CN113652501A - Mixed sample detection method for detecting purity of Chinese cabbage seeds based on mSNP technology - Google Patents

Abstract

The invention relates to a mixed sample detection method for detecting the purity of Chinese cabbage seeds based on a mSNP technology, which is carried out by utilizing a primer pair 1F/R-22F/R, wherein the gene sequence of the primer pair 1F/R-22F/R is shown in SEQ ID No. 1-44; the invention adopts the mSNP technology, and can detect more SNP variations under the condition of unchanging an amplicon; the mixed sample method is adopted for detection, the amplification workload is reduced, the sequencing cost is reduced, the detection speed is accelerated, and the detection of 1440 seeds can be completed at most in one day. The method directly reads the polymorphism of the mononucleotide by using a sequencing technology, directly judges the purity result by a program, has visual and reliable result, and avoids the influence of subjective factors during the seed development period and the result judgment.

Description

Mixed sample detection method for detecting purity of Chinese cabbage seeds based on mSNP technology

Technical Field

The invention belongs to the field of seed purity detection, and particularly relates to a mixed sample detection method for detecting the purity of Chinese cabbage seeds based on a mSNP technology.

Background

Chinese cabbage (Brissica caulestis L.ssp. pekinesis) also called cabbage, yellow bud, cabbage, and belongs to Brassicaceae Brassica. The Chinese cabbage originates from China, has more than five thousand years of cultivation history, is rich in germplasm resources and various in ecological types, and is one of the main traditional vegetables in China. In the 70 s of the 20 th century, the utilization of heterosis dominates the breeding of new varieties of Chinese cabbage, and great results are obtained. In order to breed a good new variety in a short time, breeders will select a few high-quality backbone parents, so that the genetic basis of the variety tends to be narrow continuously. The difference of the varieties directly affects the production, and the Chinese cabbage hybrid is often biologically mixed by the parental inbred line seeds or other varieties of seeds. The purity of the seeds is the main index of the quality of the seeds, is defined as the percentage of the number of the seeds of the variety in the number of the seeds of the crop sample to be tested, and the purity of the hybrid seeds must be identified before being packaged and sold.

Since the 80 s, the identification of seed purity is developed from conventional morphological feature identification, physicochemical identification, biochemical identification and further applied to molecular marker identification, and the development from an apparent level, a protein level to a nucleic acid level is realized. Morphological identification is the earliest method applied, and identification is carried out according to the shape of seeds, the shape of seedlings and the shape of plants. The traditional field shape identification is an arbitration method for seed purity identification, the method can refer to a plurality of shapes, the result is reliable, but the method has long required period and high cost and is easy to be limited by seasons, environment, human factors and the like. The physical and chemical identification is mainly used for distinguishing oat varieties and is rarely reported in the identification of Chinese cabbage. Biochemical identification includes isoenzyme and protein electrophoresis techniques. The biochemical markers have tissue specificity, few available spectral bands, limited spectral band difference and unstable band type difference in different organs and different growth periods, so that the stability and accuracy of results are reduced, and the requirements of detecting more and more varieties cannot be met. The molecular marker is a marking technology which develops rapidly after form and biochemical marking, and has the advantages of difficult influence of time environment, good polymorphism, accurate result and the like. Molecular markers can be divided into three major classes: the first is a marking technology based on enzyme digestion, such as RFLP, which has stable polymorphism but complex operation, good cost and less polymorphism; secondly, the PCR reaction is used as a basic marking technology, such as RAPD, SSR, SCAR and the like, and the marking has low cost, simple and convenient operation and poor stability; and thirdly, the technology combining enzyme digestion and PCR (polymerase chain reaction), such as AFLP (amplified fragment Length polymorphism), the marker has the advantages of RFLP and RAPD (random amplified polymorphic DNA), and has high reliability and high efficiency, small DNA consumption, complex operation steps and high cost.

Disclosure of Invention

The invention aims to overcome the defects of the prior art and provides a mixed sample detection method for detecting the purity of Chinese cabbage seeds based on the mSNP technology, which is efficient, accurate and low in cost.

In order to achieve the purpose, the technical scheme adopted by the invention is as follows:

the first technical scheme is as follows:

a primer group for purity detection of Chinese cabbage seeds in the mSNP technology is characterized by comprising a primer pair 1F/R, a primer pair 2F/R, a primer pair 3F/R, a primer pair 4F/R, a primer pair 5F/R, a primer pair 6F/R, a primer pair 7F/R, a primer pair 8F/R, a primer pair 9F/R, a primer pair 10F/R, a primer pair 11F/R, a primer pair 12F/R, a primer pair 13F/R, a primer pair 14F/R, a primer pair 15F/R, a primer pair 16F/R, a primer pair 17F/R, a primer pair 18F/R, a primer pair 19F/R, a primer pair 20F/R, a primer pair 21F/R and a primer pair 22F/R; wherein each primer pair consists of a forward primer and a reaction primer;

in the primer pair 1F/R, the sequence of the F primer is shown as SEQ ID No.1, and the sequence of the R primer is shown as SEQ ID No. 2;

in the primer pair 2F/R, the sequence of the F primer is shown as SEQ ID No.3, and the sequence of the R primer is shown as SEQ ID No. 4;

in the primer pair 3F/R, the sequence of the F primer is shown as SEQ ID No.5, and the sequence of the R primer is shown as SEQ ID No. 6;

In the primer pair 4F/R, the sequence of the F primer is shown as SEQ ID No.7, and the sequence of the R primer is shown as SEQ ID No. 8;

in the primer pair 5F/R, the sequence of the F primer is shown as SEQ ID No.9, and the sequence of the R primer is shown as SEQ ID No. 10;

in the primer pair 6F/R, the sequence of the F primer is shown as SEQ ID No.11, and the sequence of the R primer is shown as SEQ ID No. 12;

in the primer pair 7F/R, the sequence of the F primer is shown as SEQ ID No.13, and the sequence of the R primer is shown as SEQ ID No. 14;

in the primer pair 8F/R, the sequence of the F primer is shown as SEQ ID No.15, and the sequence of the R primer is shown as SEQ ID No. 16;

in the primer pair 9F/R, the sequence of the F primer is shown as SEQ ID No.17, and the sequence of the R primer is shown as SEQ ID No. 18;

in the primer pair 10F/R, the sequence of the F primer is shown as SEQ ID No.19, and the sequence of the R primer is shown as SEQ ID No. 20;

in the primer pair 11F/R, the sequence of the F primer is shown as SEQ ID No.21, and the sequence of the R primer is shown as SEQ ID No. 22;

in the primer pair 12F/R, the sequence of the F primer is shown as SEQ ID No.23, and the sequence of the R primer is shown as SEQ ID No. 24;

in the primer pair 13F/R, the sequence of the F primer is shown as SEQ ID No.25, and the sequence of the R primer is shown as SEQ ID No. 26;

in the primer pair 14F/R, the sequence of the F primer is shown as SEQ ID No.27, and the sequence of the R primer is shown as SEQ ID No. 28;

In the primer pair 15F/R, the sequence of the F primer is shown as SEQ ID No.29, and the sequence of the R primer is shown as SEQ ID No. 30;

in the primer pair 16F/R, the sequence of the F primer is shown as SEQ ID No.31, and the sequence of the R primer is shown as SEQ ID No. 32;

in the primer pair 17F/R, the sequence of the F primer is shown as SEQ ID No.33, and the sequence of the R primer is shown as SEQ ID No. 34;

in the primer pair 18F/R, the sequence of the F primer is shown as SEQ ID No.35, and the sequence of the R primer is shown as SEQ ID No. 36;

in the primer pair 19F/R, the sequence of the F primer is shown as SEQ ID No.37, and the sequence of the R primer is shown as SEQ ID No. 38;

in the primer pair 20F/R, the sequence of the F primer is shown as SEQ ID No.39, and the sequence of the R primer is shown as SEQ ID No. 40;

in the primer pair 21F/R, the sequence of the F primer is shown as SEQ ID No.41, and the sequence of the R primer is shown as SEQ ID No. 42; in the primer pair 22F/R, the sequence of the F primer is shown as SEQ ID No.43, and the sequence of the R primer is shown as SEQ ID No. 44.

Further, the primer pair 1F/R-22F/R is obtained by mSNP technology.

The second technical scheme is as follows:

a mixed sample detection method for detecting the purity of Chinese cabbage seeds according to the primer group comprises the following steps:

step 1, selecting materials: selecting 1 or more Chinese cabbage varieties; at least 96 seeds are adopted for each sample of the Chinese cabbage;

Step 2, accurately quantifying the genomic DNA of the Chinese cabbage;

step 3, synthesizing primers in the primer group, wherein when synthesizing a forward primer and a reverse primer in each primer pair, 10 primers with different target labels are synthesized; then mixing the primers according to the specified label combination to prepare a primer mixed solution;

step 4, taking the Chinese cabbage genome DNA as a template, and respectively carrying out one-round PCR amplification on the Chinese cabbage genome DNA by using the primer mixed solution to obtain a target region;

step 5, mixing the obtained PCR amplification products in equal amount;

step 6, screening fragments of the mixed product;

step 7, digesting the single-stranded DNA in the screened system;

step 8, purifying the digested product;

step 9, configuring a two-round PCR system in the system obtained in the step 8;

step 10, purifying the products of the two rounds of PCR to complete the preparation of a sequencing library;

step 11, mixing the sequencing library with the same quality, and then performing on-machine sequencing to obtain sequencing data;

step 12, splitting the sample according to the label combination again for the obtained test data;

and step 13, identifying the genotype result of the target locus of the test sample, and judging the purity of the seed according to the genotype condition of the locus.

Further, when synthesizing a forward primer and a reverse primer in a primer pair, synthesizing 10 primers with different target labels;

in the tag combination of each primer pair, the tag sequence of the forward primer is different from the tag sequence of the reverse primer.

Further, in step 3, in each primer pair, tag sequences of the synthesized 10 tagged forward primers are respectively shown as SEQ ID Nos. 49-58;

in each primer pair, the tag sequences of the synthesized 10 reverse primers with tags are respectively shown as SEQ ID Nos. 59-68.

Further, 10 pairs of labeled primers were synthesized from each pair of primers, and the label combination of the forward primer and the reverse primer was selected from any one or more of the primers shown in Table 1.

Table 1: label combination mode

Further, in the step 3, the F primers in the primer pairs 1F/R-22F/R also comprise an F-terminal universal primer, and the sequence of the F-terminal universal primer is shown as SEQ ID No. 45; the R primers in the primer pairs 1F/R-22F/R also comprise an R-terminal universal primer, and the sequence of the R-terminal universal primer is shown as SEQ ID No. 46;

the sequence of the Frimer F used in the two-round PCR in the step 9 is shown as SEQ ID No.47,

the sequence of the Primer R used is shown as SEQ ID No. 48.

Further, when there are a plurality of varieties of Chinese cabbage, the sequence of Primer R further includes a barcode sequence for discriminating the varieties of Chinese cabbage.

Further, in step 2, in the tag combination of each primer pair, the tag sequence of the forward primer is different from the tag sequence of the reverse primer.

Further, in the step 1, extracting the genomic DNA of the Chinese cabbage seeds by using a Chinese cabbage seed genomic DNA extraction kit.

Further, in step 4, the round of PCR amplification system: 8 mul of primer mixed solution; the dosage of DNA is 100 ng; 3. mu.l of Ttase; adding water to complement 45 mu l;

the one-round PCR amplification procedure: 3min at 95 ℃; (95 ℃ for 30s, 60 ℃ for 4min, 72 ℃ for 30s)28 cycles; 4min at 72 ℃.

Further, in step 6, the mixed product is subjected to fragment screening, specifically the following operations:

step 6.1, adding magnetic beads with the volume 0.4 times that of one round of PCR, blowing and beating the mixture up and down by using a pipettor, uniformly mixing, standing for 2min, adsorbing the mixture by using a magnetic frame until the solution is clarified, and transferring the supernatant into a new tube;

step 6.2, adding magnetic beads with the volume 0.6 times that of one round of PCR, blowing and beating the mixture up and down by using a pipettor, uniformly mixing, standing for 2min, adsorbing by using a magnetic frame until the solution is clarified, and removing the supernatant;

Step 6.3, adding a magnetic bead suspension with the volume 0.9 time that of one round of PCR, re-suspending the magnetic beads, standing for 2min, adsorbing by a magnetic frame until the solution is clarified, and removing the supernatant;

and 6.4, adding 100 mu l of ethanol with the volume concentration of 80%, repeatedly adsorbing the magnetic beads on different two surfaces by using a magnetic frame to fully wash the magnetic beads, adsorbing for 2min by using the magnetic frame, removing the supernatant, and standing at room temperature until the ethanol is completely volatilized.

In step 7, digesting the single-stranded DNA in the system obtained after screening, the specific operation steps are as follows:

step 7.1, adding 20 mul of water into the obtained product, and uniformly mixing the magnetic beads;

step 7.2, adsorbing magnetic beads, and transferring 16 mu l of supernatant into a new EP tube;

step 7.3, adding 2 ul of Exo I and 2 ul of 10 × Reaction Buffer into the system;

and 7.4, the digestion program of the digestion system is as follows: 30min at 37 ℃; 15min at 85 ℃;

in step 8, the specific operation steps for purifying the digested product are as follows:

step 8.1, adding 0.9 time of magnetic beads, blowing and beating the mixture up and down by using a pipettor, uniformly mixing, standing for 2min, adsorbing by using a magnetic frame until the solution is clarified, and removing the supernatant;

8.2, adding magnetic bead resuspension liquid with equal PCR volume, resuspending magnetic beads, standing for 2min, adsorbing by a magnetic frame until the solution is clarified, and removing supernatant;

And 8.3, adding 100 mu l of ethanol with the volume concentration of 80%, repeatedly adsorbing the magnetic beads on two different surfaces by using a magnetic frame to fully wash the magnetic beads, adsorbing for 2min by using the magnetic frame, removing the supernatant, and standing at room temperature until the ethanol is completely volatilized.

Further, in step 9, the two-round PCR system: 10 μ l of the enzyme tretase; primer F; primer R; H2O18 μ l;

the two-round PCR procedure: 3min at 95 ℃; (95 ℃ 15s, 58 ℃ 15s, 72 ℃ 30s) for 12 cycles; 4min at 72 ℃;

further, in step 10, the two rounds of PCR products are purified using 0.80 times of magnetic beads, specifically as follows:

step 10.1, adding 0.8 time of magnetic beads, blowing and beating the mixture up and down by using a pipettor, uniformly mixing, standing for 2min, adsorbing by using a magnetic frame until the solution is clarified, and removing the supernatant;

step 10.2, adding magnetic bead resuspension liquid with equal PCR volume, resuspending magnetic beads, standing for 2min, adsorbing by a magnetic frame until the solution is clarified, and removing supernatant;

step 10.3, adding 100 mul of 80% ethanol, repeatedly adsorbing magnetic beads on two different surfaces by using a magnetic frame to fully wash the magnetic beads, adsorbing for 2min by using the magnetic frame, removing supernatant, and standing at room temperature until the ethanol is completely volatilized;

step 10.4, adding 23 μ l of Elution Buffer, fully suspending the magnetic beads, standing for 2min at room temperature to elute DNA, adsorbing the magnetic beads by a magnet, and adsorbing the obtained supernatant DNA solution into a new tube to obtain a sequencing library; the Elution Buffer is 10mM Tris-HCl and has the pH value of 8.0-8.5.

Compared with the prior art, the invention has the following beneficial effects:

mSNP technique: the invention adopts mSNP technology, a plurality of SNPs are corresponded in one amplicon, the information obtained by each amplicon fragment is utilized to the maximum extent, and the SNP variation as much as possible can be detected under the condition that the amplicon is not changed. And haplotypes can be formed among the SNPs, so that the detection efficiency of variation is improved. Therefore, variation in and among the mSNP loci can be adopted, and two modes of haplotypes and SNP can be adopted for detection, so that the detection of genetic variation is more precise, and the accuracy and sensitivity of marker identification are improved. In the patent, 22 pairs of primer pairs are adopted, more than 100 actually detected variation information exists, and more polymorphism sites meeting the requirements can be screened for purity identification analysis. Compared with the conventional SNP detection, the method reduces the use of the primer pairs and reduces the cost.

The cost is low: by adopting the mSNP technology, more SNP variations can be detected under the condition that an amplicon is not changed; by adopting the scheme of at least 96 test sample products mixed sample detection after one round of amplification, the workload of two rounds of amplification is reduced, and the sequencing cost is reduced.

High efficiency: by adopting a mixed sample detection scheme, after one round of amplification, at least 96 detection samples are mixed and subjected to subsequent amplification and sequencing, and the detection of 1440 seeds can be completed within one day at most. Compared with other detection methods, the method is simple to operate, does not need field planting, experimental operation with large workload and detection difficulty and the like, and can quickly detect the purity of the seeds.

And (3) accuracy: the method directly reads the polymorphism of the mononucleotide by using a sequencing technology, directly judges the purity result by a program, has visual and reliable result, and avoids the influence of subjective factors during the seed development period and the result judgment.

Drawings

FIG. 1 is a flow chart of the mixed sample detection method of the present invention.

Detailed Description

Example 1: method for obtaining specific primer

The method for obtaining the specific primer specifically comprises the following steps:

the method utilizes whole genome re-sequencing data of the Chinese cabbage, adopts BWA-mem (http:// bio-bw. sourceforce. net /) to be attached back to a Chinese cabbage reference genome, and utilizes GATK (https:// software. broadinstruction. org/GATK /) to carry out single nucleotide variation identification.

The identified single nucleotide variation site set is screened, the minimum allelic variation frequency is more than 0.02, the heterozygosity rate is less than 15%, the deletion rate is less than 20%, the single nucleotide variation sites are merged, the number of the screened single nucleotide sites is positioned in a section of 2-10, namely, mSNP (poly single nucleotide polymorphism) sites, compared with the traditional SNP (single nucleotide polymorphism) sites, the mSNP sites can utilize the information obtained by each primer pair to the maximum extent, namely, the SNP sites are detected as many as possible under the condition that the primer pairs are not changed, and all SNPs in the same primer pair can also be combined into a type, so that the polymorphism of the SNP sites is higher. For example, there are two A/T variations in a SNP, which can be distinguished by 3 polymorphisms AA, AT, TT, if the mSNP site is detected, there can be 8 (AGC, AGA, ATA, ATC, TGC, TGA, TTA, TTC) polymorphisms if there are 3 SNPs in a primer pair (A/T, G/T, C/A). This allows for more precise detection of genetic variation while improving the accuracy and sensitivity of marker identification. The total number of segments screened by this patent for higher polymorphism is 43.

And (3) designing primers for 43 target sections, and screening the specificity of the primers to obtain 22 pairs of chromosome specific primers, wherein the total number of the primers is 145 single nucleotide variation sites. From the comprehensive consideration of detection cost and practicality, 22 pairs of primers are finally selected and mixed to detect the purity of the Chinese cabbage seeds according to the principle of 5-10% diversity among Chinese cabbage samples, and about 140 SNP loci can be detected in total.

In the invention, 22 groups of specific primer pairs are obtained in total, namely the primer pairs 1F/R-22F/R, and the gene sequences of the primer pairs 1F/R-22F/R are shown as SEQ ID Nos. 1-44.

Example 2: primer group for detecting purity of Chinese cabbage seeds

The primer group for detecting the purity of the Chinese cabbage seeds comprises a primer pair 1F/R-22F/R, wherein the primer pair 1F/R-22F/R not only comprises specific primer sequences shown as SEQIDNo.1-44, but also comprises a universal primer sequence, and the F-end universal primer sequence of an F primer in the primer pair 1F/R-22F/R is shown as SEQIDNo.45; the sequence of the R-end universal primer of the R primer in the primer pair 1F/R-22F/R is shown as SEQ ID No. 46;

example 3: the method for obtaining the primer mixed solution comprises the following steps:

after obtaining the specific primer, designing a specific tag sequence, and then performing primer synthesis again, where the specific tag sequence is added during primer synthesis, in this embodiment, 96 specific tag combinations are adopted, specifically:

Synthesizing 10 primers with different target labels from each specific primer according to the combination condition of the specific labels, wherein the sequence form of the primers with the target labels is shown in table 2, taking 10 mu l of each primer from all F (forward primers) and all R (reverse primers) with the target labels, and metering to 10 ml; the concentration of each primer is 0.1 mu M, and primer pairs containing 96 groups of specific label combinations, namely primer mixed liquor, are prepared in the embodiment;

TABLE 2 primer sets

"FF" is an F-terminal universal primer sequence, and the F-terminal universal primer sequence is AACGACATGGCTACGATCCGACTT, as shown in SEQ ID No. 45;

"RR" is R terminal general primer sequence, the R terminal general primer sequence is CTAAGACCGCTTGGCCTCCGACTT, as shown in SEQ ID No. 46.

Wherein "YY" is a tag sequence,

in each primer pair, the tag sequences of the synthesized 10 forward primers with tags are respectively CCTTC, ACCGA, ATGTG, AATGC, TTCGG, AAGGT, CCCAT, ATGGA, ACGAT and CTCTG, namely respectively shown as SEQIDNo.49-58;

in each primer pair, tag sequences of 10 synthesized reverse primers with tags are respectively ATCCG, TATCG, ACTCG, TAACC, CTTAC, TCCTA, ACACT, TACGT, TCACG and ACGCA, namely respectively shown as SEQIDNo.59-68.

In each pair of primer pairs, 10 labeled primer pairs are synthesized, and the label combination mode of the forward primer and the reverse primer is selected from any one or more of the following table 2.

Example 4: identification of pure species

Selecting materials, namely selecting 2 parts of Chinese cabbages (96 seeds are selected from each part of Chinese cabbages), respectively numbering the Chinese cabbages to be 18-19 and 18-20, extracting the genomic DNA of the Chinese cabbages, and accurately quantifying the extracted DNA by adopting a Chinese cabbage seed genomic DNA extraction kit produced by Shijiazhuang Boruidi biotechnology limited.

Step 2, taking the genomic DNA of the Chinese cabbage seeds as a template, and carrying out one-round PCR amplification by using a primer mixed solution to obtain a target region;

the one-round PCR amplification system comprises the following steps: 8. mu.l of the primer mixture obtained in example 3; the dosage of DNA is 100 ng; 3. mu.l of Ttase; water was added to make up 45. mu.l.

The one-round PCR amplification procedure: 3min at 95 ℃; (95 ℃ for 30s, 60 ℃ for 4min, 72 ℃ for 30s)28 cycles; 4min at 72 ℃.

And 3, mixing the obtained PCR amplification products in equal quantity, wherein the PCR amplification products can be mixed only if the amplification products are specific labels with different combinations, and the PCR amplification products can be directly mixed according to the ratio of the system 1:1 during mixing. After equal mixing, purifying the product after mixing, namely screening fragments, and the specific steps are as follows;

Step 3.1, adding magnetic beads with the volume 0.4 times that of one round of PCR, blowing and beating the mixture up and down by using a pipettor, uniformly mixing, standing for 2min, adsorbing the mixture by using a magnetic frame until the solution is clarified, and transferring the supernatant into a new tube;

step 3.2, adding magnetic beads with the volume 0.6 times that of one round of PCR, blowing and beating the mixture up and down by using a pipettor, uniformly mixing, standing for 2min, adsorbing by using a magnetic frame until the solution is clarified, and removing the supernatant;

step 3.3, adding a magnetic bead suspension with the volume 0.9 time that of the PCR for one round, re-suspending the magnetic beads, standing for 2min, adsorbing by using a magnetic frame until the solution is clarified, and removing the supernatant;

and 3.4, adding 100 mu l of ethanol with the volume concentration of 80%, and repeatedly adsorbing the magnetic beads on two different surfaces by using a magnetic frame to fully wash the magnetic beads. Adsorbing with magnetic frame for 2min, removing supernatant, and standing at room temperature until ethanol volatilizes completely;

the magnetic beads are: novozan magnetic bead

Step 4, digesting single-stranded DNA in the screened system;

in the system containing magnetic beads obtained in step 3, the following operations were performed:

step 4.1, adding 20 mul of water into the obtained product, and uniformly mixing the magnetic beads;

step 4.2, adsorbing magnetic beads, and transferring 16 mu l of supernatant into a new EP tube;

step 4.3, add Exo I2. mu.l, 10 Reaction Buffer 2. mu.l to the system.

And 4.4, the digestion procedure of the system is as follows: 30min at 37 ℃; 15min at 85 ℃.

And 5, purifying the digested product:

step 5.1, adding 0.9 time of magnetic beads, blowing and beating the mixture up and down by using a pipettor, uniformly mixing, standing for 2min, adsorbing by using a magnetic frame until the solution is clarified, and removing the supernatant;

step 5.2, adding magnetic bead resuspension liquid with equal PCR volume, resuspending magnetic beads, standing for 2min, adsorbing by a magnetic frame until the solution is clarified, and removing supernatant;

and 5.3, adding 100 mu l of ethanol with the volume concentration of 80%, and repeatedly adsorbing the magnetic beads on two different surfaces by using a magnetic frame to fully wash the magnetic beads. Adsorbing with magnetic frame for 2min, removing supernatant, and standing at room temperature until ethanol is completely volatilized.

And 6, configuring a two-round PCR system in the system obtained in the step 5:

configuring a two-round PCR system in the system containing the magnetic beads obtained in the step 5, and performing two-round PCR amplification;

the two-round PCR system: 10 μ l of the enzyme tretase; primer F; primer R; h₂O 18μl

The two-round PCR procedure: 3min at 95 ℃; (95 ℃ 15s, 58 ℃ 15s, 72 ℃ 30s) for 12 cycles; 4min at 72 ℃.

The sequence of the Primer F is shown as SEQ ID No.47 and is GAACGACATGGCTACGATCCGACTT; the sequence of the Primer R is shown as SEQ ID No.48 and is TGTGAGCCAAGGAGTTGTTGTCTTCCTAAGACCGCTTGGCCTCCGACTT;

Since 2 parts of Chinese cabbage varieties are adopted in the embodiment, in order to distinguish samples, the sequence of Primer R comprises a unique Barcode sequence Barcode in addition to the sequence shown as SEQ ID No. 48;

the sequence of the barcoded Primer R is:

TGTGAGCCAAGGAGTTGxxxxxxxxxxTTGTCTTCCTAAGACCGCTTGGCCTCCGACTT；

where "xxxxxxxx" is a unique Barcode used to identify the sample to distinguish the specimens.

The Barcode sequences of 2 parts of Chinese cabbage variety samples in the embodiment are CGGCTAAA and TCCCCGTG respectively; namely shown as SEQ ID No.69-70 respectively.

Step 7, purifying the products of the two-round PCR amplification by using 0.80-time magnetic beads to complete the preparation of a sequencing library;

step 7.1, adding 0.8 time of magnetic beads, blowing and beating the mixture up and down by using a pipettor, uniformly mixing, standing for 2min, adsorbing by using a magnetic frame until the solution is clarified, and removing the supernatant;

step 7.2, adding magnetic bead resuspension liquid with equal PCR volume, resuspending magnetic beads, standing for 2min, adsorbing by a magnetic frame until the solution is clarified, and removing supernatant;

and 7.3, adding 100 mu l of ethanol with the volume concentration of 80%, and repeatedly adsorbing the magnetic beads on two different surfaces by using a magnetic frame to fully wash the magnetic beads. Adsorbing with magnetic frame for 2min, removing supernatant, and standing at room temperature until ethanol is completely volatilized.

Step 7.4 add 23. mu.l of Elution Buffer, suspend the beads well, and let stand at room temperature for 2min to elute the DNA. Adsorbing the magnetic beads by a magnet, and adsorbing the obtained supernatant DNA solution into a new tube to obtain a sequencing library (the solution Buffer is 10mM Tris-HCl, and the pH value is 8.0-8.5);

and 8, mixing the sequencing library with the same quality, and performing computer sequencing to obtain sequencing data.

And 9, identifying the genotype result of the target DNA, respectively selecting and detecting the synthesized seeds from 96 seeds for a subsequent purity judgment basis, and judging the purity of the seeds according to the genotype condition of the site with high polymorphism, wherein the detection result of the embodiment is shown in Table 3.

TABLE 3 test results

Sample numbering	Number of selfed seeds	Purity of seed	Conclusion
				18-19	3	96.74％	The same general identificationDetermine the result
18-20	3	96.77％	Results of conventional identification

Seed purity program interpretation principle:

firstly, judging whether each locus is hybridized/outcrossed or selfed, wherein the judgment standard is as follows: and calculating the proportion of the genotype type of a batch of seeds at each site. If the genotype at this site is only one and homozygous, this site is discarded because it cannot be judged whether it is selfed or crossed. If the percentage of one heterozygous genotype exceeds 90%, judging as hybridization; if the genotype of a sample at the site is homozygous, the sample is judged to be self-bred; and if the hybrid genotype is other, judging the cross.

Then, the sample is subjected to judgment of selfing, outcrossing and hybridization. And finally, counting the overall situation of the batch of seeds.

Purity calculation, expressed as percentage of purity of a batch of seeds:

the embodiments described above are only preferred embodiments of the invention and are not exhaustive of the possible implementations of the invention. Any obvious modifications to the above would be obvious to those of ordinary skill in the art, but would not bring the invention so modified beyond the spirit and scope of the present invention.

Sequence listing

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<212> DNA

<213> Artificial sequence (unknown)

<400> 9

caacaattca caaacaagat cacgtctc 28

<210> 10

<211> 27

<212> DNA

<213> Artificial sequence (unknown)

<400> 10

ccaaacacaa caaactcgaa atcgacg 27

<210> 11

<211> 26

<212> DNA

<213> Artificial sequence (unknown)

<400> 11

ggttttactc aaagggaggc tttgac 26

<210> 12

<211> 24

<212> DNA

<213> Artificial sequence (unknown)

<400> 12

cacatcttca ggcgcaacat aagg 24

<210> 13

<211> 28

<212> DNA

<213> Artificial sequence (unknown)

<400> 13

tttttgtatt ttcgcaactc aagggaaa 28

<210> 14

<211> 26

<212> DNA

<213> Artificial sequence (unknown)

<400> 14

ggaaaaagtg cacaaaaagc tctgtt 26

<210> 15

<211> 29

<212> DNA

<213> Artificial sequence (unknown)

<400> 15

tatatggacc ttcaacaaca atcaagcat 29

<210> 16

<211> 30

<212> DNA

<213> Artificial sequence (unknown)

<400> 16

actccagtta taggaccata gattttggat 30

<210> 17

<211> 20

<212> DNA

<213> Artificial sequence (unknown)

<400> 17

acagcttttg tcgcggtctc 20

<210> 18

<211> 29

<212> DNA

<213> Artificial sequence (unknown)

<400> 18

ctaaacccta gagcttaaaa acctccaag 29

<210> 19

<211> 23

<212> DNA

<213> Artificial sequence (unknown)

<400> 19

gtcctcaagg acgaaggcaa cac 23

<210> 20

<211> 23

<212> DNA

<213> Artificial sequence (unknown)

<400> 20

gccttccagt agcccaaaac atg 23

<210> 21

<211> 27

<212> DNA

<213> Artificial sequence (unknown)

<400> 21

cgtcatatgg aagtagtcat gctttca 27

<210> 22

<211> 23

<212> DNA

<213> Artificial sequence (unknown)

<400> 22

ggtaggcatg accagatgtg tgc 23

<210> 23

<211> 28

<212> DNA

<213> Artificial sequence (unknown)

<400> 23

aaaccctaaa acagagagga ggaaatgg 28

<210> 24

<211> 27

<212> DNA

<213> Artificial sequence (unknown)

<400> 24

ctctgaactt tacagtggat tcagcat 27

<210> 25

<211> 23

<212> DNA

<213> Artificial sequence (unknown)

<400> 25

cgcattctga ggcaggaaga ttc 23

<210> 26

<211> 26

<212> DNA

<213> Artificial sequence (unknown)

<400> 26

agttcataag ccctgtgtgt ttctca 26

<210> 27

<211> 24

<212> DNA

<213> Artificial sequence (unknown)

<400> 27

agaaatgctc ctcaggtgtc aaga 24

<210> 28

<211> 25

<212> DNA

<213> Artificial sequence (unknown)

<400> 28

ctcaagtttt tccggtggaa gaaga 25

<210> 29

<211> 23

<212> DNA

<213> Artificial sequence (unknown)

<400> 29

tgggctctac caacatacca ctc 23

<210> 30

<211> 26

<212> DNA

<213> Artificial sequence (unknown)

<400> 30

ctcaggagac aagaaagaga ctcgtc 26

<210> 31

<211> 25

<212> DNA

<213> Artificial sequence (unknown)

<400> 31

ccacatcagc aaagttgtaa acgca 25

<210> 32

<211> 26

<212> DNA

<213> Artificial sequence (unknown)

<400> 32

caaagatcca cgagataacg caaacc 26

<210> 33

<211> 23

<212> DNA

<213> Artificial sequence (unknown)

<400> 33

gtgtcaacga tggctccact tat 23

<210> 34

<211> 25

<212> DNA

<213> Artificial sequence (unknown)

<400> 34

cgagatcggc tttgttgagc tttaa 25

<210> 35

<211> 23

<212> DNA

<213> Artificial sequence (unknown)

<400> 35

gcataggaca cctcgtgttc ttg 23

<210> 36

<211> 26

<212> DNA

<213> Artificial sequence (unknown)

<400> 36

cccttaacgg aacagaaacg gttagc 26

<210> 37

<211> 26

<212> DNA

<213> Artificial sequence (unknown)

<400> 37

ctgaagtgct catcttcatg tttcgt 26

<210> 38

<211> 31

<212> DNA

<213> Artificial sequence (unknown)

<400> 38

tcgaaaacaa gttttagtat cttcccaaga a 31

<210> 39

<211> 25

<212> DNA

<213> Artificial sequence (unknown)

<400> 39

gagacctcgt attcgacttt gtgtt 25

<210> 40

<211> 28

<212> DNA

<213> Artificial sequence (unknown)

<400> 40

ctcctttgtc taaggtttgt tcaaagcg 28

<210> 41

<211> 31

<212> DNA

<213> Artificial sequence (unknown)

<400> 41

agcgttggag ataaagtctt taaagtaagg a 31

<210> 42

<211> 24

<212> DNA

<213> Artificial sequence (unknown)

<400> 42

agacagctcc caacatggtt tacg 24

<210> 43

<211> 30

<212> DNA

<213> Artificial sequence (unknown)

<400> 43

gatatatcat cactatcagc agctgtgaac 30

<210> 44

<211> 23

<212> DNA

<213> Artificial sequence (unknown)

<400> 44

gggatggaca cgactgtgat tct 23

<210> 45

<211> 24

<212> DNA

<213> Artificial sequence (unknown)

<400> 45

aacgacatgg ctacgatccg actt 24

<210> 46

<211> 24

<212> DNA

<213> Artificial sequence (unknown)

<400> 46

ctaagaccgc ttggcctccg actt 24

<210> 47

<211> 25

<212> DNA

<213> Artificial sequence (unknown)

<400> 47

gaacgacatg gctacgatcc gactt 25

<210> 48

<211> 49

<212> DNA

<213> Artificial sequence (unknown)

<400> 48

tgtgagccaa ggagttgttg tcttcctaag accgcttggc ctccgactt 49

<210> 49

<211> 5

<212> DNA

<213> Artificial sequence (unknown)

<400> 49

ccttc 5

<210> 50

<211> 5

<212> DNA

<213> Artificial sequence (unknown)

<400> 50

accga 5

<210> 51

<211> 5

<212> DNA

<213> Artificial sequence (unknown)

<400> 51

atgtg 5

<210> 52

<211> 5

<212> DNA

<213> Artificial sequence (unknown)

<400> 52

aatgc 5

<210> 53

<211> 5

<212> DNA

<213> Artificial sequence (unknown)

<400> 53

ttcgg 5

<210> 54

<211> 5

<212> DNA

<213> Artificial sequence (unknown)

<400> 54

aaggt 5

<210> 55

<211> 5

<212> DNA

<213> Artificial sequence (unknown)

<400> 55

cccat 5

<210> 56

<211> 5

<212> DNA

<213> Artificial sequence (unknown)

<400> 56

atgga 5

<210> 57

<211> 5

<212> DNA

<213> Artificial sequence (unknown)

<400> 57

acgat 5

<210> 58

<211> 5

<212> DNA

<213> Artificial sequence (unknown)

<400> 58

ctctg 5

<210> 59

<211> 5

<212> DNA

<213> Artificial sequence (unknown)

<400> 59

atccg 5

<210> 60

<211> 5

<212> DNA

<213> Artificial sequence (unknown)

<400> 60

tatcg 5

<210> 61

<211> 5

<212> DNA

<213> Artificial sequence (unknown)

<400> 61

actcg 5

<210> 62

<211> 5

<212> DNA

<213> Artificial sequence (unknown)

<400> 62

taacc 5

<210> 63

<211> 5

<212> DNA

<213> Artificial sequence (unknown)

<400> 63

cttac 5

<210> 64

<211> 5

<212> DNA

<213> Artificial sequence (unknown)

<400> 64

tccta 5

<210> 65

<211> 5

<212> DNA

<213> Artificial sequence (unknown)

<400> 65

acact 5

<210> 66

<211> 5

<212> DNA

<213> Artificial sequence (unknown)

<400> 66

tacgt 5

<210> 67

<211> 5

<212> DNA

<213> Artificial sequence (unknown)

<400> 67

tcacg 5

<210> 68

<211> 5

<212> DNA

<213> Artificial sequence (unknown)

<400> 68

acgca 5

<210> 69

<211> 8

<212> DNA

<213> Artificial sequence (unknown)

<400> 69

cggctaaa 8

<210> 70

<211> 8

<212> DNA

<213> Artificial sequence (unknown)

<400> 70

tccccgtg 8

Claims (10)

1. A primer group for detecting purity of Chinese cabbage seeds based on an mSNP technology is characterized by comprising a primer pair 1F/R, a primer pair 2F/R, a primer pair 3F/R, a primer pair 4F/R, a primer pair 5F/R, a primer pair 6F/R, a primer pair 7F/R, a primer pair 8F/R, a primer pair 9F/R, a primer pair 10F/R, a primer pair 11F/R, a primer pair 12F/R, a primer pair 13F/R, a primer pair 14F/R, a primer pair 15F/R, a primer pair 16F/R, a primer pair 17F/R, a primer pair 18F/R, a primer pair 19F/R, a primer pair 20F/R, a primer pair 21F/R and a primer pair 22F/R; wherein each primer pair consists of a forward primer and a reaction primer;

In the primer pair 1F/R, the sequence of the F primer is shown as SEQ ID No.1, and the sequence of the R primer is shown as SEQ ID No. 2;

in the primer pair 2F/R, the sequence of the F primer is shown as SEQ ID No.3, and the sequence of the R primer is shown as SEQ ID No. 4;

in the primer pair 3F/R, the sequence of the F primer is shown as SEQ ID No.5, and the sequence of the R primer is shown as SEQ ID No. 6;

in the primer pair 4F/R, the sequence of the F primer is shown as SEQ ID No.7, and the sequence of the R primer is shown as SEQ ID No. 8;

in the primer pair 5F/R, the sequence of the F primer is shown as SEQ ID No.9, and the sequence of the R primer is shown as SEQ ID No. 10;

in the primer pair 6F/R, the sequence of the F primer is shown as SEQ ID No.11, and the sequence of the R primer is shown as SEQ ID No. 12;

in the primer pair 7F/R, the sequence of the F primer is shown as SEQ ID No.13, and the sequence of the R primer is shown as SEQ ID No. 14;

in the primer pair 8F/R, the sequence of the F primer is shown as SEQ ID No.15, and the sequence of the R primer is shown as SEQ ID No. 16;

in the primer pair 9F/R, the sequence of the F primer is shown as SEQ ID No.17, and the sequence of the R primer is shown as SEQ ID No. 18;

in the primer pair 10F/R, the sequence of the F primer is shown as SEQ ID No.19, and the sequence of the R primer is shown as SEQ ID No. 20;

in the primer pair 11F/R, the sequence of the F primer is shown as SEQ ID No.21, and the sequence of the R primer is shown as SEQ ID No. 22;

In the primer pair 12F/R, the sequence of the F primer is shown as SEQ ID No.23, and the sequence of the R primer is shown as SEQ ID No. 24;

in the primer pair 13F/R, the sequence of the F primer is shown as SEQ ID No.25, and the sequence of the R primer is shown as SEQ ID No. 26;

in the primer pair 14F/R, the sequence of the F primer is shown as SEQ ID No.27, and the sequence of the R primer is shown as SEQ ID No. 28;

in the primer pair 15F/R, the sequence of the F primer is shown as SEQ ID No.29, and the sequence of the R primer is shown as SEQ ID No. 30;

in the primer pair 16F/R, the sequence of the F primer is shown as SEQ ID No.31, and the sequence of the R primer is shown as SEQ ID No. 32;

in the primer pair 17F/R, the sequence of the F primer is shown as SEQ ID No.33, and the sequence of the R primer is shown as SEQ ID No. 34;

in the primer pair 18F/R, the sequence of the F primer is shown as SEQ ID No.35, and the sequence of the R primer is shown as SEQ ID No. 36;

in the primer pair 19F/R, the sequence of the F primer is shown as SEQ ID No.37, and the sequence of the R primer is shown as SEQ ID No. 38;

in the primer pair 20F/R, the sequence of the F primer is shown as SEQ ID No.39, and the sequence of the R primer is shown as SEQ ID No. 40;

in the primer pair 21F/R, the sequence of the F primer is shown as SEQ ID No.41, and the sequence of the R primer is shown as SEQ ID No. 42;

In the primer pair 22F/R, the sequence of the F primer is shown as SEQ ID No.43, and the sequence of the R primer is shown as SEQ ID No. 44.

2. The mixed sample detection method for detecting the purity of the Chinese cabbage seeds by using the primer group according to claim 1, which is characterized by comprising the following steps of:

step 1, selecting materials: selecting 1 or more Chinese cabbage varieties; at least 96 seeds are adopted in each Chinese cabbage sample;

step 2, accurately quantifying the genomic DNA of the Chinese cabbage;

step 3, synthesizing primers in the primer group in claim 1, wherein when synthesizing a forward primer and a reverse primer in each primer pair, 10 primers with different target labels are synthesized; then mixing the primers according to the specified label combination to prepare a primer mixed solution;

step 4, taking the Chinese cabbage genome DNA as a template, and respectively carrying out one-round PCR amplification on the Chinese cabbage genome DNA by using the primer mixed solution to obtain a target region;

step 5, mixing the obtained PCR amplification products in equal amount;

step 6, screening fragments of the mixed product;

step 7, digesting the single-stranded DNA in the screened system;

step 8, purifying the digested product;

Step 9, configuring a two-round PCR system in the system obtained in the step 8;

step 10, purifying the products of the two rounds of PCR to complete the preparation of a sequencing library;

step 11, mixing the sequencing library with the same quality, and then performing on-machine sequencing to obtain sequencing data;

step 12, splitting the sample according to the label combination again for the obtained test data;

and step 13, identifying the genotype result of the target locus of the test sample, and judging the purity of the seed according to the genotype condition of the locus.

3. The mixed sample detection method for detecting the purity of Chinese cabbage seeds as claimed in claim 2, wherein,

in the step 3, the F primers in the primer pairs 1F/R-22F/R also comprise an F-end universal primer, and the sequence of the F-end universal primer is shown as SEQ ID No. 45; the R primers in the primer pairs 1F/R-22F/R also comprise an R-end universal primer, and the sequence of the R-end universal primer is shown as SEQ ID No. 46;

in step 9, the sequence of Frimer F used in the two rounds of PCR is shown in SEQ ID No. 47; the sequence of Primer R used in the two-round PCR is shown in SEQ ID No. 48.

4. The mixed sample detection method for detecting the purity of Chinese cabbage seeds as claimed in claim 3, wherein,

when the variety of the Chinese cabbage is multiple, the sequence of the Primer R also comprises a barcode sequence for distinguishing the variety of the Chinese cabbage.

5. The mixed sample detection method for detecting the purity of the Chinese cabbage seeds as claimed in claim 2, wherein in the step 2, in the label combination of each primer pair, the label sequence of the forward primer is different from the label sequence of the reverse primer.

6. The mixed sample detection method for detecting the purity of Chinese cabbage seeds as claimed in claim 2, wherein,

in the step 1, extracting the genome DNA of the Chinese cabbage seeds by adopting a Chinese cabbage seed genome DNA extraction kit.

7. The mixed sample detection method for detecting the purity of Chinese cabbage seeds as claimed in claim 2, wherein,

in step 4, the round of PCR amplification system: 8 mul of primer mixed solution; the dosage of DNA is 100 ng; 3. mu.l of Ttase; adding water to complement 45 mu l; the one-round PCR amplification procedure: 3min at 95 ℃; (95 ℃ for 30s, 60 ℃ for 4min, 72 ℃ for 30s)28 cycles; 4min at 72 ℃.

8. The mixed sample detection method for detecting the purity of Chinese cabbage seeds as claimed in claim 2, wherein,

in step 6, the mixed product is subjected to fragment screening, specifically the following operations:

step 6.1, adding magnetic beads with the volume 0.4 times that of one round of PCR, blowing and beating the mixture up and down by using a pipettor, uniformly mixing, standing for 2min, adsorbing the mixture by using a magnetic frame until the solution is clarified, and transferring the supernatant into a new tube;

Step 6.2, adding magnetic beads with the volume 0.6 times that of one round of PCR, blowing and beating the mixture up and down by using a pipettor, uniformly mixing, standing for 2min, adsorbing by using a magnetic frame until the solution is clarified, and removing the supernatant;

step 6.3, adding a magnetic bead suspension with the volume 0.9 time that of one round of PCR, re-suspending the magnetic beads, standing for 2min, adsorbing by a magnetic frame until the solution is clarified, and removing the supernatant;

and 6.4, adding 100 mu l of ethanol with the volume concentration of 80%, repeatedly adsorbing the magnetic beads on different two surfaces by using a magnetic frame to fully wash the magnetic beads, adsorbing for 2min by using the magnetic frame, removing the supernatant, and standing at room temperature until the ethanol is completely volatilized.

In step 7, digesting the single-stranded DNA in the system obtained after screening, the specific operation steps are as follows:

step 7.1, adding 20 mul of water into the obtained product, and uniformly mixing the magnetic beads;

step 7.2, adsorbing magnetic beads, and transferring 16 mu l of supernatant into a new EP tube;

step 7.3, adding 2 ul of Exo I and 2 ul of 10 × Reaction Buffer into the system;

and 7.4, the digestion program of the digestion system is as follows: 30min at 37 ℃; 15min at 85 ℃;

in step 8, the specific operation steps for purifying the digested product are as follows:

step 8.1, adding 0.9 time of magnetic beads, blowing and beating the mixture up and down by using a pipettor, uniformly mixing, standing for 2min, adsorbing by using a magnetic frame until the solution is clarified, and removing the supernatant;

8.2, adding magnetic bead resuspension liquid with equal PCR volume, resuspending magnetic beads, standing for 2min, adsorbing by a magnetic frame until the solution is clarified, and removing supernatant;

and 8.3, adding 100 mu l of ethanol with the volume concentration of 80%, repeatedly adsorbing the magnetic beads on two different surfaces by using a magnetic frame to fully wash the magnetic beads, adsorbing for 2min by using the magnetic frame, removing the supernatant, and standing at room temperature until the ethanol is completely volatilized.

9. The mixed sample detection method for detecting the purity of Chinese cabbage seeds as claimed in claim 2, wherein,

in step 9, the two-round PCR system: 10 μ l of the enzyme tretase; primer F; primer R; H2O 18 μ l;

the two-round PCR procedure: 3min at 95 ℃; (95 ℃ 15s, 58 ℃ 15s, 72 ℃ 30s) for 12 cycles; 4min at 72 ℃.

10. The mixed sample detection method for detecting the purity of Chinese cabbage seeds as claimed in claim 2, wherein,

in step 10, the two rounds of PCR products are purified using 0.80 times of magnetic beads, as follows:

step 10.1, adding 0.8 time of magnetic beads, blowing and beating the mixture up and down by using a pipettor, uniformly mixing, standing for 2min, adsorbing by using a magnetic frame until the solution is clarified, and removing the supernatant;

step 10.2, adding magnetic bead resuspension liquid with equal PCR volume, resuspending magnetic beads, standing for 2min, adsorbing by a magnetic frame until the solution is clarified, and removing supernatant;

Step 10.3, adding 100 mul of 80% ethanol, repeatedly adsorbing magnetic beads on two different surfaces by using a magnetic frame to fully wash the magnetic beads, adsorbing for 2min by using the magnetic frame, removing supernatant, and standing at room temperature until the ethanol is completely volatilized;

step 10.4, adding 23 μ l of Elution Buffer, fully suspending the magnetic beads, standing for 2min at room temperature to elute DNA, adsorbing the magnetic beads by a magnet, and adsorbing the obtained supernatant DNA solution into a new tube to obtain a sequencing library; the Elution Buffer is 10mM Tris-HCl and has the pH value of 8.0-8.5.

Images