A method for batch capture of promoters

A promoter and protein factor technology, applied in the fields of biotechnology and plant genetic engineering, can solve problems such as limited quantity and quality, inability to meet the needs of crop molecular breeding, and inability to directly obtain promoters at one time

Active Publication Date: 2019-08-02
RICE RES ISTITUTE ANHUI ACAD OF AGRI SCI
View PDF2 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, compared with other organisms, the gene discovery of plants is still quite limited in terms of quantity and quality, which is far from meeting the needs of molecular breeding of crops.
In particular, the research and discovery of promoters are mostly based on the analysis, understanding, isolation and expression of individual genes, making it difficult to achieve large-scale and systematic development
[0005] There are also some methods for finding promoters in plant genes in the prior art. However, the methods in the prior art often estimate the possible existence of promoters through software calculations, and cannot directly obtain a large number of promoters at one time.

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
  • A method for batch capture of promoters
  • A method for batch capture of promoters
  • A method for batch capture of promoters

Examples

Experimental program
Comparison scheme
Effect test

Embodiment Construction

[0034] The present invention will be described below with reference to specific examples. Those skilled in the art can understand that these examples are only used to illustrate the present invention and do not limit the scope of the present invention in any way.

[0035] The experimental methods in the following examples are conventional methods unless otherwise specified. The medicinal raw materials, reagent materials, etc. used in the following examples are all commercially available products unless otherwise specified.

[0036] The present invention mainly utilizes the improved chromatin immunoprecipitation technique. Using the chromatin immunoprecipitation technique to isolate plant gene promoter fragments requires a nucleic acid binding protein that can continuously and effectively initiate transcription. The nucleic acid binding protein used in the present invention is RNA polymerase type II (Pol II) in the gene transcription device. OsTBP2 (ACCESSION code: AF464907, ...

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

PropertyMeasurementUnit
wavelengthaaaaaaaaaa
emission peakaaaaaaaaaa
Login to view more

Abstract

The invention provides a method for capturing promoters in batches. The method uses the complex of "DNA-protein factors" formed in the promoter region when plant genes are transcribed, and applies the improved chromosomal immunoprecipitation technique to capture the unknown plant DNA sorting out of gene promoter fragments. The present invention utilizes the property that the protein factors OsTBP2 and OsTFIIB tightly bind to the TATA box short-chain conserved sequence on the promoter to initiate transcription, and generates specific antibodies for these two factors, combined with chromatin immunoprecipitation (ChIP), to specifically target A technique for capturing promoter fragments of unknown plant genes. This technology utilizes the characteristic of a short-chain conserved sequence of the TATA box contained in most promoters, combined with the newly developed chromatin immunoprecipitation technique (ChIP) in recent years to isolate unknown plant gene promoter fragments, it is relatively easy Achieving large-scale capture of plant promoters has high commercial value.

Description

technical field [0001] The invention relates to the technical fields of biotechnology and plant genetic engineering. Specifically, the present invention relates to a method capable of capturing promoters from plants in batches. This method utilizes the "DNA-protein factor" complex formed in the promoter region when plant genes are transcribed, through improved chromosomal immunity Co-precipitation technique, using antibodies specific for protein factors in the complex, to isolate unknown gene promoter fragments from plant genomes. Background technique [0002] In the process of plant growth and development, the regulatory sequence of the gene, namely the promoter, plays a decisive role in the formation and growth of the specific tissue structure of the plant in different growth stages, as well as the stress response to external biotic and abiotic factors. The conserved sequence in the promoter region is the target of transcription factors, and the specific combination of th...

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
Patent Type & Authority Patents(China)
IPC IPC(8): C12Q1/6869G01N33/68
CPCC12Q1/6851C12Q1/6897G01N33/68C12Q2531/113
Inventor 杨剑波王常霖魏鹏程李娟李浩杨亚春李莉许蓉芳
Owner RICE RES ISTITUTE ANHUI ACAD OF AGRI SCI
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products