Gene dvrpt1 with salt tolerance function, its encoded protein and its application
A technology that encodes proteins and genes, used in applications, genetic engineering, plant genetic improvement, etc.
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Embodiment 1
[0023] Embodiment one: Dunaliella viridis DvRPT1 Cloning and analysis of the full-length coding region
[0024] Dunaliella viridis D. viridis The EST sequence (Expressed Sequence Tag) of the cDNA library induced by different concentrations of salt was analyzed, and a salt-induced expression sequence (Contig 6774) was found, from which a Dunaliella viridis 26S proteasome regulatory subunit RPT1 gene was isolated and named for DvRPT1 . The full length of the Contig 6774 sequence is 1737 bp, containing DvRPT1 Complete open reading frame (ORF), eukaryotic translation conserved Kozak sequence (gcc atg c) and poly(A) structure (see sequence listing).
Embodiment 2
[0025] Embodiment two: Dunaliella viridis DvRPT1 Encoded protein structure, evolution analysis and location prediction
[0026] The analysis results of Vector NTI software showed that the gene encoded a protein with 433 amino acids, the molecular weight of the protein was 48.3 kDa, and the isoelectric point was 6.8. The encoded protein belongs to the 26S proteasome regulatory subunit RPT1 protein family. The sequence 32-430 AA of DvRPT1 is the conserved domain of RPT1. RPT1 is the regulatory subunit of the 26S proteasome, located in the base structure of the 26S proteasome, and has ATPase activity. The 178-345 AA of the DvRPT1 sequence is the conserved domain of ATP-binding protein, which can combine with ATP to release energy to help deubiquitination of ubiquitination-labeled proteins, thereby entering the base structure of the proteasome to achieve protein degradation.
[0027] figure 1 for the present invention DvRPT1 The evolution analysis diagram of the protein enco...
Embodiment 3
[0029] Embodiment three: Dunaliella viridis DvRPT1 Functional analysis in yeast mutants
[0030] (1) Construction of yeast expression vector
[0031] will first contain DvRPT1 The Contig 6774 sequence of the complete ORF was ligated into a yeast expression vector: We ligated the Contig 6774 sequence using the restriction enzyme Eco R I and xho I, construct into yeast expression vector pAJ401 after enzyme digestion, obtain recombinant plasmid pAJ401::6774.
[0032] (2) Transform yeast
[0033]The recombinant plasmid pAJ401::6774 was transformed into yeast salt-sensitive mutant G19 (Mat∂, ura3 his3 trp1 ade2 ena1△::ena4△) using LiAc heat shock transformation method.
[0034] (3) Phenotypic identification of yeast transformants
[0035] The basic medium used is AP medium, and the required amino acids are added. The screening marker was uracil auxotrophy. The vector was transferred to the phenotype display medium of the pAJ401 transformant, and 2% galactose was added as...
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