Published online 8 September 2004
Nucleic Acids Research, Vol. 32 No. 16 © Oxford University Press 2004; all rights reserved
Rapid tagging of endogenous mouse genes by recombineering and ES cell complementation of tetraploid blastocysts
Department of Biochemistry and Molecular Genetics, Schools of Medicine and Dentistry, University of Alabama at Birmingham, Birmingham, AL 35294, USA
* To whom correspondence should be addressed. Tel: +1 205 934 5294; Fax: +1 205 934 2889; Email: ttownes{at}uab.edu
Received July 16, 2004; Revised and Accepted August 20, 2004
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ABSTRACT |
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 TOP ABSTRACT INTRODUCTIONMATERIALS AND METHODSRESULTS AND DISCUSSIONCONCLUSIONSREFERENCES |
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The construction of knockin vectors designed to modify endogenous genes in embryonic stem (ES) cells and the generation of mice from these modified cells is time consuming. The timeline of an experiment from the conception of an idea to the availability of mature mice is at least 9 months. We describe a method in which this timeline is typically reduced to 3 months. Knockin vectors are rapidly constructed from bacterial artificial chromosome clones by recombineering followed by gap-repair (GR) rescue, and mice are rapidly derived by injecting genetically modified ES cells into tetraploid blastocysts. We also describe a tandem affinity purification (TAP)/floxed marker gene plasmid and a GR rescue plasmid that can be used to TAP tag any murine gene. The combination of recombineering and tetraploid blastocyst complementation provides a means for large-scale TAP tagging of mammalian genes.
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INTRODUCTION |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTS AND DISCUSSIONCONCLUSIONSREFERENCES |
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In recent years, protein–protein interactions in Saccharomyces cerevisiae have been studied on a genome-wide level (1–4). This large-scale approach is possible because endogenous, protein-encoding genes in yeast are easily tagged with sequences that facilitate protein complex purification. The high efficiency of homologous recombination in this organism permits modifications of endogenous genes with electroporated PCR products containing only 40 bp of homology. The modified genes are expressed at normal levels; therefore, physiologically relevant protein complexes are formed in vivo and these complexes can be easily purified.
Similar studies have not been performed in mammalian cells because the efficiency of homologous recombination is several orders of magnitude lower. Two novel technologies that have been developed in the past few years make large-scale tagging of mammalian genes possible. The first technology is recombineering. This method utilizes strains of Escherichia coli that contain inducible recombination (red) genes of bacteriophage 
to carry out efficient, homologous recombination between short, terminal homology regions on a PCR product and sequences on a bacterial artificial chromosome (BAC) (5,6). Several groups have used this technology to construct standard, conditional and knockin gene-targeting vectors for embryonic stem (ES) cell modifications (7,8).
The second technology is ES cell complementation of tetraploid embryos (9–11). This method allows mice to be cloned directly from ES cells. F1 hybrid ES cells are injected into tetraploid blastocysts and implanted into pseudopregnant foster mothers. The animals that are born after 18 days are derived totally from injected cells. If ES cells containing tagged genes are injected, primary tissues could be used directly for protein purification. In this paper, we combine recombineering and ES cell complementation of tetraploid blastocyts to produce knockin mice with a tagged allele in 3 months. The protocol is applicable to any mouse gene and provides a method for large-scale tagging of mouse genes.
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MATERIALS AND METHODS |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTS AND DISCUSSIONCONCLUSIONSREFERENCES |
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BAC transfer
The Erythroid Kruppel-like factor (EKLF) BAC DNA (75 kb) was purified from the E.coli strain DH10B by the miniprep method (12). Five hundred nanograms of this DNA was electroporated into the E.coli recombineering strain DY380 and chloramphenicol-resistant colonies were obtained. EKLF BAC DNA prepared from DH10B and DY380 was digested with EcoRI, KpnI and SalI and separated on agarose gels to confirm that no DNA rearrangements occurred.
Plasmids
The TAPR plamid was constructed by assembling DNA fragments containing tandem affinity purification (TAP) (1,13), floxed PGK/Hyg (14) and KanR. The gap-repair (GR) plasmid was constructed by inserting the MCI/TK gene (15) into pBlueScript (Stratagene). The sequence of these two plasmids and the plasmids themselves are available upon request.
Recombineering
The procedure for recombineering was essentially as described previously (5). E.coli DY380 harboring the EKLF BAC was grown at 30°C to an OD600 = 0.4–0.6 in Luria–Bertani Medium (LB) in the presence of 20 µg/ml chloramphenicol. The cells were then shifted to 42°C for 15 min to induce expression of recombination proteins Beta, Exo and Gam, followed by chilling in ice water for 10 min. Electrocompetent cells were prepared by washing the cells three times with 10% glycerol. Five hundred nanograms of PCR products were boiled for 1 min per 500 bp and then chilled in ice-cold water. The denatured DNA fragments were electroporated into 50 µl of ice-cold competent cells. After electroporation, 1 ml of LB medium was added to the cuvette, and the culture was incubated at 30°C for 3 h with shaking. The cells were then plated on selective media or pools of cells.
ES cell culture
V6.5 F1 hybrid ES cells (11) were maintained using standard methods (16).
Tetraploid blastocyst complementation
HA–EKLF–TAP mice were produced by tetraploid embryo complementation as described previously (10,11) with the following modifications. Briefly, B6D2F1 female mice (The Jackson Laboratory, Bar Harbor, ME) were hormonally ovulated and bred to stud B6D2F1 males. During the following morning, fertilized eggs were collected in M2 media (MR-015-D, Specialty Media, Phillipsburg, NJ) and incubated overnight at 37°C, 5% CO2 in KSOM plus amino acids media (MR-106-D, Specialty Media) to two-cell embryos. Two-cell diploid embryos were fused individually to produce one-cell tetraploid embryos using a 100 µs, 100 V pulse from a CF-150/B electrofuser (Biological Laboratory Equipments, Hungary) with hand-held, insulated electrodes in M2 media. Ninety-nine percent of the two-cell embryos were converted to one-cell tetraploid embryos within 45 min by this simple procedure. Tetraploid embryos were incubated at 37°C, 5% CO2 for 50 h to blastocysts in KSOM plus amino acids media. Approximately 90% of tetraploid embryos produced blastocysts with an excellent blastocoele cavity. The ES cells were injected into tetraploid blastocysts with the aid of a Piezo Impact Drive Unit micromanipulator (PMM-150FU, Primetech, Ibaraki, Japan). Injected tetraploid blastocysts were transferred to the uterus of pseudopregnant CD1® female recipients (Charles River Laboratories, Wilmington, MA). Approximately 10% of tetraploid blastocysts that were injected with genetically modified ES cells yielded live-born pups. Forty percent of these pups survived to adulthood. Approximately 25% of tetraploid balstocysts that were injected with unmodified V6.5 ES cells yielded live-born pups and 50% of these pups survived to adulthood.
Primers
The sequences of all the primers used in this paper are listed below. Primers for TAPR plasmid construction: Bam-TAP-F, 5'-GGAGGATCCATGGAAAAGAGAAGATG-3'; Bam-TAP-R, 5'-ACTGGATCCTCAGGTTGACTTCCCCGC-3'. Primers for HA tagging: HA-KLF-5', 5'-TAGCCCATGAGGCAGAAGAGAGAGAGGAGGCCTGAGGTCCAGGGTGGACACCAGCCAGCC-3'; KLF+79, 5'-AGTCCTCCTGGGTGTCCAGAA-3'. Primers for TAP tagging: KLF-L8-TAP-F2, 5'-tcgtcccttctgctgtggcctctgcccacgtgctttttcacgctctgaccacttagctctgcacatgaagcgtcacctcgcaggtgctggagccggtgcagggTCCATGGAAAAGAGAAGATG-3'; EKLF–TAP-R5, 5'-tataatggctcatcttttgggatacggtccttggatccactcttatttcatccccagtccttgtgcaggatcactcaTCGAATTCCTGCAGATAACTTC-3'. Primers for GR: pBSTK-GAP-F, 5'-ctctgtatagctttgactgtctgggaactcactctatagatcaggctggtTGACCATGATTACGCCAAGC-3'; pBSTK-GAP-R, 5'-cacagccattgagagaaactcacccaagaacttatgaggttcctgtggcaTCCGCTCACAATTCCACACAAC-3'. Primers for PCR screening: EKLF-F, 5'-GAGAGAAGCCTTATGCCTGC-3'; EKLF-R, 5'-TCTGGTGGTCTATATTGCTG-3'; KLF-188, 5'-AGACGCACACCACACACATA-3'; HA-R, 5'-AGTCGGGCACGTCGTAAG-3'; KLF+96, 5'-CCTCCCACACACTCACACT-3'; KLF-9F2, 5'-GCAGCAGCAGTAGTTTCATC-3'; TAP-R2, 5'-CGCCTGAGCATCATTTAG-3'; ES-R1, 5'-AGGGTCACCTAGTGCTTCCA-3'; Kan-F2, 5'-GCCTTCTTGACGAGTTCTT-3'.
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RESULTS AND DISCUSSION |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTS AND DISCUSSIONCONCLUSIONSREFERENCES |
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The generation of knockin mice in 3 months is illustrated by tagging the endogenous murine EKLF gene with HA and TAP (1,13). EKLF is a C2H2 zinc finger transcription factor that is essential for the globin gene regulation (17–20). To study the cellular localization of EKLF during development and to define protein complexes containing EKLF in primary mouse tissues, we inserted an HA tag at the 5' end and a TAP tag at the 3' end of the endogenous mouse EKLF gene. In this paper, we report the method utilized to produce HA/EKLF/TAP knockin mice rapidly. The overall strategy is illustrated in Figure 1.
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An EKLF BAC clone in DH10B was obtained from the BACPAC Resources Center at Children's Hospital Oakland Research Institute (CHORI). BAC DNA was purified and electroporated into E.coli DY380, which harbors the
phage red system (5,6). To insert a TAP tag (with an 8 amino acid linker) into the 3' end of the EKLF gene, two long oligonucleotides were used to amplify by PCR a TAPR (TAP Recombineering) plasmid containing the following cassette: linker/TAP/loxP-PGK/Hyg/KanR-loxP. The 5' 79 or 77 bases of the two primers are homologous to sequences either immediately upstream or immediately downstream of the EKLF stop codon (TGA) (Figure 1) and the 3' 20 or 22 bases are homologous to sequences at the ends of the TAPR cassette. The 3.9 kb PCR fragment was gel purified and electroporated into DY380/EKLF BAC after the induction of the recombination system by a 15 min incubation at 42°C. Thirty kanamycin-resistant colonies were obtained and PCR with primers EKLF-F and EKLF-R (Figure 2A) was used to identify homologous recombinants. As shown in Figure 2A, the 4084 bp band that was predicted for homologous recombinants was observed in four colonies. Twenty-one colonies contained only a 372 bp band and, therefore, were non-homologous recombinants. The remaining five clones were mixtures of homologous and non-homologous recombinants. Homologous recombinants were derived from these five clones when the original EKLF BAC was lost after further growth and isolation of single colonies. We then purified BAC DNA from the nine homologous recombinants and sequenced the TAP tag and the PGK/Hyg gene. Three of the nine BACs contained the correct sequences.
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An HA tag was inserted at the 5' end of the EKLF gene in one of these clones by recombineering. Two methods were used to prepare an HA DNA fragment for electroporation into DY380 cells containing the TAP-tagged EKLF BAC clone. First, a 202 bp fragment containing HA–(11 amino acid linker)–EKLF sequences was derived by PCR amplification of an HA–linker–EKLF plasmid (21). This fragment contained an HA–linker sequence plus 60 bp of homology upstream and 79 bp of homology downstream of the EKLF ATG. Second, a 148 bp fragment containing the HA–linker sequence plus 50 bp of homology upstream and downstream of the EKLF ATG was derived by annealing two partially overlapping 98 base oligonucleotides (48 base overlap) and by extending these primers with T4 DNA polymerase. The fragments were gel-purified and electroporated into DY380 cells containing the TAP-tagged EKLF BAC clone. Correctly recombineered BACs were identified by sib selection. Pools of 100 cells and 10 cells were prepared by serial dilution, expanded by overnight growth and screened by PCR for homologous recombinants using an EKLF upstream primer (KLF-188) and a primer from within the HA tag (HA-R). Data for the first method of HA tagging are shown in Figure 2A. All the 100-cell pools and 13 of the 32 10-cell pools were positive for homologous recombinants. Four of the 10-cell pools were streaked on plates and individual colonies were examined by PCR. Four homologous recombinants were identified and sequencing confirmed that three of these clones contained the correct HA sequence. A similar efficiency of homologous recombination was observed using the second HA tagging method (data not shown).
The modified gene (HA–EKLF–TAP) with 
6.0 kb of sequence upstream of HA and 1.0 kb of sequence downstream TAP was rescued from the HA–EKLF–TAP BAC clone by GR (Figure 1). The GR vector was a 5.0 kb DNA fragment generated by PCR amplification of a GR plasmid containing an ampicillin-resistance gene, a ColE1 replicon and a pMCI/TK gene (15). Two long primers were utilized for PCR. The 5' 50 bases of the two primers were homologous to sequences either 6.0 kb upstream of HA or 1.0 kb downstream of TAP and the 3' 20 or 22 bases were homologous to sequences at the ends of the linearized GR plasmid. The 5.0 kb PCR fragment was gel-purified and electroporated into induced DY380 containing the HA–EKLF–TAP BAC. Nine ampicillin/kanamycin-resistant colonies were picked and the DNA prepared from these colonies was digested with NotI, EcoRI, HindIII and XhoI. As shown in Figure 2B, the restriction patterns of all nine clones indicated that the 18.3 kb plasmid contained correctly captured HA–EKLF–TAP with the appropriate homology regions. Sequence analysis of the junctions between HA–EKLF–TAP and the GR plasmid vector in these clones confirmed that the predicted structure was produced (data not shown).
To replace the wild-type EKLF gene with HA–EKLF–TAP in ES cells, one of the capture plasmids was linearized by NotI digestion and electroporated into hybrid B6/129 F1 ES cell line V6.5 (11). After 8 days of selection in hygromycin and gancylovir, eight ES cell colonies were obtained. Genomic DNA from these colonies was analyzed by PCR with primers Kan-F2 and ES-R1. As shown in Figure 3A (ES 3' PCR), colonies designated ES5 and ES7 (lanes 10 and 12) produced a 1.6 kb band that is predicted for homologous recombination. PCR amplification of HA–EKLF–TAP BAC DNA was used as a positive control (lane 1), and PCR amplifications of linearized capture plasmid (lane 2) and wild-type V6.5 ES cell DNA (lane 3) served as negative controls.
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Correct targeting at the 5' end was assessed by PCR amplification of genomic ES cell DNA using a TAP primer (TAP-R2) and a primer (KLF-9F2) derived from the sequence upstream of the 6 kb homology (Figure 3A, ES 5' PCR). As expected, ES5 and ES7 (lanes 4 and 5) produced a 9.1 kb band which was identical to the one generated by the HA–EKLF–TAP BAC DNA control (lane 1). A 9.1 kb PCR fragment was not observed with wild-type V6.5 cell DNA (lane 2). Southern blot analysis of ES5 and ES7 DNA confirmed that one EKLF allele was replaced with HA–EKLF–TAP in these cells (Figure 3B). Lanes 4 (ES5) and 5 (ES7) of Figure 3B demonstrate that both ES cell clones contain the 4.1 kb wild-type allele and the 7.7 kb knockin allele. Control lanes 1 and 2 are the wild-type and knockin EKLF BAC DNA, respectively, and lane 3 is wild-type ES cell DNA.
Mice containing the HA–EKLF–TAP knockin allele were rapidly produced by the method of tetraploid embryo complementation. The production of mice by this method precludes the generation of chimeric mice that must be bred to demonstrate germline transmission. ES5 and ES7 cells were injected into tetraploid blastocysts and 121 of these blasts were transferred to the uteri of foster mothers. Twelve pups were born alive and five survived to adulthood. All were heterozygous for the HA–EKLF–TAP allele and no chimerism was observed. Each animal was derived entirely from the modified ES cells.
All the steps described above were completed in 3 months. To demonstrate that HA–EKLF–TAP is functional in vivo, we derived mice that were homozygous for the knockin. Heterozygous HA–EKLF–TAP males were bred to C57B6 females that express CRE recombinase from the cytomegalovirus promoter and the offspring were mated. Tail DNA from one litter of six pups was analyzed by PCR with 5' primers KLF-188 and KLF+96, and the results are illustrated in Figure 4A (lanes 4–9). One of six pups was homozygous for HA–EKLF–TAP (lane 7). The six tail DNAs were also analyzed by PCR with 3' primers EKLF-F and EKLF-R (lanes 6–11, Figure 4A). The segregation pattern was the same as observed above, and the same pup was homozygous for HA–EKLF–TAP (lane 9). Multiple litters were genotyped and, as expected, one-fourth of the pups were homozygous for HA–EKLF–TAP. Blood smears and hematological values (data not shown) were normal in these animals; therefore, HA–EKLF–TAP is functional in vivo.
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Western Blot analysis of bone marrow cell extracts with an anti-HA monoclonal antibody confirmed HA–EKLF–TAP expression. Bone marrow cells from wild-type and HA–EKLF–TAP homozygous mice were separated into Ter119+ and Ter119– fractions on a MACS column (Miltenyi Biotech) using anti-Ter119 antibody linked to magnetic beads. Whole-cell protein extracts from these cells were analyzed. As shown in Figure 4B, two bands with molecular weights of
65 and 70 kDa were detected in the Ter119+ bone marrow cell fraction from HA–EKLF–TAP mice (lane 5) but not in Ter119+ cells from wild-type mice (lane 3). Low levels of the HA–EKLF–TAP doublet were also observed in the Ter119– fraction from HA–EKLF–TAP mice (lane 4). Similar bands were detected in a positive control sample derived from COS cells transfected with a HA–EKLF–TAP cDNA clone, pDZ17 (lane 2), but no protein was detected in whole-cell extracts prepared from COS cells transfected with a control vector pSG5 (lane 1). These results demonstrate that EKLF is expressed predominately in Ter119+ hematopoietic cells from the bone marrow. The cellular localization of EKLF in bone marrow cells was tested by immunofluorescence microscopy. Bone marrow cells were prepared from wild-type and HA–EKLF–TAP homozygous mice and stained with PE-conjugated anti-Ter119 antibody. Ter119+ cells were then purified by FACS sorting, and stained with FITC-conjugated anti-HA monoclonal antibody. Figure 4C illustrates fluorescent, digital sections of these cells. The bottom left panel, which illustrates the merge of Hoechst, anti-Ter119-PE and anti-HA-FITC stains, demonstrates that HA–EKLF–TAP is localized in the nucleus in adult bone marrow erythroid cells.
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CONCLUSIONS |
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TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTS AND DISCUSSIONCONCLUSIONSREFERENCES |
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The combination of recombineering and tetraploid blastocyst complementation (5,6,10,11) provides a method to produce knockin mice in 3 months. The novel plasmids described in this paper permit rapid TAP tagging of any gene in the murine genome. We anticipate that the use of this strategy will enable large-scale tagging of mouse genes and systematic identification of protein complexes during development.
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ACKNOWLEDGEMENTS |
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We thank Dr Don Court for the E.coli recombineering strain DY380. We are grateful to Dr Rudolf Jaenisch for the V6.5 ES cells and members of the Townes laboratory for helpful discussions. This work was supported by NHLBI grants to T.M.R. and T.M.T., and a NIGMS grant to N.P.H.
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