Genetically modified mice expressing humanized PD-1
Provided is a method for preparing a PD-1 gene-modified humanized animal model. The method utilizes the CRIPSR/Cas9 technique to replace partial fragments of a mouse PD-1 gene with fragments of a human PD-1 gene using homologous recombination by constructing a targeting vector, thereby preparing a gene-modified humanized mouse. This mouse can normally express a PD-1 protein containing the functional domain of the human PD-1 protein, and can be used as an animal model for mechanism research regarding PD-1, PD-L1 and other signals, for screening regulators, and for toxicological research. The method has an important and high application value in studies on functions of the PD-1 gene and in the development of new drugs.
1. A genetically modified mouse whose genome comprises a nucleic acid sequence encoding a chimeric programmed cell death 1 (PD-1) protein comprising the amino acid sequence of SEQ ID NO: 17 operably, linked to a promoter of the mouse PD-1 gene, and wherein the mouse functionally expresses the chimeric PD-1.
2. The genetically modified mouse of claim 1 , wherein the mouse has a C57BL/6 background.
3. The genetically modified mouse of claim 1 , wherein the genome of the mouse comprises a nucleic acid sequence that has at least 80% homology to the nucleic acid sequence of SEQ ID NO: 21 operably linked to the promoter of the mouse PD-1 gene.
4. A cell or tissue isolated from the genetically modified mouse of claim 1 .
5. The genetically modified mouse of claim 1 , wherein the genome of the mouse comprises the nucleic acid sequence of SEQ ID NO: 21 operably linked to the promoter of the mouse PD-1 gene.
6. The genetically modified mouse of claim 1 , wherein the genome of the mouse further comprises a nucleic acid sequence encoding a humanized CTLA-4.
7. A method of preparing a genetically modified mouse, the method comprising:
1) providing a plasmid comprising a human PD-1 gene fragment that comprises a nucleic acid sequence that has at least 80% homology to the nucleic acid sequence of SEQ ID NO: 21 flanked by a 5′ homology arm and a 3′ homology arm, wherein the 5′ and 3′ homology arms target exon 2 of a mouse PD-1 gene;
2) providing two small guide RNAs (sgRNAs) that target the nucleic add sequences of SEQ ID NO: 1-4 and SEQ ID NO: 5-8;
3) modifying the genome of a mouse embryo using the plasmid of step 1), the sgRNAs of step 2) and Cas9; and
4) transplanting the embryo obtained in step 3) into a recipient mouse such a transgenic mouse is obtained, wherein the transgenic mouse has a genome comprising a nucleic acid sequence encoding a chimeric programmed cell death 1 (PD-1) protein comprising the an acid sequence of SEQ ID NO: 17 operably linked to a promoter of the mouse PD-1 gene, and wherein the mouse functionally expresses the chimeric PD-1.
8. The method of claim 7 , wherein the 5′ homology arm has the nucleic acid sequence of SEQ ID NO: 18, and the 3′ homology arm has the nucleic acid sequence of SEQ ID NO: 24.
9. A method of evaluating a drug for the treatment of cancer, the method comprising:
a) administering a drug to a genetically modified mouse that has a tumor, and
b) determining whether the drug inhibits the tumor,
wherein the genetically modified mouse has a genome comprising a nucleic acid sequence encoding a chimeric programmed cell death 1 (PD-1) protein comprising the amino add sequence of SEQ ID NO: 17 operably linked to a promoter of the mouse PD-1 gene, and wherein the mouse functionally expresses the chimeric PD-1.
10. The method of claim 9 , wherein the tumor expresses human PD-L1.
11. The method of claim 9 , wherein the genome of the mouse further comprises a nucleic acid sequence encoding a humanized CTLA-4.
12. The method of claim 9 , wherein the drug is an anti-human PD-1 antibody.
13. The method of claim 9 , wherein the sgRNAs target the nucleic acid sequences of SEQ ID NO: 3 and SEQ ID NO: 8.