A kind of gene of transcription factor lcbhlh52 of Liriodendron tulipifera and its application
A transcription factor, the technology of Liriodendron, applied in application, genetic engineering, plant genetic improvement, etc., to achieve the effect of enhancing tolerance
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Embodiment 1
[0029] Example 1: Analysis of the bHLH family of Liriodendron tulipifera and the cloning of the LcbHLH52 gene
[0030] Download model plant Arabidopsis (https: / / www, arabidopsis.org) and rice (http: / / rapdb.dna.affrc.go.jp) databases to obtain bHLH family sequences, 177 and 135. Then use the protein domain alignment software HMMER3.0 to build a model to find out the potential bHLH family sequences of Liriodendron tulipifera, and then use BLASTP to compare the candidate bHLH family sequences of Liriodendron tulipifera. Finally, LcbHLH52 transcription factor was selected for cloning and sequencing.
[0031] 1. Extraction and quality detection of total RNA
[0032] Before extracting total RNA, all containers used in the extraction process need to be treated without RNase, in order to remove the interference of genomic DNA. Soak plastic utensils such as centrifuge tubes, grinding tools such as mortar and pestle, and tweezers in 0.1% DEPC water overnight, drain the water, wrap it ...
Embodiment 2
[0086] Embodiment 2: Construction of Liriodendron LcbHLH52 gene expression vector
[0087] 1. Design of enzyme digestion primers
[0088] According to the Pcambia2301 plasmid map ( image 3 ) and the characteristics of the LcbHLH52 gene coding region, using the software Primerpremier 5.0 to design the primers containing the restriction site for the LcbHLH52 gene ORF. Searching the restriction site of LcbHLH52 gene ORF through software, it is found that there is no restriction site of KpnI and BamHI in the ORF of LcbHLH52 gene, and the double restriction primers of KpnI and BamHI can be designed as follows:
[0089] LcbHLH52-KpnI-F: 5′-GGggtaccATGGAAATAGATGAACATGG-3′,
[0090] LcbHLH52-BamHI-R: 5'-CGggatccCTACATGCATCTCCCTCC-3'.
[0091] 2. PCR amplification of the enzyme-cut fragment of the target gene
[0092] Same as "4, PCR amplification target gene sequence fragment" in Example 1
[0093] 3. Electrophoresis detection and recovery of amplified products
[0094] Same as...
Embodiment 3
[0121] Example 3: Genetic transformation of Arabidopsis thaliana by the LcbHLH52 gene mediated by Agrobacterium
[0122] 1. Freezing and thawing into Agrobacterium
[0123] (1) Melt Agrobacterium EHA105 competent cells on ice, add 2 μL of the extracted plant expression vector plasmid, and pipette the tip to mix;
[0124] (2) Ice bath for 30 minutes, freeze in liquid nitrogen for 1 minute, and then bathe in water at 37°C for 5 minutes;
[0125] (3) Add 700 μL LB liquid medium, shake at 28°C, 200 rpm for 3 hours;
[0126] (4) Centrifuge at 4000rpm for 3min, leaving a little supernatant;
[0127] (5) Mix the remaining bacterial liquid after transformation, and apply it on the LB solid medium containing Kan;
[0128] (6) Inverted culture at 28°C for 3 days
[0129] (7) Identification of positive clones.
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