Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Corn drought-inducible promoter and activity analysis

A technology of drought induction and promoter sequence, which is applied in the field of plant drought-inducible expression vectors, can solve problems such as plant growth retardation, and achieve the effect of increasing yield

Inactive Publication Date: 2012-04-18
JILIN UNIV
View PDF2 Cites 4 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, overexpression of the DREB1A gene also resulted in plant growth retardation under normal growth conditions; in contrast, gene expression driven by the stress-inducible promoter rd29A not only made plants more stress tolerant but also had minimal effects on their growth. negative impact

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Corn drought-inducible promoter and activity analysis
  • Corn drought-inducible promoter and activity analysis
  • Corn drought-inducible promoter and activity analysis

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0036] Example 1: Cloning of the Drought-Inducible Promoter of the Maize Drought Response Protein Gene CKS2

[0037] The promoter of the corn drought response protein gene CKS2 (promoter sequence comprises the DNA nucleotide sequence of the -1bp to -1444bp region relative to the transcription start site of SEQ ID NO: 1), in the corn drought response protein gene CKS2 identified in the 5' untranslated region sequence.

[0038] The maize drought response protein gene CKS2 is registered in NCBI GenBank (accession number: GU556566.1), and the sequence listing shows the DNA sequence of the plant drought-inducible promoter and 5' untranslated region of the above-mentioned gene of the present invention. exist figure 1 In , the start codon ATG for protein synthesis is underlined, and the base T of the transcription start site is shown with +1. And use the promoter analysis website to analyze the core elements of the promoter. The Promoter Analysis website is http: / / bioinformatics.p...

Embodiment 2

[0042] Example 2: Construction of Plant Drought Inducible Vector

[0043] The promoter of the maize drought response protein gene CKS2 cloned in Example 1 and the 5' untranslated region ZmCKS2Pro of 219 bp (see the sequence listing) were inserted into the vector to construct a plant drought-inducible vector.

[0044] More specifically, the plant expression vector pCAMBIA1301 and the recombinant plasmid pMD 18-T::ZmCKS2Pro were respectively digested with PstI and NcoI inside the cloned sequence, and then inserted into the PstI and NcoI restriction sites of the vector pCAMBIA1301. The vector is called pCAMBIA 1301::Zm CKS2Pro, which is used to drive the expression of GUS gene, which was identified by enzyme digestion ( image 3 ) obtained the promoter fragment, which was the same as the expected result.

[0045] exist Figure 4 Among them, the gene GUS encoding β-glucuronidase was used as the reporter gene, and the selection marker was hygromycin resistance gene. In addition,...

Embodiment 3

[0046] Example 3: Identification of the activity of a maize drought-inducible promoter

[0047] The vector pCAMBIA 1301::ZmCKS2Pro constructed in Example 2 was transferred into Agrobacterium tumefaciens EHA105 by heat shock transformation method, and the plasmid was extracted and identified by enzyme digestion.

[0048] In order to identify the drought-inducible activity of the promoter, the method of Jefferson et al. (EMBO J, 1987) was used to test the activity of GUS after drought treatment of the embryos of maize after Agrobacterium infection.

[0049] More specifically, soak the corn seeds to accelerate germination, then cut the seeds in half longitudinally, induce culture with 20% PEG for 24 hours, put the corn seeds in the GUS detection solution at 37°C overnight, GUS detection solution: 3mg / ml X- gluc (5-bromo-4-chloro-3-indole-β-D-glucuronide), 50mM sodium phosphate buffer solution (PH=7.0), 10mM EDTA, 0.5mM potassium ferricyanide, 0.5mM ferrocyanide Potassium chlorid...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

A corn drought-inducible promoter and activity analysis belong to the technical field of bioengineering. The invention provides an obtained corn drought-inducible promoter sequence, a drought-inducible plant expression vector for corn transformation and genetically modified plants transformed by plant expression vector; the corn drought-inducible promoter sequence contains a DNA (deoxyribonucleic acid) nucleotide sequence from the -1bp region to the -1444bp region relative to the transcription start site of SEQ ID NO: 1; the drought-inducible plant expression vector contains the corn drought-inducible promoter sequence and a 5' untranslated region of a corn drought-responding protein gene; the genetically modified plants transformed by the plant expression vector contain the corn drought-inducible promoter sequence and the 5' untranslated region of the corn drought-responding protein gene; and PCR (polymerase chain reaction) primers of SEQ ID NO: 2 and SEQ ID NO: 3 are suitable for amplifying the sequence DNA segment containing the SEQ ID NO: 1. The corn drought-inducible promoter can be used for promoting the high-efficiency expression of drought-resistant genes and in drought-resistant genetically modified plants, and has a positive significance in solving the problem in grain production in arid regions and increasing grain yield.

Description

technical field [0001] The invention belongs to the technical field of bioengineering, and specifically relates to a drought-inducible promoter sequence derived from the corn drought-responsive protein gene CKS2 and highly expressed in plants, a plant drought-inducible expression vector containing the promoter sequence, and the application of the The promoter produces transgenic plants. Background technique [0002] Adversity stress is one of the most important factors and challenges affecting food production in agricultural production. Factors such as soil degradation, lack of fresh water, climate (elephant) and other factors lead to deduction of barren, saline-alkali, and tidal flat land (more than 1.5 billion mu) with zero output, and crops directly caused by adversity stress such as saline-alkali, drought, and low temperature every year Production cuts still exceed about 20 percent of total output. Among these adversity factors that seriously affect crop production, dr...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): C12N15/113C12N15/82C12N15/84A01H5/00C12N15/11
Inventor 潘洪玉王凤婷刘金亮张世宏张桂珍贾承国李桂华
Owner JILIN UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com