CN111100951B - A09 chromosome major QTL locus of cabbage type rape oil content character, SNP molecular marker and application - Google Patents
A09 chromosome major QTL locus of cabbage type rape oil content character, SNP molecular marker and application Download PDFInfo
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- C12Q2600/00—Oligonucleotides characterized by their use
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Abstract
The invention provides an A09 chromosome major QTL locus of cabbage type rape oil content character, which is positioned between 29763871 th base and 30109732 th base of A09 chromosome of cabbage type rape. Preferably, the contribution rate to the oil content character of the brassica napus is 11.32%. Closely linked to the first SNP molecular marker, which is located at base 29763871, is C or G, the mutation results in polymorphism. Closely linked to a second SNP molecular marker, which is located at base 30109732, A or G, the mutation results in polymorphism. Closely linked to the peak SNP molecular marker, it is located at 30096360 base, A or C, and the mutation results in polymorphism. Also provides a related SNP molecular marker and application thereof. The A09 chromosome major QTL locus has high contribution rate to the oil content character of the cabbage type rape, plays a key role in regulating the oil content of the cabbage type rape, can be used as map-based cloning and molecular marker auxiliary selection, and is suitable for large-scale popularization and application.
Description
Technical Field
The invention relates to the technical fields of molecular biology and rape breeding, in particular to the technical field of cabbage type rape oil content traits, and specifically relates to an A09 chromosome major QTL locus, SNP molecular markers and application of the cabbage type rape oil content traits.
Background
The demand of edible oil in China is increased rigidly at the speed of 100 ten thousand tons per year, the demand of vegetable oil in 2025 is expected to be 3.5-4.0 times of the production capacity in the existing country, but the arable land resources in China are continuously reduced, so that the improvement of the unit yield of oil crops is a fundamental way for realizing the increase of the total yield of oil. Rape is the first large oil crop in China, the annual seeding area exceeds 1 hundred million mu, the total yield is more than 1500 ten thousand tons, and the rape seed oil accounts for more than 55 percent of the total edible vegetable oil in China. At present, the planting area and yield of the rape industry in China continuously appear to be declining for years, the industrial safety is lowered year by year, and China is the largest oil import country in the world. The improvement of the unit yield level to promote the income increase of farmers is a core measure for promoting the development of rape industry in China and guaranteeing the supply safety of edible vegetable oil.
At present, the rape yield level in China is lower, and the planting enthusiasm of farmers is influenced. The regional trial yield level of the winter rape variety examined by the Chinese home in 2001-2016 is 2.26-3.75 tons/hm 2 Is far lower than that of new variety test of 2013-2015 Canadian by 4.06 tons/hm 2 Yield level of (2); in recent years, the production unit of rape field production in China is about 1.92 tons/hm 2 And the European Union is 3.12 tons/hm 2 Canadian is 2.24 tons/hm 2 . Because the rape single yield is low, the economic benefit is low, the enthusiasm of farmers for planting rape is influenced, and the normal development of the rape industry is restricted. There is a need in production to create new varieties of ultra-high yield canola with unit yield levels exceeding those of the european union and canada.
The mature seed of rape contains approximately 45% of stored oil, 25% of protein and 10% of soluble sugar. Seed oil content is an important agronomic trait for yield formation, and is also a key determinant of rape quality, and as the demand of rape seed oil in food and non-food applications is continuously increasing, how to increase rape seed oil content has been receiving great attention.
The oil content of the brassica napus is quantitative inheritance character controlled by multiple genes, the influence of environmental factors is large, and the conventional breeding means can hardly achieve the breeding goal.
Therefore, it is necessary to provide a major QTL locus of the oil content trait of brassica napus, which has a high contribution rate to the oil content trait of brassica napus, plays a key role in regulating the oil content of brassica napus, and can be used as a map-based cloning and molecular marker-assisted selection.
Disclosure of Invention
In order to overcome the defects in the prior art, the invention aims to provide an A09 chromosome major QTL locus of the oil content character of the brassica napus, which has high contribution rate to the oil content character of the brassica napus, plays a key role in regulating the oil content of the brassica napus, can be used as map cloning and molecular marker assisted selection, and is suitable for large-scale popularization and application.
The invention further aims to provide the SNP molecular marker of the A09 chromosome major QTL locus of the oil content character of the brassica napus, which can detect the oil content of the brassica napus, can predict the oil content of the brassica napus, can effectively select the oil content of the brassica napus, can be used for molecular marker-assisted breeding of the brassica napus with high oil content, accelerates the progress of the high oil content breeding of the brassica napus, and is suitable for large-scale popularization and application.
The invention further aims to provide the SNP molecular marker of the A09 chromosome major QTL locus of the oil content character of the brassica napus, which has the advantages of ingenious design, simple and quick detection, low cost, no environmental influence and suitability for large-scale popularization and application.
The invention further aims to provide an application of the SNP molecular marker of the A09 chromosome major QTL locus of the oil content character of the brassica napus, which can detect the oil content of the brassica napus, predict the oil content of the brassica napus, effectively select the oil content of the brassica napus, can be used for molecular marker assisted breeding of the brassica napus with high oil content, accelerate the progress of the high oil content breeding of the brassica napus and is suitable for large-scale popularization and application.
The invention also aims to provide an application of the SNP molecular marker of the A09 chromosome major QTL locus of the oil content character of the brassica napus, which has the advantages of ingenious design, simple and quick detection, low cost, no environmental influence and suitability for large-scale popularization and application.
In order to achieve the above object, in a first aspect of the present invention, there is provided an a09 chromosomal main QTL locus for oil content trait of brassica napus, wherein the a09 chromosomal main QTL locus for oil content trait of brassica napus is located between base 29763871 and base 30109732 of a09 chromosome of brassica napus.
Preferably, the contribution rate of the A09 chromosome major QTL locus of the oil content character of the brassica napus to the oil content character of the brassica napus is 11.32%.
Preferably, the main effect QTL locus of A09 chromosome of the oil content character of the brassica napus is closely linked with a first SNP molecular marker, the first SNP molecular marker is positioned at the 29763871 base, the 29763871 base is C or G, and the mutation leads to polymorphism.
Preferably, the main effect QTL locus of A09 chromosome of the oil content character of the brassica napus is closely linked with a second SNP molecular marker, the second SNP molecular marker is positioned at the 30109732 base, the 30109732 base is A or G, and the mutation leads to polymorphism.
Preferably, the main effect QTL locus of the A09 chromosome of the oil content character of the brassica napus is closely linked with a peak SNP molecular marker, the peak SNP molecular marker is positioned at the 30096360 base of the A09 chromosome of the brassica napus, the 30096360 base is A or C, and the mutation leads to polymorphism.
In a second aspect of the present invention, there is provided a SNP molecular marker for the major QTL site of the a09 chromosome of a brassica napus oil content trait, which is characterized in that the SNP molecular marker is located at the 29763871 th base of the a09 chromosome of the brassica napus, the 29763871 th base is C or G, and the mutation results in polymorphism.
In a third aspect of the invention, the application of the SNP molecular marker of the A09 chromosome major QTL locus of the oil content trait of the brassica napus in detecting the oil content of the brassica napus, predicting the oil content of the brassica napus, selecting the oil content of the brassica napus or performing molecular marker assisted breeding of the brassica napus with high oil content is provided.
In a fourth aspect of the present invention, there is provided a SNP molecular marker for a major QTL site of the a09 chromosome of a brassica napus oil content trait, wherein the SNP molecular marker is located at the 30109732 th base of the a09 chromosome of the brassica napus, the 30109732 th base is a or G, and the mutation results in polymorphism.
In a fifth aspect of the invention, the application of the SNP molecular marker of the A09 chromosome major QTL locus of the oil content trait of the brassica napus in detecting the oil content of the brassica napus, predicting the oil content of the brassica napus, selecting the oil content of the brassica napus or performing molecular marker assisted breeding of the brassica napus with high oil content is provided.
In a sixth aspect of the present invention, there is provided a peak SNP molecular marker at the major QTL site of the a09 chromosome of brassica napus oil content trait, wherein the peak SNP molecular marker is located at the 30096360 base of the a09 chromosome of brassica napus, the 30096360 base is a or C, and the mutation results in polymorphism.
In a seventh aspect of the invention, the application of the peak SNP molecular marker of the A09 chromosome major QTL locus of the oil content trait of the brassica napus in detecting the oil content of the brassica napus, predicting the oil content of the brassica napus, selecting the oil content of the brassica napus or performing molecular marker assisted breeding of the brassica napus with high oil content is provided.
The beneficial effects of the invention are mainly as follows:
1. the main effect QTL locus of the A09 chromosome of the oil content character of the cabbage type rape is positioned between 29763871 th base and 30109732 th base of the A09 chromosome of the cabbage type rape, has high contribution rate to the oil content character of the cabbage type rape, plays a key role in regulating the oil content of the cabbage type rape, can be used as map-based cloning and molecular marker auxiliary selection, and is suitable for large-scale popularization and application.
2. The SNP molecular marker of the main effect QTL locus of the A09 chromosome of the cabbage type rape comprises the SNP molecular marker of the 29763871 th base of the A09 chromosome of the cabbage type rape, the SNP molecular marker of the 30109732 th base of the A09 chromosome of the cabbage type rape and the peak SNP molecular marker of the 30096360 th base of the A09 chromosome of the cabbage type rape, which can detect the oil content of the cabbage type rape, can predict the oil content of the cabbage type rape, can effectively select the oil content of the cabbage type rape, can also be used for molecular marker assisted breeding of the cabbage type rape with high oil content, accelerates the progress of high oil content breeding of the cabbage type rape, and is suitable for large-scale popularization and application.
3. The SNP molecular marker of the A09 chromosome major QTL locus of the oil content trait of the brassica napus comprises an SNP molecular marker of a 29763871 base of the A09 chromosome of the brassica napus, an SNP molecular marker of a 30109732 base of the A09 chromosome of the brassica napus and a peak SNP molecular marker of a 30096360 base of the A09 chromosome of the brassica napus, and the SNP molecular marker is ingenious in design, simple and quick to detect, low in cost, free from environmental influence and suitable for large-scale popularization and application.
4. The application of the SNP molecular marker of the main effect QTL locus of the A09 chromosome of the cabbage type rape oil content character comprises the application of the SNP molecular marker of the 29763871 base of the A09 chromosome of the cabbage type rape, the application of the SNP molecular marker of the 30109732 base of the A09 chromosome of the cabbage type rape and the application of the peak SNP molecular marker of the 30096360 base of the A09 chromosome of the cabbage type rape, which can detect the oil content of the cabbage type rape, can predict the oil content of the cabbage type rape, can effectively select the oil content of the cabbage type rape, can also be used for molecular marker assisted breeding of the cabbage type rape with high oil content, accelerates the progress of the high oil content breeding of the cabbage type rape and is suitable for large-scale popularization and application.
5. The application of the SNP molecular marker of the A09 chromosome major QTL locus of the oil content trait of the brassica napus comprises the application of the SNP molecular marker of the 29763871 base of the A09 chromosome of the brassica napus, the application of the SNP molecular marker of the 30109732 base of the A09 chromosome of the brassica napus and the application of the peak SNP molecular marker of the 30096360 base of the A09 chromosome of the brassica napus, and the SNP molecular marker is ingenious in design, simple and quick to detect, low in cost, free from environmental influence and suitable for large-scale popularization and application.
These and other objects, features and advantages of the present invention will become more fully apparent from the following detailed description, the accompanying drawings and the claims, and may be learned by the practice of the invention as set forth hereinafter, the product and the combination thereof as set forth hereinafter.
Drawings
FIG. 1 is a schematic diagram showing the distribution results of oil content traits of brassica napus of the present invention.
FIG. 2 is a schematic diagram of allele analysis by using a peak SNP molecular marker of the A09 chromosome major QTL locus of the oil content trait of brassica napus in the present invention.
Detailed Description
Through intensive researches, the inventor firstly discloses an A09 chromosome major QTL locus of the oil content character of the brassica napus and SNP molecular markers thereof, and can effectively improve the oil content of the brassica napus.
The main effect QTL locus of the A09 chromosome of the oil content character of the cabbage type rape is positioned between 29763871 th base and 30109732 th base of the A09 chromosome of the cabbage type rape.
Preferably, the contribution rate of the A09 chromosome major QTL locus of the oil content character of the brassica napus to the oil content character of the brassica napus is 11.32%.
Preferably, the main effect QTL locus of A09 chromosome of the oil content character of the brassica napus is closely linked with a first SNP molecular marker, the first SNP molecular marker is positioned at the 29763871 base, the 29763871 base is C or G, and the mutation leads to polymorphism.
Preferably, the main effect QTL locus of A09 chromosome of the oil content character of the brassica napus is closely linked with a second SNP molecular marker, the second SNP molecular marker is positioned at the 30109732 base, the 30109732 base is A or G, and the mutation leads to polymorphism.
Preferably, the main effect QTL locus of the A09 chromosome of the oil content character of the brassica napus is closely linked with a peak SNP molecular marker, the peak SNP molecular marker is positioned at the 30096360 base of the A09 chromosome of the brassica napus, the 30096360 base is A or C, and the mutation leads to polymorphism.
Also provides a SNP molecular marker of the main effect QTL locus of the A09 chromosome of the oil content character of the cabbage type rape, which is positioned at the 29763871 th base of the A09 chromosome of the cabbage type rape, the 29763871 th base is C or G, and the mutation leads to polymorphism. Namely the first SNP molecular marker.
The application of the SNP molecular marker of the A09 chromosome major QTL locus of the cabbage type rape oil content character in detecting the oil content of the cabbage type rape, predicting the oil content of the cabbage type rape, selecting the oil content of the cabbage type rape or carrying out molecular marker assisted breeding of the cabbage type rape with high oil content is also provided.
Also provides a SNP molecular marker of the main effect QTL locus of the A09 chromosome of the oil content character of the cabbage type rape, which is positioned at the 30109732 th base of the A09 chromosome of the cabbage type rape, the 30109732 th base is A or G, and the mutation leads to polymorphism. The second SNP molecular marker is the second SNP molecular marker.
The application of the SNP molecular marker of the A09 chromosome major QTL locus of the cabbage type rape oil content character in detecting the oil content of the cabbage type rape, predicting the oil content of the cabbage type rape, selecting the oil content of the cabbage type rape or carrying out molecular marker assisted breeding of the cabbage type rape with high oil content is also provided.
Also provides a peak SNP molecular marker of the main effect QTL locus of the A09 chromosome of the oil content character of the brassica napus, which is positioned at the 30096360 base of the A09 chromosome of the brassica napus, wherein the 30096360 base is A or C, and the mutation leads to polymorphism.
The application of the peak SNP molecular marker of the A09 chromosome major QTL locus of the cabbage type rape oil content character in detecting the oil content of the cabbage type rape, predicting the oil content of the cabbage type rape, selecting the oil content of the cabbage type rape or carrying out molecular marker assisted breeding of the cabbage type rape with high oil content is also provided.
The invention will be further illustrated with reference to specific examples. It is to be understood that these examples are illustrative of the present invention and are not intended to limit the scope of the present invention. The experimental procedures, which do not address the specific conditions in the examples below, are generally carried out according to conventional conditions such as those described in J.Sam Brookfield et al, molecular cloning guidelines, third edition, scientific Press, 2002, or according to the manufacturer's recommendations.
Example 1 determination of phenotype of oil content trait in Brassica napus
1. Determination of oil content phenotype of related populations
(1) Performing field test analysis on agronomic and quality traits of 627 parts of core germplasm materials (from a seed pool of Guizhou oil-saving vegetable research institute), and selecting 300 cabbage type rape high-generation lines from all over the world to form natural populations, wherein the natural populations comprise 98 parts of resources, 110 parts of breeding materials, 92 parts of varieties or parents; divided into regions, wherein 246 parts belong to China and 54 parts belong to foreign sources. Phenotype identification of 2 points in 3 years is completed in Qinghai county, qinghai county and Qinghai county, weiyuan Zhen rape base in Guiyang city.
(2) The seedling is directly planted, the row spacing is 40cm, the plant spacing is 25cm, the row length is 3.5m, and 4 rows are arranged in each cell. And planting protection rows around the test material field.
(3) Oil content: after the plants were matured normally, 10 brassica napus plants were taken per cell and the oil content of each matured clean seed was measured in% using a near infrared scanner. The phenotypic values of all environments for 300 parts of material were averaged and the results were summarized as follows:
TABLE 1 average of oil content phenotype values for all environments of 300 parts of material
The oil content distribution results of the related groups show that the oil content character expression distribution is continuous distribution and normal distribution, and the oil content character belongs to quantitative characters and has main effective gene sites, as shown in figure 1.
2. Acquisition of high quality SNP datasets for related populations
The CTAB method is adopted to extract the total DNA of the leaves, and the specific method is as follows:
placing tender leaves in 10% ethanol for rinsing; then shearing 0.1-0.2g of blades, putting the blades into a grinding bowl, rapidly grinding the blades into powder by utilizing liquid nitrogen, and loading the powder into a 2mL centrifuge tube; 700. Mu.L of preheated DNA extract was added; mixing, placing into 65 deg.C water bath for 1 hr, and mixing for 1 time every 10-15 min; 700. Mu.L of the mixture (phenol: chloroform: isoamyl alcohol=25:24:1) was added and mixed by gentle inversion for 10min; centrifuging at room temperature for 15min at 10 000Xg; sucking the supernatant into a new 2mL centrifuge tube; adding an equal volume of the mixture (chloroform: isoamyl alcohol=24:1), mixing the mixture upside down, standing for 5min, centrifuging for 15min at 10000 Xg, and sucking the supernatant into a new centrifuge tube by using a gun; adding 2 times volume of absolute ethyl alcohol, mixing, standing at-20deg.C for 1 hr, centrifuging for 10min, and discarding supernatant; adding 500 mu L of precooled 75% ethanol to wash the precipitate, and removing supernatant; washing and precipitating for 2 times continuously, and airing; 100. Mu.L of a solution containing 2% RNase A was added thereto, and the mixture was allowed to stand at 37℃for 1 hour and then at 4℃overnight; extracting the DNA solution again with an equal volume of the mixture (chloroform: isoamyl alcohol=24:1), mixing the mixture upside down, standing the mixture for 10min, centrifuging the mixture for 15 or 20min at 10 x g, removing RNase A, sucking the supernatant (about 60 μl), and centrifuging the supernatant again for 1min; detecting the concentration, quality and integrity of the DNA by agarose gel electrophoresis (0.8%) and an ultraviolet spectrophotometer; the absorbance 260/280 ratio was determined to be between 1.8 and 2.0 for all DNA samples. The DNA samples were then dry-ice shipped to sequencing companies (wara gene technologies limited) with a sequencing depth of approximately 9× per material.
After obtaining high quality DNA according to the above description, sequencing company (Huada gene technologies Co., ltd.) performs 9 Xdepth of coverage sequencing and then returns data, which is subjected to sequencing quality assessment using FastQC software, and then to adapter and low quality reads filtering of the sequenced sequence. And (3) obtaining clean data of double-end sequencing of each material, performing mapping and mutation detection by using bwa software and GATK software, obtaining a total SNP data set of the related population, and performing SNP data set quality filtration according to the minimum allele frequency of not less than 0.05, the deletion rate of not more than 0.1 and the heterozygosity rate of not more than 0.15, so as to finally obtain a high-quality population SNP data set for subsequent analysis.
3. Whole genome association analysis
Performing format conversion on the VCF file of the high-quality SNP data set generated in the last step by using plink software, then performing total-gene association analysis on the obtained oil content phenotype and the SNP data set by using EMMA software to obtain a P value of each site of the oil content property, wherein when the P value is less than 5 multiplied by 10 -6 The SNP with the minimum P value is the peak SNP, the materials are grouped according to different allele types of the peak SNP in the population, variance analysis is carried out, and the percentage of the ratio of the inter-group variance to the total variance is the contribution rate of the peak SNP.
By analysis, the interval of the main effect QTL locus of the oil content character of the brassica napus is limited between 29763871 th base and 30109732 th base of an A09 chromosome of the brassica napus, the corresponding SNP is chra09_29763871 (C/G), chra09_30109732 (A/G), and the peak SNP is: the contribution rate of the QTL to the oil content character of the brassica napus is 11.32 percent (the materials are grouped according to different allele types of peak SNP, single-factor variance analysis is carried out, and the percentage of the group variance divided by the total variance is the contribution rate).
The peak SNPs for the oil content trait are: chra09— 30096360 (a/C), the corresponding oil content phenotypes are grouped as: when SNP at the chra09_30096360 position is AA, the average oil content of the material is 43.08%; at AC, the average oil content of the material was 42.02%; the average oil content of the material at CC is 40.20%, as shown in FIG. 2.
One of the boundary SNPs for oil content traits is: chra09— 29763871 (C/G), the corresponding oil content phenotypes are grouped as: when SNP at the chra09_29763871 position is CC, the average oil content of the material is 40.14%; at CG, the average oil content of the material was 39.64%; at TT, the average oil content of the material was 43.37%, and the contribution rate of the boundary SNP was 15.61%.
Another boundary SNP for oil content traits is: chra09— 30109732 (a/G), the corresponding oil content phenotypes are grouped as: when SNP at the chra09_30109732 position is AA, the average oil content of the material is 40.03%; at AG, the average oil content of the material was 41.45%; at GG, the average oil content of the material was 43.75%, and the contribution rate of the boundary SNP was 15.90%.
The whole genome sequence of Brassica napus has been published, see http:// www.genoscope.cns.fr/brassicana pus/. The 400bp sequences (total 801 bp) before and after the chrAl09_ 29763871 (C/G) are shown in SEQ ID NO. 1, the 400bp sequences (total 801 bp) before and after the chrAl09_ 30109732 (A/G) are shown in SEQ ID NO. 2, and the 400bp sequences (total 801 bp) before and after the chAl09_ 30096360 (A/C) are shown in SEQ ID NO. 3. The specific primer for detecting the SNP locus can be designed by a person skilled in the art according to the sequence by adopting a conventional method, so that the genotype of the SNP locus is detected, the oil content of the brassica napus can be predicted, the oil content of the brassica napus can be effectively selected, the method can be used for molecular marker assisted breeding of the brassica napus with high oil content, and the progress of the high oil content breeding of the brassica napus is accelerated.
Therefore, the invention detects a major QTL locus of the oil content character of the brassica napus on chromosome A09 of the brassica napus through phenotype analysis and whole genome re-sequencing of the oil content character, and then carries out whole genome association analysis, and the contribution rate of the major QTL locus to the oil content of the brassica napus is 11.32%. The main effect QTL locus of the oil content character of the brassica napus is positioned between 29763871 th base and 30109732 th base of an A09 chromosome of the brassica napus, the boundary obvious SNP is chra09_29763871 (C/G), chra09_30109732 (A/G), the peak SNP is chra09_30096360 (A/C), and the SNP molecular marker closely linked with the main effect QTL locus can be used for detecting the oil content of the brassica napus, can be used for predicting the oil content of the brassica napus, can be used for effectively selecting the oil content of the brassica napus, can also be used for molecular marker assisted breeding of the brassica napus with high oil content and accelerating the progress of the high oil content breeding of the brassica napus.
The SNP molecular marker disclosed by the invention is used for carrying out molecular marker assisted selection, so that the identification method is simple, the selection efficiency is high, and the oil content of the brassica napus can be predicted. The selection target is clear and is not influenced by the environment. Can identify the single plants of the cabbage type rape with high oil content in early growth period of the cabbage type rape, and eliminate other single plants.
In conclusion, the A09 chromosome major QTL locus of the oil content trait of the brassica napus has high contribution rate to the oil content trait of the brassica napus, plays a key role in regulating the oil content of the brassica napus, can be used as map cloning and molecular marker auxiliary selection, and is suitable for large-scale popularization and application.
It will thus be seen that the objects of the present invention have been fully and effectively attained. The functional and structural principles of the present invention have been shown and described in the examples and embodiments may be modified at will without departing from such principles. Therefore, this invention includes all modifications encompassed within the spirit of the following claims and the scope of the following claims.
Sequence listing
<110> institute for rape in Guizhou province
<120> A09 chromosome major QTL locus of cabbage type rape oil content character, SNP molecular marker and application
<160> 3
<210> 1
<211> 801
<212> DNA
<213> Brassica napus (Brassica napus, L.)
<220>
<221> misc_feature
<222> (1)...(801)
<223> genomic sequences comprising 400bp sequences before and after chra09_29763871 (C/G)
<400> 1
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tagatattct cacaagaata ttttctctgt ccttacactc gaaggaagac atatcaggat 120
gaacgttaat aatatttcgt tgaaccaaga agtcagtttc cgagaacagg tgtcgtcctt 180
gttgaaccga gcagcgtccg aggcagcgaa caatcctaga aagttctaca cgacacaggc 240
taatttttcc acagtccaga ctttgtacgt cttggctcag tgcactcctg atcttactac 300
acgagactgt ttgacctgtt tgcgatcgtc catcaaggga atgcctctta acagatacgg 360
aggaagactt ctctggccta gttgtaatac aaggtacgag cttaacaaat tctacaacga 420
aaccgccatt agaacatctc ctccacgatt tggtaaactc ccttcctttg tttattttct 480
tcctcaagat tagcaatatt ctttttaatc cttattttag caaatgatac attatttaat 540
acacagggaa aggcgggaat tcaaatgtgt tagtcgtatc cgtcgttgtg cctataatag 600
tggttgttct aattctcgga gcttgttatt gcttccttgc aaagagagca aagaagactt 660
ctgatactgc accagacttt gatggtaatg attcgaatgt gctaacattg ggttagatta 720
atttgttcgt tctttttttt tctttttatg attagtataa tgaatttcat tgtgcaacag 780
gagatgggat aacaaccata g 801
<210> 2
<211> 801
<212> DNA
<213> Brassica napus (Brassica napus, L.)
<220>
<221> misc_feature
<222> (1)...(801)
<223> genomic sequences comprising 400bp sequences before and after chra09_30109732 (A/G)
<400> 2
ttctttaaca aaaaatctat tccacttaca cgttacactc aacccaaacc acatatatat 60
aacattgctt acgtacatta tagattatat ataagagcaa tttcaaataa aaccaaaata 120
tattagaaag ttcactattt tgttttgtaa taaaagatta tcaaaaaaat taaagtatac 180
agcatatata atagagtcaa cgtacaaaaa tcaaataaaa ctaatacaaa ataaaaacta 240
atacagtaaa aacaaaaaga ttactaattg tattctgaaa tttaatctaa taacatttat 300
tccaaaaaaa aacaataggt agatgcagaa taacttttct aacctgaacc atcagctgcc 360
atgaaacgtc taagactttc agttacgttt tcagcatctg acggcattcc aacgtttcct 420
ttacaaaaaa actaataaca ttaagttaat tgcaactaac agtgaactaa attatagtgt 480
ggttatttaa cccaaaggga aaaaaatgag acaagtaaaa tctttcacaa cttttacccg 540
cattgcaacg aagtaattcc aataacagga agagctaagt agtacaaata aataacaagt 600
agcatgtgga cttaaaaata tgaatacact tttagaaatt tacacccaat aatgagatta 660
tgactctttt caccatgttt agagtgggaa ttgagtgttt cgaattgttc ttattatact 720
ctgtctgaac attaatatta cataaaacac atacgacccc acattaacga cacatacata 780
cttttaaatt ttaatattta a 801
<210> 3
<211> 801
<212> DNA
<213> Brassica napus (Brassica napus, L.)
<220>
<221> misc_feature
<222> (1)...(801)
<223> genomic sequences comprising 400bp sequences before and after chra09_30096360 (A/C)
<400> 3
aggaaggtgc aaggtgcttt gattcattga ctgctgatta cgggatcgtt cccgaccaag 60
aacattactc atgtctgata gatctcctag gtcgtgccgg ttgttttgaa gagttgatga 120
gcaggatcga gaaaatgcct tttagaccag acgagcacat ctggaatgca atcctaggag 180
tatccagaat ccatggaaat atggaactgg agaaaaaagt ggcggaagag ctgattaaac 240
tggacgcaga gcaaaaagaa gaagcttcaa gaagatgatc ctcggacaag aagatgcatt 300
ttctgtaaat tttcttcccg tgaggattgt acactactgt taaaagcctg caaaagcaga 360
gggaagttat aggtgttgtg gtgatatttt tttttagcag cttcaaaagt tttgtaagtg 420
tagcagagct aacgaactac aactgtcgaa ttctttcttt cttttttttt ccttactgga 480
ggcaattttt caaacgaaaa gattaatatt tctggtttga tttgtaatgg ctaagttact 540
acagaacaat ggagatggtc ggtgtgaaag acgtggacaa aatatttatc ttgggtctct 600
tctaaatttt acttatgtgg taaaccaaaa ggcaaccaaa caaagcaaat aaccggttat 660
gtctaaaccg gtgactaagt tgtcactgcc atgagagaaa aataactaca cccacattca 720
acgcaagata tatattaggt ttttggtatg ggtactacat ttttcatcac attaaaaaga 780
aaaacggaag agaagcaaaa g 801
Claims (6)
1. A SNP molecular marker of a main effect QTL locus of an A09 chromosome of a cabbage type rape oil content character is characterized in that the nucleotide sequence of the SNP molecular marker is shown as SEQ ID NO. 1, the 401 st base of the nucleotide sequence is C or G, and the mutation leads to polymorphism.
2. The use of the SNP molecular marker of the A09 chromosome major QTL locus of the oil content trait of brassica napus according to claim 1 in detecting the oil content of brassica napus, predicting the oil content of brassica napus, selecting the oil content of brassica napus or performing molecular marker assisted breeding of brassica napus with high oil content.
3. A SNP molecular marker of a main effect QTL locus of an A09 chromosome of a cabbage type rape oil content character is characterized in that the nucleotide sequence of the SNP molecular marker is shown as SEQ ID NO. 2, the 401 st base of the nucleotide sequence is A or G, and the mutation leads to polymorphism.
4. The use of the SNP molecular marker of the A09 chromosome major QTL locus of the oil content trait of brassica napus according to claim 3 in detecting the oil content of brassica napus, predicting the oil content of brassica napus, selecting the oil content of brassica napus or performing molecular marker assisted breeding of brassica napus with high oil content.
5. A peak SNP molecular marker of a main effect QTL site of an A09 chromosome of a cabbage type rape oil content character is characterized in that the nucleotide sequence of the peak SNP molecular marker is shown as SEQ ID NO. 3, the 401 st base of the nucleotide sequence is A or C, and the mutation leads to polymorphism.
6. The use of the peak SNP molecular marker of the A09 chromosome major QTL locus of the oil content trait of brassica napus according to claim 5 in detecting the oil content of brassica napus, predicting the oil content of brassica napus, selecting the oil content of brassica napus or performing molecular marker assisted breeding of brassica napus with high oil content.
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Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105505925A (en) * | 2016-01-10 | 2016-04-20 | 华中农业大学 | Molecular marker closely linked with oil content QTL of cabbage type rape |
| CN110527738A (en) * | 2019-08-28 | 2019-12-03 | 中国农业科学院油料作物研究所 | Main effect QTL site, SNP marker and its application of cabbage type rape seed oleic acid content |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105505925A (en) * | 2016-01-10 | 2016-04-20 | 华中农业大学 | Molecular marker closely linked with oil content QTL of cabbage type rape |
| CN110527738A (en) * | 2019-08-28 | 2019-12-03 | 中国农业科学院油料作物研究所 | Main effect QTL site, SNP marker and its application of cabbage type rape seed oleic acid content |
Non-Patent Citations (2)
| Title |
|---|
| Liezhao Liu et al .A high-density SNP map for accurate mapping of seed fibre QTL in Brassica napus L.《Plos One》.2013,全文. * |
| 周龙华 ; 蒋立希 ; .SNP分子标记及其在甘蓝型油菜中应用的研究进展.农业生物技术学报.2016,(第10期),全文. * |
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