A kind of transcription repression structure domain, its coding gene and its application
A technology encoding genes and domains, applied in the field of bioengineering, can solve problems such as low activity and inability of transgenic plants to survive, and achieve the effect of reducing transcriptional activation activity
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Embodiment 1
[0021] Example 1. Construction of a recombinant expression vector based on pCIMBIA1300-35S.
[0022] Extract the RNA of Arabidopsis Col-0, reverse transcribe it into cDNA as a template, and perform PCR amplification with the following primers:
[0023] TCP7F: 5'GCTCTAGAaccATGTCTATTAACAACAAC 3' (SEQ ID NO: 4);
[0024] TCP7-3R: 5'CGGGATCCTTAATCCGGAAGACGTGGATCTTCCTCTCTTC 3' (SEQ ID NO: 5);
[0025] TCP7-6R: 5'CGGGATCCTTACAAATTAAGATCCGGAAGACGTGGATCTTCCTCTCTTC 3' (SEQ ID NO: 6);
[0026] TCP7-9R: 5'CGGGATCCTTAAGAAGCAAGCAAATTAAGATCCGGAAGACGTGGATCTTCCCTCTCTTC3' (SEQ ID NO: 7);
[0027] TCP7-12R: 5'CGGGATCCTTAACCGGATAAAGAAGCAAGCAAATTAAGATCCGGAAGACGTGGATCTTCCTCTCTTC 3' (SEQ ID NO: 8);
[0028] TCP7-13R: 5'CGGGATCCTTAACCGGATAAAGAAGCAAGCAAATTAAGATGACCCGGAAGACGTGGATCTTCCTCTCTTC 3' (SEQ ID NO: 9);
[0029] Insert the fragments into the pCIMBIA1300-35S vector Xba I and Bam H I restriction site 35S:TCP7-3 / 6 / 9 / 12 / 13AA Six sets of recombinant expression vectors.
Embodiment 2
[0030] Example 2. Construction of transformants.
[0031] After the obtained six sets of recombinant expression vectors were sequenced correctly, the constructed plasmids were respectively transformed into Agrobacterium GV3101 to obtain transformants.
Embodiment 3
[0032] Embodiment 3, acquisition of transgenic plants.
[0033] Transgenes were introduced into Arabidopsis thaliana by flower dipping method (Clough and Bent, 1998). The specific steps of the soaking method are as follows:
[0034] Pick a single colony and inoculate it in 5 ml YEB (Rif 50 mg / L, Kana 100 mg / L) and culture overnight at 30°C. Inoculate at 1:100 in 300 ml YEB (Rif 50 mg / L, Kana 100 mg / L) and expand until OD600=1.0-1.2.
[0035] To collect the bacteria, collect the bacteria into a 500 ml sterilized centrifuge bottle, centrifuge at 4000 rpm at room temperature for 20 min.
[0036] Discard the supernatant. Resuspend the bacteria in the transformation medium (1 / 2MS, 5% sucrose, 0.5 g / L MES, 10 μg 6-BA, adjust the pH to 5.7 with KOH, ready-to-use, without sterilization), add an appropriate amount of transformation medium to OD600=0.8-0.85. Add 0.03% silwet L-77.
[0037] Remove the siliques and flowers from the plants. Compact the soil with 4-6 pots of plants r...
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