438.
The invention also provides a method for constructing a transgenic tobacco plant. An RNAi expression vector of gene NtTCTP is firstly constructed, and then the recombinant expression vector is transformed into tobacco via Agrobacterium-mediated transformation, and screening is performed to obtain transgenic tobacco plants. Preferably the starting vector is pBin438.
The present invention also provides the use of the gene NtTCTP in the improvement of tobacco varieties.
The invention also provides the use of the gene NtTCTP in breeding of PVY-resistant tobacco.
The present invention further provides an expression vector carrying an expression cassette that inhibits the tobacco gene NtTCTP.
Preferably, the expression vector carries the nucleotide sequence represented by SEQ ID NO: 3.
The present invention obtains the translationally controlled tumor protein gene NtTCTP by cloning from tobacco, and the gene has a full length of 507 bp, and encodes a protein containing 168 amino acids; and the present invention studies the role of the gene in the process of resisting PVY in tobacco. The gene is silenced in the cultivated tobacco, and the tobacco shows stronger resistance to the PVY, which can reach immune levels. The gene is overexpressed in the cultivated tobacco, and tobacco becomes more sensitive to the PVY. It is demonstrated that the gene plays an important role in the process of resisting PVY in tobacco and can be used in the breeding of PVY-resistant plants such as tobacco.
The RNAi expression vector of gene NtTCTP is constructed in the present invention, and the tobacco is genetically transformed through Agrobacterium-mediated transformation. The result shows that after the gene is silenced in tobacco, the resistance of tobacco against PVY can be increased by 50%-80%.
The following examples are intended to illustrate the present invention but not to limit the scope of the present invention. Unless otherwise specified, the examples are carried out under conventional experimental conditions, such as those described in Sambrook J & Russell D W, Molecular Cloning: a Laboratory Manual (2001), or the conditions recommended in the manufacturer's instructions.
1. Experimental Materials
1.1 Cultivated Tobacco Variety “Shanxi Tobacco” was Provided by the Breeding Engineering Center of Guizhou Institute of Tobacco Science.
1.2 Reagents
LA Taq DNA polymerase and restriction enzymes were purchased from TaKaRa. A DNA gel purification recovery kit was purchased from Tiangen Biochemical Technology (Beijing) Co., Ltd. T4 DNA ligase was purchased from NEB; and pGEM-T vector was purchased from Promega Biotech Co., Ltd. ABI PRISM™ Optical 96-Well Reaction Plates and Optical Caps were purchased from ABI; Escherichia coli DH5a, Agrobacterium tumefaciens EHA105, and the plant expression vector pBin438 were all commercially available products. DNA synthesis and sequencing were completed by Huada Gene Technology Services Co., Ltd.
2. Experimental Methods
After logging in NCBI, primers for amplifying the full length gene were designed based on the full length sequence of the tobacco TCTP gene in Genbank (Accession NO: KM507327.1), and the restriction enzyme cutting sites BamH I and Sal I were added. The designed primer sequences were as follows:
2.2 Full Length Amplification of the Tobacco Gene NtTCTP
The total RNA of “Shanxi tobacco” leaves was extracted, and subjected to reverse transcription to synthesize a first strand of cDNA. The following reagents were added into a 0.2 ml centrifuge tube to perform the PCR reaction:
The PCR reaction procedure was as follows: heating the lid, pre-denaturing at 95° C. for 5 minutes; then performing 35 cycles of denaturing at 95° C. for 30 s, annealing at 55° C. for 30 s, and extending at 72° C. for 30 s.
The DNA fragment obtained by amplification was sequenced, with the result shown in SEQ ID NO: 1.
1. Construction of Gene NtTCTP-Overexpressed Vectors
1.1 the plant expression vector pBin438 and the full length amplified PCR products were separately double-enzyme digested with Sal I and BamH I, and the enzyme digestion system was as follows:
1.2 The enzyme digested products were detected by 1% agarose gel electrophoresis, and the enzyme digested PCR products and the large fragments of the vector pBin438 were recycled and ligated. The recycled products were directionally ligated in the following proportions. The ligation system was as follows:
Ligation was performed at 16° C. for 16 hours or longer, so as to improve the ligation efficiency.
1.3 Transformation of Agrobacterium Tumefaciens with Recombinant Plasmid
1) 0.5 to 1.0 μL of DNA was taken, added into the competent cells of Agrobacterium tumefaciens, and gently mixed; the mixture was kept in ice bath for 5 min, then quickly put into liquid nitrogen and frozen for 5 min;
2) the mixture was thawed in a 37° C. water bath, and added with 800 μL YEB liquid medium, and then cultured under shaking at 28° C. and 100 r/min for 4 h;
3) the mixture was centrifuged for 5 minutes at 4000 r/min, and most supernatant was discarded with about 100 μL left to suspend the bacteria;
4) the suspended bacteria was coated on solid YEB medium containing 40 mg/L rifampicin (Rif), 50 mg/L streptomycin (Sm) and 100 mg/L kanamycin (Km), and cultured at 28° C. for 48 to 96 h.
2. Construction of Silencing Vector
The forward sequence and the reverse complementary sequence of a 330 bp fragment from 1st bp to 330th bp of the tobacco gene NtTCTP was connected through an intermediate sequence, and the restriction enzyme cutting sites BamH I and Sal I were added. The designed sequence was synthesized by Sangon Biotech, Shanghai, and the synthesized sequence was represented by SEQ ID NO: 3. The synthesized fragment was digested with enzymes BamH I and Sal I, and ligated with the pBin438 vector which was digested in the same manner, so as to construct a final silencing vector.
3. Agrobacterium tumefaciens-Mediated Genetic Transformation of Tobacco
Tobacco leaf dishes were pre-cultured for 2-3 days, and then infected with Agrobacterium tumefaciens EHA105 containing the plant expression vector. After co-culture for 3 to 4 days, the leaf dishes were taken out and sterilized for 2 to 3 h in a liquid medium containing a bactericide, and then transferred to a screening medium for screening and differentiation culture. The resistant buds began to form via differentiation about 3 weeks later. When the resistant buds grew to a height of 3 to 4 cm, they were cut from the base of the explants and inoculated onto a rooting medium for rooting culture. After the root system of the plantlets was developed, acclimatizating and transplanting were performed. A large number of resistant plants that survived after transplanting were obtained. Plants that are positive in PCR detection were transplanted into large flower pots until the seeds were harvested.
Minimal medium: MS medium, pH 5.8, 0.8% agar.
Screening medium: minimal medium+25 mg/L Km+100 mg/L cephalosporin.
Differentiation medium: minimal medium+1.0 mg/L 6-BA+0.1 mg/L NAA, pH 5.8, 0.75% agar.
Rooting medium: MS medium+0.5 mg/L NAA, pH 5.8, and 0.75% agar.
Transgenic materials, TCTP gene-overexpressed strains O2 and O7, and TCTP gene-silenced strains Ri16 and Ri20 were obtained.
1. Materials and Methods
1.1 Experimental Materials
The gene NtTCTP overexpressed transgenic tobacco strains O2 and O7 constructed in Example 2.
The gene NtTCTP-silenced transgenic tobacco strains Ri16 and Ri20 constructed in Example 3.
The PVY strain was a PVY necrosis strain (N strain).
1.2 Experimental Methods
1.2.1 Preparation of PVY inoculum: fresh diseased leaves were added to a crusher, and crushed together with a small amount of phosphate buffer solution; the diseased leaf residue was filtered off with gauze, and the fresh juice was taken to prepare the PVY inoculum.
1.2.2 PVY inoculation: the inoculation period was the 4-leaf stage of the tobacco. 2 to 3 young leaves of the tobacco plant to be inoculated were selected and gently rubbed with sandpaper to generate light graze, and then the PVY inoculum was brushed on the rubbed leaves by a brush.
1.2.3 Data investigation: the time at which the plant was most severely diseased was selected to investigate the incidence rate and the disease grade of PVY.
The grade of disease was investigated according to the following standards:
Grade 0: The whole plant was disease-free or had leaves mottled very slightly.
Grade 1: 1/10 to ⅓ of the leaves showed slight necrosis of small veins, or stipple streak symptom and slight deformation occurred, the rest leaves of the whole plant were asymptomatic, and the plants had no obvious dwarfing.
Grade 2: ⅓ to ½ of the leaves showed stipple streaks or vein necrosis, most of the small veins of the diseased leaves were necrotic, resulting in a large area of leaf yellowing and withering, and the plant dwarfed to ⅔ or more of the height of normal plants.
Grade 3: ½ to ⅔ of the leaves showed relatively serious vein necrosis or more than ⅔ of the leaves showed stipple streak necrosis, single leaves were withered in a large area, and a few leaves fell off. Or the leaves of the whole plant began to turn yellow.
Grade 4: the leaves of the whole plant showed serious vein necrosis or deformation and atrophy of leaves, about ⅔ of the leaves were wilted and sheded, the diseased plant dwarfed to ½ to ⅓ of the height of normal tobacco plants, or the whole plant was withered.
Disease index DI=[Σ(number of diseased plants at each grade×the value of the disease grade)/(total number of investigated plants×the value of the highest grade)]×100
2. Experimental Results
(1) Validation of the Expression of NtTCTP Gene in Different Tobacco Strains
Western Blot validation showed that, the TCTP gene was not expressed in the two silenced strains Ri16 and Ri20, indicating that the TCTP gene was successfully silenced, and the expression levels in 2 overexpressed strains O2 and O7 both exceeded that in the control (WT), indicating that the TCTP gene overexpression was also successfully constructed (
(2) Identification Results on Disease Resistance in the NtTCTP Gene-Overexpressed and Gene-Silenced Strains
14 days after inoculation, the status of the disease was investigated. Both silenced strains Ri16 and Ri20 were immune, and showed no disease, with a disease index of 0, and the disease resistance was greatly improved. However, the overexpressed strains O2 and O7 showed necrosis more serious than the wild type control (WT), and the disease was more serious (
The above results indicated that silencing TCTP gene in tobacco can enhance the resistance of plants against PVY, and the gene has important application value.
Although the present invention has been described above in detail with general description and specific embodiments, it is obvious to a person skilled in the art that some modifications or improvements can be made on the basis of the present invention. Therefore, these modifications or improvements made without departing from the spirit of the present invention all fall within the protection scope of the present invention.
The activity of the tobacco gene NtTCTP provided by the present invention is closely related to the resistance of tobacco against PVY. By construction of RNAi expression vector of the gene NtTCTP and genetic transformation via Agrobacterium-mediated transformation, it is shown that, after the gene is silenced in tobacco, the resistance of tobacco against PVY is enhanced, and the resistance can be increased by 50%-80%.
| Number | Date | Country | Kind |
|---|---|---|---|
| 201510858859.0 | Dec 2015 | CN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2016/104255 | 11/1/2016 | WO | 00 |
