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Construction method and application of inducible transgenic mouse cardiomyopathy animal model

A technology of transgenic mouse and construction method, applied in the field of transgenic, can solve the problems of difficult and accurate identification of myocarditis and cardiomyopathy, potential risk of virus, long modeling time, etc., so as to avoid modeling waiting period and low maintenance cost. , the effect of high modeling success rate

Active Publication Date: 2020-07-28
SUZHOU UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Disadvantages of this method: (1) The modeling time is too long, and it is reported in the literature that it takes more than one year at most; (2) There is a great potential risk in the use of the virus itself; (3) Myocarditis and The boundary of cardiomyopathy is not easy to accurately identify, and the feasibility is poor
Disadvantages of this method: (1) There is no uniform standard for the dosage of doxorubicin at present. Insufficient dosage may lead to modeling failure, while excessive dosage may lead to direct death; (2) intraperitoneal injection requires certain technical training. There is a certain failure rate due to the differences in the techniques of the operators
[0011] To sum up, there are obvious deficiencies in the current main cardiomyopathy animal models and modeling methods, and the current cardiomyopathy animal models cannot choose whether to induce cardiomyopathy according to actual needs.

Method used

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  • Construction method and application of inducible transgenic mouse cardiomyopathy animal model
  • Construction method and application of inducible transgenic mouse cardiomyopathy animal model
  • Construction method and application of inducible transgenic mouse cardiomyopathy animal model

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0051] Using the human calpain-1 plasmid as a template, the calpain-1 fragment was specifically amplified by PCR, and TetO, α-MHC promoter nucleic acid sequence and mitochondrial signal peptide sequence were added to its 5' end (see sequence table SEQ ID No.1 ). The PCR product and the eukaryotic expression vector (Alpha-MyHC clone 26 plasmid, for its preparation method refer to the journal Journal of Biological Chemistry.1991May 15; 266 (14): 9180-5) were digested with restriction endonuclease Not I respectively, and gelatinized Recovery, T4DNA ligase ligation, transformation of recombinant plasmid into E.coli DH5α, extraction of plasmid and identification by PCR, enzyme digestion and sequencing. The successful sequencing is the expression vector containing calpain-1 gene. figure 1 It is a structural schematic diagram of the expression vector containing the calpain-1 gene of the present invention. In the figure, MTS represents the mitochondrial signal peptide sequence, Huma...

Embodiment 2

[0053] The expression vector of calpain-1 gene successfully obtained in Example 1 was injected into the fertilized mouse egg by microinjection technique, and then implanted into the uterus of the recipient mouse. The progeny transgenic mice (Tg-mtCapn1) identified as positive by PCR were selected and mated with transgenic mice specifically expressing tTA (Tg-tTA) or transgenic mice specifically expressing rtTA (Tg-rtTA), . PCR and Western Blot identification were performed on the progeny after hybridization, and transgenic mice (Tg-mtCapn1 / tTA or Tg-mtCapn1 / rtTA) with myocardial specificity and mitochondrial selective overexpression of calpain-1 were selected. figure 2 It is a hybridization schematic diagram taking Tg-tTA mice as an example.

[0054] When screening the first generation of Tg-mtCapn1 positive transgenic mice by PCR, mouse endogenous G protein signaling 7 was selected as an internal reference, as follows:

[0055] 1. Primers

[0056] Transgenic PCR primer F1...

Embodiment 3

[0094] The model built by the present invention can choose whether to induce cardiomyopathy according to actual needs. For Tg-mtCapn1 / tTA mice, the expression of calpain-1 can be inhibited by tetracycline or doxycycline intervention to block the occurrence of cardiomyopathy; For Tg-mtCapn1 / rtTA, tetracycline or doxycycline can promote the expression of calpain-1 to induce cardiomyopathy. The following takes Tg-mtCapn1 / tTA transgenic mice as an example to illustrate, and the specific method is as follows:

[0095] A certain number of wild-type (WT) and Tg-mtCapn1 / tTA transgenic mice (TG) were selected, and the Tg-mtCapn1 / tTA transgenic mice were divided into three groups, and the following interventions were carried out from the 0th week: the normal control group ( TG-Ctrl), adding 0.2mg / ml doxycycline in drinking water to continuously shut down the overexpression of calpain-1 (TG-Doxy) and adding 0.2mg / ml doxycycline in drinking water to shut down the overexpression of calpain...

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Abstract

The invention relates to an expression vector containing a calpain-1 gene. The expression vector comprises a Tet operon, an alpha-MHC promoter nucleotide sequence, a mitochondrial signal peptide sequence and a gene segment of calpain-1 which are connected in sequence. The invention further provides a construction method of an inducible transgenic mouse cardiomyopathy animal model. The constructionmethod comprises the following steps: importing the expression vector containing the calpain-1 gene into oosperms of a mouse, and transferring the oosperms into the uterus of the receptor mouse for gestation, thus obtaining the positive offspring transgenic mouse; and mating the positive offspring transgenic mouse with a transgenic mouse with specific expression of tTA or a transgenic mouse withspecific expression of rtTA, and picking out the inducible transgenic mouse cardiomyopathy animal model from the hybrid offsprings. The invention further discloses applications of the transgenic mousecardiomyopathy animal model obtained through the construction method in screening medicines for treating cardiomyopathy. According to the technical scheme provided by the invention, the modeling success rate is high, the phenotype is stable, the cost is ow, and whether inducting for the generation of cardiomyopathy is needed or not can be selected according to the actual demands.

Description

technical field [0001] The invention relates to the field of transgenic technology, in particular to a construction method and application of an inducible transgenic mouse cardiomyopathy animal model. Background technique [0002] Cardiomyopathy is a kind of myocardial disease caused by various reasons, characterized by myocardial enlargement, thickening and hardening. It is often manifested clinically as cardiac mechanical / electrical activity disturbance and abnormal hypertrophy or dilation of the ventricle. With the development of the disease, it can eventually evolve into heart failure. In recent years, the incidence of cardiomyopathy has been increasing year by year in the world, and it has become one of the most common clinical heart diseases in my country. The pathogenesis of cardiomyopathy is complex, the course of the disease is hidden, the prognosis is extremely poor, and there is a lack of specific treatment methods. It seriously endangers the health of the popula...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12N15/85C12N15/66C12N15/70A01K67/027
CPCA01K67/0275A01K2217/072A01K2227/105A01K2267/0375C12N15/66C12N15/85
Inventor 彭天庆黄一帆曹婷郑东张露露
Owner SUZHOU UNIV
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