Promoter from rice and application thereof
A technology of promoter and rice, applied in the fields of genetic engineering and rice breeding, can solve problems such as restricting the promotion and development of transgenic crops, achieve good application prospects, avoid unnecessary waste, and increase the effect of local expression.
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Embodiment 1
[0033] Example 1: Cloning of the promoter of the OsHDT702 gene
[0034] Using the japonica rice variety "Zhonghua 11" as the experimental material, genomic DNA was extracted by CTAB method.
[0035] According to the sequence of rice gene OsHDT702 (Genebank accession number: AK072845) known in NCBI, primers were designed from the 1776 bp sequence upstream of the initiation codon ATG, and PCR amplification was performed using genomic DNA as a template. The amplification primer is HDT702P-F: AT AAGCTT GTGCTCGTGCCGTCGTCCTT (the underlined part is the Hind III restriction site); HDT702P-R: AT CTGCAG TCTCCTCGCCGTGCTCCTCT (the underlined part is the restriction site of Pst I). The PCR reaction was carried out in a 50ul system, and the reaction parameters were: pre-denaturation at 94°C for 5min; denaturation at 94°C for 30s, annealing at 56°C for 45s, extension at 72°C for 2min, 35 cycles; extension at 72°C for 5min. The PCR amplified product was separated by 1.0% agarose gel ele...
Embodiment 2
[0037] Example 2: Analysis of cis-acting elements on HDT702P sequence
[0038] Put the HDT702P sequence on the PLACE promoter analysis website ( http: / / www.dna.affrc.go.jp / PLACE / ) on cis-acting element analysis. The result is as figure 2 As shown, the sequence of HDT702P contains multiple anther-specific expression cis-acting elements and various hormone-responsive elements.
Embodiment 3
[0039] Example 3: Obtaining and identification of rice transfected with PCAMBIA1391Z-HDT702P vector
[0040] 1. Construction of PCAMBIA1391Z-HDT702P vector
[0041] The positive clone that sequencing is correct among the embodiment 1 extracts plasmid, the plasmid of extracting and pcambia1391Z vector (its structure such as image 3 Shown) Digest with Hind III and Pst I at the same time, recover the target fragment, use T4 ligase to connect the target DNA fragment and the PCAMBIA1391Z vector digested with Hind III and Pst I, and you can get the GUS gene containing HDT702P and its downstream gene The expression vector PCAMBIA1391Z-HDT702P. There is a Sac I restriction site at about 900 bp upstream of the HDT702P fragment, but PCAMBIA1391Z does not have a Sac I restriction site, so a small fragment of 900 bp will be obtained by cutting the fusion vector with Hind III and Sac I to identify a positive plasmid; Figure 4 As shown, lanes 1, 3, 5, and 7 correspond to positive plasmi...
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