Liriodendron chinensis LhPIN3 genes and application thereof
A technology of hybridizing Liriodendron tulipifera and genes, which is applied in application, genetic engineering, plant genetic improvement, etc., can solve the problems of insufficient auxin and achieve good application prospects
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Embodiment 1
[0028] Using the hybrid Liriodendron tulipifera as material, total RNA was extracted and reversed into cDNA, corresponding primers were designed for PCR, after agarose gel electrophoresis, the target band was recovered, connected with pMD19-T vector, transformed into Escherichia coli, sequenced and analyze. Pick positive clones for plasmid extraction, add restriction sites, and simultaneously double-enzyme cut with the vector pBI121, ligate under the action of T4 ligase, transfer into Agrobacterium GV3101, and pass through the flower organs after Arabidopsis reaches the right age. The soaking transformation method was used for transformation, and the phenotypes of the regenerated plants of T1, T2 and T3 generation transgenic homozygous were observed.
[0029] (1) Extraction of total RNA
[0030] Using the lateral buds of the hybrid tulip tree as material, according to the NORGEN kit ( Norgen Biotek ) for RNA extraction, and the reagents and consumables used are all treated ...
Embodiment 2
[0045] Example 2 Gene function verification
[0046] First build the tulip tree LhPIN3 Expression vector, transformed into Arabidopsis pin1 In mutants, the observation of Liriodendron LhPIN3 Can the mutant restore the phenotype, compare the phenotype difference between the two, speculate that Liriodendron LhPIN3 Function; construction of 35S: PIN3 expression vector, transformed into Arabidopsis wild type, observed phenotype, speculated that Liriodendron chinensis LhPIN3 Function.
[0047] 1) Construction of the carrier
[0048] The Escherichia coli strain used in the present invention is E. coli JM109 (purchased from Biovector (Dalian) Co., Ltd.); the expression vector is pBI 121 (purchased from Biovector Co., LTD).
[0049] The specific process is as follows:
[0050] 1. Through PCR in LhPIN3 XbaI and SmaI restriction sites were added upstream and downstream of the gene, respectively. The PCR system and reaction conditions are the same as the full-length amplificatio...
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