Regulatory protein HbMYB85 synthesized by virtue of rubber tree lignin as well as encoding gene and application of regulatory protein HbMYB85
A technology of lignin and genes, applied in application, genetic engineering, plant genetic improvement, etc., can solve the problems of poor physical and mechanical properties, crispness, low density, etc., and achieve the effect of promoting the synthesis and accumulation of lignin
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Embodiment 1
[0042] Embodiment 1, the discovery of HbMYB85 protein and its coding gene
[0043] Obtain the EST sequence database of leaves, stems, roots, flowers, and latex of rubber trees, screen out high-abundance expression DNA fragments in stems, and conduct homologous comparison analysis with existing DNA fragments to determine an EST assembled sequence of about 1000bp (contig ). A pair of specific primers were designed based on contig: 5'-GCATTAGTGGAACTTGTTCAT-3' and 5'-TTTTCTCACTACGTACGTACG-3'. Total RNA was extracted from the bark of the rubber variety "Reyan 7-33-97" and reverse transcribed into cDNA. Using cDNA as a template, specific primers were used for PCR amplification. The amplified product was subjected to 1% agarose electrophoresis, and the target band was recovered and cloned into the pMD18-T vector for sequencing.
[0044] Sequencing results showed that the amplified product contained a gene encoding a new protein.
[0045] The new protein discovered was named HbMYB8...
Embodiment 2
[0046] Embodiment 2, the expression level comparison of HbMYB85 gene in Hevea different parts
[0047] Total RNA was extracted from the leaves, stem top, stem middle, stem lower part, cortex and xylem of the rubber variety "Reyan 7-33-97", and the total RNA was reverse transcribed into cDNA. The CFX96 (Bio-Rad company) real-time fluorescent quantitative PCR detection system was used to analyze the expression level of HbMYB85 gene in different parts of rubber tree.
[0048] The primers used for real-time fluorescent quantitative PCR detection of HbMYB85 gene are as follows:
[0049] HbMYB85-QTF: 5'-AGAGGCCTTCTAACTGAAGCA-3';
[0050] HbMYB85-QTR: 5'-TTTATGGAAGGATTCATGCG-3'.
[0051] The amplification reaction program of real-time fluorescence quantitative PCR: pre-denaturation at 95°C for 3min; denaturation at 95°C for 10s, annealing at 60°C for 10s, extension at 72°C for 30s, 39 cycles.
[0052] The relative expression level of HbMYB85 gene was normalized with 18S gene as in...
Embodiment 3
[0054] Example 3, Subcellular localization analysis of HbMYB85 protein
[0055] Sequence 2 of the sequence listing is inserted between the XbaI and EcoRI restriction sites of the pCAMBIA1205-GFP vector from the 69th-899th nucleotide at the 5' end to obtain the recombinant plasmid pCAMBIA1205-GFP-HbMYB85.
[0056] The pCAMBIA1205-GFP vector or the recombinant plasmid pCAMBIA1205-GFP-HbMYB85 were respectively introduced into the EHA105 Agrobacterium strain to obtain the recombinant Agrobacterium.
[0057] The recombinant Agrobacterium was treated with 150 μM acetosyringone and 10 mM MgCl 2 MES buffer (pH5.6, 10mM) resuspended, adjust OD 600nm =0.8, and then injected into tobacco leaves, cultured for 2 days and then observed under a laser confocal microscope with 488nm excitation.
[0058] see results figure 2 . Unlike GFP, the fluorescence of HbMYB85-GFP is mainly concentrated in the nucleus. The results showed that HbMYB85 protein had nuclear localization properties.
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