Figures
Abstract
Mouse embryonic stem (ES) cells are derived from the inner cell mass of blastocyst stage embryos and are used primarily for the creation of genetically engineered strains through gene targeting. While some inbred strains of mice are permissive to the derivation of embryonic stem cell lines and are therefore easily engineered, others are nonpermissive or recalcitrant. Genetic engineering of recalcitrant strain backgrounds requires gene targeting in a permissive background followed by extensive backcrossing of the engineered allele into the desired strain background. The inbred mouse strain DBA/2J is a recalcitrant strain that is used as a model of many human diseases, including glaucoma, deafness and schizophrenia. Here, we describe the generation of germ-line competent ES cell lines derived from DBA/2J mice. We also demonstrate the utility of DBA/2J ES cells with the creation of conditional knockout allele for Endothelin-2 (Edn2) directly on the DBA/2J strain background.
Citation: Reinholdt LG, Howell GR, Czechanski AM, Macalinao DG, MacNicoll KH, Lin C-S, et al. (2012) Generating Embryonic Stem Cells from the Inbred Mouse Strain DBA/2J, a Model of Glaucoma and Other Complex Diseases. PLoS ONE 7(11): e50081. https://doi.org/10.1371/journal.pone.0050081
Editor: Anand Swaroop, National Eye Institute, United States of America
Received: July 26, 2012; Accepted: October 15, 2012; Published: November 27, 2012
Copyright: © 2012 Reinholdt et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by EY011721 (SWMJ), The Barbara and Joseph Cohen Foundation, The Pew Charitable Trust, Kathryn W. Davis and family, and donors of National Glaucoma Research – a program of the American Health Assistance Foundation (GRH). SWMJ is an Investigator of the Howard Hughes Medical Institute. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
The development of gene targeting technologies and the availability of a well-annotated mouse genome sequence allows the function of individual gene(s) to be assessed in a temporal and spatial manner. Historically, the resources for genetically engineering mice have been available for a limited number of strains, including C57BL/6J (B6) and 129Sv/ImJ (129), and are more recently emerging for C57BL/6N. Resources include ES cell lines, a vast number of null and conditional alleles through the Knockout Mouse Project (KOMP) and Cre driver lines to ablate the function of individual genes in specific cell types. A major advantage of the mouse as an animal model is the availability of well-characterized inbred strains that enable functional genomics on defined genetic backgrounds. Currently, however, exploiting the full utility of mice to study human diseases is hampered by the lack of gene targeting resources for multiple inbred mouse strains.
DBA/2J is a common inbred mouse strain critical in studying a diverse range of human diseases. For example, it is widely used as an inherited model of glaucoma. Glaucoma is a neurodegenerative disorder that affects 70 million people worldwide. Clinically, no treatments that specifically target retinal ganglion cell (RGC) death are in use, as the mechanisms involved are not well understood. However, we and others have used DBA/2J extensively to identify processes involved in glaucomatous RGC death and to test potential neuroprotective treatments for human glaucoma [1], [2], [3], [4], [5], [6], [7], [8], [9], [10], [11], [12]. Secondly, DBA/2J is used to model temporal lobe epilepsy (TLE) and schizophrenia (SZ) in combination. Psychotic episodes and cognitive impairment are among the most debilitating and common comorbidities of TLE, while SZ patients are more prone to seizures than the general population. To study the overlap between both disease pathologies animal models that combine epileptic seizures with select endophenotypes of schizophrenia are essential and DBA/2J is one of the few animal models that meet these criteria [13], [14]. Finally, DBA/2J is used to model other complex diseases including deafness, cardiovascular disease and host response to infections (e.g. [15], [16], [17], [18], [19]).
Phenotypes are often very different between mouse strains with diverse genetic backgrounds and the strain characteristics of DBA/2J are often contrasted with other genetically distinct inbred strains such as C57BL/6J. These defined genetic backgrounds provide an excellent system for mapping modifier genes [20], [21], [22]. To study these differences a number of DBA/2J-relevant resources have been generated. For instance, a genome-wide panel of congenic strains has been created that contain portions of DBA/2J chromosomes on a C57BL/6J background [23]. These 65 strains contain more than 95% of the DBA/2J genome. Also, DBA/2J is one parent in two sets of recombinant inbred lines that have been generated, AKXD (the other parent being AKR/J) and BXD (the other parent being C57BL/6J). Recombinant inbred (RI) strains such as these are especially useful for mapping complex traits, since they create an immortalized mapping population that allows researchers to phenotype as many animals per genome as desired over extended periods of time. AKXD strains have been used to study a variety of diseases including murine lymphoma and glaucoma [24], [25]. The more widely used BXD strains have been used to understand the genetics of a variety of diseases and biological systems including aging, the immune system and iron regulation [26], [27], [28], [29], [30]. Much of this work has been made available through GeneNetwork (formerly WebQTL) an on-line resource to study complex gene networks and phenotypes [31].
(A) In each round of derivation, 11–60% of embryos gave rise to stable embryonic stem cell lines (see also Table 1). (B) Approximately ∼20% of lines were male with normal chromosome counts, regardless of culture conditions. (C) All of the ES cell lines, regardless of culture conditions, expressed the essential pluripotency markers NANOG, SSEA-1 and OCT-3/4 (POU5F1).
(A–D) Representative images and FLOW analysis of 3i (AC175, A,C) and 1i lines (AC216, B,D) immunolabeled with an antibody to NANOG. Robust NANOG expression was characteristic of lines derived and cultured in 3i conditions.
Stable ES cell lines for gene targeting are available only for inbred strains from which stable ES cells lines can be consistently derived from the inner cell mass of blastocyst stage embryos. These permissive inbred strains include B6 and 129 derived strains [32], [33]. However, DBA/2J is one of many inbred strains that are considered recalcitrant to ES cell derivation because pluripotent embryonic stem cells (ES cells) are not easily derived [32], [33] from the inner cell mass of blastocyst stage embryos. Therefore, ES cell lines for gene targeting are simply not available. This severely hampers the ability to use DBA/2J mice to assess the role of specific genes in many human diseases. Previously, introducing mutant alleles into DBA/2J mice required targeting of the allele in an available ES cell line (usually B6- or 129-derived), followed by extensive backcrossing of the mutation to DBA/2J (for greater than 10 generations to replace the ES cell genome with a DBA/2J genome). Even after extensive backcrossing, a substantial interval of ES cell-derived DNA will remain surrounding the targeted gene, potentially confounding analysis of the phenotype.
DBA/2J ES cells were injected into C57BL/6J-derived blastocyst. Estimated percentage of coat derived from DBA/2J ES cells (dilute brown agouti) was used to determine the percent chimerism in each pup.
Previous attempts to derive ES cell lines from DBA/2J mice have failed and therefore the DBA/2J strain is considered to be recalcitrant to ES cell derivation [33]. However, recent advances in stem cell biology have revealed that embryonic stem cells derived from the inner cell mass of some strains and some species (like the laboratory rat) have a limited capacity to maintain pluripotency and self-renewal in culture without consistent inhibition of signaling pathways that promote early differentiation [34], [35]. Therefore, addition of small molecule inhibitors of fibroblast growth factor (FGF)/mitogen-activated protein kinase (MEK)/extracellular signal-related kinase pathways and of glycogen synthase kinase 3 (Gsk3) have proven highly effective for successful derivation of ES cells from rats and from a recalcitrant mouse strain (NOD) [36]. Taking advantage of this renewed understanding of ES cell pluripotency, we surmised that recalcitrance in DBA/2J is likely due to the same underlying differentiation pathways. By inhibiting these pathways we successfully derived germ line competent ES cells. Using these cells, we have generated the first engineered allele in the DBA/2J genome.
Methods
Mouse Strains, Breeding and Husbandry
All DBA/2J mice used in this study were obtained from either The Jackson Laboratory production facility (Bar Harbor, ME) or from our research colony. Our DBA/2J colony is routinely crossed with DBA/2J mice from The Jackson Laboratory production facility to prevent genetic drift. Mice were housed in a 14 h light to 10 h dark cycle under previously described conditions [37]. The Jackson Laboratory Animal Care and Use Committee approved all of the experiments in this study.
(A) A targeting construct was generated that included loxP sites flanking exon 2 (e2) of the Edn2 gene. Exon 2 contains part of the key functional domain for Edn2, and removal of exon 2 induces a frameshift for protein translation (B) Correct targeting at the 5′ end of the Edn2 gene was assessed using Xba1 restriction digests and southern blotting. The presence of the Neomycin (NEO) selectable marker incorporates an additional Xba1 restriction enzyme site in the targeted allele, generating a 6.6 kb fragment (Flox) compared to the normal 8.7 kb fragment (WT). Black arrows indicate clones correctly targeted at the 5′ end. (C) An example of a chimeric mouse generated as a result of injection of targeted DBA/2J ES cell clones into C57BL/6J blastocysts. (D–E) Chimeric male mice were mated with DBA/2J females and offspring genotyped for the heterozygous presence of the loxP sites in intron 1 (WT = 481 bp, Flox = 631 bp, see Methods). White arrows indicate mice that carry the floxed allele of Edn2. (D). See methods for primer information. As expected, 100% of heterozygous mutant offspring had the DBA/2J coat color (dilute brown agouti, E).
Generation of DBA/2J-derived ES Cells
Embryo harvest and inner cell mass (ICM) outgrowth.
Embryos from natural DBA/2J matings were collected at 3.5 days post coitum by flushing uteri with M2 medium (Millipore). Blastocysts were transferred directly to MEF feeder layers (cell cycle arrested mouse embryonic fibroblasts) in 4-well IVF (in vitro fertilization) culture dishes, 1–2 blastocysts per well. Morulae were cultured overnight in KSOM/M16 (Millipore) medium and the resulting blastocysts were transferred to MEF feeder layers the following day. Blastocysts were then cultured at 37°C, 5% CO2 for 8–10 days. During the first 4 days, blastocysts were undisturbed to allow for zona hatching and attachment of the embryos to the feeder layers. During days 5–10, the media were replaced every other day and inner cell mass (ICM) outgrowth was observed. The media conditions of ICM outgrowth were either ‘1i outgrowth media’ or ‘3i media’.
ES cell media.
DMEM (Dulbecco’s Modified Eagle’s Medium, 4500 mg/L glucose and sodium bicarbonate, without L-glutamine and sodium pyruvate, Sigma), 15% fetal calf serum (Lonza), penicillin (100 units)/streptomycin (100 µg) (Life Technologies), Glutamax (1X, Life Technologies), 0.1 mM beta-mercaptoethanol, non-essential amino acids (1X, Life Technologies), sodium pyruvate (1 mM, Life Tecnologies), leukemia inhibitory factor (LIF, ESGRO 1000 U/ml, Chemicon).
1i outgrowth media.
ES cell media (as described above) containing KOSR (knockout serum replacement, Life Technologies) in place of fetal calf serum, and PD98059 (MAP kinase inhibitor, 50 µM, Calbiochem [32]) with LIF (1000 U/ml).
3i media.
serum free media (as described in [34]] containing 3 inhibitors (PD17304 (FGF receptor tyrosine kinase inhibitor, 100 nM, Stemgent), PD0325901 (MEK kinase inhibitor, 1 µM, Stemgent) and CHIR99021 (glycogen synthase kinase-3 inhibitor, 3 µM)), and LIF (leukemia inhibitory factor, ESGRO 1000 U/ml, Chemicon).
Disaggregation and culture.
After 8–10 days, each outgrowth was given a unique identification number (AC###) and mechanically disaggregated. Disaggregated fragments were plated onto new MEF feeder layers in the same media type used for outgrowth (except for 1i media where KOSR was replaced with serum). After ∼2 days of growth, each emergent cell line was enzymatically dissociated using 0.05% trypsin EDTA (Life Technologies) and re-plated (P1). Light microscopy was used to monitor cell dissociation and trypsin exposure time was adjusted accordingly (usually 2–4 minutes depending on the culture conditions and cell line).
Emergent cell lines grown in 3i serum free media required less exposure (∼2 minutes) to 0.05% trypsin for dissociation and trypsin inhibition (using an equal volume of defined trypsin inhibitor, DTI, Life Technologies). Each cell line was expanded to P4 and any lines with overt differentiation or poor growth were discarded.
ES Cell Line Characterization
Karyotypic analysis.
ES cells were grown in 60 mm culture dishes until sub-confluent. Approximately 1–2 hours after media replacement, colcemid (0.02 mg/ml) was added to the media and the cells were incubated at 37°C, 5% CO2 for three hours. Cells were trypsinized, re-suspended by slow addition 0.56% KCl with constant agitation and incubated for 30–60 minutes. Cells were then fixed with ice-cold 3∶1 methanol:glacial acetic acid. Fixed cell suspensions were added dropwise to the surface of clean, moist glass slides and slides were air dried at 37°C for 1–2 days. Slides were mounted with Vectashield® hard set mounting reagent with DAPI (4′, 6-diamidino-2-phenylindole) (Vector Laboratories). A Spectral Karyotyping Microscope (SKY, Applied Spectral Imaging, Ltd.) was used to automatically scan slides for mitotic chromosome spreads and images were digitally captured. Chromosomes were counted in at least 40 well-spread, well-isolated nuclei and sex chromosomes were identified by morphology and distribution of heterochromatin (as assessed by DAPI, which preferentially binds A-T rich DNA).
Immunolabeling.
Sub-confluent ES cells were fixed with 4% paraformaldehyde (PFA) for 20 minutes and washed 3×5 minutes with phosphate buffered saline (PBS). Fixed cells were then blocked with 5% fetal bovine serum (FBS), 0.1% triton-X for 15 minutes, incubated with primary antibody for 4 hours and washed 3×5 minutes with PBS. Secondary antibody incubations were 2 hours, and subsequent washes were 3×5 minutes with PBS, incubation with DAPI (2 mg/ml) for 10 minutes and 2×5 minute washes with PBS. Primary antibodies were anti-OCT 3/4 (1∶250, Santa Cruz Biologicals, #sc-5279), anti-NANOG (1∶250, Abcam, #ab21603) and anti-SSEA-1 (1∶250, Santa Cruz Biologicals, #sc-21702). Secondary antibodies were goat anti-mouse IgG Alexa Fluor® 488 (1∶1000, Life Technologies) and goat anti-rabbit IgG Alexa Fluor® 488 (1∶1000, Life Technologies). All antibodies were diluted with PBS, 1% FBS. All incubations and washes were performed at room temperature with gentle rocking. Labeled cells were visualized and images were collected with a Zeiss Axio Observer Z1 inverted microscope and a Zeiss AxioCam CCD camera.
To prepare and immunolabel ES cells for flow cytometry, cells were washed, counted and fixed in 4% PFA (100 µl per 1×10∧6 cells) for 15 minutes at room temperature. Cells were then washed 2×5 minutes in PBS, 1% FBS and stored in 1 ml aliquots at 1×10∧6 cells/ml for up to 72 hours at 4°C. For antibody labeling, cells were transferred to 12×75 mm polypropylene tubes, permeabilized for 15 minutes (Perm/Wash Buffer, BD Biosciences), incubated with mouse Fc block (purified rat IgG2b anti-mouse CD16/CD32 monoclonal antibody, BD Biosciences) for 15 minutes, split and then incubated with either rat anti-Nanog Alexa Fluor® 647 (50 µg/ml, eBioscience) or rat IgG2a isotype control Alexa Fluor® 647 (eBioscience). Post-labeling washes were 2×5 minutes in PBS, 1% FBS and cells were resuspended in 400 µl of PBS, 1% FBS. Immunolabeled cells were then analyzed using a FACSCalibur flow cytometer (BD Biosciences).
Microinjection and Chimera Production for Parental ES Cell Lines
Each parental ES cell line (AC203, AC216, AC173 and AC175) was tested for germ line competence by microinjection. For each line, ∼12 ES cells were microinjected into 50 C57BL/6J (black, a/a, The Jackson Laboratory stock #00664) host blastocysts and 6 ES cells were injected into 8 cell C57BL/6J embryos by the laser assisted method using a Hamilton Thorne XYClone. Male coat color chimeras were generated from both injection methods. Male chimeras were bred to DBA/2J females (dilute brown, a/a Tyrp1b/Tyrp1b Myo5ad/Myo5ad, The Jackson Laboratory stock #000671) and germ line transmission of the DBA/2J ES cell line was assessed by calculating the % dilute brown offspring over three litters for each fertile male chimera.
Generation of EDN2 Targeting Construct, pMCS-EDN2-DTA
A Frt-Loxp (FL) was inserted in intron 1 and a LNL (Loxp-Neo-Loxp) cassette was inserted in intron 2 of Edn2 gene on a BAC clone (RP23-265J18) by BAC recombineering so that exon 2 of Edn2 gene was flanked by two loxp sites. A gene targeting vector, pMCS-EDN2-DTA, was constructed by retrieving a 10 kb long homology arm (5′ to FL), LNL, and a 2 kb short homology arm (end of LNL to 3′) into a plasmid vector carrying the DTA (Diphtheria toxin alpha chain) negative selection marker.
Targeting DBA/2J ES Cells with Edn2 Conditional Knockout Construct
Prior to targeting, the following parameters for DBA/2J ES cell line AC173 were established; geneticin sensitivity (150 µg/mL), required working concentration of trypsin inhibitor (0.25 mg/mL), and compatibility of serum free media with available MEF stocks (irradiated at passage 3 or lower). In preparation for electroporation, pMCS-EDN2-DTA was prepared using a mini-prep kit (Qiagen) and DNA linearized with NotI. Electroporation was performed using the BTX ECM 830 electroporator. Ten million DBA/2J ES cells (line AC173, P9) were electroporated with 20 µg of DNA at a concentration of 3.8 µg/uL. Cells were plated onto 60 mm dishes in 3i media. Selection with geneticin at 150 µg/mL was started the following day and continued for 9 days. Plates were then switched back to media not containing selection antibiotic until day 12 post electroporation. On day 12, colonies from half the 60 mm plates were picked, selecting each independent colony into a separate 96 well. Colonies from the remaining 60 mm plates were picked on day 13 for a total of 46 colonies. Clones were expanded into two sets of 96 well plates to allow for a stock freeze of one set of 96 well plates and lysate preparation for their duplicates for Southern blot screening. Clones were maintained on MEFs due to poor growth of the DBA/2J line in the absence of MEFs. A total of 43 clones were frozen.
Confirmation of Correct Targeting by Southern Blotting
For each of the 43 clones, Southern blotting was used to assess correct targeting of the 5′ end of the Edn2 locus. A 622bp 5′ probe was generated upstream of the Edn2 gene (forward primer, GATGTGGGTGGCCAGTGGC; reverse primer, GCTGGGAGCAGAGGCCAGGTG). DNA from each of the 43 clones was digested with Xba1. Correct integration of the targeting construct introduced a novel XbaI site to generate a 6.6 kb band after digestion compared to an 8.7 kb band for non-targeted clones. Five of the 43 clones were correctly targeted on the 5′ end (clones 5, 32, 33, 34, and 36), a targeting efficiency of approximately 11.5% of tested clones. For these five clones, Southern blotting was again used to assess correct targeting at the 3′ end. A 1001 bp 3′ probe was generated by PCR (forward primer, AGTAGACAGTGGACAGTTCC; reverse primer, CAAAAGTGTCCCAAGAGAACAGT). Correct integration of the targeting construct at the 3′ end disrupted an EcoRI site to generate a 16.2 kb band after digestion compared to a 15.2 kb band for non-targeted clones. Clones 33 and 36 were identified as properly targeted on both ends. (All primers shown 5′ to 3′).
Microinjection of Targeted Clones and Confirmation of Germ Line Transmission
For microinjection of EDN2-targeted AC173 ES cell lines, the correctly targeted clones (33 and 36) were thawed from 96 well plates to 12 well MEF plates using 3i media and injected into C57BL/6J blastocysts (∼12 ES cells per embryo). Both clones were at passage 22 at the time of injection. Passage number indicates the total number of trypsin exposures from the emergence of the ES cell line (see Disaggregation and culture above). In total, 149 injected blastocysts (approximately half from each of clone 33 and 36) were transferred into 13 pseudopregnant B6(Cg)-Tyr<c-2J>/J recipients (albino). For clone 33, 3 chimeric pups were produced (all male) and for clone 36, 2 chimeric pups (1 male and 1 female). Percentage chimerism ranged from 20–50% for both clones (based on coat color).
Mouse Genotyping
To determine the presence or absence of the EDN2flox allele, Edn2-Intron2-F (CATAGAGCGGTGAGGCCACAG) and Edn2-Intron2-R: (AAGTTGGCACCCTTGGTGTTC) primers were used. The primers amplify a region of intron 2 that includes the first loxP site (Edn2+ allele, 113bp; Edn2flox allele, 259bp).
Results
DBA/2J ES Cell Derivation
To define the most efficient protocol for derivation of ES cell lines from DBA/2J, we tested two media conditions that have been previously shown to promote ES cell derivation efficiency and ES cell pluripotency for other recalcitrant mouse strains. These media were tested in parallel over two rounds of derivation. The first medium, ‘1i’, was standard mouse ES cell medium, including LIF (leukemia inhibitory factor) and a single inhibitor of MAP kinase/ERK kinase, PD98059. This medium was previously shown to promote ES cell derivation efficiency from the recalcitrant CBA mouse strain [32]. More recently, several laboratories have had great success deriving ES cells not only from recalcitrant mouse strains (e.g. NOD), but also recalcitrant species (rat) by using defined serum free culture conditions combined with inhibitors of MEK kinase, FGF receptor tyrosine kinase and glycogen synthase kinase-3 [34], [35], [38]. Therefore, the second media condition, ‘3i’ was serum free media, including LIF and 3 inhibitors, PD17304 (FGF receptor tyrosine kinase inhibitor), PD0325901 (MEK kinase inhibitor, 1 µM, Stemgent) and CHIR99021 (glycogen synthase kinase-3 inhibitor) [34]. Finally, to promote growth of the inner cell mass and to minimize trophoblast differentiation, FBS was excluded from the 1i media during the inner cell mass (ICM) outgrowth stage.
Comparing Derivation Media
ES cell lines were derived from a total of 112 DBA/2J embryos over 2 rounds of derivation (derivation 1 and derivation 2) as shown in Table 1. Regardless of the media used, ES cell derivation efficiency (number of established ES cell lines/number of embryos) was comparable to permissive strains like C57BL/6J and significantly better than has been previously reported for DBA/2J, 1–6% [33]. From a total of 36 ES cell lines, 9 were euploid (>70% normal chromosome counts over 40 nuclei) male lines. These 9 lines were further characterized to select a subset of lines for germ line testing (Figure 1). All 9 ES cell lines showed expression of alkaline phosphatase and the pluripotency markers NANOG, SSEA-1 and OCT 3/4 (POU5F1), however ES cell lines that were derived and cultured in 1i medium showed variable expression of NANOG compared to ES cell lines derived and cultured in 3i medium. This variable expression was evident both qualitatively by immunofluorescence microscopy and quantitatively by flow cytometry, where a broad range of NANOG expression was consistently present in 1i cultures, including a fraction of ES cells with NANOG expression as low as background (Figure 2).
Assessing Chimerism and Germ Line Efficiency
The capacity of an ES cell line to contribute to the germ line of a chimeric animal is the gold standard test of pluripotency for mouse ES cell lines and a pre-requisite for any ES cell line to be used to generate genetically engineered mice. Four DBA/2J ES cell lines were selected for germ line testing based on media conditions (two 1i ES cell lines and two 3i ES cell lines), NANOG expression, and chromosome counts (those with the highest percent of euploid nuclei were favored). These were AC203 (1i, 86% euploid), AC216 (1i, 86% euploid), AC175 (3i, 78% euploid) and AC173 (3i, 86% euploid). All four ES cell lines successfully contributed to chimeras and to the germ line, as determined by coat color (Table 2, Figure 3). The 2 ES cell lines derived and grown in 3i conditions (AC175 and AC173) produced larger percentages of coat color chimeras upon injection into C57BL/6J host embryos, consistent with the more robust expression of the pluripotency factor NANOG in these ES cell lines (Table S1).
Testing Gene Targeting Efficiency in DBA/2J ES Cells
The DBA/2J strain is a widely used mouse model of glaucoma. Glaucoma is characterized by the degeneration of retinal ganglion cells and the degeneration of the optic nerve. We have shown previously that Endothelin-2 (Edn2), a component of the endothelin system is upregulated in monocytes and microglia-like cells in the retina and optic nerve during glaucoma [4], [5]. Given that no conditional allele was available for Edn2 on a DBA/2J background, Edn2 was selected as the gene of interest to assess targeting capabilities for the newly derived DBA/2J ES cells. A targeting construct was generated and used to target the AC173 ES cell line (one of the parental lines with robust NANOG expression and a high degree of chimerism in earlier tests, Figure 4). After targeting and subsequent colony expansion, 43 clones were assessed for correct targeting of the Edn2 locus. Five of the 43 clones (11%) were correctly targeted on the 5′ end, two of which were also correctly targeted on the 3′ end. These two clones (Edn2-clone33 and Edn2-clone36) were injected into C57BL/6J blastocysts and chimeric pups obtained. Chimerism for mice derived from either clone ranged from 20–50% (Table S1). Male chimeric mice were bred to DBA/2J females and approximately 50% of offspring were heterozygous for the conditional Edn2 allele. More than 20 mice heterozygous have been aged for 6–12 months. They have a healthy appearance with no gross adverse phenotypes or premature death.
Discussion
We have demonstrated that ES cells can be derived from DBA/2J mice and that these ES cells are competent to contribute to the germ line both at low passages and higher passages, post-targeting. Moreover, we report the first use of these DBA/2J ES cells to generate a genetically engineered mouse strain. While both media conditions used to derive DBA/2J ES cells favored successful derivation of germ line competent cells, serum free 3i media promoted more robust NANOG expression and higher percentages of coat color chimeras. This is likely due to inhibition of FGF signaling through more efficient inhibition of phospho-ERK combined with the restorative effects of glycogen synthase kinase inhibition [34]. A recent study indicates that inhibition of the FGF receptor tyrosine kinase through PD173074 is not necessary in combination with PD0325901, hence 2i media was equally effective for maintenance of pluripotency in ES cells [39]. Efficient inhibition of FGF signaling promotes the pluripotent ground state of embryonic stems cells, the hallmark of which is NANOG expression [40].
Serum free, 3i culture conditions are frequently used in the absence of MEFs feeder layers since the leukemia inhibitory factor provided by the MEF’s can instead be added to the culture medium. However, we found that in the absence of feeders, emergent ES cell lines in serum free, 3i medium were loosely adherent, despite the use of gelatin-coated plates. This made them subsequently difficult to manipulate during gene targeting. Therefore, MEF feeder layers were used throughout our derivation, culture and targeting of DBA/2J ES cells regardless of the culture media used. We found that use of low passage MEFs that have been previously screened for tolerance to serum free culture was critical for maintenance of our serum free, 3i DBA/2J ES cells, especially during drug selection post-targeting where feeder layers are exposed, long term to serum free culture conditions.
The availability of DBA/2J ES cells will enable genetic manipulation of genes of interest directly on a DBA/2J background. As we have shown with the Edn2 gene, it is possible to generate conditional alleles without the need for costly and time-consuming backcrossing from other genetic backgrounds (commonly C57BL/6J or 6N). Targeting constructs for many genes are available through the Knockout Mouse Project. Although many constructs were generated using C57BL/6N, many will be useful for generation of conditional alleles directly in DBA/2J ES cells. This will greatly aid in the ability to test the role(s) of specific genes of interest. Importantly, this ability means that no congenic interval that is derived from the original strain and that can confound experiments will surround the targeted gene.
In summary, the derivation of ES cells from DBA/2J mice will accelerate the ability to generate genetically engineered DBA/2J mice. These resources will aid in the understanding of and the development of improved therapies for a wide variety of human diseases including glaucoma, deafness and schizophrenia.
Supporting Information
Table S1.
Additional chimerism and germ line data transmission data, including laser assisted microinjection data.
https://doi.org/10.1371/journal.pone.0050081.s001
(XLSX)
Acknowledgments
The authors would like to thank Scientific Services at The Jackson Laboratory, in particular John Kulik, Stephanie Dion and Charles Lerner from Microinjection and Leslie Goodwin from Molecular Biology.
Author Contributions
Conceived and designed the experiments: LR GRH LRD SJ. Performed the experiments: LR GRH AC DM KM CSL. Analyzed the data: LR GRH SWMJ. Contributed reagents/materials/analysis tools: LR GH CSL LRD SWMJ. Wrote the paper: LR GH LRH SWMJ.
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