Methods for genetic diversification in gene conversion active cells
View Patent ↗The invention relates to a modified lymphoid cell having gene conversion fully or partially replaced by hypermutation, wherein said cell has no deleterious mutations in genes encoding paralogues and analogues of the RAD51 protein, and wherein said cell is capable of directed and selective genetic diversification of a target nucleic acid by hypermutation or a combination of hypermutation and gene conversion. The invention also relates to a method for diversifying any transgenic target gene in said cell. Preferably, the target gene is integrated into the immunoglobulin light or heavy chain locus by targeted integration.
1. A method for producing a hypermutated transgenic target nucleic acid sequence comprising
a) transfecting a chicken immunoglobulin expressing B lymphoid cell with a genetic construct comprising a target nucleic acid sequence flanked by nucleic acid sequences homologous to an endogenous V gene immunoglobulin locus;
b) integrating said genetic construct comprising said target nucleic acid sequence into said endogenous V gene immunoglobulin locus of said chicken immunoglobulin expressing B lymphoid cell, wherein said chicken immunoglobulin expressing B lymphoid cell comprises a functional activation-induced deaminase (AID) protein, and functional XRCC2, XRCC3, and RAD51 proteins or their analogues; and
c) culturing said chicken immunoglobulin expressing B lymphoid cell transgenic for said target nucleic acid to produce said hypermutated transgenic target nucleic acid sequence.
2. The method according to claim 1 , wherein an endogenous V-gene segment or a fragment thereof in said endogenous V-gene immunoglobulin locus of said chicken immunoglobulin expressing B lymphoid cell is replaced with said transgenic target nucleic acid sequence.
3. The method according to claim 1 , wherein said chicken immunoglobulin expressing B lymphoid cell is capable of homologous recombination and DNA repair.
4. The method according to claim 1 , wherein said chicken immunoglobulin expressing B lymphoid cell is a chicken Bursal lymphoma cell.
5. The method according to claim 1 , wherein said chicken immunoglobulin expressing B lymphoid cell is a DT40 cell or a derivative thereof.
6. The method according to claim 1 , wherein said target nucleic acid sequence encodes a protein or possesses a regulatory activity.
7. The method according to claim 1 , wherein said target nucleic acid sequence encodes a protein selected from the group consisting of an immunoglobulin chain, a selection marker, a DNA-binding protein, a DNA-binding protein fragment, an enzyme, a receptor protein, and a receptor protein fragment.
8. The method according to claim 1 , wherein said target nucleic acid sequence is a human immunoglobulin V-gene segment or a part thereof.
9. The method according to claim 1 , wherein said target nucleic acid sequence comprises a transcription regulatory element or an interfering RNA (RNAi) sequence.
10. The method according to claim 9 , wherein said transcription regulatory element is a promoter.
11. The method according to claim 1 , further comprising (d) identifying said chicken immunoglobulin expressing B lymphoid cell containing said hypermutated transgenic target nucleic acid sequence.
12. The method according to claim 11 , wherein said identifying said chicken immunoglobulin expressing B lymphoid cell containing said hypermutated transgenic target nucleic acid sequence comprises identifying a protein encoded by said hypermutated transgenic target nucleic acid sequence on the surface of said chicken immunoglobulin expressing B lymphoid cell, within said chicken immunoglobulin expressing B lymphoid cell, or outside of said chicken immunoglobulin expressing B-lymphoid cell.
13. The method according to claim 1 , further comprising modulating hypermutation of said target nucleic acid sequence with a DNA repair or recombination factor other than a XRCC2, XRCC3, and RAD51 protein or their analogue.
14. The method according to claim 13 , wherein said DNA repair or recombination factor is a RAD54 protein.
15. The method according to claim 1 , wherein said chicken immunoglobulin expressing B lymphoid cell has no pseudo-V gene segment.
16. The method according to claim 1 , wherein hypermutation is at a rate above an order of 10 −9 to 10 −10 bp −1 generation −1 .
17. The method according to claim 1 , wherein hypermutation is at a rate between 10 −5 to 10 −3 bp −1 generation −1 .
18. The method according to claim 11 , wherein a gene product of said hypermutated transgenic target nucleic acid sequence has an optimized desired activity.
19. The method according to claim 11 , wherein said identifying further comprises (e) culturing said chicken immunoglobulin expressing B lymphoid cell under appropriate conditions to express a mutated gene product encoded by said hypermutated transgenic target nucleic acid sequence; (f) identifying said cultured chicken immunoglobulin expressing B lymphoid cell that expresses said mutated gene product having a desired activity; (g) establishing a clonal population of cells from said cultured chicken immunoglobulin expressing B lymphoid cell; and (h) selecting from said clonal population a cell that expresses a gene product of said hypermutated transgenic target nucleic acid sequence having an improved desired activity.
20. The method according to claim 19 , wherein steps (f) through (h) are iteratively repeated.
21. The method according to claim 19 , further comprising inhibition of hypermutation.
22. The method according to claim 21 , wherein said inhibition of hypermutation is by down-regulation of the expression of a trans-acting regulatory factor.
23. The method according to claim 22 , wherein said trans-acting regulatory factor is activation-induced deaminase (AID).
24. The method according to claim 5 , wherein said chicken immunoglobulin expressing B lymphoid cell has no pseudo-V gene segment.
25. The method according to claim 1 , wherein said chicken immunoglobulin expressing B lymphoid cell is a DT40 AID R ΨV − cell.