Efficient generation of expression cell lines through the use of scorable homeostatic reporter genes
The present invention provides methods for site-specific recombination in a cell, as well as vectors which can be employed in such methods. The methods and vectors of the present invention can be used to obtain persistent gene expression in a cell and to modulate gene expression. One preferred method according to the invention comprises contacting a cell with a vector comprising an origin of replication functional in mammalian cells located between first and second recombining sites located in parallel. Another preferred method comprises, in part, contacting a cell with a vector comprising first and second recombining sites in antiparallel orientations such that the vector is internalized by the cell. In both methods, the cell is further provided with a site-specific recombinase that effects recombination between the first and second recombining sites of the vector.
1 . A cellular expression system comprising:
a. at least one integration cassette comprising
i. a promoter operably linked to
ii. an exchangeable reporter segment comprising a scorable homeostatic reporter element, which comprises at least one scorable reporter gene, the scorable homeostatic reporter element linked at its 5′ end to a first frt recombinase recognition site, and at its 3′ end to a second frt recombinase recognition site;
wherein the integration cassette is capable of stable and random insertion into one or more discrete genomic positions in a host cell, thereby creating a recombinant cell population;
b. at least one target cassette comprising an exchangeable target segment comprising:
i. a third frt recombinase recognition site, capable of recognizing the first frt recombinase recognition site in the integration cassette;
ii. a target element; and
iii. a fourth frt recombinase recognition site, capable of recognizing the second frt recombinase recognition site in the integration cassette;
wherein the target element is linked at its 5′ end to the third frt recombinase recognition site, and at its 3′ end to the fourth frt recombinase recognition site; and
c. at least one rec element encoding FLP recombinase activity recognizing the frt recombinase recognition sites of a and b,
wherein introduction of the rec element and the target cassette to the recombinant cell population results in site-specific substitution of the exchangeable reporter segment with the exchangeable target segment at one or more discrete genomic positions.
2 . The cellular expression system of claim 1 , in which the rec element is included in the integration cassette.
3 . The cellular expression system of claim 1 in which the rec element is included in the target cassette.
4 . The cellular expression system of claim 1 in which the scorable reporter gene encodes a scorable homeostatic reporter selected from the group consisting of CD4 and/or CD8.
5 . The cellular expression system of claim 1 in which the host cell is selected from the group consisting of mammalian cells, yeast cells, or bacterial cells.
6 . The cellular expression system of claim 1 in which the integration cassette further comprises a polycistronic element.
7 . The cellular expression system of claim 1 in which the integration cassette further comprises an internal ribosome entry site (IRES) sequence.
8 . The cellular expression system of claim 1 in which the integration cassette further comprises a tag.
9 . The cellular expression system of claim 1 in which the target element further comprises a target gene and a selectable marker gene.
10 . The cellular expression system of claim 1 in which the target cassette further comprises a polycistronic element.
11 . The cellular expression system of claim 1 in which the target cassette further comprises a tag.
12 . The cellular expression system of claim 1 further comprising a second integration cassette and a second target cassette.
13 . The cellular expression system according to claim 12 , wherein
a. the second integration cassette comprises
i. a promoter operably linked to
ii. an exchangeable reporter segment comprising a scorable homeostatic reporter element, which comprises at least one scorable reporter gene, the scorable homeostatic reporter element linked at its 5′ end to a fifth frt recombinase recognition site, and at its 3′ end to a sixth frt recombinase recognition site;
wherein the second integration cassette is capable of stable and random insertion into one or more discrete genomic positions in a host cell, thereby creating a recombinant cell population; and
b. the second target cassette comprises an exchangeable target segment comprising:
i. a seventh frt recombinase recognition site, capable of recognizing the fifth frt recombinase recognition site in the second integration cassette;
ii. a target element; and
iii. an eighth frt recombinase recognition site, capable of recognizing the sixth frt recombinase recognition site in the second integration cassette;
wherein the target element is linked at its 5′ end to the seventh frt recombinase recognition site, and at its 3′ end to the eighth frt recombinase recognition site
14 . The cellular expression system according to claim 12 in which a rec element is included in the second integration cassette or in the second target cassette.
15 . The cellular expression system of claim 12 in which each of the target elements encodes one subunit of a protein complex.
16 . The cellular expression system of claim 15 in which the protein complex is an antibody.
17 . A method for selecting a transformed cell population, comprising:
a. introducing the integration cassette as in claim 1 (a) into a population of host cells to create a transformed cell population, wherein each cell of the transformed population comprises at least one integration cassette stably inserted at one or more discrete genomic positions;
b. scoring the level of expression of the scorable homeostatic reporter element in one or more cells of the transformed host cell population; and
c. selecting from the transformed host cell population one or more cells scoring a predetermined level of expression.
18 . The method of claim 17 , wherein the population of host cells is selected from the group consisting of mammalian cells, yeast cells, or bacterial cells.
19 . The method of claim 17 , further comprising isolating a single cell from the population of transformed cells scoring a predetermined level of expression for the scorable homeostatic reporter element, and expanding the single cell to form a clonal cell population, wherein said integration cassette is stably inserted at the same discrete genomic position within each cell of the clonal cell population.
20 . The method of claim 17 , further comprising introducing to the clonal cell population:
a. a first target cassette as in claim 1 (b); and
b. a rec element encoding FLP recombinase activity recognizing the frt recognition sites of the integration cassette and the target cassette;
wherein the exchangeable target segment is substituted for the exchangeable reporter segment.