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Method for constructing B6-Chr1<ZZ2>/Xiao mouse model through replacing No. 1 chromosome based on ZZ2 mus musculus source

A b6-chr1zz2, chromosome replacement technology, applied in the determination/inspection of microorganisms, biochemical equipment and methods, animal husbandry, etc., can solve the problems of too simple, small number of alleles, single source and so on

Inactive Publication Date: 2014-12-03
DONGHUA UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The fundamental reason is that the current experimental animal strains all come from a small number of primitive ancestors (pet mice), which brings a problem: for each gene, in the population (such as all hundreds of mouse experimental strains) considered as a group) the number of alleles is small, much lower than that of Mus musculus musculus subspecies in the natural state
[0004] Especially considering that the population itself belongs to a group with high genetic heterogeneity, it is often too simple to evaluate drug effects and other effects with simple inbred mouse models.
The single source of genetic background of existing inbred mice often makes a drug effective in mice but ineffective in large populations; or the opposite result

Method used

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  • Method for constructing B6-Chr1&lt;ZZ2&gt;/Xiao mouse model through replacing No. 1 chromosome based on ZZ2 mus musculus source
  • Method for constructing B6-Chr1&lt;ZZ2&gt;/Xiao mouse model through replacing No. 1 chromosome based on ZZ2 mus musculus source
  • Method for constructing B6-Chr1&lt;ZZ2&gt;/Xiao mouse model through replacing No. 1 chromosome based on ZZ2 mus musculus source

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Experimental program
Comparison scheme
Effect test

Embodiment 1

[0033] 1. Identification of ZZ2 mice

[0034] The ZZ2 mouse genome was sequenced and identified as Mus musculus musculus subspecies.

[0035] 2. Construction of backcross population

[0036] (a) The ZZ2Mus musculus musculus subspecies mouse ZZ2 was crossed with the inbred mouse C57BL / 6J with known genetic background to obtain the F1 generation.

[0037] (b) F1 generation mice were backcrossed with B6 to obtain F2 generation, and the whole chromosome 1 heterozygous mice were screened by genotyping.

[0038] (c) F2 generation mice were backcrossed with B6. After 10 generations of backcrossing and screening by the same method, a population of mice in which chromosome 1 was heterozygous and the rest of the chromosomes were homozygous for the B6 genotype was formed.

[0039] 3. Identification of backcrosses

[0040] From NCBI (National Center for Biotechnology Information), 29 SNP sites covering chromosome 1 were selected on average. The phenotypes of the SNP sites in the two st...

Embodiment 2

[0061] (1) Determination of traits

[0062] Screened pure line B6-Chr1 ZZ2 / Xiao mouse model screens dozens of biological characteristics from multiple perspectives such as external morphology, internal physiology, overall development, blood physiology and biochemistry, and conducts abnormal phenotypes and genes based on existing trait data and genetic background diversity. Type analysis, share various germline resources and biological data, further develop my country's unique experimental animal resources, and provide a breakthrough for the research of corresponding disease genes and prevention methods.

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Abstract

The invention relates to a method for constructing a B6-Chr1<ZZ2> / Xiao mouse model through replacing the No.1 chromosome based on a ZZ2 mus musculus source. The method comprises the steps as follows: a ZZ2 mus musculus is hybridized with a mouse C57BL / 6J, so as to obtain a F1-generation mouse; secondly, the F1-generation mouse is backcrossed with the C57BL / 6J, and a F2-generation mouse is obtained; thirdly, a mouse of which the No. 1 chromosome is in a heterozygosis state is screened out through genotyping; fourthly, the F2-generation mouse is backcrossed with the C57BL / 6J; fifthly, the same method is adopted for backcross until a 10-generation is screened out, and a mouse group of which the No.1 chromosomes are in the heterozygosis state while the other chromosomes are all pure C57BL / 6J genotypes is formed; sixthly, the DNA of the genes of the backcross mouse is identified; finally, when the backcross mouse with the No.1 chromosome in the heterozygosis state of ZZ2 and B6 is subjected to the 10-generation backcross, homologous genes carrying the No.1 chromosome of the ZZ2 mus musculus is bred and introduced into an inbred strain, and the mouse model is obtained through brother-sister selfing and gene identification.

Description

technical field [0001] The invention belongs to the field of animal model construction, in particular to a chromosome 1 replacement B6-Chr1 derived from ZZ2 Mus musculus ZZ2 / Xiao mouse model construction method. Background technique [0002] Mus musculus Mus musculus originated in South Asia and migrated to various parts of Asia and Europe about 500,000 to 1,000,000 years ago, forming three main subspecies of Mus musculus, M.m.musculus, M.m.castaneus and M.m.domesticus. Although all three subspecies of Mus musculus are ancestors of today's laboratory mice, the common classical inbred mouse genome is primarily derived from M.m. domesticus. There are at least two subspecies of Mus musculus, M.m.castaneus and M.m.musculus, in China. There are large differences between the genetic structure of Mus musculus populations in my country and the current experimental mouse strains, so it is a very important supplementary resource for related gene research. [0003] Although there ...

Claims

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Application Information

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IPC IPC(8): A01K67/02C12Q1/68
Inventor 李凯高遄晁天柱徐福意周宇荀肖君华
Owner DONGHUA UNIV
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