Original Research ARTICLE
Screening for stress-resistance mutations in the mouse
- 1Department of Cell and Developmental Biology, University of Colorado Denver, Aurora, CO, USA
- 2Charles C. Gates Regenerative Medicine and Stem Cell Biology Program, University of Colorado Denver, Aurora, CO, USA
- 3Department of Pediatrics, University of Colorado Denver, Aurora, CO, USA
- 4Department of Integrative Physiology, University of Colorado Boulder, Boulder, CO, USA
- 5Institute for Behavioral Genetics, University of Colorado Boulder, Boulder, CO, USA
- 6Biofrontiers Institute, University of Colorado Boulder, Boulder, CO, USA
Longevity is correlated with stress resistance in many animal models. However, previous efforts through the boosting of the antioxidant defense system did not extend life span, suggesting that longevity related stress resistance is mediated by other uncharacterized pathways. We have developed a high-throughput platform for screening and rapid identification of novel genetic mutants in the mouse that are stress resistant. Selection for resistance to stressors occurs in mutagenized mouse embryonic stem (ES) cells, which are carefully treated so as to maintain pluripotency for mouse production. Initial characterization of these mutant ES cells revealed mutations in Pigl, Tiam1, and Rffl, among others. These genes are implicated in glycosylphosphatidylinositol biosynthesis, NADPH oxidase function, and inflammation. These mutants: (1) are resistant to two different oxidative stressors, paraquat and the omission of 2-mercaptoethanol, (2) have reduced levels of endogenous reactive oxygen species (ROS), (3) are capable of generating live mice, and (4) transmit the stress resistance phenotype to the mice. This strategy offers an efficient way to select for new mutants expressing a stress resistance phenotype, to rapidly identify the causative genes, and to develop mice for in vivo studies.
Stress resistance is a trait intimately linked to increased life span and health span in multiple species, including yeast, fruit flies, worms, and mice (Lithgow et al., 1995; Harshman and Haberer, 2000; Fabrizio et al., 2001; Johnson et al., 2002; Murakami et al., 2003). In mammals, the Ames and Snell dwarf mice are long-lived and have increased resistance toward multiple stressors, including paraquat (PQ), hydrogen peroxide, UV, and heavy metals (Salmon et al., 2005). Knocking out the growth hormone receptor (GHR) gene in mice produced a similar effect, extending the life span and concurrently exhibiting resistance to multiple forms of stress (Salmon et al., 2005). These long-lived mutants highlight the importance of the IGF-1 signaling pathway in modulating life span and in the coordinated modification of stress resistance. Interestingly, dietary restriction, a proven way to extend life span, also imparts the animal with increased resistance to multiple stresses (Masoro, 2000), possibly through a SIRT1 (Cohen et al., 2004) or mTOR (Blagosklonny, 2010) pathway. Naked mole rats, the longest-lived rodent, also appear to possess enhanced resistance to multiple stresses (Salmon et al., 2008). Although seemingly utilizing different mechanisms, these long-lived rodents converge to a common stress-resistance phenotype. These facts implicate stress resistance as a surrogate for (and perhaps as a mediator of) longevity (Perez-Campo et al., 1998; Lithgow and Walker, 2002).
Longevity genes identified in lower organisms have provided candidate orthologs for studying their impact on life span in mammals. Although this strategy yielded significant insight into the genetics of aging, it suffers from the limitation that only orthologs of mammalian genes can be identified. To overcome this bottleneck, we developed an unbiased genetic approach to identify new genes and pathways that mediate stress resistance and longevity in the mouse. Selections for increased stress resistance as a surrogate marker for extended lifespan have been performed efficiently in lower organisms (e.g., yeast, fruit flies, and nematodes) (Kennedy et al., 1995; Harshman and Haberer, 2000; De Castro et al., 2004). This approach, however, is cost-prohibitive and logistically implausible in mice. Herein, we describe our use of mouse embryonic stem (ES) cells to identify mutations that confer increased stress resistance. Novel manipulations allow these cells to become intact mice (Chick et al., 2009), which can be used for multiple tests of increased longevity and reduced rates of aging. The use of ES cells has several advantages: (1) it allows the screening of vast numbers of independent mutations for the phenotype of interest; (2) genetic tools are widely available to manipulate the genome of the cells; and (3) stress-resistant ES cells can readily be converted into living mice for whole-animal studies.
In our previous studies we demonstrated that mice derived from stress-resistant ES cells retained the stress-resistance Phenotype in tail skin fibroblast and were able to transmit increased stress resistance to their offspring (Chick et al., 2009). In these initial proof-of-principal studies, we used N-ethyl-N-nitrosourea (ENU) to generate a highly mutagenized ES cell population, which facilitated the isolation of stress-resistant mutants (Chick et al., 2009). Although the screen was successful, it suffered from two drawbacks. First, cells that had been exposed to the stressor were no longer competent to form mouse embryos; second, the ENU-induced point mutations were not capable of being mapped with sufficient resolution as to allow the mutant genes to be identified. We overcame the loss of pluripotency by developing a sib-selection method, which allowed the development of fertile adult mice (Chick et al., 2009). Herein, we have employed a transposon: piggyBac (PB) as a mutagen to facilitate gene identification. We report here the recovery of 7 PB-mediated, stress-resistant mutants identified via mass-selection for paraquat (PQ) resistance. These stress-resistant ES cells retained germline competence and are being converted into living mice for further in-depth investigations. The genes responsible for stress resistance are implicated in diverse functions including NADPH oxidase (Nox) activities, inflammation, and protein anchoring. These new mutants will be valuable animal models to investigate how those mutations affect stress resistance and their potential roles in extension of both life and health-span.
Materials and Methods
ES Cell Culture
We generated a mouse ES cell lines with a F1 hybrid background (C57BL/6J × 129X1/SvJ), designated as Blmtet/tet C9, in which the expression of Bloom Syndrome helicase like protein (Blm) genes could be turned off by doxycycline (Supplemental Figure 1). The transient knock out of Blm will increase the rate of loss of heterozygosity, allowing for the generation of homozygous mutations in culture (Yusa et al., 2004) so that recessive mutations could be captured in our screen. C9 ES cells were cultured in ES cell medium with the composition as follow: Knock-Out DMEM (Life Technologies), 15% FBS, 1000 unit/ml of leukemia inhibitory factors (ESGRO, Millipore), 100 μM nonessential amino acids, 2 mM GlutaMAX, 55 μM 2-mercaptoethanol, and 25 unit/ml penicillin/streptomycin. With the exception for selection for stress resistance, ES cells were cultured on feeder layers of mitomycin C-inactivated primary mouse embryonic fibroblast (PMEF). We routinely passage the ES cells every other day in a ratio of 1:8–1:10.
Cloning of piggyBac polyA Trap Vector (PB-UPA)
The unbiased polyA (UPA) trap vector was cloned by routine restriction digestion, or PCR, and ligation so that genetic elements were put in the order of splice-acceptor (SA) from the Bcl2 gene, bovine growth hormone polyA signal (bGHpA), phosphoglycerate kinase (PGK) promoter, neomycin resistant cassette (neo), internal ribosomal entry site (IRES), and splice-donor (SD) from the Hprt gene. This UPA trap was then subcloned into pCyL50 (a gift from the Wellcome Trust Sanger Institute) at the XhoI site which is flanked by the 3′ and 5′ long terminal repeat (LTR) of PB. The resulting piggyBac-unbiased polyA-trap vector was designated as PB-UPA (Figure 1A).
Figure 1. Methods used in ES-cell mutagenesis and selection for stress resistance. (A) Anatomy of the piggyBac (PB)-UPA vector. A UPA Trap vector containing a splice acceptor (SA), the bovine growth hormone poly-adenylate signal (pA), the phosphoglycerate kinase (PGK) promoter, the neomycin phosphotransferase gene (neo), an internal ribosomal entry site (IRES), and a splice donor (SD) with ATG (in 3 different reading frames) was cloned into the piggyBac transposon vector, flanked by the 3′ and 5′ long terminal repeats (PB 3′ and PB 5′) to yield PB-UPA. Gene-trapping occurs when the PB-UPA inserts into the intron of a gene. The exon upstream of the insertion site splices to the SA of PB-UPA and the transcription will be terminated by the pA. At the same time, the expression of neo, driven by PGK, will be possible when the SD splices to the downstream exons and acquires the endogenous polyA signal from the trapped gene, conferring G418 resistance to the cell and allowing selection of ES cells carrying the PB-UPA vector. (B) Method of mutagenesis in ES cells and selection for stress-resistant clones. ES cells were co-transfected with PB-UPA and PB transposase (mPBase) by electroporation, followed by plating into 96-well plates. Gene-trapped clones were selected by G418 resistance. Once confluent, wells were divided into a master and a replicate set. The master was frozen down and the other set was further divided into two, one for selection of resistance to paraquat (PQ) and the other for DNA isolation and gene identification. PQ-resistant cells were selected by exposure to 10 μM PQ for 7 days. Putative stress-resistant colonies were recovered and the site of PB insertion determined by Sp-PCR. Primers were then designed to screen the replica DNA library to determine the well containing the desired PQR clone, which could be subsequently recovered from the frozen master. Because each well on the master plate contains a mixture of about 9 clones, a subcloning step was performed to isolate the pure clonal line of PQR ES cells. These cells are used for various stress-resistance assays and for mouse production.
Mutagenesis in ES cells
C9 ES cells (5 × 106) were electroporated with 1 μg of PB-UPA and 20 μg of mPB transposase (a gift from the Wellcome Trust Sanger Institute) (Cadinanos and Bradley, 2007) to generate gene-trap clones, which were selected by G418 resistance. Six electroporations were performed and pooled so as to generate approximately 9000 gene-trap clones. Transfected cells were plated evenly into ten 96-well plates which contain, on average, 9 unique gene-trap clones per well under G418 (150 μg/ml) selection. Each plate represented is a sub-library of gene-trapped clones and was handled separately. When the gene-trapped ES cells were grown to near confluency (typically after 7 days), half of the cells were frozen as the master stock. The rest were replica-plated into another 96-well plate for the isolation of DNA and selection for stress-resistant cells (Figure 1B). This replica-plating strategy allows us to preserve replica clones of ES cells that have not been through stress treatment. These protocols are crucial for maintaining pluripotency of the mutant ES cells, allowing the production of fertile mice.
Selection for Stress Resistance
Prior to stress selection, gene-trapped ES cells from each sub-library were expanded on a 100-mm culture plate in the presence of doxycyline (1 μg/ml) for 12–14 days, to generate Blm-deficient daughter cells harboring homozygous mutations. Next, doxycycline-treated cells from each sub-library (6 × 106 cells) were plated onto a 150-mm gelatinized culture dish (totally 10) and exposed to 10 μM PQ for 7 days. Colonies of surviving cells typically arose 7 days after reinstating normal culture medium; these colonies were isolated, expanded, and analyzed.
Isolation of Genomic DNA and Splinkerette-PCR
Genomic DNA of stress-resistant ES cells was isolated using Qiagen's GenePure kit and splinkerette PCR was performed as described (Uren et al., 2009). PCR products, which constitute the junction fragments at the insertion site of the PB transposon, were cloned (TOPO-TA, Life Technologies, Carlsbad, CA) and sequenced. The DNA sequence flanking the transposon thus obtained was aligned with the mouse genome using BLAST to identify the integration site and the gene being disrupted.
Clone Isolation on the Master Plate
Based on the trapped gene information from the PQ-resistant ES clone, primer pairs were designed to screen genomic DNA to locate the replica ES clone on the master plate, which had not been exposed to PQ. Isolation of genomic DNA on 96-well plate was performed as described (Ramirez-Solis et al., 1992) and 2 μl of the DNA was used for PCR. A primer annealing to the upstream genomic region of the PB insertion site and a primer annealing to the long terminal repeat (LTR) of PB were employed for PCR (Supplemental Table 1A). After the well containing the replica clone of the PQ-resistant ES cells had been identified in the master plate, the entire master well of ES cells was thawed and expanded. Because each well contained a mixture of about 9 different clones, a subcloning step was performed by seeding 1000 cells onto a 100-mm culture dish followed by picking 192 individual colonies. Correct clones were then identified by PCR. These clonal lines of ES cells were used for subsequent characterization and mouse production.
Generation of Homozygous ES Mutant Clones
To induce homozygosity of the mutation in culture, we treated the heterozygous mutant ES cells with doxycycline (1 μg/ml) for 12–14 days, during which time the cells were passaged every 48 h. Next, 1 × 106 cells were seeded onto a 100-mm culture plate containing 2 mg/ml of G418 to select homozygous clones. Surviving cells under high G418 treatment were then trypsinized and 1000 cells were plated onto another 100-mm plate. This low density of cells ensures recovery of single clones. Typically after 7 days, we hand-picked 96 individual colonies to a 96-well plate and identified homozygous clones by PCR using a 3-primer strategy (Supplemental Table 1A).
Remobilization of piggyBac Transposon
Inserted PB transposons could be remobilized by transient expression of PB transposase. Excision of the PB element causes reversion to the original wild-type DNA sequence and the associated loss of PQR would be tested. Gene-trapped ES cells (5 × 106) were electroporated with 20 μg of an expression plasmid containing PB transposase and a puromycin-resistance cassette (mPB-Puro). Transfected ES cells were selected with puromycin (1 μg/ml) for 2 days to enrich for clones with reversion. Individual ES cell colonies were picked and analyzed for G418 sensitivity (conferred by the loss of PB-gene-trap cassette) and genotyped by PCR.
Total RNA from ES cells were isolated by Qiagen RNeasy kit. The first strand cDNA was then synthesized from the total RNA using the High Capacity cDNA Reverse Transcription kit (Applied Biosystem). Gene specific primers (Supplemental Table 1B) were then used to amplify the mutant transcript resulting from PB-UPA insertion. The PCR products were cloned and sequenced to verify the mutations in the transcripts.
Copy Number and Gene Expression Analysis
The number of copies of PB inserted into PQR ES cells was assessed by qPCR using a probe that anneals to the neomycin resistant gene (neo). The expression level of the genes in these cells was assessed by reverse transcription (RT)-qPCR, using a probe set that spans two exons between which the PB had been inserted (Supplemental Table 2).
Assessment of Stress-Resistant ES Cells
ES cells (2.5 × 105) were plated onto a 60-mm gelatinized culture dish with culture medium containing PQ (10 μM) or omission of 2-mercaptoethanol (a reducing agent normally required for culturing ES cells) and cultured for 48 h. After that, the total number of viable cells (those that excluded trypan blue) was counted. PQ at 10 μM kills about half of the wild-type ES cells in 48 h and is an optimal concentration for measuring stress resistance. The percentage of cells surviving stress treatment was calculated based on the total viable cells recovered divided by the total cells seeded. The parental clone C9 and a known stress-resistant clone, 4C11 (Chick et al., 2009), were included in the assay as controls.
Reactive Oxygen Species (ROS) Measurement
Cultured cells were trypsinized and resuspended in Hank's balanced salt solution (HBSS) containing 8 μM of 5-(and 6-)chloromethyl-2′,7′-dichlorodihydroflurorescein diacetate, acetyl ester (CM-H2DCFDA) (Life Technologies, Carlsbad, CA) and incubated for 15 min with shaking followed by plating onto a 96-well plate (20,000 cells/ 100 μl/well) for an additional 15 min incubation. The fluorescence signal was then measured using the well-scanning mode by a BioTek H1 fluorescence plate reader. Afterward, Hoechst 33342 dye (Life Technologies, Carlsbad, CA) was added to each well (1 μg/ml) and incubated at room temperature for 1 h to stain the total DNA, as a normalization factor for cell number. The ROS content was expressed as the ratio of relative fluorescent unit (RFU) of DCFDA to that of Hoechst.
Generation of Mice
Clones of resistant ES cells recovered from the master plates were used for embryo injection by the Transgenic and Gene Targeting core at the University of Colorado Denver. About 15–20 ES cells were injected into each individual C57BL/6 blastocyst. Fifteen blastocysts were then transferred to the uterus of a pseudopregnant female (strain ICR). Male chimera (indicated by the ES cells specific agouti coat color) recovered from the litter were mated with several young virgin C57BL/6J females to test for germ-line transmission. All animal work was approved by the IACUC.
Fibroblast Stress-Resistance Assay
Tail skin fibroblasts were isolated from 3-month old mice and cultured as described (Salmon et al., 2005). They were frozen at passage 3. Eight wild-type fibroblast lines and eight PiglPB/+ fibroblast lines were thawed at the same time, and cultured on 60-mm plates for 24 h. After that, they were trypsinized, counted, and plated onto a 96-well plate at 15,000 cells per well (6 wells per line), and allowed to attach overnight. Cells were then exposed to 4 mM PQ for 6 h, after which normal media were reinstated for an overnight recovery. Next morning, cell viability was measured by MTT assay, with untreated cells serving as controls. Viability after PQ treatment was expressed as percentage of live cells with respect to the untreated cells.
We are interested in identifying novel mouse genes that lead to resistance to multiple stressors. When multi-stress-resistant mutant strains were selected in C. elegans, these strains were frequently found to slow the rate of aging and to extend life span (De Castro et al., 2004). Here we have developed a strategy for selecting similar mutations in mouse embryonic stem (ES) cells, as a means of identifying novel mouse genes that mediate both stress resistance and slowed aging. Importantly, as previously indicated, mutant ES cells are capable of developing into a whole mouse carrying the stress resistance phenotype (Chick et al., 2009), allowing for investigation of the mechanisms underlying stress resistance, as well as testing its relationship with aging and life extension.
Mutagenesis by the piggyBac Transposon-Mediated UPA Trap
In an earlier study using ENU mutagenesis to generate stress-resistant mutants, we did not attempt to identify the point mutants causing this phenotype because of the great difficulty it would entail. In this study, we employed a method by which these mutations can be rapidly identified and cloned using transposon-mediated mutagenesis. A gene-entrapment cassette was incorporated into the PB transposon to mutate coding genes in the mouse genome. We chose to employ a poly-A trap rather than a promoter trap because promoter trap will only trap actively transcribed genes, which is estimated to be 60% of the genome in ES cells, under normal conditions (Skarnes et al., 2004). In contrast, a poly-A trap would trap genes regardless of transcriptional activity, in theory giving us the potential to screen for mutations in all genes in the genome. A major drawback of the conventional poly-A trap is the strong bias toward trapping the last exon, appeared to be mediated by an endogenous nonsense-mediated decay (NMD) mechanism (Baker and Parker, 2004). By incorporating the unbiased poly-A trap (UPA) strategy in our PB-UPA transposon to suppresses NMD (Shigeoka et al., 2005), we were able to eliminate biased trapping.
We transfected C9 ES cells with the PB-UPA transposon (1 μg) and mPB transposase (20 μg) by electroporation. Approximately 0.03% of ES cells were stably integrated with PB-UPA, trapping a gene. Transfected ES cells were distributed evenly into ten 96-well plates and exposed to G418 to select gene-trapped clones. After 4 days of G418 selection, most of the non-trapped ES cells were killed while the surviving clones, on average about 9 clones per well, were proliferating. Each plate contained a unique set of gene-trapped clones, designated as a sub-library (C9PA-01 to C9PA10). Each was handled separately in downstream processing. The combined library contained approximately 9000 gene-trapped clones in total (Table 1). To better preserve pluripotency, this master library was frozen at early passage, soon after making a replica set. We used this replica set of cells for stress selection and mutation identification.
Selection for Paraquat Resistance
Prior to stressor treatment, replicated ES cells from each sub-library were expanded in the presence of doxycycline (dox) to generate clones of homozygous mutants. Dox-treated cells (6 × 106 cells per 150-mm culture dish per sub-library in a total of 10 dishes) were cultured in the presence of PQ to isolate resistance mutants. PQ was chosen as our primary stressor because it kills cells effectively and cleanly, which facilitated the unambiguous isolation of surviving clones. Moreover, PQ was used in a similar strategy to identify longevity mutants in invertebrate species. We found that both the omission of the feeder layer and a low density of cells were crucial for the selection, otherwise non-resistant ES cells would not be killed by the stressors. After a 7-day exposure to PQ, we observed that surviving ES cell colonies, which varied in number, appeared in nine of the culture dishes. We picked at least 10 colonies from each of those dishes and a total of 96 putative stress-resistant colonies were isolated. Colonies isolated from the same dish frequently harbored the same gene-trap mutations indicating that they arose from a single clone. The observation of multiple PQ resistant (PQR) sibling colonies within a given dish strongly suggests a prevalent stress-resistance phenotype associated with that clone. Since colonies isolated from the same sub-library usually contained identical mutations, we analyzed only 2 colonies from each sub-library. These PQR colonies were analyzed by Splinkerette PCR to identify the trapped gene. For two putative PQR clones isolated from two separate sub-libraries, we failed to locate the PB insertion site, presumably due to difficulty in PCR amplification, and they were excluded from further testing. Clones with successfully identified gene-trapped mutation were further characterized and reported here. Overall, by screening a total of 6 × 107 cells (9000 unique gene trapped clones), we identified 7 mutant clones that were resistant to PQ (Table 1). Both recessive and dominant mutations could be captured at this point because daughter cells carrying homozygous mutations co-exist with the parental heterozygotes.
Identification of the Genes Trapped in PQ-Resistant Clones
Trapped genes in the PQR ES cell colonies were identified by Splinkerette PCR and sequence analysis. Splinkerette PCR, although very efficient, still suffers from spurious amplification producing non-specific products. We carefully verified the putative integration site by ascertaining that the consensus TTAA site used by PB transposition was present in the amplified genomic DNA sequence. Junction fragments passing this criterion were used for BLAST analysis to identify the trapped genes. Seven PQR clones were identified, containing gene-trap mutations in the Pigl, Tiam1, Rffl, Cybasc3, Ttc37 genes, as well as two uncharacterized genes, AU019990, and 4933439C10Rik (Table 2). All of the PB integrations were found in the introns of these genes, as expected for a poly-A trap, in which the disruption of transcripts were likely caused by aberrant splicing (Figure 2B).
Figure 2. Analysis of mutational events. (A) Genotyping of the PB-mediated gene-trap mutants. A 3-primer methodology was used to analyze PB mutant clones. Flanking primers a and b will amplify an endogenous genomic fragment. However, in the PB allele, the distance between a and b is so large that no PCR product will be formed, under a short extension; instead primers a and c (annealing to the PB) will produce a product. Allele specific PCR product was visualized on an agarose gel. (B) Genomic location of PB insertion. PQR ES clones with the PB insertion site shown graphically (not in scale). The red vertical bar represents the site of PB insertion. Black horizontal bars under the exons represent the DNA sequence being transcribed into mRNA; the yellow box and green box represent the PB-UPA splice acceptor (SA) sequence and the splice donor (SD), respectively. The thin lines between these bars illustrate the joining of these DNA sequences. Mutant mRNA was detected by reverse transcription (RT) and PCR amplification with primer pairs as indicated by the blue arrows. These RT-PCR products were analyzed on an agarose gel showing the expected size. The DNA sequence of the RT-PCR product was determined and presented as an electropherogram showing the expected splicing events. (C) Gene expression level in mutant ES cells. Specific gene expression level in mutant cells was compared to the wild-type cells (C9) as measured by RT-qPCR. Error bars represent SD of means (n = 3). (D) Predicted protein truncation in Pigl and Tiam1 mutants. Mutant Pigl protein is predicted to have the C terminal truncated, retaining 79 N-terminal amino acids. His49, Asp52, and His157 are critical residues for enzymatic activity. TM, transmembrane domain. Mutant Tiam1 protein is predicted to be a truncation retaining 665 residues at the N terminal. PH, pleckstrin homology domain; RBD, Ras-binding domain; PDZ, PSD-95 Disks large/ZO-1 homology domain; DH, Dbl-homology domain.
PQ selection and cloning of the PB insertion sites can be finished within a month, providing a rapid means to identify stress-resistance genes. The PQR ES cells isolated directly from stress selection, however, are not suitable for downstream characterization and mouse production. First, we are concerned that dox-induced Blm knock-out and exposure to PQ might have induced lesion to the cells, which would compromise phenotypic analysis. Second, exposure to stressor alone diminishes pluripotency of the ES cells resulting in the failure of mouse production (Chick et al., 2009). The current replica plating strategy addressed both of these concerns by preserving unchallenged replicate clones separately in the master plates. After the PQR clones were identified, we designed primers, specific to the trapped allele, to screen the DNA from the 96-well replica plates to locate the master wells containing the desired mutant clones. PQR gene-trapped clones thus purified were used for subsequent studies in which we focused on the Pigl, Tiam1, and Rffl mutants.
Characterization of the Pigl, Tiam1, and Rffl Gene-Traps
Pigl, Tiam1, and Rffl gene-trapped ES cells were recovered from the master plate. They are morphologically indistinguishable and have a similar proliferation rate comparable to the wild-type ES cells (C9). All three clones have a single PB insertion, as determined by qPCR with the TaqMan probe binding to the neo, and are heterozygous with respect to the gene-trap mutations. The use of C9 ES cells containing the BLM deletion allowed us to easily generate homozygous clones in cell culture to analyze how this affects the stress-resistance phenotype. In addition, PB provided a molecular tag for us to easily genotype the cells by PCR using a 3-primer setup to differentiate wild-type, heterozygote, and homozygote (Figure 2A). By treating cells with doxycycline and selecting with an increased concentration of G418 (2 mg/ml), one homozygous Rffl clone was recovered from 96 colonies analyzed. No homozygote was isolated from the Pigl and Tiam1 clones after analyzing 300 individual colonies (Supplemental Table 3). The low efficiency of LOH induction in Pigl and Tiam1 may be due to a homozygous lethal phenotype. It is also possible that there is an intrinsically low level of somatic recombination in these chromosomal regions.
To confirm that the PB insertion causes an alteration at the mRNA level, we examined the mutant transcript by RT-PCR. In the Pigl and Tiam1 mutants, as predicted, the transcripts were altered by splicing to the splice acceptor (SA) provided by PB-UPA, leading to a truncation in the encoded mRNA (Figure 2B). For the Rffl mutant, the PB-UPA was inserted into the intron region upstream of the initiating codon in exon 2. Sequence analysis showed that the splicing event did not alter the coding sequence of exon 2 and the downstream exons (Figure 2B); thus, the transcript is expected to be intact.
The PiglPB/+ mutant showed a 50% reduction in wild-type transcript level, as determined by RT-qPCR (Figure 2C). Based on the mRNA sequence data, PB insertion at intron 1 of Pigl contributed to a truncated protein retaining 79 amino acids (out of 252) at the N-terminal (Figure 2D). The distal part of the protein containing deacetylase activity (AA44–AA167) was predicted to be lost. However, the transmembrane domain (AA5–AA26) and the cytoplasmic portion (up to AA79) that are critical for ER localization (Pottekat and Menon, 2004) were still intact. The mutant PIGL protein retained the His49 and Asp52 residues, but lost the His157 residue. These three amino acids are highly conserved and thought to be important for deacetylase activity (Urbaniak et al., 2005).
The Tiam1PB/+ mutant showed a 50% reduction in wild-type transcript level, determined by RT-qPCR (Figure 2C). Based on the mRNA sequence data, Tiam1 mutants are also predicted to produce a C-terminal truncated protein. The transcription of exons upstream to the PB insertion produced an N-terminal portion of the protein, consisting of 665 amino acids (out of a full length of 1591 amino acid) (Figure 2D). The PHn domain, which is important for membrane location was retained but the catalytic (DH) and other domains (RBD, PDZ, PHc) (Mertens et al., 2003) were lost, suggesting the mutant Tiam1 has likely lost all the function, as well.
When the transcript level of the RfflPB/+ mutant was analyzed by RT-qPCR, a 7-fold increase of expression was observed when compared to the wild-type cells. Homozygous RfflPB/PB mutant cells showed a 12-fold increase in expression (Figure 2C). Sequence analysis indicated that the splice donor (SD) in the PB-UPA spliced to the second exon of Rffl, and produced a bi-cistronic transcript driven by the PGK promoter. The mRNA sequence of Rffl is expected to be unchanged. The elevated expression could be explained by the stronger PGK promoter taking over the endogenous promoter to drive Rffl expression to a level higher than the wild-type.
Resistance to Oxidative Stress
Next, we assessed the stress resistance of the mutant ES cell clones. This test would help to confirm the resistance observed is due to the gene-trap. Given that normal ES cells are sensitive to oxidative stress, the reducing agent 2-mercaptoethanol is included in the media during routine culture. Omission of 2-mercaptoethanol kills the majority of the cells. We tested our mutant ES cells in 2 different stress conditions: (1) media without 2- mercaptoethanol, and (2) media with 10 μM PQ. Cells were cultured under stress for 2 days, after which the number of viable cells was counted. Compared to the wild-type ES cells (C9), PiglPB/+, Tiam1PB/+, and RfflPB/+ heterozygotes exhibited resistance to both of these stressors. Interestingly, RfflPB/PB homozygotes appeared to have stronger resistance compared to its respective heterozygotes, suggesting that the level of Rffl expression correlates with stress resistance. When the PB insertions from these heterozygotes were removed, resistance to both stressors was lost (Figures 3A,B), confirming that the gene-trapping event is the causal factor for stress resistance. In culture, these resistant ES cell clones were able to form colonies under stressor treatment while non-resistant ES cells rarely did (Figure 3C). The observation of a stress-resistance phenotype in the heterozygous state suggested that all of the PQR mutations are dominant.
Figure 3. Stress resistance in mutant ES cells. (A) Resistance to 2-mercaptoethanol (2-ME) withdrawal. (B) Resistance to paraquat (PQ). Shown are the parental wild-type ES cells (C9: yellow), a stress-resistant control ES cell clone, (4C11: red), recovered from a previous study (Chick et al., 2009), and three gene-trap clones (gray). Cells were subjected to stress treatment for two days, after which the number of viable cells was counted. Pigl, Tiam1, and Rffl heterozygotes (PB/+: dark gray) exhibit resistance to both of these stressors. Rffl homozygotes (PB/PB: black) exhibit stronger stress resistance compared to the heterozygotes. Resistance to both stressors was lost when the PB insertions were removed (+/+: light gray). Error bars represent SD of mean (n = 4). *p < 0.001, #p = 0.01 between the gene-trap clones and the wild-type parental C9, evaluated by Student's t-test. (C) ES cell colonies formation under PQ (10 μM) treatment. Stress-resistant ES clones were able to form colonies in culture under PQ treatment while the number and size of colonies from the wild-type clone were significantly reduced.
Next, we investigated whether or not the PQR phenotype may correlate with ROS level in these cells. When measuring basal cellular ROS level by CM-H2DCFDA, we observed all three resistant clones exhibited a lower level of ROS (Figure 4). The reduction of ROS may be a common feature of cells resistant to oxidative stresses (Brunet-Rossinni, 2004) and may also contribute to longevity (Perez-Campo et al., 1998).
Figure 4. Endogeneous reactive oxygen species (ROS) level in stress-resistant ES cells. The ROS level of the wild-type parental C9 ES cells and three stress-resistant ES cell clones were analyzed by fluorescence spectrophotometry using the CM-H2DCFDA fluorescent dye normalized against Hoeshst 33342 which stained for total DNA of the cells in a given well. The fluorescence unit emitted from the CM-DCFDA was divided by the signal emitted from the DNA-bound Hoechst and expressed as a relative fluorescence unit (RFU). Error bars represent s.e.m. of means (n = 18). The P values evaluated by two tailed Student's t-test between the wild-type cells and each of the stress-resistant lines are indicated.
After confirming that these gene-trapped ES cells were stress resistant, we injected the PiglPB/+ and Tiam1PB/+ ES cells into blastocysts to generate mouse chimeras. From a single injection session, we recovered 4 chimeras of the Pigl mutant; two of them showed germline transmission. Two chimeras were recovered from the Tiam1 mutant and also showed germline transmission (Supplemental Table 4). These results confirmed that PQR ES cells mutagenized by the PB-UPA mutagenesis vector retained germline competency, thus allowing the potential for production of stress-resistant mice. Both the Pigl and Tiam1 chimeras and their respective F1 heterozygous pups are outwardly normal and fertile (Figure 5). Breeding is currently underway to generate a cohort of Pigl and Tiam1 mice for whole animal studies.
Figure 5. Pigl gene-trap mutant mice. (A) PiglPB/+ male chimera. A fertile, germline competent chimera produced by microinjection of PiglPB/+ ES cells is shown. The chimerism was exhibited in the ES cell specific coat color (agouti) on a non-agouti host background (C57BL/6). (B) F1 pups from PiglPB/+ chimera. One of the litters produced by crossing a wild-type inbred C57BL/6 female with the PiglPB/+ chimera is shown. The agouti progeny indicated germline transmission. Further genotyping by PCR confirmed the inheritance of the gene-trapped Pigl allele.
Recapitulation of Stress-Resistance Phenotype in the PiglPB/+ Mice
Intercross of the PiglPB/+ heterozygotes consistently produced small litters (average 5 pups), from which no live homozygous PiglPB/PB pups were identified, suggesting that homozygous Pigl gene-trap mutations are embryonic lethal. We have isolated tail snips from both the PiglPB/+ heterozgyotes and the wild-type littermates at 3-months of age to culture fibroblasts for assessing cellular resistance to stressors. PiglPB/+ fibroblasts have lower ROS content than wild-type and are more resistant to PQ-induced cell death (Figure 6). These observations indicate that the stress-resistance phenotype in ES cells was recapitulated in the mice, demonstrating the feasibility of making stress-resistant mouse by forward genetic screen in ES cells. Currently, Pigl mice are being investigated for several aging parameters including measurement of life span. Those studies will be presented in future communications.
Figure 6. Characterization of PiglPB/+ fibroblasts. (A) ROS level. Tail skin fibroblasts isolated from wild-type (WT) and PiglPB/+ mice were stained with CM-H2DCFDA and the fluorescence was normalized against Hoechst. The ROS content was expressed as relative fluorescence unit (RFU). The P value was evaluated by two tailed Student's t-test (n = 8). (B) PQ resistance. Tail skin fibroblasts from wild-type (WT) and PiglPB/+ mice were exposed to 4 mM PQ for 6 h, after which the viability of the cells were measured by MTT assays. The percentage of live cells after PQ treatment was calculated by the ratio of the absorbance obtained from the PQ-treated cells and that from the un-treated cells. The P value was evaluated by one tailed Student's t-test (n = 8). Each dot or square represent one individual mouse.
The use of a selectable mutant phenotype in ES cells, followed by conversion of these cells into living mice with the same phenotype, offers a novel and efficient method for performing a large-scale, high-throughput forward genetic screen to produce mouse mutants for any phenotype that can be studied in cells. A major advantage of such a screen is that it is unbiased, allowing the discovery of unexpected mutants and novel mutational events. Based on the large body of evidence that stress resistance is closely linked to life extension, both across and within species, we selected for stress-resistant ES cells as a surrogate, at the cellular level, for longevity mutants. Here we report on this novel strategy to create ES cells that are resistant to oxidative stress. Using a piggyBac-mediated gene-trap as the mutagen, we were able to quickly generate a total of 9000 gene-trap clones. The current collection has not yet fully captured all of the coding genes in the mouse genome (23,139 genes, based on the GRCm38 assembly on Ensembl). We envision that a full coverage can readily be achieved by accumulating mutants over repeated independent mutagenesis experiments.
The diploid nature of mammalian cells has been a limiting factor in conducting genetic studies because inactivation of one allele usually is insufficient to yield an observable phenotype due to the compensatory effect of the unaffected allele. Recessive mutations must exist in the homozygous state for them to be detected. To allow the discovery of recessive mutations causing stress resistance, we adopted the method of knocking out the Bloom syndrome helicase like protein (Blm) (Guo et al., 2004; Yusa et al., 2004; Trombly et al., 2009). Loss of Blm increases the rate of sister chromatid exchange (SCE) leading to a loss of heterozygosity (LOH) in the segment being exchanged. By culturing heterozygous mutant cells under Blm-deficient conditions, one can generate daughter cells harboring homozygous mutations. However, constitutive knock out of Blm in long-term culture leads to genome instability; thus we employed the tet-off strategy (Bond et al., 2000) to transiently turn off Blm during our genetic screen (Yusa et al., 2004).
The piggyBac transposon used here is superior to several other transposons (e.g., Sleeping Beauty), both for randomness and for transposition efficiency (Wu et al., 2006). It is not uncommon for a cell to receive multiple piggyBac insertions, which is correlated with the dose of transposon used in transfection (Wang et al., 2009). We observed that 0.03% of cells were captured by the gene-trap when transfected with 1 μg of PB-UPA. Increasing the amount of transposon DNA generally increases the number of gene-trapped clones; the fraction of cells carrying a gene trap increased to 0.18% when 5 μg of PB-UPA was used. However, the incidence of multiple transposon integrations within the same cell is also increased accordingly (Wang et al., 2009). We conclude that using 1 μg of transposon yields a reasonable number of gene-trap clones, while maintaining predominantly a single PB insertion per cell. To simplify genetic analysis, we have so far limited our analyses to mutants carrying a single PB insertion.
The use of F1 hybrid ES cells strain is another contributing factor to making this method work. Because the ultimate goal is to make stress-resistant mice from these mutant cells, the ability of the mutant ES cells to maintain pluripotency is critical. In our studies, cells need to go through multiple experimental manipulations, each of which can diminish such potential. Compared to ES cells derived from inbred strains, F1 hybrid ES cells retain exceptional developmental potential (Eggan et al., 2001), even after multiple rounds of in vitro manipulation such as serial gene targeting (Nyabi et al., 2009), chemical mutagenesis (Chen et al., 2000), and irradiation-induced chromosomal deletion (Chick et al., 2005). As demonstrated here, our hybrid ES cells have gone through targeted manipulations of the Blm gene followed by transposon-mediated gene entrapment and still maintain pluripotency, allowing mouse formation.
Generation of mutants by a polyA-trap has offered several advantages in selection for stress resistance. The polyA-trap captures both active and dormant genes in ES cells, while a promoter-trap only captures active genes. Stress-responsive genes that are not expressed in normal culture will escape from the promoter-trap and will not be identified in the screen. The inclusiveness of the polyA-trap is an important factor to consider in a screen where differential gene expression would be induced, such as the case we found here. While the promoter-trap usually induces loss-of-function, the polyA-trap could produce loss-of-function, partial loss-of-function, and gain-of-function alleles, depending on the integration site of the vector. In most cases, the poly-A trap will result in a C-terminal truncation of the protein; depending on the insertion site, the size of truncation may vary, which could produce a variety of functional outcomes. For example, a protein may retain some function even when a domain is deleted and the resulting phenotype could be different from a total loss of the same protein. To further improve the versatility of gene trapping, we eliminated the bias associated with the conventional polyA-trap, in which the last exon was preferentially trapped, by employing the UPA design. Consistent with a previous report (Shigeoka et al., 2005), we also found that our PB-UPA trap does not show such bias. In some cases, the PB-UPA trap was inserted into the first intron, resulting in a large truncation.
In this study, six out of seven PQR clones are predicted to have gene-trap mutation causing protein truncation. Quite unexpectedly, we also identified a mutation leading to an over-expression of the Rffl gene. This increase of expression was produced by the insertion of the PB-UPA trap in close proximity to the first coding exon, thereby replacing the endogenous promoter with the strong PGK promoter provided by the gene-trap cassette. This example illustrates that the PB-UPA trap is quite versatile in inducing multiple forms of mutations, making it the vector of choice for mutagenesis and multi-allelic analysis.
Mutant Gene Ontology
The seven clones of stress-resistant ES cells recovered from the screen have mutations in genes of diverse functions. Two of them are novel genes without information on function in the literature. We focused on three mutants with mutations in known genes.
The T cell lymphoma invasion and metastasis inducing protein 1 (Tiam1) knock out was first shown to reduce skin tumorigenesis in mice (Malliri et al., 2002). Subsequent studies showed that the Tiam1 knock out reduces the level of intracellular reactive oxygen species (ROS) (Rygiel et al., 2008). Tiam1 activates RAC1, a subunit of the NADPH oxidase complex (Nox1, Nox2, and Nox3 isoforms), and in turn mediates ROS generation. The Nox family of enzymes is one of the major sources of ROS in a variety of cell types, and has recently been shown to have strong implications in inducing oxidative stress and damage. Many studies suggested that Nox activities could contribute to oxidative stress in various tissues, including the microglia (Qin et al., 2013), the vasculature (Lassegue and Griendling, 2010), liver (Kono et al., 2000), and the lung (Sato et al., 2002). Furthermore, Nox-dependent superoxide production can contribute to atherosclerosis (Judkins et al., 2010) and Hungtinton's disease (Valencia et al., 2013). In contrast, inhibiting Nox activity appears to provide protection against oxidative-stress-induced damage in neurons during cerebral ischemia (Kleinschnitz et al., 2010), in cardiac myocytes during pressure overload (Kuroda et al., 2010), and in mouse proximal tubule (MPT) cells under high glucose challenge (Sedeek et al., 2010). These studies highlight the importance of Nox in modulating oxidative stress in a broad range of tissues and the onset and progression of age-related disease. Consistent with data previously reported (Rygiel et al., 2008), we observed reduced ROS level in the Tiam1PB/+ ES cells, presumably through the reduction of Nox activities. The capture of the Tiam1 mutant, a regulator of Nox, illustrates that our screen is successful in identifying a relevant genes that modulate the oxidative state of the cells.
Another hit was Pigl (phosphatidylinositol glycan anchor biosynthesis, class L). This gene encodes for an enzyme catalyzing the second step of the biosynthesis of the glycosylphosphatidylinositol (GPI) anchor. PIGL catalyzes the deacetylation of N-acetylglucosaminyl-phosphatidylinositol at the cytosolic side of endoplasmic reticulum (ER). The deacetylated glucosaminyl-phosphatidylinositol is flipped into the lumen of ER for further maturation to a full GPI anchor and transferred to proteins that have a GPI attachment signal at the C terminus by GPI transamidase. GPI anchored proteins are then transported to plasma membranes and membranes of cellular organelles. PIGL mutations, causing GPI deficiency, lead to the CHIME syndrome (Ng et al., 2012), a collective systemic disorders characterized by colobomas, congenital heart defects, early onset migratory ichthyosiform dermatosis, mental retardation, and ear anomlies. Patients with CHIME syndrome (a recessive trait) commonly have a homozygous Leu167Pro mutation, in exon 5 of the PIGL gene; heterozygotes have no disease phenotype. The mouse PiglPB/+ mutant ES cells we recovered have a predicted early termination after exon 1, producing a putative truncated PIGL protein. However, the N-terminal portion of the mutant protein is still localized to the ER. In the heterozygous state, we did not observe global GPI deficiency in these cells as measured by fluorescent aerolysin (FLARE) staining using flow cytometry (data not shown). The stress-resistance phenotype in PiglPB/+ ES cells may be mediated by a modification of the composition of GPI-anchored proteins on the plasma membrane or the secretion of a subset of proteins without proper attachment of the GPI anchor (Murakami et al., 2012). The possibility of protein secretion from these PiglPB/+ ES cells is of particular interest because we observed that occasionally these PiglPB/+ ES cells can rescue surrounding non-resistant cells from PQ treatment (unpublished observation). We also observed ROS reduction in PiglPB/+ ES cells but how the Pigl mutation mediate such an effect is currently unknown.
Rififylin (Rffl) (also known as Carp-2) encodes a RING domain-containing ubiquitin protein ligase (E3), a potential negative regulator of TNF-induced NF-kB activation. Rffl targets receptor interacting protein (RIP) for ubiquitination and degradation resulting in a downregulation of NF-kB transcriptional activity so as to prevent sustained inflammatory reaction (Liao et al., 2008). The RfflPB/PB ES cells have a 12-fold increase of Rffl expression; we speculate that overexpression of Rffl might decrease NF-kB activity which was suggested by Liao et al., and as such, might attenuate TNFα-dependent inflammatory response and apoptosis. However, while increasing Rffl expression appeared to reduce NF-kB activity, knocking out of Rffl did not alter the induction of NF-kB by TNFα (Ahmed et al., 2009). The precise role of Rffl in modulating NF-kB dependent inflammatory response remains to be clarified.
In summary, we illustrate the generation and isolation of mutant ES cells resistant to oxidative stresses via a novel forward-genetic approach. This phenotype-driven screen in ES cells has been successful in isolating stress-resistant mutants. Initial interrogation of the mutated genes suggests some of them have known physiological roles in modulating stress responses (e.g., ROS level and inflammatory state). These newly identified genes offers considerable promise as novel longevity genes in the mouse. Although we have only demonstrated the use of PQ for selection, we believe this strategy is useful in identifying novel genetic factors that confer resistance to virtually any stressor such as ER stress, heat shock, as well as cytotoxic stress such as heavy-metal exposure. Thus, this forward genetic screen has broad implication in a many field of study. Current efforts in our lab focus on generating additional PB-UPA trap libraries covering the whole genome and to exhaustively screen for additional stress-resistant mutants. We are also generating mice from these stress-resistant ES cells for whole-animal studies.
Wallace S. Chick, Michael Ludwig, David Kitzenberg, and Thomas E. Johnson conceived of the experiments. Wallace S. Chick, Michael Ludwig, David Kitzenbery, Xiaoyun Zhao, and Kristina Williams performed the experiments. Wallace S. Chick and Thomas E. Johnson wrote the manuscript with input from Michael Ludwig, David Kitzenberg, and Kristina Williams.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
This work is supported by the Butcher Grant from the UC (Wallace S. Chick, Thomas E. Johnson) and the NIH/NIA R01 AG041801 (Wallace S. Chick, Thomas E. Johnson).
The Supplementary Material for this article can be found online at: http://www.frontiersin.org/journal/10.3389/fgene.2014.00310/abstract
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Keywords: embryonic stem cells, stress resistance, mice, forward genetics, piggyBac transposon, gene-trap, paraquat
Citation: Chick WS, Ludwig M, Zhao X, Kitzenberg D, Williams K and Johnson TE (2014) Screening for stress-resistance mutations in the mouse. Front. Genet. 5:310. doi: 10.3389/fgene.2014.00310
Received: 10 July 2014; Paper pending published: 06 August 2014;
Accepted: 19 August 2014; Published online: 08 September 2014.
Edited by:Robert Joseph Shmookler Reis, Central Arkansas Veterans Healthcare Service, USA
Reviewed by:Kaoru Tominaga, Jichi Medical University, Japan
Jianxin Lu, Wenzhou Medical College, China
Copyright © 2014 Chick, Ludwig, Zhao, Kitzenberg, Williams and Johnson. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Wallace S. Chick, Department of Cell and Developmental Biology, University of Colorado Denver, 12800 East 19th Avenue, Aurora, CO 80045, USA e-mail: firstname.lastname@example.org