Methods and products for producing engineered mammalian cell lines with amplified transgenes

Abstract

Methods of inserting genes into defined locations in the chromosomal DNA of cultured mammalian cell lines which are subject to gene amplification are disclosed. In particular, sequences of interest (e.g., genes encoding biotherapeutic proteins) are inserted proximal to selectable genes in amplifiable loci, and the transformed cells are subjected to selection to induce co-amplification of the selectable gene and the sequence of interest. The invention also relates to meganucleases, vectors and engineered cell lines necessary for performing the methods, to cell lines resulting from the application of the methods, and use of the cell lines to produce protein products of interest.

1 - 19 . (canceled) 
     
     
         20 . A method for inserting an exogenous sequence into an amplifiable locus of a mammalian cell comprising:
 (a) providing a mammalian cell having an endogenous target site proximal to a selectable gene within the amplifiable locus, wherein the endogenous target site comprises:
 (i) a recognition sequence for an engineered meganuclease; 
 (ii) a 5′ flanking region 5′ to the recognition sequence; and 
 (iii) a 3′ flanking region 3′ to the recognition sequence; and 
   (b) introducing a double-stranded break between the 5′ and 3′ flanking regions of the endogenous target site;   (c) contacting the cell with a donor vector comprising from 5′ to 3′:
 (i) a donor 5′ flanking region homologous to the 5′ flanking region of the endogenous target site; 
 (ii) an exogenous sequence; and 
 (iii) a donor 3′ flanking region homologous to the 3′ flanking region of the endogenous target site; 
   
       whereby the donor 5′ flanking region, the exogenous sequence and the donor 3′ flanking region are inserted between the 5′ and 3′ flanking regions of the endogenous target site by homologous recombination to provide a modified cell. 
     
     
         21 . The method of  claim 20 , further comprising growing the modified cell in the presence of a compound that inhibits the function of the selectable gene to amplify the copy number of the selectable gene. 
     
     
         22 . The method of  claim 20 , wherein the exogenous sequence comprises a gene of interest. 
     
     
         23 . The method of  claim 20 , wherein the endogenous target site is downstream from the 3′ regulatory region of the selectable gene. 
     
     
         24 . The method of  claim 23 , wherein the endogenous target site is 0 to 100,000 base pairs downstream from the 3′ regulatory region of the selectable gene. 
     
     
         25 . The method of  claim 20 , wherein the endogenous target site is upstream from the 5′ regulatory region of the selectable gene. 
     
     
         26 . The method of  claim 25 , wherein the endogenous target site is 0 to 100,000 base pairs upstream from the 5′ regulatory region of the selectable gene. 
     
     
         27 . The method of  claim 20 , wherein the selectable gene is glutamine synthetase (GS) and the locus is methionine sulphoximine (MSX) amplifiable. 
     
     
         28 . The method of  claim 20 , wherein the selectable gene is dihydrofolate reductase (DHFR) and the locus is Methotrexate (MTX) amplifiable. 
     
     
         29 . The method of  claim 20 , wherein the selectable gene is selected from the group consisting of Dihydrofolate Reductase, Glutamine Synthetase, Hypoxanthine Phosphoribosyltransferase, Threonyl tRNA Synthetase, Na,K-ATPase, Asparagine Synthetase, Ornithine Decarboxylase, Inosine-5′-monophosphate dehydrogenase, Adenosine Deaminase, Thymidylate Synthetase, Aspartate Transcarbamylase, Metallothionein, Adenylate Deaminase (1,2), UMP-Synthetase and Ribonucleotide Reductase. 
     
     
         30 . The method of  claim 29 , wherein the selectable gene is amplifiable by selection with a selection agent selected from the group consisting of Methotrexate (MTX), Methionine sulphoximine (MSX), Aminopterin, hypoxanthine, thymidine, Borrelidin, Ouabain, Albizziin, Beta-aspartyl hydroxamate, alpha-difluoromethylornithine (DFMO), Mycophenolic Acid, Adenosine, Alanosine, 2′deoxycoformycin, Fluorouracil, N-Phosphonacetyl-L-Aspartate (PALA), Cadmium, Adenine, Azaserine, Coformycin, 6-azauridine, pyrazofuran, hydroxyurea, motexafin gadolinium, fludarabine, cladribine, gemcitabine, tezacitabine and triapine. 
     
     
         31 - 54 . (canceled) 
     
     
         55 . A recombinant meganuclease comprising a polypeptide having at least 75%, 85%, 90%, 95%, 97%, 98% or 99% sequence identity to SEQ ID NO: 9. 
     
     
         56 . The recombinant meganuclease of  claim 55 , having the sequence of the meganuclease of SEQ ID NO: 9. 
     
     
         57 . A recombinant meganuclease which recognizes and cleaves a recognition site having at least 75%, 85%, 90%, 95%, 97%, 98% or 99% sequence identity to SEQ ID NO: 7. 
     
     
         58 . The recombinant meganuclease of  claim 57 , wherein the meganuclease recognizes and cleaves a recognition site of SEQ ID NO: 7. 
     
     
         59 - 70 . (canceled)