Transgenic mouse model of B cell malignancy
View Patent ↗A transgenic non-human animal, such as a mouse, has a genome that include a nucleic acid construct having at least one transcriptional regulatory sequence capable of directing expression in B cells of the animal, wherein the transcriptional regulatory sequence is operably linked to a nucleic acid encoding a miR155 gene product. A method of testing the therapeutic efficacy of an agent in treating or preventing a lymphoproliferative condition includes assessing the effect(s) of the agent on a transgenic non-human animal.
1. A transgenic mouse whose genome comprises a nucleic acid construct comprising at least one transcriptional regulatory sequence capable of directing expression in B cells of the mouse, wherein said transcriptional regulatory sequence is operably linked to a nucleic acid encoding a miR155 gene product comprising a nucleotide sequence having at least 90% sequence identity to SEQ ID NO: 1 and/or SEQ ID NO: 2, wherein said mouse exhibits a B cell malignancy.
2. The transgenic mouse of claim 1 , wherein the at least one transcriptional regulatory sequence comprises a VH promoter.
3. The transgenic mouse of claim 1 , wherein the at least one transcriptional regulatory sequence comprises an Ig heavy chain-Eμ enhancer.
4. The transgenic mouse of claim 1 , wherein the nucleic acid encodes a miR155 gene product comprising SEQ ID NO: 1 and/or SEQ ID NO:2.
5. The transgenic mouse of claim 2 wherein the VH promoter is derived from mouse.
6. The transgenic mouse of claim 3 , wherein the Ig heavy chain-Eμ enhancer is derived from mouse.
7. The transgenic mouse of claim 1 , wherein the B cell malignancy is a leukemia, lymphoma or neoplasm.
8. The transgenic mouse of claim 1 , wherein the nucleic acid construct comprises the 3′ UTR and poly(A) sequence of the β-globin gene.
9. The transgenic mouse of claim 1 , wherein the B cell malignancy exhibits characteristics of human acute lymphoblastic leukemia, human lymphoblastic lymphoma or a combination thereof.
10. A transgenic mouse whose genome comprises a nucleic acid construct comprising a VH promoter and an Ig heavy chain-Eμ enhancer, operably linked to a nucleic acid encoding a miR155 gene product comprising SEQ ID NO: 1 and/or SEQ ID NO:2.
11. A method of determining whether an agent affects a B cell malignancy, comprising:
a) administering said agent to a transgenic mouse whose genome comprises a nucleic acid construct comprising at least one transcriptional regulatory sequence capable of directing expression in B cells of the mouse, operably linked to a nucleic acid encoding a miR155 gene product comprising a nucleotide sequence having at least 90% sequence identity to SEQ ID NO: 1 and/or SEQ ID NO: 2, wherein said mouse exhibits a B cell malignancy; and
b) after said agent has been administered to said transgenic mouse, comparing one or more symptoms and/or indications of said B cell malignancy in said mouse to those of a control mouse of the same genotype, wherein the control mouse has not been administered said agent, wherein a difference in the detectability and/or rate of appearance of said one or more symptoms and/or indications of said B cell malignancy in said transgenic mouse, relative to said control mouse, is indicative of the agent affecting the B cell malignancy.
12. A method of testing the therapeutic efficacy of an agent in treating a B cell malignancy, comprising:
a) administering said agent to a transgenic mouse whose genome comprises a nucleic acid construct comprising at least one transcriptional regulatory sequence capable of directing expression in B cells of the mouse, operably linked to a nucleic acid encoding a miR155 gene product comprising a nucleotide sequence having at least 90% sequence identity to SEQ ID NO: 1 and/or SEQ ID NO: 2, wherein said mouse exhibits a B cell malignancy; and
b) after said agent has been administered to said transgenic mouse, comparing one or more symptoms and/or indications of said B cell malignancy in said mouse to those of a control mouse of the same genotype, wherein the control mouse has not been administered said agent, wherein if said agent inhibits, prevents and/or reduces said one or more symptoms and/or indications of said B cell malignancy in said mouse, relative to said control mouse, then said agent is considered to have therapeutic efficacy in treating or preventing a B cell malignancy.
13. The method of claim 12 , wherein the at least one transcriptional regulatory sequence comprises a VH promoter, an Ig heavy chain-Eμ enhancer or a combination thereof.
14. The method of claim 12 , wherein the transcriptional regulatory sequence is derived from mouse.
15. The method of claim 12 , wherein the nucleic acid comprises the nucleotide sequence of SEQ ID NO:1 and/or SEQ ID NO:2.
16. The method of claim 12 , wherein the B cell malignancy is selected from the group consisting of acute lymphoblastic leukemia, B cell lymphoma, B cell neoplasm and a combination thereof.
17. The method of claim 12 , wherein the B cell malignancy exhibits characteristics of human acute lymphoblastic leukemia, human lymphoblastic lymphoma or a combination thereof.
18. The method of claim 13 , wherein the at least one transcriptional regulatory sequence comprises a VH promoter, an Ig heavy chain-Eμ enhancer or a combination thereof.
19. The method of claim 13 , wherein the transcriptional regulatory sequence is derived from mouse.
20. The method of claim 13 , wherein the nucleic acid comprises the nucleotide sequence of SEQ ID NO: 1 and/or SEQ ID NO:2.
21. The method of claim 13 , wherein the B cell malignancy is selected from the group consisting of acute lymphoblastic leukemia, B cell lymphoma, B cell neoplasm and a combination thereof.
22. The method of claim 13 , wherein the B cell malignancy exhibits characteristics of human acute lymphoblastic leukemia, human lymphoblastic lymphoma or a combination thereof.