Method for Creating New Germplasm of Male Sterile Crop by Gene Editing and Application Thereof

Abstract

A method for creating a new germplasm of a male sterile crop by gene editing and an application thereof are provided. In this method, the gene editing is performed on an exon region of a Ty-5 gene, and a deletion of DNA sequence is introduced by using a repair mechanism of plants themselves to double-strand breaks (DSBs), causing a loss of function of Ty-5 gene, thereby obtaining a male-sterile character. The method can be applied without being limited by crop categories. After the gene editing is performed on Ty-5 genes of various crops, new germplasms can be quickly obtained. The new germplasms have the same agronomic characters as the previous materials, and only differ in sexual aspect, which effectively solves the problem of the lack of male sterile materials and unstable fertility in natural resources.

Description

TECHNICAL FIELD

The present invention belongs to the technical field of gene editing technology for crop breeding, and particularly relates to a method for creating a new germplasm of a male sterile crop by a gene editing and an application thereof.

BACKGROUND

Crop male sterility is a phenomenon of normal pollination failure due to inability to produce pollen or abort pollen, which is caused by abnormal male organs resulting from physiological or genetic reasons of sexually propagated crops. Because crop male sterility can avoid the artificial emasculation in the pollination process in crop heterosis breeding, a lot of labor input is saved. Meanwhile, crop male sterility significantly improves the purity of hybrid varieties, and creates varieties with heterosis.

Male sterility technology plays an important role in the utilization of heterosis, and obtaining stable male sterility materials has important application value. Male sterility can be divided into nucleus male sterility and nucleus-cytoplasmic male sterility according to a genetic model and position of male-sterile character in cells. At present, male sterility has been applied in crops such as rice, corn, wheat, cabbage, pepper and the like. However, in many crops, male sterility is not used for production mainly due to problems like lack of male sterile resources and stability of male-sterile character of male sterile materials. It is found that the male sterile line material with natural mutation is the main source of male sterile materials. In addition, male sterile materials can be obtained by distant hybridization, artificial mutagenesis, and cell engineering. With the development of biotechnology, it has become possible to create male sterile materials through genetic engineering.

The gene Ty-5 is a tomato yellow leaf curl virus resistance gene in tomato, and is also a surveillance factor for monitoring a peptide chain synthesis process. The gene Ty-5 exists in all crops. In the present application, the new germplasm of male sterility can be created rapidly by performing a gene editing on the gene Ty-5. The development of gene editing technology provides a powerful weapon for the utilization of Ty-5 gene in heterosis breeding. The current gene editing technologies mainly include zinc finger nuclease technology, transcription activator-like effector nuclease technology, and the latest CRISPR/CAS9 gene editing technology. Gene editing realizes the recognition and cleavage of specific DNA sequences, and the introduction of different types of mutations such as deletion, substitution, and insertion of bases at double-strand breaks (DSBs) of DNA, achieving fixed-point editing of DNA.

SUMMARY

In view of the problems of the shortage of male sterile materials and the low purity of hybrid varieties, and the current situation of long time and high cost of conventional breeding, gene editing technology is applied to Ty-5 gene according to the present invention, so as to rapidly create a new germplasm of a male sterile crop while retaining agronomic characters of an original male fertile material.

In order to solve the above technical problems, the following technical solutions of the present invention are used.

(1) All of the existing gene editing methods can be used for the editing of Ty-5 in this study. In the present invention, only CRISPR/Cas9 technology is used for the gene editing of Ty-5. A deletion of DNA sequence is introduced by using a repair mechanism of plants themselves to DSBs, causing a loss of function of Ty-5 gene, thereby obtaining a male-sterile character;

(2) gRNA target sites are selected in an exon region of Ty-5 gene. According to the principle of CRISPR/Cas9 target anchor, the 18-20 bp upstream of the protospacer-associated motif (PAM) as the target site, i.e., (5′-N18-20NGG-3′, NGG is a PAM sequence, and N18-20 represents a recognition sequence of 18-20 bp);

(3) Oligo sequence primers are designed based on the recognition sequence:

Target-Sense:
5′-TTG-NNNNNNNNNNNNNNNNNNN (N represents gRNAsense
sequence)
Target-Anti:
5′-AAC-NNNNNNNNNNNNNNNNNNN N represents the
reverse complement of gRNA sense)

The primers are respectively diluted to a concentration of 10 μM, 5 μL of each of the above primers is taken, and 15 μL of water is added for a uniform mixing to form a mixed solution. The mixed solution is placed at 95° C. for 3 minutes, then slowly cooled to 25° C., and finally kept at 16° C. for 5 minutes to complete a synthesis of an oligo dimer;

(4) A CRISPR/Cas9 kit VK005-14 from VIEWSOLID BIOTECH, Beijing is selected, 1 μL of synthesized oligo dimer, 1 μL of Cas9/gRNA vector, 1 μL of Solution 1, 1 μL of Solution 2, and 6 μL of H₂O are mixed uniformly to form a mixed solution, and a reaction is performed on the mixed solution at 16° C. for 2 h;

(5) After ligation, the vector is transferred into E. coli competent state, a single clone is picked for plasmid sequencing analysis. A sequencing primer is sqprimer: 5′-GATGAAGTGGACGGAAGGAAGGAG-3′, and a positive plasmid is transferred to Agrobacterium GV3101;

(6) A cotyledon of the crop is used as an explant, a plant regeneration is carried out by a leaf disc method, Agrobacterium GV3101-mediated transformation is performed, and a regenerated plant is obtained by hygromycin resistance screening;

(7) Primers that can amplify the target site are designed according to upstream and downstream sequences of the target site, and the regenerated plant DNA is extracted to be used as a template for PCR amplification. The amplified products are sequenced, and a sequencing analysis is performed on the regenerated plants to determine whether a gene editing occurs and whether an editing type is homozygous mutation;

(8) After the sequencing analysis, a pollen content and germination identification is performed on homozygous gene edited strains. The results show that the homozygous edited Ty-5 plants created by the gene editing are new male sterile germplasms.

Compared with the prior art, the advantages of the present invention are as follows:

(1) The method for creating a new germplasm of a male sterile crop of the present invention can be applied without being limited by crop categories. After the gene editing is performed on Ty-5 genes of various crops, new germplasms can be quickly obtained. The new germplasms have the same agronomic characters as the previous materials, and only differ in sexual aspect, which effectively solves the problem of the lack of male sterile materials and unstable fertility in natural resources.

(2) As compared to a conventional breeding method, materials treated by the method of the present invention can obtain male-sterile characters more quickly.

(3) As compared to a conventional breeding method, materials treated by the method of the present invention can better retain the agronomic traits of the acceptor material.

(4) The new male sterile germplasm created by the present invention is a powerful supplement to existing materials.

(5) Performing a hybrid seed production by using the materials created by the male sterility creating method of the present invention can greatly reduce the labor requirement and improve the purity of the hybrid seed.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a diagram showing a regenerated plant after a gene editing amplified by a gene editing primer;

(M: 100 bp Marker; 1: regenerated plant No. 1 after the gene editing; 2: regenerated plant No. 2 after the gene editing; 3: wild type Money maker material);

FIG. 2 is a diagram showing results of a sequencing of each material band amplified by a CRISPR5-F primer;

(a: regenerated plant No. 1; b: a sequencing result of a wild type moneymaker; c: regenerated plant No. 2; triangle boxes indicate sequence deletions of the regenerated plant No. 1 and the regenerated plant No. 2, respectively); and

FIG. 3 is a diagram showing a comparison of pollen germination;

(a: regenerated plant No. 1; b: wild type moneymaker; c: regenerated plant No. 2).

DETAILED DESCRIPTION OF THE EMBODIMENTS

The technical solutions of the present invention will be clearly and completely described with reference to the drawings in the embodiments. It is obvious that the described embodiments are only a part of the embodiments of the present invention, but not all embodiments. All other embodiments obtained by those of ordinary skill in the art based on the embodiments of the present invention without creative work should be considered as falling within the scope of the present invention.

A method for creating a new germplasm of a male sterile crop through a gene editing, includes the following steps:

(1) Materials

Material of moneymaker having normal stamen fertility;

CRISPR/Cas9 Kit: a CRISPR/Cas9 Kit VK005-14 from VIEWSOLID BIOTECH, Beijing was selected;

T carrier: TransGen Biotech, Beijing. (CT301-01);

DNA Extraction Kit: TIANGEN Biotech (Beijing) Co., Ltd. (DP305);

Agrobacterium competent state: GV3101;

Primer synthesis and sequencing were completed by GenScript Biotech Corp. (Nanjing).

(2) Selection of gRNA Target Sites

The full length sequence of the Ty-5 gene (as shown in SEQ ID NO: 1) includes a total of 16 exons, and the second exon sequence was selected for the design of the gRNA target site in the present embodiment. The length of target sequence is 19 bp (as shown in SEQ ID NO: 2). The primers were designed based on the target sequence:

Target-F: 5′-TTG-AGAAGAAGCTGATGATCTA-3′, as shown
in SEQ ID NO: 3,
Target-R: 5′-AAC-TAGATCATCAGCTTCTTCT-3′, as shown
in SEQ ID NO: 4;

(3) Oligo Dimer Synthesis:

The Target primers were respectively diluted to a concentration of 10 μM, 5 μL of each of the above primers was taken, and 15 μL of water was added for a uniform mixing to obtain a mixed solution. The mixed solution was placed at 95° C. for 3 minutes, slowly cooled to 25° C., and then kept at 16° C. for 5 minutes, so as to complete the synthesis of oligo dimer;

(4) Construction of CRISPR/Cas9 Recombinant Vector and Transformation of Agrobacterium

The reaction system was as follows: 1 μL of synthesized oligo dimer, 1 μL of Cas9/gRNA vector, 1 μL of Solution 1, and 1 μL of Solution 2, and 6 μL of H₂O were mixed homogeneously to obtain a mixed solution, and the mixed solution reacted at 16° C. for 2 h. The ligated vector was transformed into Escherichia coli competent Trans1-T1, and coated on a plate for placing overnight. A single colony was selected for extracting the plasmid, and a sequence analysis was performed on the plasmid. The sequencing primer was sqprimer: 5′-GATGAAGTGGACGGAAGGAAGGAG-3′, as shown in SEQ ID NO: 5. The plasmid was extracted from the colony with the correct sequencing result, and transferred into the Agrobacterium GV3101 by a freeze-thaw method.

(5) Tomato Transformation:

The main steps were as follows:

Pre-culture preparation of explants: Cotyledons that had just emerged from the seed coat were selected for transformation. The cotyledons were cut and placed in 50-100 mL of MS liquid medium. The stalk ends and tips of the cotyledons were excised and placed in D1 medium, and the cotyledons were placed upside down for culture in D1 medium. The culture dish was pre-incubated for 2 days in a constant temperature culture chamber (16 L/8 D) at 24° C.

Co-culture: 5 μL of 0.074 M acetosyringone was added to each 10 mL of MS liquid medium, 5 mL of the MS liquid medium (+AS) was taken to wash Agrobacterium colonies, the bacterial solution OD600 was diluted to a concentration of 0.3-0.4, and the bacterial solution was added to the pre-cultured (2 days) cotyledons. After infecting the cotyledons for 8-10 minutes by Agrobacterium, the excess bacterial solution was removed. The cotyledons were transferred to the D1 medium containing filter paper. The cotyledons were inversely placed (the lower surface of the cotyledon faces upwards) for incubation at 24° C. for 2 days in the dark.

Screening: the sterile cotyledons were transferred to a 50 mL centrifuge tube, washed twice with sterile water, and washed once with +Car; the cotyledons were inversely placed (back up) on the differentiation medium 2Z, 20-30 leaves were placed per culture dish to ensure the growth space required for cotyledons. The double-layer sealing film was used for sealing, and a cultivation was performed at 24° C. for 10 days (16 L/8 D). On the tenth day, the cotyledons were transferred to fresh 2Z medium plates, and then subcultured every 2-3 weeks. The callus appeared after 2-3 weeks. The initial buds appeared within 4-6 weeks. When the buds began to appear, the explants were subcultured every 2 weeks, and the medium was 1Z selective medium.

Rooting: the shoots were picked from the explants and placed in a 100 mL sterile vial containing 40 mL of MMSV medium (containing 0.5 mg/L IBA, 15 mg/L hygromycin and 200 mg/L Timentin). Roots began to appear after cultured for around 2 weeks. When the plants grown large enough, the seedlings were transplanted into small plastic pots containing a mixture of vermiculite and soil, and watered with nutrient water. A total of 2 transformed tomato seedlings were obtained by tomato transformation.

6. Regenerated Plant Detection after Gene Editing:

Leaf DNA of two regenerated plants and wild type moneymaker materials were extracted separately, and the following amplification primers were used:

CRISPR5-F: 5′-TCCATTGAACTGAAGCAAATCTC-3′, as shown
in SEQ ID NO: 6;
CRISPR5-R: 5′-GCTAATAATGCTAAGCCCTCACA-3′, as shown
in SEQ ID NO: 7.

The length of the amplified fragment was about 450 bp, and the product after PCR amplification was subjected to an agarose gel electrophoresis to determine whether the size of the strip was correct (FIG. 1). The electrophoresis bands showed that the regenerated plants and wild type moneymaker materials could amplify a 450 bp band, and the three PCR products amplified by the regenerated plants and wild materials were sequenced by CRISPR5-F primers to detect the variation of the base sequence of the gene editing site (FIG. 2). The results showed that, as compared to wild type moneymaker materials, using the regenerated plants No. 1 and No. 2 resulted in sequence variation at the gene editing site. However, the variation type of the plant No. 1 was heterozygous mutation, and a 13 bp deletion occurred in one of the double-stranded DNA; the variation type of the plant No. 2 was homozygous mutation, and a 6 bp deletion occurred respectively at a same site of the double-stranded DNA.

7. Comparison of Pollen Content and Germination

The pollens of two regenerated plants and wild type moneymaker were collected, and incubated on the germination medium for 4 h at 26° C. in the dark. The pollen contents and the germination thereof of various materials were compared and observed under a microscope (FIG. 3). Through the germination comparison test, the pollen content of regenerated plant No. 1 was equal to that of wild type moneymaker, while the pollen content of regenerated plant No. 2 was significantly reduced. By the comparison of pollen germination, no pollen germination was observed in plant No. 2 after cultured for 4 h, but pollen germination was observed respectively in regenerated plant No. 1 and wild type moneymaker. It can be seen that homozygous variation (plant No. 2) can greatly reduce plant pollen content and stop pollen germination.

In summary, the present invention provides a method for creating a new germplasm of a male sterile crop by a gene editing. Through performing a gene editing on the Ty-5 gene exon region, the homozygous edited plant was obtained, which is a new male sterile germplasm.

SEQ ID NO: 1

The full-length sequence of the Ty-5 gene in the tomato material moneymaker, the underlined sequence is the intron sequence, and the shadow indicates the gene recognition site.

ATGAAGATTGTTCGTAGAGACTTTGTTCCTGATGGTTCTGGTAGTGTAAAGGTAACTTTTTTATCTCTATA
ATTGTTGTTTAAATCTATAATTCGAGTAATTTTCGTGATTTTTTGAAACCCCAGATGAAGAAAACGTTAAAATT
TTGCTTATAATCTGATAGCTGAAGGTGATACTGTATTAGCTGTTACTGTTAGGTATTGCACTTTTGCTCAATTT
TATTAGTGTGAGGGCTTAGCATTATTAGCAATTTTTTTGGGATAAATAAGTAATTTTTATTCGCGTATGTAATA
AGTTTGAGATTTTGTAGAAAAACATGTTTTTACTATAAGAAGCATTTAGTTTATACTACTCCCTTACTCCGTTA
CAATTTGTTTGTTTGGTTTTGAATTGTCACGAGTTTTTTAAAAAAGAGAGTAAAGAACGACTTTTGAATCTCAT
GGTCTTTAAACTAAAGAGATTGTGGGATGTACGGAATTTGGTCTTTTATCTTGTGCTATTAAATATGGTAGGT
GGAAAGTCGAATAGAAGAGTTGCCAAATAAGGAAAGAGACATTATTTTTGGAACAAACTAAAAAGAAAAGT
AGGATAAACAAATTAAAACAGGGGGAGTATTTGGTTTCTCATCGGTGCTACAAGAATTACTAAAAAGCTAGC
GTCTTGCCTTTTTTAAAAAGAAATTTTGATCCTGAAAGATGGAGTTTTTAATTTGAATATGGATGTCACTTGCT
AATTAGGTTCGAATTCTGTTCATTCGAAAGCTTGGAGCTTTTTACTTTGTTTATAACTACATAGTTGATTCTCT
ACACTTGTTAATGTTTCTCATCCTGTTGAGTTGATTGAAAATTTATGTTTTTTGGATAACATATTAATTGCTCTC
GTTCTCGTAAATGTCTAATTTCTGCATCAATTTTTGTTGTTTTATTCGTTGATTAGCTAATTCTTAGAAAATGTA
GTGTTCTGTGATGTGCGAAAGTAATCTATAAATAGTTAGACTCTAATCAGATTTGTGCTAAATTCTAGTTAAA
TTTGTCTAAATTGGCCTGAGATGAGTTTATATAAACTGTGGAGTTACATGGTCAGTGAGGATTCATTTATACG
ACCTGAACTTGCTTGGACTGAGGTGTTGTTGTTATTGTTGTTTGCTGAAATTGTGAATGACAATGTTACTATAA
GGAAAATGGATTTTGAGCATAGTGTGAGTCTCTACTGATTACACAGGTTGATAATAGTATTGTTATATTTGTTT
TGCTTAAAGCTTAGGGGAAGACTCTTTTTTAATGTTGAGAGCAACTTTCTTTTGCAAATTATGCTATGTGGGTC
TTTGCTGATTGTTAACACGGTTTAGCTTGTCACAACACAACCTACTGGAAGCTGGTTAAATTTTGCTTGTAATT
TCTTGTAGGAAGGTCCTGAGGGAAGCTGCTTCTGGAGGAAGAGATGCTGAACGAGTGAAACTGAAATTGGAA
ATTAAAGTTGAGGTAAGGATATATTAGACATCCAGCATCATTCAGTTGTGGGGTGCGGGCCTTGGTTAGAACT
TTGTTTTAGCTTCCAGCATAAGGTGTTTTAATATAAATTGAAAGATAAAACTTTGAAATCAATTAACTATAGA
GAAGAATCTACTAAGGATAGAGAGGAGACTTTTCTTTGTCTTCCTTTTCCAATGTGGTCGAGATGAAGTATTT
TTGGGCAGTTTGATGAATTTTGAGGATATCAATACAACCCGTGTATGACATATGCATGATAAATTGTCACATA
ACAATGCTCCATTTCTAACTAATCTCAATAAATGCGATGTTGATAGTTTTGTTACCATAGTAATGATGACAATT
GTAATGTGACTGGAAAGTAGGAAATAGATAGTGCTCTTTCTAGAGTTTTTATTTGAATATATTCCACTCCAAT
GTGGTATAATATAATCAATTTGGTGTTTTAGAATGTGGAGTATGACAAAGAAGGTTCTGCCTTGCGTATTCGC
GGGAAGAATATTCTGGAGAATGAACATGTAAAGGTGTGTATTCTTCAACTTAATCCTTTTGGATAAATTCCTA
ATATTGATGCTGCAACAAAAATGTATCTAATTATTTTATTGCAGATAGGGGCCTTTCACACTCTGGAAATTGA
GCAACACAGACCTTTTGTGCTAAGAAAGGTACAATGCTGTGTTTTGATTCTTTTGCAACTATCACTCTGTTTTC
TTTTAAAAATTTTGAGGTATATTATTTGCACTTTAAAAGCTATCAAGCTGGTGATATATGTTCTTTAGGATTGC
AGCTCTAACCTATGTTTCTCAGACTCTTCAAAAATGTCAACTGGTGCATGTCGGATTCTCCAAAAATAGCGTG
TTTTGGAATATCCGACATGGGTGCGGCATTGTAAGTGAAGAGTCCGCAACTTAGGCTCTAACAAGTAAAAAA
ATCTGTAAAGTTATTCATGTAATTTACATTATTATTATAAAATCCCCGGAAAAAGAAGAAGAGTACCTTTTTTT
TCTTTAATAACCTTGGTATCCGGGCCAGTTTGTGCACACTTCGACCACTTCCACCAACACAGCTACCGCCTAC
AGGGTAACTCTTTCCATCAAGGTTTTGACAAATAAGAAGAAATTGTCTAGTGTTTTTCGCCTCTGGTTGGATTT
GAACCTAAGATCTTATGACTCTTAACTCACTTCATTGGCCGCTAGACCATACCCCTTGGGTGCAGTTACTTGA
AACTAAGTTTAATTTTTCCCGCTAAATTTCAGTTGTCCCGCCGCTGACACCCCTTCGAGGCATCTCGTGTTCCT
GTCCTTTGACGTAGTTCACATCCTGCACGAAAGGTGTACATACGATACCTCCTTTCTGTCTCTAGATGGAACA
ACCCTTCTACATTAATGATGATTCCACCTTGGTTATCATCATGACTAATTCCATGCCAAATAAGCCAAGAAAT
AGCTACACATTTTCGGCACACACCAAAAAAGGGAACCCGAAGTATATTGTCGTTGATTTCTCATAAACAAGTG
TACAATGGTTCGAAAATTATCCGAAAGCATTAATGCTTATTAAGCTATTATTAACTCCTATATTATACATTCTA
TGGACTTTGGTCTGAGGGGGCTAGTTTCTTTTCTCAGCTTGTTTCTTTGTAGTTTGAAGGATCTATGCCCCCTA
GTTCGTCCAACACAGGTAGGGCTGAGGCATGATAAGATAAGTGACGGTTTGTGTAGCCTAGGTAATATATAC
TTAAGTGATGCAACAATATAAGTTCAGGTAGGGGAAATTCTTCTCGTACACATAGGAGTACATGGAATTTGGT
AAGATTTCTTGATTTTTTTCTGCATTATACAAAGTTGCTGCATAGATTAAGTATAACTAAATAAGTGTCTTTTT
ATAATTAGAGGCTAATGAGTCATAGAAGTTGAATTAGGAGATAATCATTTGTAGTTGTAACTAGAGGTTTCTA
TAGGAAATTGAGGAGTATCCCAATCGAAATATAAATGCCTAAAAATGTCTGGGCTAAGAATTACATGTGAAC
TTGATGTCTGGGCTAAGAATTACATGTGAACTTGAAATTATATTGATCGGGTACAGGTCGAATGAAATTTTCC
ATAATTTCTTTTACTACTGGATTTATTACTTAAAAGGGTATAAACTTATCAAAATAAGATTTCTTAGAAGGTAT
GCGTGCTTTTATTTAAAACTTTTGTTTATGTATAATCCTATCTAATGCATGTACATGAATTATTTTGAATTTATT
TTTACTCAAAGTAATCGTTATTTTCCTGTGTCATCTTCCTTATTATTTTTGTATATTCTATTTGTTTAGCAAATAT
ATGAGCATCTTGTTTGTTTCAATCTTAGTCTTACCTGAACATAGTTGATTTATACGAAAGCTTATACATATATG
AGTTCTGACTTGCATTATCTGATTTAGGTGGTCTGGGACTCACTGGCACGGGAGGTTCTTCGTCAAGCTTCTGG
TATTTTTCACAGTGCACTTTAACAAAGTTATATTTTTATTTGTTCAAGTGTTGCCATTAACTTTATCTGCAATAT
TAGGCATTTTAGTTCATAGCCTGACTTTTCATCCATAACTTATCAAGTTCTATAACATGTTGCTGCTTCTTTTTA
GTACATTGACATGATTGTGAAACCACTTTATAGGTGCATTATTCTTAGATGGATTGTTTCAGTCTAGGTGTCTT
TTAGCCCTTATGTTGCAGAGGTTTTCTTCTTTACTCGTACACTTGCAGTGAGAACATGATTATTCGCTGCAAGT
ACATGTGTGTTGCAGAGTGCTTTTGAACTGATGAGAAGTTTCCTATATAATTGTTGATATTCAGCTATATTGAT
TCCAACATGGATATGTGTTTGTAACTTTGTACTGCTCTTAGATTTACCGTTTCAATATGCTGAATACGGTTTTC
CTTTTTGATGATTCAGATCCATCTGCAAGTGCTGATCTGGCTGTGGTTCTGATGCAAGAAGGATTGGCACACA
TTCTTCTTATTGGTAAAAGGTAAGCTTGACAATCTCATAGTCCTATGAATACAAGTTTTAAACAGATCTTGAG
CATCTCCTTTTCTTGTATTTAAACGAGATGTAATAGTTTAAAAGTCGAATGATTATGTCAGAATTTCTATATGT
TGAGGCTGAGTTAAGTGTTAACTAGATTGTATGGCATAATTTTACCTTATGTACTTGTTACTGTTGTCTGAACA
GTGTGACTATCACCCGTTCTCGTATAGAGTCTTCTATACCGCGCAAGCATGGACCGGCTATTGCAGGTTATGA
TAAGGTGAGTCTCTTACTTCTTTTTGTTTCATCTTTTGTATAATTTAATTATTTTGAACATGACGTCAAGTGAAA
TTGTGTTCTTAATTTTGATTTGCAGGCGTTAAATAAATTCTTTGACAATGTTCTACAGGTAGACTTTTGTCAAC
TTTCTTGATGTTGCTTAATTTCCAGAAGCAATATGTTATAGGTTCTTATTTCTGTTGCAGGCCTTTGTCAAGCAT
GTTGATTTCAAAGTAGTTCGCTGTGCTGTGATTGCAAGTCCAGGATTCACCAAGGTATTTTTTGTATAGTTACA
CTTCTTAGCTAGTCATACTTTTATGCTATGTTACAAGGGGTAGAACTTGCATATCTAATTATATCTGTACTATG
CATATGTTAATTCAGTTGTGACATTTAAACTTTTTTGTGTTGAATGTGCAGGATCAGTTTCATCGTCACCTGTT
GTTGGAAGCCGAGAGGAAGCAACTAAGACCTATAATAGAAAATAAGTCACGCATAATTCTTGTCCATACAAC
CTCGGGATACAAGTATGCCCTTCTTTCTCTCTCTCCTTGCCCTTCATCTGACATCTCAAAACGAGTCAATACAT
TTTTGTGCAAACCATATGATGTTAGACATGCGTGCTAGTCTAAAATTGACTAATATGTAGCAATACATTTTTGT
GTACGCGATTCTCTCGTCAGTACTGCTATTTTAGTACAAATCGCCTTTATTATTTGTCTATTGTAGTTGATATGT
AAAAGTTCAATTATTATCCAGCACGGGTGTTTAAGGCCGAGAGTTTTTTTTTTCCCTCGTTTTACAGACATAGT
TTGAAAGAGGTTATGGATGCCCCAAATGTAATGACTATGATAAAAGATACAAAAGCTGCCAAAGAGGTACCT
TCTGACCCTTGTCCAACTTGATATGATCTTTAATCTTTATTCTTGTGTTTGTTCAAGTCTTTTTTCGTATTTTTTG
GGAATAACTGTTTTCCTTTCTCTTCCAATCTTAATCAGGTTCAAGCCCTAAAGGATTTTTTCAACATGCTTTCA
AATGTTAGGTTCTATCCTTGGTCTCAATGTTCTATTTATATTTTTCTTAATAACTTTGGATGTTTCAGATTTTTA
TCTATCATATGCTAAGAGTAAACACAGATTGTTTGGTTTTGAATTTATTTGTTTGCTTTTTTTGGTGTTTATCGG
TTATCTTGGGTTCTGTAAGAGGCCTGAGAGTTTCAAATAAAAGTTTGAGGTGTTTAACTATGCATGACGGATA
TCCCTGTTTAAGGAGAGGTGGACTAATCTGAAATATTTCTAGATTAAGAACAGATACGTTGTGTTATGATGGG
CAGCTGGTGATATTGTTATCTCTGCGTGTGCCTTTTTTTAGGCCTTTCTACCAATTGAATGCTGAAAATTCATTT
GCAACCAACCTTGGTTGAATTTATTTTCAGCAAGGATCCGTCATAATTCTCAGATATCCAATCATCAACAACT
TTGAACTTCTATTAAATTTTAGGGCATCTCAGTTGTGTTCTTTCATCTTTTGATTTTATATGCAATTTTACTGTA
GTAATAGGAGTATCTCTCTTCAATGCTTTGGCCATATCGGTACGAGAGAATTTATCATCTGATGTGCCCTCTCC
TTTACTTTTTTGCAGACAGAAAATACGATAAGGAAGTCTTAATTAAAAATATGCGTGTGCTTGATTTTCTGGTT
TTAAGGATATTTAGGTCTAAAAACTATAGTTACATTACATAATTTAGGGATGCTAGATGTAGAGGTCTTTTGC
TAGAGCGAGTGCTTGTTTGAACCCCCCGCCCCGCCCCGCATATTTCATGAATTATGATATTAATTGGATATTTA
TGATACCGCTTTTCAAGCTTTCTGAAGAAACTAAGAAGGATAACATCTTTATTTAAAAACTTTTTTCCCTCTCT
TGTTATAACTTCTTGCAATAAATGTAGTCATGTCCCTTTTTCTGGATCTCTTAACATTTATATTAATGAGCCCCT
GCATGAAGTTTACTTCCAGTTGTCAACAAATAGATCCTTGTAGTGTGTTTCTTTACCCGAAACTTGTGAAAATT
GAAGTTACTTTATTTGGACTTCTCTAGGATCCTGATCGTGCATGCTATGGACCAAAGCATGTTGAAGTTGCCC
ATGAGCGTCTGGCTATTCAGACACTTCTCATTACTGACGAGCTCTTTAGGTGAGTATCTTATGGTCCCAGGTTA
ATGGGGGCTTTATGAGCAATAAAATTAAACTGTATATAGCTTGATATAAATTTGCAACTCGTGGCATATTTCA
AGTTCATAAGTATCTCTTTTTACGTGCTTAGCTTTTAAAATCGACATCTTTGGTTCATAGGATAATATGTAAAC
ATGTATAACTATCTTCAAATCTCAACCAGTTATGTATGGGCCATTTCACTCGTGCTGTATATATATAGTTGGTT
GATATCGTACATGAGAAATATCCAACTTCTTTTGATCTGTTGACAGGAGTTCTGATGTAGAAACGAGGAAAAA
GTATGCTAATTTGGTCGATTCAGTCAAGGATTCAGGTGGTACTGCTCTCATTTTCTCGTCAATGCATGTCTCCG
GAGAACGTGAGTATATACAATTCCTGTTAATTTCTTTTTCCTCCCAGCATTTTCATCTCTGCCTTTCCCTGTCGC
CCCCTAGTAATGCTTAGAATGGTATTTTCCTTCTGTGCACATATTCATTGTCCCATAGTCGCTTCAAATCCTTTT
TCCTTCCTACGAACACACGTTCTTTACTGCATATTTGTCAAGGCTGATTAAAACAACTTTTGGTTTTCGTCACA
GAATTGAATCAGCTAACCGGCATTGCTGCAATCCTTCGTTTTCCTTTGCCGGAGCTGGAAGACATTGAGATGT
GA

Although the embodiments of the present invention have been shown and described, it is should be understood for those of ordinary skill in the art, various variation, modifications, substitutions, and improvements may be made to these embodiments without departing from the principle and spirit of the present invention, and the scope of the present invention is limited by the accompanying claims and their equivalents.

Claims

1. A method for creating a germplasm of a male sterile crop by a gene editing, comprising: performing the gene editing on an exon region of a Ty-5 gene, andintroducing a DNA sequence deletion by using a repair mechanism of plants to double-strand breaks (DSBs), so as to reach a loss of function of the Ty-5 gene, thereby obtaining a male-sterile character.

2. The method according to claim 1, wherein the gene editing is performed on the Ty-5 gene by using a CRISPR/Cas9 technology.

3. The method according to claim 2, further comprising the following steps: (1) selection of gRNA target sitesselecting gRNA target sites in the exon region of the Ty-5 gene, according to a principle of the CRISPR/Cas9 technology, selecting a 18-20 bp upstream of a protospacer-associated motif (PAM) as the gRNA target sites, wherein the gRNA target sites are 5′-N18-20NGG-3′, NGG is a PAM sequence, and N18-20 represents a recognition sequence of the 18-20 bp;(2) designing oligo sequence primers based on the recognition sequence as follows:Target-Sense: 5′-TTG-NNNNNNNNNNNNNNNNNNN, wherein N represents a gRNAsense sequence;Target-Anti: 5′-AAC-NNNNNNNNNNNNNNNNNNN, wherein N represents a reverse complement of the gRNAsense sequence;diluting the oligo sequence primers to a concentration of 10 μM, taking 5 μL of each of the oligo sequence primers, and adding 15 μL water to the oligo sequence primers for mixing uniformly to obtain a first mixed solution, placing the first mixed solution at 95° C. for 3 minutes, slowly cooling down the first mixed solution to 25° C., and keeping the first mixed solution at 16° C. for 5 minutes to complete a synthesis of an oligo dimer;(3) construction of CRISPR/Cas9 recombinant vector and transformation of Agrobacterium selecting a CRISPR/Cas9 kit VK005-14 from VIEWSOLID BIOTECH, Beijing, uniformly mixing 1 μL of the oligo dimer, 1 μL of a Cas9/gRNA vector, 1 μL of Solution 1, 1 μL of Solution 2, and 6 μL of H2O to obtain a second mixed solution, reacting the second mixed solution at 16° C. for 2 h;transferring a ligated vector into E. coli competent state, picking a single clone for a plasmid sequencing analysis, a sequencing primer is sqprimer: 5′-GATGAAGTGGACGGAAGGAAGGAG-3′, as shown in SEQ ID NO: 5, and transferring a positive plasmid to Agrobacterium GV3101;(4) crop transformationusing a cotyledon of a crop as an explant, carrying out a plant regeneration by a leaf disc method, carrying out a positive Agrobacterium GV3101-mediated transformation, performing a hygromycin resistance screening to obtain a regenerated plant.

4. The method according to claim 3, further comprising the following steps: (1) regenerated plant detection after gene editing:designing primers amplifying the gRNA target sites according to upstream and downstream sequences of the RNA target site, extracting DNA of the regenerated plant, using the DNA as a template for a PCR amplification to obtain amplified products, sequencing the amplified products, and performing a sequencing analysis on the regenerated plant to determine whether the gene editing occurs and whether an editing type is a homozygous mutation;(2) after the sequencing analysis, identifying a pollen content and germination of homozygous gene edited strains; wherein, results show that a homozygous edited Ty-5 plant created by the gene editing is a male sterile germplasm.

5. A male sterile germplasm prepared by the method of claim 1.

6. The male sterile germplasm according to claim 5, wherein the gene editing is performed on the Ty-5 gene by using a CRISPR/Cas9 technology.

7. The male sterile germlasm according to claim 5, wherein the method further comprises the following steps: (1) selection of gRNA target sitesselecting gRNA target sites in the exon region of the Ty-5 gene, according to a principle of CRISPR/Cas9 target anchor, selecting a 18-20 bp upstream of a protospacer-associated motif (PAM) as the gRNA target sites, wherein the gRNA target sites are 5′-N18-20NGG-3′, NGG is a PAM sequence, and N18-20 represents a recognition sequence of the 18-20 bp;(2) designing oligo sequence primers based on the recognition sequence as follows:Target-Sense: 5′-TTG-NNNNNNNNNNNNNNNNNNN, wherein N represents a gRNAsense sequence;Target-Anti: 5′-AAC-NNNNNNNNNNNNNNNNNNN, wherein N represents a reverse complement of the gRNAsense sequence;diluting the oligo sequence primers to a concentration of 10 μM, taking 5 μL of each of the oligo sequence primers, and adding 15 μL water to the oligo sequence primers for mixing uniformly to obtain a first mixed solution, placing the first mixed solution at 95° C. for 3 minutes, slowly cooling down the first mixed solution to 25° C., and keeping the first mixed solution at 16° C. for 5 minutes to complete a synthesis of an oligo dimer;(3) construction of CRISPR/Cas9 recombinant vector and transformation of Agrobacterium selecting a CRISPR/Cas9 kit VK005-14 from VIEWSOLID BIOTECH, Beijing, uniformly mixing 1 μL of the oligo dimer, 1 μL of a Cas9/gRNA vector, 1 μL of Solution 1, 1 μL of Solution 2, and 6 μL of H2O to obtain a second mixed solution, reacting the second mixed solution at 16° C. for 2 h;transferring a ligated vector into E. coli competent state, picking a single clone for a plasmid sequencing analysis, a sequencing primer is sqprimer: 5′-GATGAAGTGGACGGAAGGAAGGAG-3′, as shown in SEQ ID NO: 5, and transferring a positive plasmid to Agrobacterium GV3101;(4) crop transformationusing a cotyledon of a crop as an explant, carrying out a plant regeneration by a leaf disc method, carrying out a positive Agrobacterium GV3101-mediated transformation, performing a hygromycin resistance screening to obtain a regenerated plant.

8. The male sterile germlasm according to claim 5, wherein the method further comprises the following steps: (1) regenerated plant detection after gene editing:designing primers amplifying the gRNA target sites according to upstream and downstream sequences of the gRNA target site, extracting DNA of the regenerated plant, using the DNA as a template for a PCR amplification to obtain amplified products, sequencing the amplified products, and performing a sequencing analysis on the regenerated plant to determine whether the gene editing occurs and whether an editing type is a homozygous mutation;(2) after the sequencing analysis, identifying a pollen content and germination of homozygous gene edited strains; wherein, results show that a homozygous edited Ty-5 plant created by the gene editing is a male sterile germplasm.