Molecular marker for authenticating zizania latifolia turcz. phenotype characteristics, and application and acquisition method thereof
A technology for molecular marker and water bamboo separation, applied in the field of molecular biology, can solve the problems of decreased taste, quality of water bamboo, inedible, etc., and achieves the effect of eliminating interference and shortening the research period.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0046] Embodiment 1: Classification of test materials and phenotypic characteristics
[0047] The following test materials come from Jinhua Academy of Agricultural Sciences, Zhejiang Province, Jinyun County Agricultural Bureau, Lishui City, Zhejiang Province, Yuyao City Agricultural Science Research Institute, Ningbo City, Zhejiang Province, Suzhou Academy of Agricultural Sciences, Jiangsu Province, and Tongxiang City, Jiaxing City, Zhejiang Province. Dongjia Zizania Cooperative, Shengzhou Puhui Vegetable Cooperative in Shaoxing City, Zhejiang Province, Vegetable Research Institute of Huangyan District, Taizhou City, Zhejiang Province, and School of Life Sciences, China Jiliang University, Hangzhou City, Zhejiang Province. Samples were collected in autumn 2016, autumn 2017, summer 2018, and autumn 2018.
[0048] Table 1 Variety, phenotype and source of tested samples
[0049]
[0050]
[0051]
[0052]
Embodiment 2
[0053] Example 2: Population Analysis
[0054] 1) Genomic DNA of Ustilago smut was extracted by CTAB method, the DNA concentration was measured with a nucleic acid micrometer, and the DNA quality was detected by agarose gel electrophoresis. with ddH 2 O was diluted to 100ng / μL and stored at -20°C.
[0055] 2) Send the DNA of 47 Zizania zizania varieties with different phenotypes to next-generation resequencing. The reference genome is the MT-type genome of Ustilago sativa, WGS INSDC: JTLW00000000.1.
[0056] 3) Sequencing data were compared to the reference genome using GATK, SAMTOOLS, and BWA software to obtain SNP data files. A total of 321659 SNP sites were obtained.
[0057] 4) All samples of Ustilago smut samples participating in the SNP scanning were numbered into two types, A and B, which represent two types of normal Zizania and gray Zizania respectively. By extracting the Genotype data from the SNP scanning results, output the SNP data of A and B into SNP c a / b f...
Embodiment 3
[0058] Embodiment 3: SNP site identification
[0059] 1) Among the 1330 screened SNP sites, one SNP site was selected at every interval of 20 as the verification site. At the same time, due to the quality of the reference genome sequencing, it was necessary to exclude the SNP sites in the relatively late contig of the reference genome. A total of 39 SNP sites that could be used for verification were screened out, and relevant primers were designed.
[0060] 2) AS-PCR (allele-specific PCR), AS-PCR uses the principle that the base mismatch at the 3' end of the primer can interrupt the PCR extension program and cause no amplification product. important role. In this example, 40 pairs of AS-PCR primers are designed, and all primers are attached in Table 2
[0061] Table 2 Allele-specific PCR primer sequence list
[0062]
[0063]
[0064]
[0065]
[0066]
[0067] 3) In this example, 8 different phenotypes of the same species of Zizania smut DNA were used as tem...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com