Protein GPA4 related to plant glutelin transportation and storage and encoding gene and application thereof
A related protein and gluten technology, which is applied to the plant gluten transport and storage related protein GPA4 and its encoding gene and application field, can solve the problems of unknown function and the like
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Embodiment 1
[0047] Example 1. Discovery of related proteins and their coding genes for plant gluten sorting
[0048] 1. Phenotype analysis and genetic analysis of gpa4 mutant of rice gluten sorting
[0049] In 9311 60 The silty mutant gpa4-1 was selected from the Co radiation mutant library, and the silty mutant gpa4-2 was selected from the Kinmaze MNU-treated mutant library. The two mutants were allelic variants of the same gene. Compared with the wild type, the main feature of gpa4 is the grain quality and opacity (see figure 2 ). Scanning electron microscope analysis confirmed that the starch granules in gpa4-1 were loose (see figure 2 ), which may be the main cause of endosperm opacity. In addition, the SDS-PAGE analysis of the mature seeds of the mutant showed that the mutation of the gene resulted in a sharp increase in the 57-kDa gluten precursor, and the corresponding mature acidic and basic subunits decreased, along with the globulin content. Decreased, gliadin showed no significa...
Embodiment 2
[0089] Example 2. Obtaining and identification of transgenic plants
[0090] 1. Recombinant expression vector construction
[0091] Using rice Kinmaze cDNA as a template, PCR amplification was performed to obtain the coding region of GPA4 gene. The PCR primer sequence is as follows:
[0092] primer3: (The underline is the BamHI restriction site)
[0093] 5'CTGCAGGTCGAC GGATCC ATGGTTTCCTTCGAGATG 3'(SEQ ID NO. 6)
[0094] primer4: (the underline is the BamHI restriction site)
[0095] 5'TAGAATTCCCGG GGATCC CTACACTGGAACCCGTTT 3'(SEQ ID NO. 7)
[0096] The above-mentioned amplified product contains the coding region of the gene, and the PCR product is recovered and purified. The PCR product was cloned into the vector pCUbi1390 using Infusion Recombination Kit (Clontech) to construct pCUbi1390-GPA4. Recombination reaction system (2.5μL): PCR product 0.5μL (50-100ng), pCUbi1390 vector 1.0μL (30-50ng), 5×Infusionbuffer 2.0μL, Infusion enzyme mix 0.5μL. After a short centrifugation, the mi...
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