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

Transcription activator-like effector nucleases, and encoding genes and application thereof

A transcriptional activation, one-to-one technology, applied in the field of genetic engineering, to achieve strong specificity, high accuracy, and high targeting efficiency

Inactive Publication Date: 2012-07-11
ZHEJIANG UNIV
View PDF1 Cites 26 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, unlike the specific triplet bases recognized by each zinc finger protein, each RVDs on TALEs can only recognize one base

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
  • Transcription activator-like effector nucleases, and encoding genes and application thereof
  • Transcription activator-like effector nucleases, and encoding genes and application thereof
  • Transcription activator-like effector nucleases, and encoding genes and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0053] Example 1 Design of TALENs target sequence

[0054] 1. Download the goat and sheep BLG genome sequences from NCBI (GenBank ID: Z33881.1 for goats, X12817.1 for sheep), and select exon2 as the target;

[0055] 2. Design primers and PCR amplify the target site fragments on the genome, and sequence them, wherein, the PCR primers and sequencing primers are shown in Table 1;

[0056] Table 1

[0057]

[0058] 3. Design TALENs recognition sequence:

[0059] According to the sequence obtained by sequencing, the recognition sequence of TALENs is determined according to the following principles:

[0060] (1) The 0th base is T (the base before the first one in the recognition sequence is the 0th position)

[0061] (2) The last base is T

[0062] (3) The length of the recognition sequence is between 14-19

[0063] (4) The length of the spacer sequence (Spacer) between the two recognition sequences is controlled between 14-21 (12 or 13 can also be used, but the efficiency m...

Embodiment 2

[0067] Example 2 Connection between recognition modules of TALENs and construction of recombinant vector

[0068] 1. Acquisition of TALENs identification module (modular)

[0069] (1) Synthesize four recognition modules NI, NG, HD, and NK that recognize bases A, T, C, and G, respectively. The sequences are shown in Table 3.

[0070] table 3

[0071]

[0072] (2) The four fragments are connected into the pEASY-B vector (purchased from Beijing Quanshijin Company), and the connection method is:

[0073] ① Take 3 μl of PCR product;

[0074] ②Add 1μl pEASY-B vector;

[0075] ③25℃, 7min;

[0076] ④Transform DH5a competent cells and coat with kanamycin plate;

[0077] ⑤Pick clones, extract plasmids in small quantities, digest with enzymes, sequence, and finally obtain the identification modules NI, NG, HD, NK connected to the vector pEASY-B.

[0078] 2. Identify connections between modules

[0079] Connection strategy: Take the connection of 19 identification modules as an ...

Embodiment 3

[0153] Example 3 Transfection of plasmids

[0154] 1. Add 100 μl Matrigel to each well of a 6-well plate, shake it back and forth to make it cover the bottom of the entire well, and place it in 5% CO 2 30min in the incubator.

[0155] 2. Aspirate the culture medium in the T25 bottle for culturing IPS cells, and once in PBS, add 1mL of 0.25% trypsin, shake back and forth to make it evenly cover the bottom of the bottle, and place in 5% CO 2 5min in the incubator.

[0156] 3. After digestion, add 1ml 10% DMEM to neutralize trypsin, transfer the digested cells to a 15ml centrifuge tube, count the cells, and centrifuge at 1200rpm for 5min.

[0157] 4. Resuspend the cells with an appropriate amount of 4*Dox ES0, take 2 million IPS cells and place them in a 6-well plate that has been covered with Matrigel, and add 2ml of fresh 4*Dox ES0.

[0158] 5. Passage and transfect at the same time.

[0159] 6. Transfect the constructed BLG-TALEN-L1, BLG-TALEN-L2, BLG-TALEN-L3, BLG-TALEN-R...

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 pair of transcription activator-like effector nucleases, and encoding genes and application thereof. The pair of transcription activator-like effector nucleases (TALEN) is obtained by fusing a pair of deoxyribonucleic acid (DNA) recognition proteins and two heterologous subunits of a Flavobacterium okeanokoites 1(Fok 1) DNA incision enzyme and can recognize two adjacent loci on goat or sheep beta lactoglobulin gene (BLG) exon2 specifically. When the transcription activator-like effector nucleases are transferred to a host cell simultaneously, the exon2 loci of the BLG gene of the host cell can be targeted by the transcription activator-like effector nucleases, and the targeted loci are subjected to genetic mutation, so that the targeted modification of the goat or sheet BLG gene is realized, and the transcription activator-like effector nucleases have the advantages of high specificity, high targeting efficiency, high accuracy and the like.

Description

technical field [0001] The invention relates to the field of genetic engineering, in particular to a pair of transcription activator-like effector nucleases and their coding genes and applications. Background technique [0002] It has always been the dream of many scientists to modify the genome according to human wishes. Specifically delete or add the sequences we need on the endogenous genome. On the one hand, various animal models can be constructed for basic biological research and disease mechanism research. On the other hand, animal reactors can be produced to produce what we need cheaply. Biological components that are difficult to obtain from other sources. [0003] Among them, the use of large animal mammary glands to produce medicinal or health-care proteins not only has huge economic value, but also has social value such as greatly reducing overall medical costs. The principle of the large animal mammary gland is to knock the target protein into the high-efficie...

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 Applications(China)
IPC IPC(8): C07K14/00C12N15/11C12N9/22C12N15/55C12N15/63C12N5/10
Inventor 肖磊赵金龙
Owner ZHEJIANG 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