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

A transgenic method using wheat anthers as receptors

A technology of transgenic plants and receptors, applied in the field of transgenic, can solve the problems of complex chromosome composition and slow stability of transgenic offspring, and achieve the effect of improving the efficiency of resource innovation

Inactive Publication Date: 2011-12-14
CROP RES INST SHANDONG ACAD OF AGRI SCI +1
View PDF1 Cites 10 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, wheat is an allohexaploid with complex chromosomal composition, and its genome is nearly 40 times that of rice and maize. Transgenic offspring with diploids such as immature embryos, mature embryos, and shoot apical meristems as recipients are slow to stabilize. easy to form chimeras

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 transgenic method using wheat anthers as receptors
  • A transgenic method using wheat anthers as receptors
  • A transgenic method using wheat anthers as receptors

Examples

Experimental program
Comparison scheme
Effect test

experiment example 1

[0038] Experimental example 1, transformation of anther by gene gun

[0039] 1. Separation and pretreatment of anthers

[0040] 1. Preparation of 0.3M mannitol pretreatment solution: Weigh 54.65 grams of analytically pure mannitol, dissolve it in 1000 ml of ultrapure water, and after autoclaving, add 200 mg of cephalosporin sterilized by suction filtration per liter.

[0041] 2. Preparation of medium for anther callus induction: solid medium was poured three days in advance, 200 mg of cephalosporin was added per liter, poured into a 3.5 mm culture dish, and the culture medium plate was checked for contamination. The specific formula is shown in Table 2.

[0042] 3. The wheat anther donor variety is K35, observe the anther development period under a microscope, and take figure 2 The anthers at the single-nuclei margin stage as shown (at this time, the top of the ear is about 10cm away from the flag leaf auricle), put them into a petri dish filled with 0.3M mannitol pretreatme...

experiment example 2

[0057] Experimental example 2. Anther recovery culture and selection of regenerated seedlings and chromosome doubling

[0058] 1. Anther recovery culture and selection of regenerated seedlings

[0059] 1. Put the bombarded anthers in the aseptic operating table, press Figure 4 The method shown was transferred to the callus induction medium, and after 3 days of dark culture at 32°C, it was changed to dark culture at 28°C for about 4 weeks to obtain embryoid bodies.

[0060] 2. Transfer the embryoid bodies of about 1 to 2 mm to the regeneration medium added with G418 (the G418 in the regeneration medium shown in Table 2 should be filtered and sterilized and added to the regeneration medium after autoclaving), and light Intensity 5000lux, 16 hours of light per day at 25°C for regeneration culture, see Figure 5 .

[0061] 3. Transfer the regenerated green shoots to 1 / 2 MS medium added with 25 mg / L G418, and continue to screen for 2 weeks.

[0062] 2. Strong seedling cultivat...

experiment example 3

[0071] Experimental example 3. Analysis of Gus gene expression in transgenic offspring

[0072] 1. Preparation of Gus tissue staining solution mother solution: 0.2M sodium phosphate buffer; 200mg X-gluc dissolved in 400ul DMSO; 0.1M potassium ferrocyanide; 0.1M potassium ferricyanide; 0.5M Na2- EDTA

[0073] 2. Preparation of Gus tissue staining solution: 1000ml of 0.2M sodium phosphate buffer; 1ml of 0.1M potassium ferrocyanide and 0.1M potassium iron cyanide; 8ml of 0.5M Na2-EDTA; dissolved in DMSO 200mg X-gluc in water; 90ml water, dilute to 200ml.

[0074] 3. Gus tissue staining: Take the tissue to be tested, cut or cut it, put it into a 5ml centrifuge tube, completely submerge it in Gus staining solution, shake overnight at 37°C, wash it with 70% ethanol 2~3 times the next day, Observe the gus gene expression intensity.

[0075] Such as Figure 8 , Figure 9 B and Figure 10 Shown in A, transform the positive plant of pCAMBIA1301, its grain ( Figure 8 ),root tip( ...

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

The invention discloses a transgenic method using wheat anthers as receptors. The method provided by the invention comprises the following steps: 1) using plant anthers as receptors to carry out gene transformation with a gene gun method to obtain transformed anthers; 2) culturing the transformed anthers obtained in step 1) to obtain embryoid bodies, The embryoid bodies are then cultured to obtain haploid regenerated shoots. The present invention establishes a wheat transgenic technology system with anthers as receptors, in vitro moisturizing of anthers, adhesion and fixation of anthers during gene gun bombardment, gold powder particle size for preparing bullets, bullet coating effect, bombardment distance and haploid Chromosome doubling and other processes have been systematically studied, and transgenic plants with homozygous genotypes can be obtained in contemporary times.

Description

technical field [0001] The invention relates to a transgenic method using wheat anthers as receptors. Background technique [0002] In 1991, Vasil et al introduced the bar gene into wheat by gene gun-mediated method, and obtained the world's first wheat transgenic plant. In the following year, Weeks et al. introduced the gus gene and bar gene into wheat using the gene gun-mediated method, and established a more mature technical system for gene gun transformation of young wheat embryos by optimizing different parameters in the process of gene gun transformation. Afterwards, wheat gene transformation has made significant progress. Different methods were used to introduce multiple genes into wheat immature embryos, and a batch of wheat transgenic plants were obtained, which provided data for the genetic research of exogenous genes. However, compared with rice, corn and other crops, wheat is the most difficult food crop for genetic transformation, and the research on wheat gene...

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): C12N15/87A01H4/00A01H5/00
Inventor 李根英夏先春何中虎高洁李玉莲郭凤芝樊庆琦隋新霞黄承彦
Owner CROP RES INST SHANDONG ACAD OF AGRI SCI
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