Methods for the genetic modification of endogenous genes in animal cells by homologous recombination

• US 5,614,396 A
• Filed: 02/22/1994
• Issued: 03/25/1997
• Est. Priority Date: 06/14/1990
• Status: Expired due to Fees

• Current Assignee: Baylor College of Medicine (Baylor College)
• Original Assignee: Baylor College of Medicine (Baylor College)
• Inventors: Davis, Ann, Hasty, Paul, Bradley, Allan
• Primary Examiner(s): Crouch, Deborah
• Application Number:
  US08/200,011
• Time in Patent Office: 1,127 Days
• Field of Search: 435/240.1, 435/172.3, 800/2, 935/71
• US Class Current: 435/463
• CPC Class Codes: A01K 2217/05 Animals comprising random inserted nucleic acids (transgenic)
• CPC Class Codes: A01K 67/0275 Genetically modified vertebrates, e.g. transgenic
• CPC Class Codes: C12N 15/8213 Targeted insertion of genes into the plant genome by homologous recombination
• CPC Class Codes: C12N 15/902 using homologous recombination

Abstract

A method for producing animal cells, chimeric or transgenic non-human animals which contain a desired gene sequence inserted into a predetermined gene sequence. The method permits the production of animal cells and non-human animals which have subtle and precise modifications of gene sequence and expression relative to natural non-human animals.

Claims

1. A method for producing a desired mammalian cell which contains a desired gene sequence inserted within a predetermined gene sequence of said cell'"'"'s genome, which method comprises:

A. introducing into a mammalian cell a DNA molecule comprising;

i) said desired gene sequence;

ii) two regions of homology which flank said desired gene sequence wherein said regions are sufficiently homologous with said predetermined gene sequence to undergo homologous recombination with said predetermined gene sequence of said mammalian cell; and

iii) at least one selectable gene sequence located within said regions of homology which flank said desired gene sequence, wherein the presence of at least on selectable gene sequence in said mammalian cell can be selected for by culturing said mammalian cell under a set of selective culture conditions;

B. permitting said introduced DNA molecule to undergo homologous recombination with said predetermined gene sequence of said mammalian cell to produce an intermediate cell, wherein said desired gene sequence has been inserted into said mammalian cell; and

C. recovering said intermediate cell by culturing said intermediate cell under said selective culture conditions;

D. culturing said intermediate cell under conditions such that said intermediate call undergoes intrachromosomal recombination or sister chromated exchange, wherein said at least one selectable gene sequence is deleted from the cell'"'"'s genome and said desired mammalian cell is produced; and

E. recovering said desired mammalian cell.

2. The method of claim 1, wherein said mammalian cells are deficient in HPRT enzyme, wherein said at least one selectable polynucleotide sequence codes for an active HPRT enzyme, and wherein said first set of selective culture conditions comprise conditions in which the presence of an active HPRT enzyme in said mammalian cells is required for growth.

3. The method of claim 1, wherein said mammalian cells are deficient in APRT enzyme, wherein said at least one selectable polynucleotide sequence codes for an active APRT enzyme, and wherein said first set of selective culture conditions comprises conditions in which the presence of an active APRT enzyme in said mammalian cells is required for growth.

4. The method of claim 1, wherein said mammalian cells are deficient in thymidine kinase enzyme, wherein said at least one selectable polynucleotide sequence codes for an active thymidine kinase enzyme, and wherein said first set of selective culture conditions comprises conditions in which the presence of an active thyroidins kinase enzyme in said mammalian cells is required for growth.

5. The method of claim 1, wherein said first selectable polynucleotide expresses an active HPRT enzyme, and said first set of selective culture conditions comprises incubation of said cell in the presence of HAT medium.

16. The method of claim 1, 6 or 11, wherein said DNA molecule is introduced into said mammalian cells by subjecting said mammalian cells and said DNA molecule to electroporation.

17. The method of claim 1, 6 or 11, wherein said desired polynucleotide is a human analog of said predetermined sequence of said mammalian cells.

6. A method for producing a desired mammalian cell which contains a desired gene sequence inserted within a predetermined gene sequence of said cell'"'"'s genome, which method comprises:

A. introducing into a mammalian cell a DNA molecule comprising;

i) said desired gene sequence;

ii) two regions of homology which flank said desired gene sequence wherein said regions are sufficiently homologous with said predetermined gene sequence to undergo homologous recombination with said predetermined gene sequence of said mammalian cell; and

iii) at least one selectable gene sequence located within said regions of homology which flank said desired gene sequence wherein presence of least one selectable gene sequence in said mammalian cell can be selected against by culturing said cell under a set of selective culture conditions;

B. permitting said introduced DNA molecule to undergo homologous recombinantion with said predetermined gene sequence of said mammalian cell to produce an intermediate cell, wherein said desired gene sequence has been inserted into said predetermined gene sequence;

C. culturing said intermediate cell thereby permitting said intermediate cell to undergo intrachromosomal recombination or sister chromatid exchange to produce a population of cells;

D. culturing said population of cells under said set of selective culture conditions, wherein said at least one selectable gene sequence is deleted from the genome of the desired mammalian cell; and

E. recovering said mammalian cell.

7. The method of claim 6, wherein said mammalian cells are deficient in HPRT enzyme wherein said at least one selectable polynucleotide sequence codes for an active HPRT enzyme, and wherein said first set of selective culture conditions comprises conditions in which the absence of an active HPRT enzyme in said mammalian cells is required for growth.

8. The method of claim 6, wherein said mammalian cells are deficient in APRT enzyme, wherein said at least one selectable polynucleotide sequence codes for an active APRT enzyme, and wherein said first set of selective culture conditions comprises conditions in which the absence of an active APRT enzyme in said mammalian cells is required for growth.

9. The method of claim 6, wherein said mammalian cells are deficient in thyroidine kinase enzyme, wherein said at least one selectable polynucleotide sequence codes for an active thyroidins kinase enzyme, and wherein said first set of selective culture conditions comprises conditions in which the absence or an active thymidine kinase enzyme in said mammalian cells is required for growth.

10. The method of claim 6, wherein said first selectable polynucleotide expresses active HPRT enzyme, and said first set of selective culture conditions comprises incubation of said cell in the presence of 6-thioguantne.

11. A method for producing a desired mammalian cell which contains a desired non-selectable gene sequence inserted within a predetermined gene sequence of said cell'"'"'s genome, which method comprises:

A) introducing into a mammalian cell under non-selective culture conditions a DNA molecule comprising;

i) said desired non-selectable gene sequence;

ii) two regions of homology which flank said desired nonselectable gene sequence wherein said regions are sufficiently homologous with said predetermined gene sequence to undergo homologous recombination with said predetermined gene sequence of said mammalian cell; and

iii) at least two selectable gene sequences located within said regions of homology which flank said desired non-selectable gene sequence, wherein the presence of at least one selectable gene sequence in said mammalian cell can be selected for by culturing said mammalian cell under a first set of selective culture conditions, and wherein the presence of least one selectable gene sequence in said mammalian cell can be selected against by culturing said cell under a second set of selective conditions;

B. permitting said introduced DNA molecule to undergo homologous recombination with said predetermined gene sequence of said mammalian cell to produce an intermediate cell, wherein said desired on-selectable gene sequence has been inserted into said predetermined gene sequence;

C. recovering said intermediate cell by culturing said intermediate cell under said first set of culture conditions;

D. culturing said intermediate call under non-selective conditions thereby permitting said intermediate cell to undergo intrachromosomal recombination or sister chromatid exchange or produce a population or cells;

E. culturing said population of cells under said second set of selective conditions to produce desired mamma cell; and

F. recovering said desired mammalian cell, wherein said desired mammalian cell has said at least two selectable gene sequences deleted from their genome.

12. The method of claim 11, wherein said mammalian cells are deficient m HPRT enzyme, wherein said at least one selectable polynucleotide sequence codes for an active HPRT enzyme, and wherein said first set of selective culture conditions comprises conditions in which the presence of an active HPRT enzyme in said mammalian cells is required for growth, and wherein said second set of selective culture conditions comprises conditions in which the absence of an active HPRT enzyme in said intermediate cells is required for growth.

13. The method of claim 11, wherein said mammalian cells are deficient in APRT enzyme wherein said at least one selectable polynucleotide sequence codes for an active APRT enzyme, and wherein said first set of selective culture conditions comprises conditions in which the presence of an active APRT enzyme in said mammalian cells is required for growth, and wherein said second set of selective culture conditions comprises conditions in which the absence of an active APRT enzyme in said intermediate cells is required for growth.

14. The method of claim 11, wherein said mammalian cells are deficient in thymidine kinase enzyme, wherein said at least one selectable polynucleotide sequence codes for an active thymidine kinase enzyme, and wherein said first set of selective culture conditions comprises conditions in which the presence of an active thyroidins kinase enzymes in said mammalian cells is required for growth, and wherein said second set of selective culture conditions comprises conditions in which the absence of an active thymidine kinase enzyme in said intermediate cells is required for growth.

15. The method of claim 11, wherein said first selectable polynucleotide expresses an active HPRT enzyme, and said first set of selective culture conditions comprises incubation or said cell in the presence of HAT medium, and wherein said second set of selective culture conditions comprises incubation of said coil in the presence of 6-thioguanine.

18. A method of producing a desired pluripotent animal cell which contains a desired gene sequence inserted within a predetermined gene sequence of said cell'"'"'s genome, method comprises:

A. introducing into a pluripotent animal cell a DNA molecule comprising;

i) said desired gene sequence;

ii) regions of homology which flank said gene sequence wherein said regions re sufficiently homologous with said predetermined gene sequence to undergo homologous recombination with said predetermined sequence of said pluripotent animal cell; and

iii) at least one selectable gene sequence located within said regions of homology which flank said desired gene sequence, wherein presence of at least one selectable gene sequence in said pluripotent animal cell can be selected for by culturing said under a set of selective culture conditions;

B. permitting said introduced DNA molecule to undergo homologous recombination with said predetermined gene sequence of said Pluripotent animal cell to produce an intermediate cell, wherein said desired gene sequence has been inserted into said predetermined gene sequence;

C. recovering said intermediate cell by culturing said intermediate cell under said selective culture conditions;

D. culturing said intermediate cell under conditions such that said intermediate cell undergoes intrachromosomal recombination or sister chromatid exchange, wherein said at least one selectable gene sequence is deleted from the cell'"'"'s genome and said desired pluripotent animal cell is produced;

E. recovering said desired pluripotent animal cell.

19. The method of claim 18, wherein said pluripotent animal cells are deficient in HPRT enzyme, wherein said at least one selectable polynucleotide sequence codes for an active HPRT enzyme, and wherein said first set of selective culture conditions comprises conditions in which the presence of an active HPRT enzyme in said pluripotent animal cells is required for growth.

20. The method of claim 18, wherein said pluripotent animal cells are deficient in APRT enzyme, and wherein said at least one selectable polynucleotide sequence codes for an active APRT enzyme, and wherein said first set of selective culture conditions comprises conditions in which the presence of an active APRT enzyme in said pluripotent animal cells is required for growth.

21. The method of claim 18, wherein said pluripotent animal cells are deficient in thymidine kinase enzyme, wherein said at least one selectable polynucleotide sequence culture for an active thyroidins kinase enzyme, and wherein said first set of selective culture conditions comprises conditions in which the presence of an active thyroidine kinase enzyme in said pluripotent animal cells is required for growth.

22. The method of claim 18, wherein said first selectable polynucleotide expresses an active HPRT enzyme, and said first set of selective culture conditions comprises incubation or said cell in the presence of HAT medium.

23. A method of introducing a desired pluripotent animal cell which contains a desired gene sequence inserted within a predetermined gene sequence of said cell'"'"'s genome, which method comprises:

A. introducing into a pluripotent animal cell a DNA molecule comprising;

i) said desired gene sequence;

ii) two regions of homology which flank said desired gene sequence wherein said regions are sufficiently homologous with said predetermined gene sequence to undergo homologous recombination with said predetermined gene sequence of said pluripotent animal cell; and

iii) at least one selectable gene sequence located within said regions of homology which flank said desired non-selectable gene sequence, wherein the presence of least one selectable gene sequence in said pluripotent animal cell can be selected against by culturing said cell under a set of selective culture conditions;

B. permitting said introduced DNA molecule to undergo homologous recombination with said pluripotent animal cell to produce an intermediate cell, wherein said desired gene sequence has been inserted into said predetermined gene sequence;

C. culturing said intermediate cell thereby permitting said intermediate cell to undergo intrachromosomal recombination or sister chromatid exchange or produce a population of cells;

D. culturing said population of cells under said set of selective culture conditions, wherein said at least one selectable gene lens sequence is deleted from the genome of the desired mammalian cell, and

E. recovering said desired pluripotent animal cell.

24. The method of claim 23, wherein said pluripotent animal cells are deficient in HPRT enzyme, wherein said at least one selectable polynucleotide sequence codes for an active HPRT enzyme, and wherein said first set of selective culture conditions comprises conditions in which the absence of an active HPRT enzyme in said pluripotent animal of cells is required for growth.

25. The method of claim 23, wherein said pluripotent animal cells are deficient in APRT enzyme, wherein said at least one selectable polynucleotide sequence codes for an active APRT enzyme, and wherein said first set of selective culture conditions comprises conditions in which the absence of an active APRT enzyme in said pluripotent animal cells is required for growth.

26. The method of claim 23, wherein said pluripotent animal cells are deficient in thymidine kinase enzyme, wherein said at least one selectable polynucleotide sequence codes for an active thyroidins kinase enzyme, and wherein said first set of selective culture conditions comprises conditions in which the absence of an active thymidine kinase enzyme in said pluripotent animal cells is required for growth.

27. The method of claim 23, wherein said first selectable polynucleotide expresses an active HPRT enzyme, and said first set of selective culture conditions comprises incubation or said cell in the presence of 6-thioguanine.

28. A method for producing a desired pluripotent cell which contains a desired non-selectable gene sequence inserted within a predetermined gene sequence of said cell'"'"'s genome, which method comprises:

A introducing into a pluripotent animal cell under non-selective culture conditions a DNA molecule comprising;

i) said desired non-selectable gene sequence;

ii) two regions of homology which flank said desired nonselectable gene sequence wherein said regions are sufficiently homologous with said predetermined gene sequence to undergo homologous recombination with said predetermined gene sequence of said mammalian cell; and

iii) at least two selectable gene sequences located within said regions homology which flank said desired non-selectable gone sequence, wherein the presence of at least one selectable gene sequence in said mammalian cell can be selected for by culturing said mammalian cell under a first set or selective culture conditions, can be selected against by culturing said cell under a second set of selective conditions;

B. permitting said introduced DNA molecule to undergo homologous recombination with said predetermined gene sequence of said pluripotent animal cell to produce an intermediate cell, wherein said desired non-selectable gene sequence has been inserted into said predetermined gene sequence;

C. recovering said intermediate cell by culturing said intermediate cell under said first set of culture conditions;

D. culturing said intermediate cell under non-selective conditions thereby permitting said intermediate cell to undergo intrachromosomal recombination or sister chromatid exchange or produce a population of cells;

E. culturing said population of cells under said second set of selective conditions to produce said desired pluripotent animal cell; and

F. recovering said desired pluripotent animal cell, wherein said desired pluripotent animal cell has said at least two selectable gene sequences deleted from their genome.

29. The method of claim 28, wherein said pluripotent animal cells are deficient in HPRT enzyme, wherein said at least one selectable polynucleotide sequence codes for an active HPRT enzyme, and wherein said frost set of selective culture conditions comprises conditions in which the presence of an active HPRT enzyme in said pluripotent animal cells is required for growth, and wherein said second set of selective culture conditions comprises conditions in which the absence of an active HPRT enzyme in said intermediate cells is required for growth.

30. The method of claim 28, wherein said pluripotent animal cells are deficient in APRT enzyme, wherein said at least one selectable polynucleotide sequence codes for an active APRT enzyme, and wherein said first set of selective culture conditions comprise conditions in which the presence of an active APRT enzyme in said pluripotent animal cells is required for growth, and whereto said second set of selective culture conditions comprises conditions in which the absence of an active APRT enzyme in said intermediate cells is required for growth.

31. The method of claim 28, wherein said pluripotent animal cells are deficient in thymidine kinase enzyme, wherein said at least one selectable polynucleotide sequence codes for an active thyroidins kinase enzyme, and wherein said first set of selective culture conditions comprises conditions in which the presence of an active thyroidine kinase enzyme in said pluripotent animal cells is required for growth, and wherein said second set of selective culture conditions comprises conditions in which the absence of an active thyroidins kinase enzyme in said intermediate cells is required for growth.

32. The method of claim 28, wherein said first selectable polynucleotide expresses an active HPRT enzyme, and said first set of selective culture conditions comprises incubation of said pluripotent animal cell in the presence of hypoxanthine, and wherein said second set of selective culture conditions comprises incubation of said intermediate cell in the presence of 6-thioguanine.