Method for generating diversity
View Patent ↗The invention relates to a method for preparing an antibody-producing cell line capable of directed constitutive hypermutation of a specific nucleic acid region, comprising the steps of: a) screening a clonal cell population for V gene diversity; b) isolating one or more cells which display V gene diversity and comparing the rate of accumulation of mutations in the V genes and other genes of the selected cells; and c) selecting a cell in which the rate of V gene mutation exceeds that of other gene mutation.
1. A method for preparing a cell line exhibiting directed constitutive hypermutation of a target nucleic acid region, comprising screening a cell population for ongoing target sequence diversification, wherein said screening comprises determining the mutation rate of the target nucleic acid region relative to the mutation rate of a non-target nucleic acid region, and selecting a cell in which the rate of target nucleic acid mutation exceeds the rate of non-target nucleic acid mutation by a factor of 100 or more, wherein the rate of mutation in the cell line is modulated by genetic manipulation of one or more DNA repair genes, and wherein said genetic manipulation is selected from the group consisting of gene deletion, conversion, and insertion.
2. A method according to claim 1 , wherein the cell line is a lymphoid cell line.
3. A method according to claim 2 , wherein the cell line is an immunoglobulin-expressing cell.
4. A method according to claim 1 , wherein the cell line expresses the target nucleic acid region in a manner that facilitates selection of cells comprising mutants of said target nucleic acid region.
5. A method according to claim 4 , wherein the cell line expresses a gene product encoded by the target nucleic acid region on the cell surface.
6. A method according to claim 1 , wherein the cell line comprises a cell type which hypermutates in vivo.
7. A method according to claim 6 , wherein the cell line is a Burkitt lymphoma, follicular lymphoma or diffuse large cell lymphoma cell line.
8. A method according to claim 1 , further comprising the steps of isolating one or more cells which display target sequence diversification, and comparing the rate of accumulation of mutations in the target sequences with that in non-target sequences in the isolated cells.
9. A method according to claim 8 , wherein the target sequence is an immunoglobulin V-gene sequence.
10. A method according to claim 9 , wherein cells of said cell population are screened by assessing loss of an expressed immunoglobulin.
11. A method according to claim 1 or 8 , wherein cells of said cell population are screened by assessment of mutation rates by direct sequencing of the target sequences.
12. A method according to claim 1 or 8 , wherein cells of said cell population are screened by an immunofluorescence technique.
13. A method according to claim 1 , wherein said one or more DNA repair genes are Rad51 analogues and/or paralogues.
14. A method according to claim 1 , wherein the DNA repair genes are selected from the group consisting of Rad51b, Rad51c and analogues and/or paralogues thereof.