Combination of SNP loci for detection of tomato gray leaf spot resistance and its application
A tomato gray leaf spot and locus technology, applied in the field of plant biology, can solve problems such as linkage burden, insufficient SNP site versatility, ineffective target gene selection, etc., achieve accurate detection, reduce field transplanting workload, and improve Effects of Breeding Efficiency
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Embodiment 1
[0084] Example 1 Screening of SNP site combinations
[0085] 1. Experimental materials
[0086] Select the variation group data of 660 representative tomato germplasm resources in the world, different source types, for SNP site screening in this example, and this tomato variation group data is mainly based on the preliminary work of the project team where the inventor is located ( Lin, T., Zhu, G., Zhang, J. et al. Genomic analyses provide insights into the history of tomato breeding[J]. Nat Genet, 2014, 46: 1220~1226; Tieman D, Zhu G, Resende M F R, et al.A chemical genetic roadmap to improved tomato flavor[J].Science,2017,355(6323):391). Among them, the genotype data of some tomato germplasm resources and the resistance phenotype data of Sm gene were obtained from the existing public database (https: / / solgenomics.net / ).
[0087] 2. Screening of SNP site combinations
[0088] Use the target gene Sm (Solyc11g018710, Solyc11g018720 and Solyc11g018730, database source: https:...
Embodiment 2
[0092] Example 2 Primer synthesis and kit preparation
[0093] 1. Primer design and screening
[0094] According to the flanking sequences of the SNP01 site to the SNP11 site provided in Example 1, for each SNP site, the principle of design and development according to KASP markers (target product 80-150bp, primers that specifically match the target region on the reference genome and are located in non- SNP-intensive regions, avoid complex sequence regions with high A\T or G\C content, etc.), use Primer3.0 software to design two forward primers upstream of the SNP site, and a reverse primer downstream.
[0095] The tomato samples to be tested include 21 randomly selected samples from germplasm resources and breeding materials with known genotypes and phenotypes as resistance, sensitivity or heterozygous controls, and finally add 3 ddH 2 O as the NTC blank control, a total of 24 copies.
[0096] DNA extraction Using conventional CTAB method or domestic magnetic bead kit to ex...
Embodiment 3
[0111] Example 3 Validation and breeding application of high-efficiency KASP marker of tomato resistance gene Sm to gray leaf spot
[0112] Based on the SNP loci provided in Example 1, this example uses the kit (including primer combination) provided in Example 2 to carry out the verification and breeding application of the high-efficiency KASP marker of the tomato gray leaf spot resistance gene Sm.
[0113] Selected 381 representative tomato samples including mainstream commercial varieties, core public germplasm of the national resource bank, intermediate breeding materials, new hybrid combinations, etc., involving large fruit tomatoes, cherry tomatoes, bunch tomatoes, fresh tomatoes, processed tomatoes and Farm varieties (landraces) and other cultivated tomatoes of different types and origins, 162 of which have obtained Sm genotype data through third-party commercial agencies using closely linked InDel markers (including 15 known phenotypes of gray leaf spot resistance) The...
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