Method for constructing fixed-point integrated exogenous DNA transgenic pigs

A technology of site-specific integration and transgenic pigs, applied in recombinant DNA technology, cells modified by introducing foreign genetic material, using vectors to introduce foreign genetic material, etc., can solve problems such as difficult to obtain KI animals

Active Publication Date: 2018-07-17
WENS FOOD GRP CO LTD +1
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  • Abstract
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  • Application Information

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Problems solved by technology

Somatic cell cloning technology is often used for transgenic large animals such as pigs, and the cloning efficiency is only 0.5% to 1.5

Method used

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  • Method for constructing fixed-point integrated exogenous DNA transgenic pigs
  • Method for constructing fixed-point integrated exogenous DNA transgenic pigs
  • Method for constructing fixed-point integrated exogenous DNA transgenic pigs

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Experimental program
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Embodiment Construction

[0069] The present invention will be described in further detail below in conjunction with the accompanying drawings.

[0070] Figure 1 to Figure 6 A method for constructing a transgenic pig with site-specific integration of exogenous DNA according to one embodiment of the present invention is schematically shown.

[0071] The construction method includes the following steps.

[0072] S1. Target screening and target binding gRNA cleavage efficiency verification

[0073] S1.1, sgRNA vector construction

[0074] According to the first intron sequence of the pig Rosa26 gene and the fifth intron sequence of the CEP112 gene, use the online website http: / / crispr.mit.edu:8079 / ? , design and synthesize sgRNA primers (as shown in Table 1). The synthesized annealing double-stranded primers were prepared and mixed according to the system in Table 2, and annealed in a PCR machine to form double-stranded DNA.

[0075] Table 1 gRNA target sites and primer design

[0076]

[0077] ...

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Abstract

The invention discloses a method for constructing fixed-point integrated exogenous DNA transgenic pigs. The method comprises the following steps: S1, performing safety target screening and target binding gRNA cleavage efficiency verification; S2, constructing a homologous arm donor plasmid and obtaining a fixed-point integrated transgenic cell line; S3, constructing the fixed-point integrated exogenous DNA transgenic pigs. The method disclosed by the invention has the benefits that a gRNA target sequence is introduced in the donor plasmid, the donor plasmid is linearized while a Cas9 nucleasecleavage target gene is induced by utilizing intracellular transcription gRNA, the test steps are significantly simplified, the labor is saved, and the co-transfection efficiency is favorably improved; carriers used for the fixed-point integration are less, a homologous arm is moderate in size, and the transgenic cell line is more favorably obtained; an efficient site-directed integration technology, a high-activity site-specific transgenic cell culture technology and a somatic cell cloning technology are combined, so that the efficient preparation of fixed-point integrated transgenic animalsis facilitated, and the breeding speed of new transgenic animal varieties is accelerated.

Description

technical field [0001] The invention belongs to the field of biotechnology, and mainly relates to a method for constructing transgenic pigs with fixed-point integration of exogenous DNA, which is applied to the preparation of transgenic animals with fixed-point integration of exogenous DNA fragments, and is suitable for breeding new varieties of long-segment multi-gene fixed-point integration transgenic animals. Background technique [0002] The acquisition of large transgenic animals relies on somatic cell cloning technology (SCNT), and the successful construction of related transgenic cell lines is a key step in obtaining large transgenic animals. Traditional transgenic techniques, such as microinjection, transposon, virus vector encapsulation and infection, etc., insert the target gene into the genome in a random way. These random integrations bring many disadvantages to the establishment and breeding of transgenic animal strains in the later stage. Therefore, there is an...

Claims

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Application Information

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IPC IPC(8): C12N15/85C12N5/10A01K67/027
CPCA01K67/0275A01K2227/108A01K2267/02C12N15/85
Inventor 吴珍芳张献伟李国玲杨化强莫健新钟翠丽石俊松贺晓燕张健李紫聪蔡更元
Owner WENS FOOD GRP CO LTD
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