Application of populus trichocarpa PtrbHLH186 gene in regulation and control of secondary xylem development of trees
A technology of Populus trichocarpa and xylem, applied in the field of genetic engineering, can solve the problems that the biological functions of genes have not been studied
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Embodiment 1
[0029] Example 1: Acquisition of Populus trichocarpa PtrbHLH186 transcription factor and construction of plant expression vector
[0030] (1) Cloning of PtrbHLH186 gene sequence
[0031] The total RNA of wild-type plants of Populus trichocarpa Nisqually-1 genotype was extracted with the plant RNA extraction kit from Qiagen, and cDNA was obtained by reverse transcription with the Takara reverse transcription kit (RR047A).
[0032] Referring to the Populus trichocarpa genome sequence information provided by the phytozome website, gene-specific primers were designed at both ends of the target gene sequence and commissioned to synthesize the primers by a biological company. The sequences of the upstream and downstream primers for PtrbHLH186 gene cloning are shown in Table 1.
[0033] Table 1 is used for the upstream and downstream primer sequences of PtrbHLH186 gene cloning
[0034]
[0035] Note: The underlined part represents the restriction site, and the protection base is ...
Embodiment 2
[0053] Example 2: Obtaining of Populus trichocarpa PtrbHLH186 overexpression plant
[0054] (1) Transformation of Agrobacterium by freeze-thaw method
[0055] ①Take out the Agrobacterium competent cells and place them on ice, add about 30ng of the plasmid into the Agrobacterium competent cells, mix well, and ice-bath for 30 minutes, then immediately put them in liquid nitrogen, freeze for 1 minute, and then immediately put them in a water bath at 37°C 3min.
[0056] ② Add 1ml of liquid LB and incubate at 28°C 180-200rpm for 2-3h.
[0057] ③Centrifuge for 15 seconds, remove the supernatant, retain 300-400 μl of the supernatant, resuspend, plate on LB (kanamycin + gentamicin) solid medium, and incubate at 28°C for about 48 hours.
[0058] ④ Pick a large clone, inoculate it in 5 ml LB (kanamycin + gentamicin) liquid medium, and culture overnight at 220 rpm at 28°C.
[0059] ⑤ Carry out PCR with the bacterial solution as a template to confirm positive clones, refer to Example 1...
Embodiment 3
[0083] Example 3: Application of Populus trichocarpa PtrbHLH186 gene in regulating the development of secondary xylem of trees
[0084] (1) Analysis of the growth phenotype of the independent resistant strains obtained in Example 2 and the wild-type plants of Populus trichocarpa
[0085] Growth phenotype analysis includes the following indicators:
[0086] Tree height measurement: Measure the height from the soil surface to the terminal buds of 1, 2, 3, and 4-month-old wild-type and transgenic greenhouse plants overexpressing PtrbHLH186, with at least 3 biological replicates of wild-type plants and transgenic plants.
[0087] Number of stem nodes: The number of stem nodes was counted for 1, 2, 3, and 4-month-old wild-type and transgenic greenhouse plants overexpressing PtrbHLH186, and wild-type plants and transgenic plants had at least 3 biological replicates.
[0088] Stem measurement: 1, 2, 3, and 4-month-old wild-type and transgenic greenhouse plants overexpressing PtrbHLH...
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