Transcription factor of tree peony psmyb12 and its coding gene and application
A technology that encodes genes and genes, applied in applications, genetic engineering, plant genetic improvement, etc., can solve problems such as lack of experimental evidence
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Embodiment 1
[0041] Embodiment 1, the cloning of peony PsMYB12 gene
[0042] 1. Gene cloning
[0043] Gene cloning was carried out using the S2 stage petals of the purple-spotted peony cultivar 'Qinghai Lake Yinbo' as material.
[0044] (1) Plant total RNA extraction
[0045] Refer to the product manual of RNAprep Pure PlantKit from Tiangen Company to extract total RNA from plant materials. The specific method is as follows:
[0046] 1) Take 50-100mg of petals in the S2 stage, quickly and fully grind them into powder in liquid nitrogen, immediately pour them into a 1.5mL EP tube, add 500μL of SL (add 5% mercaptoethanol before use), and immediately vortex vigorously Shake and mix;
[0047] 2) Centrifuge at 12,000rpm for 2min;
[0048] 3) Transfer the supernatant to the filter column CS in the collection tube, centrifuge at 12,000rpm for 2min, carefully pipette the supernatant in the collection tube into a new 1.5mL EP tube without RNase, try to avoid the tip from touching the collection...
Embodiment 2
[0108] Example 2, Comparison of expression levels of PsMYB12 gene in different stages of peony petal development and in different tissues
[0109] The purple-spotted peony variety 'Qinghai Lake Yinbo' was divided into four stages from the colorless period to the full-bloom period ( figure 1 ), samples were taken every two weeks in the first two periods, and once a week in the latter two periods. The petals of 3 different plants were taken each time as 3 independent experimental repetitions. Total RNA was extracted from all samples and reverse-transcribed into cDNA, which was used as a template for fluorescent quantitative PCR.
[0110] 1. RNA extraction
[0111] The RNA extraction method was the same as that in Example 1 above.
[0112] 2. Reverse transcription
[0113] For reverse transcription, refer to the product manual of Tiangen FastQuant RT Kit for reverse transcription, the method is as follows:
[0114] Since the concentration of RNA extracted from multi-stage sa...
Embodiment 3
[0134] Example 3, VIGS silences PsMYB12
[0135] Tobacco rattle virus (TRV) is a virus composed of two strands, TRV1 and TRV2. The VIGS carrier used in the present invention comes from tobacco rattle virus carrier (tobacco rattle virus, TRV), and TRV1 / TRV2 is a gift from Professor Ma Nan of the Ornamental Plant Postharvest and Stress Physiology Laboratory of China Agricultural University (the non-patent literature that has recorded the carrier is: Tian J,Pei H X,Zhang S,Chen J W,Chen W,Yang R Y,Meng Y L,You J,Gao J P,Ma N.2014.TRV-GFP:amodified Tobacco rattle virus vector for efficient and visualizable analysis of gene function.J Exp Bot, 65:311-322.), which has a Kanna selection marker and a 35S promoter, and pTRV2 has multiple cloning sites such as BamH I and Xho I. The modified virus is used for related research. TRV1 mainly plays the role of virus operation in plants, and TRV2 is an expression vector containing multiple cloning sites.
[0136]PsMYB12 was cloned into an ...
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