Method for imparting environmental stress tolerance to plants
An environmental and tolerance technology, applied in the field of environmental stress tolerance, can solve problems such as incompatibility, and achieve the effects of increasing production, realizing cost reduction, and cost reduction.
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Embodiment 1
[0096] (1) Selection of Arabidopsis tyrosine phosphatase (PTP) gene
[0097] In this example, a gene specified by the AGI code: At1g71860 was selected as the tyrosine phosphatase gene in Arabidopsis. In addition, this At1g71860 is known in Plant Cell, 10, 849-857, 1998 as a gene characterized by enhanced expression by high-salt concentration treatment. In this example, the possibility of growth and development under high-salt concentration conditions was investigated for a mutant in which the At1g71860 gene was suppressed.
[0098] In addition, the nucleotide sequence of the coding region of the At1g71860 gene is shown in SEQ ID NO: 1, and the amino acid sequence of the tyrosine phosphatase encoded by this gene is shown in SEQ ID NO: 2.
[0099] (2) T-DNA tag line of Arabidopsis
[0100] Arabidopsis T-DNA insertion mutants in which T-DNA was inserted into the selected At1g71860 gene, SALK_118658 and SALK_062441 obtained from Nottingham Arabidopsis Stock Center (http: / / nasc.n...
Embodiment 2
[0113] In this example, an overexpressor of the At1g71860 gene and an overexpressor of the mutant At1g71860 gene were prepared, and the possibility of growth and development under high-salt concentration conditions was investigated in the same manner as in Example 1. In addition, the mutant At1g71860 gene produced in this example encodes an amino acid sequence in which cysteine at position 175 in the amino acid sequence shown in SEQ ID NO: 2 is replaced by serine, para-oxidized glutathione and / or Or the gene for hydrogen peroxide-hyposensitivity tyrosine phosphatase.
[0114] (1) Overexpression body of At1g71860 gene
[0115] A nucleic acid fragment comprising the At1g71860 gene was cloned from Col by the following steps.
[0116] First, total RNA was recovered from Col using RNeasy Plant Mini Kit (manufactured by Qiagen). Genomic DNA was digested with DNase I (manufactured by Invitrogen), and then cDNA was prepared from 5 μg of total RNA using StrataScript First Strand cD...
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