Anthocyanin synthesis-related proteins and their application in regulating plant anthocyanin content
A technology for anthocyanin content and related proteins, applied to the application field of regulating plant anthocyanin content
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Embodiment 1
[0114] Embodiment 1, the discovery of RH1 and its coding gene RH1 gene
[0115] 1. Mutant acquisition and phenotype analysis
[0116] In The Nobel Foundation, by screening the Tnt1 insertion mutant library of Medicago truncatula, a mutant with abnormal anthocyanin synthesis was isolated and obtained. The mutant was numbered NF7599 in the Tnt1 database, and it mainly manifested in the specific accumulation of anthocyanins on leaves. The phenotype of red heart was presented, and the mutant was named red heart1(rh1). The mutant was crossed with wild-type Medicago truncatula R108 to obtain F 1 Expressed as an intermediate type with a lighter red heart, F 2 Three phenotypes were isolated from the population: wild type, intermediate type with lightened red heart and red heart phenotype, and the segregation ratio was 1:2:1 (p=0.754>0.05). It shows that for wild-type R108, the red heart trait of rh1 mutant is controlled by a semi-dominant single gene.
[0117] The leaf phenotype o...
Embodiment 2
[0138] Example 2, Functional Verification of RH1 Gene
[0139] 1. Construction of CRISPR / Cas9 genome editing vector
[0140] Using pMtU6-Cas (Meng et al., 2017, Targeted mutagenesis by CRISPR / Cas9system in the model legume Medicago truncatula, Plant Cell Rep (2017) 36:371–374) as a template, using the primer pair MtU6-F1 and MtU6-R1 Perform PCR amplification to obtain the MtU6 promoter; use primer pair 1 (composed of 40-sgRNA-F1 primers and R2 primers) and primer pair 2 (composed of 40-sgRNA-F2 primers and R2 primers) for PCR amplification, respectively, Obtain two DNA fragments encoding the sgRNA targeting the target fragment and the scaffold respectively, that is, the sgRNA1-scaffold fragment and the sgRNA2-scaffold fragment. Using the mixture of MtU6 promoter and sgRNA1-scaffold fragment as a template, PCR amplification was performed using a primer pair (composed of MtU6-F1 and R2) to obtain pMtU6::sgRNA1-scaffold fragment; using MtU6 promoter and sgRNA2-scaffold fragment ...
Embodiment 3
[0168] Embodiment 3, the anthocyanin content of Medicago truncatula of transfection RH1 gene increases
[0169] This example introduces the RH1 gene into the wild-type Medicago truncatula R108 to further illustrate that the RH1 gene can increase the anthocyanin content of Medicago truncatula, and the specific method is as follows:
[0170] 1. Construction of recombinant vector
[0171] Using the genomic DNA of the mutant rh1 as a template, PCR amplification was carried out with primers 40-PRO-EcoRI-F and 40-3'UTR-PstI-R to obtain the DNA fragment shown in sequence 3 of the sequence table; the pCAMBIA2300 The DNA fragment between the EcoRI and PstI recognition sequences was replaced with the DNA fragment shown in Sequence 3, and the resulting recombinant vector was named pCAMBIA2300-RH1pro::RH1. pCAMBIA2300-RH1pro::RH1 can express the protein shown in sequence 1 in the sequence listing. The primer sequences used are:
[0172] 40-PRO-EcoRI-F:5'-ccatgattacgaattcACTCGTATGTGGGGATT...
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