- Research article
- Open Access
ENU mutagenesis reveals that Notchless homolog 1 (Drosophila) affects Cdkn1a and several members of the Wnt pathway during murine pre-implantation development
BMC Genetics volume 13, Article number: 106 (2012)
Our interests lie in determining the genes and genetic pathways that are important for establishing and maintaining maternal-fetal interactions during pregnancy. Mutation analysis targeted to a 34 Mb domain flanked by Trp53 and Wnt3 demonstrates that this region of mouse chromosome 11 contains a large number of essential genes. Two mutant alleles (l11Jus1 and l11Jus4), which fall into the same complementation group, survive through implantation but fail prior to gastrulation.
Through a positional cloning strategy, we discovered that these homozygous mutant alleles contain non-conservative missense mutations in the Notchless homolog 1 (Drosophila) (Nle1) gene. NLE1 is a member of the large WD40-repeat protein family, and is thought to signal via the canonical NOTCH pathway in vertebrates. However, the phenotype of the Nle1 mutant mice is much more severe than single Notch receptor mutations or even in animals in which NOTCH signaling is blocked. To test the hypothesis that NLE1 functions in multiple signaling pathways during pre-implantation development, we examined expression of multiple Notch downstream target genes, as well as select members of the Wnt pathway in wild-type and mutant embryos. We did not detect altered expression of any primary members of the Notch pathway or in Notch downstream target genes. However, our data reveal that Cdkn1a, a NOTCH target, was upregulated in Nle1 mutants, while several members of the Wnt pathway are downregulated. In addition, we found that Nle1 mutant embryos undergo caspase-mediated apoptosis as hatched blastocysts, but not as morulae or blastocysts.
Taken together, these results uncover potential novel functions for NLE1 in the WNT and CDKN1A pathways during embryonic development in mammals.
Mouse chromosome (Mmu Chr) 11 shares significant synteny conservation with regions of six different human (Hsa) chromosomes: 22, 7, 2, 5, 1 and 17 . The largest domain of synteny conservation between mouse and human occurs on distal Mmu 11, which is entirely syntenic with Hsa 17 . The gene-rich domain flanked by Trp53 and Wnt3 in this region of synteny conservation contains 2545 gene structures, including 1597 predicted protein-coding genes, 450 processed RNAs and 498 pseudogenes .
A large-scale, phenotype-driven ENU (N-ethyl-N-nitrosourea) mutagenesis screen targeted to this 34 Mb region of Mmu 11 demonstrated the wide functional diversity of this linkage group [2–4]. Functional analysis of 785 total pedigrees from this ENU mutagenesis screen resulted in the discovery of a variety of mutant phenotypes, including infertility, craniofacial abnormalities, neurological defects and lethality . Subsequent studies detailed the embryonic lethal phenotypes of 45 mutant lines that fell into 40 complementation groups [3, 4]. Resequencing efforts led to the identification of causative or putatively causative lesions in 31 genes in 17 lethal lines .
Although many mutations were identified in the sequencing study, the lesions in the l11Jus1 and l11Jus4 complementation group have yet to be identified. These two alleles survive through implantation but arrest prior to embryonic day (E) 6.5 [3, 4]. Our interests lie in determining the genes and genetic pathways that are important for establishing and maintaining maternal-fetal interactions during pregnancy. Since these two mutants fail during this critical window, we undertook a positional cloning strategy to identify the causative mutations in this complementation group. Here, we present evidence that both mutant alleles have non-conservative missense mutations in the Notchless homolog 1 (Drosophila) gene, Nle1. Moreover, targeted disruption of Nle1 in mice  results in an embryonic lethal phenotype that is remarkably similar to l11Jus1 and l11Jus4, providing further supporting evidence that Nle1 is disrupted in both mutant alleles.
NLE1, which is a member of the WD40 repeat protein family, was first identified as a suppressor of the notchoid phenotype in Drosophila, and has been implicated in both positive and negative regulation of NOTCH signaling, depending upon developmental stage and species [5, 6]. Studies in Drosophila and Xenopus demonstrate that NLE1 signals via the canonical NOTCH pathway [5, 6]. In invertebrates and lower vertebrates, the NOTCH pathway is critical for directing cell fate prior to gastrulation, and also plays important, but varied roles in germ layer boundary formation. At the 4-cell stage in C. elegans, NOTCH signaling dictates an ectodermal cell fate in ABp daughter cells by repressing expression of TBX-37 and TBX-38. In sea urchins, the NOTCH pathway impacts the development and differentiation of the secondary mesenchymal cells, which are fated to produce mesodermal cells [8, 9]. In contrast, in X. laevis, induction of NOTCH signaling leads to an increase in endoderm-specific and a decrease in mesoderm-specific markers, while suppression of NOTCH signaling has the opposite consequence .
The role of NOTCH signaling during the earliest stages of mammalian development is much less clear. Several lines of evidence demonstrate that NOTCH signaling is dispensable for gastrulation in mice. Single gene and compound knockout studies of the Notch receptors and ligands results in either viable animals or embryonic lethality at mid-gestation [11–21]. Similarly, deletion of genes that block NOTCH signaling, such as Pofut1 and members of the γ-secretase complex, leads to embryonic failure after gastrulation and midline formation. POFUT1 adds O-fucose molecules to NOTCH receptors prior to their translocation to the cell surface, while Presenilin 1 and 2 are members of the γ-secretase complex [22, 23]. This complex cleaves NOTCH at the cell membrane, releasing the NOTCH intracellular domain (NICD) into the cytoplasm. The NICD translocates to the nucleus and binds to RBPJ, thereby modulating transcription of downstream target genes.
Deletion of Pofut1, which effectively blocks NOTCH signaling through inhibition of post-translational modifications to NOTCH receptors , leads to embryonic lethality at E9.5 [25, 26]. Targeted disruption of Presenilin 2 in a Presenilin 1 null background leads to embryonic lethality at E9.5. Compound mutants exhibit cardiac, somite and neurological phenotypes . Finally, deletion of the co-repressor, Rbpj, causes somitogenesis defects, placental abnormalities and marked growth delay [28, 29]. These studies demonstrate that unlike lower vertebrates and invertebrates, and despite the fact that Notch receptors and ligands are expressed prior to and during gastrulation , NOTCH signaling is dispensable prior to gastrulation in mice.
Since Nle1l11Jus1 and Nle1l11Jus4 mutants have more severe phenotypes than mutations that disrupt NOTCH signaling in mice, we hypothesized that NLE1 interacts with NOTCH and other signaling pathways during pre-implantation development. To address this hypothesis, we conducted targeted gene expression studies in homozygous mutant embryos. Surprisingly, and in contrast to studies in Xenopus and Drosophila, our data indicate that canonical NOTCH signaling is not disrupted in Nle1 mutant embryos; instead, we discovered that Cdkn1a was upregulated, while several members of the Wnt cascade were downregulated in homozygous mutant embryos. These results highlight the differences in NOTCH signaling between mammals (where canonical NOTCH signaling is dispensable for gastrulation) and other species (where NOTCH signaling is required for gastrulation) and indicate that NLE1 could play divergent roles in development that depend upon other signal transduction cascades.
Mouse strains, meiotic mapping and generation of mutant embryos
The l11Jus1 and l11Jus4 mutants were induced by ENU mutagenesis on a C57BL/6J background [3, 4], and maintained in trans using a balancer chromosome (In(11Trp53;11Wnt3)8Brd) harboring a 34 Mb inversion between Trp53 and Wnt3 that expresses the agouti protein under the Keratin 14 promoter (Figure 1A) . The inversion animals were on a 129S6/SvEvTac background. Animals carrying one copy of the balancer chromosome have light ears and tails due to ectopic agouti expression that reduces pigment [3, 4, 31, 32]. The l11Jus1 line has been continually maintained in our colony. The l11Jus4 line was resuscitated from cryopreserved spermatozoa of an l11Jus4/In(11Trp53;11Wnt3)8Brd male with a C3H/HeJ female (http://www.MMRRC.org, MMRRC:000074-UCD). Pups were genotyped at weaning and l11Jus4/C3H/HeJ males were backcrossed to In(11Trp53;11Wnt3)8Brd/Rex females on a 129S6/SvEvTac genetic background. We genotyped the progeny of both lines at least every 10 generations by microsatellite analysis or direct sequencing of the mutations to ensure that we maintained the mutations.
To generate recombinant animals for meiotic mapping it is necessary to remove the balancer chromosome. Animals heterozygous for the l11Jus1 mutation (l11Jus1/In(11Trp53;11Wnt3)8Brd) were mated to animals carrying one copy of the inversion and the dominant curly coat marker, Rex (In(11Trp53;11Wnt3)8Brd/Rex). We selected animals with a curly coat (i.e. inherited the Rex allele) and dark ears and tail (i.e. inherited the l11Jus1 mutation) for meiotic mapping. We intercrossed F1 animals to generate recombinant F2 animals, which were genotyped at several microsatellite markers (D11Mit4, 219, 245, 120, 39, 327, and 32) and single nucleotide variances (SNVs; Slc6a4, Wsb1, Rad51l3 and Rasl10b) along the 34 Mb interval (Figure 1B). Primers and PCR conditions are available upon request.
For the Notch PCR array studies, qRT-PCR analysis and caspase 3 detection, we outcrossed heterozygous males to 129S6/SvEvTac females (Taconic, Hudson, New York) to eliminate genetic interactions with Wnt3. Heterozygotes, which had dark ears and tails were mated, generating F2 blastocysts for analysis. Notch PCR array studies were conducted on N5F2 embryos (Nle1l11Jus1). qRT-PCR studies were performed on N14F2 and N15F2 (Nle1l11Jus1) and N4F2 (Nle1l11Jus4) embryos dissected at E3.5. Caspase detection assays were carried out on N15F2 (Nle1l11Jus1), as well as N14F2 or N15F2 (Nle1l11Jus4) embryos. All mouse studies were conducted in facilities approved by the American Association for the Accreditation of Laboratory Animals with the approval of the Baylor College of Medicine Animal Care and Use Committee or the Purdue University Animal Care and Use Committee.
To determine time of death and perform phenotypic studies, we examined embryos after timed matings, with the day of the vaginal plug designated E0.5. We genotyped each one as described [3, 4]. DNA was isolated by incubating whole embryos (E6.5 to E9.5) in 1 X PCR buffer (Life Technologies, Grand Island, NY) and 0.08 mg/ml Proteinase K (Life Technologies, Grand Island, NY) at 55°C for 2–3 hours. Proteinase K was inactivated by either heating to 95°C for 10 min or by phenol:chloroform:Isoamyl alcohol extraction followed by ethanol precipitation. Alternatively, embryos were incubated in 25 to 50 μl of 25 mM NaOH, 0.2 mM EDTA for 60 min at 95°C. Genomic DNA was neutralized by the addition of an equal amount of 40 mM Tris–HCl, pH 8.0 and stored at −20°C. D11Mit327 was used to genotype the embryos in a 25 μl PCR reaction under the following conditions: 1 X PCR buffer, 1.5 mM MgCl2, 0.2 mM dNTPs, 250 pmoles of each primer and 0.625 U of Taq Polymerase (Life Technologies, Grand Island, NY). After an initial denaturing step at 95°C for 5 min, D11Mit327 was amplified with the following cycling parameters: 30 cycles of 94°C for 30 s, 60°C for 30 s followed by 72°C for 30 s, with a final 5 min incubation at 72°C. Products were size fractionated on 5% Metaphor (Cambrex, Bio Science, Rockland, ME), 0.5 X TBE gels.
Deciduas were dissected at E6.5–E8.5. Implantation sites were fixed for 3 hours in Bouin’s fixative, embedded in paraffin, sectioned in 5–7 μm slices and stained in hematoxylin and eosin as described . Stained sections were analyzed under light microscopy.
Candidate gene interrogation
Exons of candidate genes were bidirectionally sequenced directly from PCR amplicons using the Big Dye® Teminator v3.1 (Life Technologies, Grand Island, NY) sequencing mix. Each amplicon contained at least one exon, plus ≥ 200 bp of flanking sequence. For the l11Jus1 mutation, genomic DNAs from 129S6/SvEvTac, C57BL/6J and l11Jus1/In(11Trp53;11Wnt3)8Brd mice were sequenced as controls. For the l11Jus4 mutation, genomic DNAs from 129S6/SvEvTac, C57BL/6J, In(11Trp53;11Wnt3)8Brd/C3H, and l11Jus4/C3H, and l11Jus4/In(11Trp53;11Wnt3)8Brd mice were sequenced as controls. Sequence data was analyzed (Sequencher; Gene Codes, Ann Arbor, MI) to identify mutations on the l11Jus1 and l11Jus4 alleles, as well as any additional sequence variants.
Notch pathway expression of l11Jus1 mutants at E3.5
We analyzed Notch pathway gene expression in homozygous mutant and homozygous wild-type blastocysts using the SAB PCR Arrays (SABiosciences/Qiagen, Frederick, MD). Embryos were washed in EmbryoMax© M2 media (M2; EMD Milllipore, Billerica, MA) and transferred into 100 μl of RNAqueous lysis buffer (RNAqueous-Micro Kit, Life Technologies, Grand Island, NY). After vortexing, we snap-froze each tube in liquid nitrogen and stored each sample at −80°. Total RNA was isolated following manufacturer’s instructions, eluting with 20 μl of nuclease-free water. We used 5 μl of RNA to generate cDNA for genotyping in a half reaction of SuperScript One-Step RT-PCR with Platinum Taq (Life Technologies, Grand Island, NY) with gene specific primers, oligo dT, and PCR primers (Table 1). We used nested PCR for sequencing (Figure 1E). We collected 45 mutant and 45 wild-type E3.5 embryos, and split embryos with the same genotype into 3 pools (i.e. biological replicates); each pool consisted of morulae, half-blastocysts, full blastocysts and hatched blastocysts. We then performed a linear amplification step on each pool using the RT2 Nano PreAMP cDNA synthesis kit (SABioscience, Frederick, MD). Each biological replicate was subdivided into 3 technical replicates. Data from each PCR plate were analyzed using an iCycler Real Time PCR detection system (Bio-Rad, Hercules, CA).
PCR array data analysis for gene expression
Cycle threshold (Ct) values were calculated for all data obtained from 18 PCR plates. We calculated the optimal threshold values based on the value for each plate by selecting the auto calculate threshold position and the PCR base-line subtracted analysis mode from the iCycler Data Analysis Software (Bio-Rad, Hercules, CA). The highest threshold position was 1415 PCR base-line subtracted relative fluorescence units (RFU). We re-analyzed each plate by entering 1415 as the user defined threshold position. Therefore, we were able to compare replicates across multiple plates using Ct values generated from the common threshold position.
We used the SABiosciences RT2 Profiler Data Analysis Software to determine gene expression profiles (http://www.sabiosciences.com/pcr/arrayanalysis.php). This software calculated fold regulation values for each gene using the relative quantification 2-ΔΔCt method . Each plate met the quality assurance criteria listed by the manufacturer for genomic DNA contamination, reverse transcription inhibition, and PCR cycling conditions. ΔCt values were normalized using the mean values of three housekeeping genes: Gusb, Hsp90ab1, and Actb. All wells with a Ct value above 29.5 cycles were excluded from the analysis. This left 65 transcripts for analysis.
Caspase 3 detection
Active caspase were detected based on a fluorescent inhibitor of caspase (FLICA) approach [35, 36]. Zona-free embryos were placed on slides and incubated with FLICA caspase 3 reagent (Image-iT™ LIVE Red caspase-3 and −7 Detection Kit, Life Technologies, Grand Island, NY) in M2 medium at 37°C for one hour. FLICA was removed and the embryos were washed with M2 media, counterstained with Hoechst dye for 3 minutes and washed with buffer provided by the manufacturer. Embryos were fixed in 1% PFA for 10 min and mounted on cover slides. Each embryo was imaged with Zeiss LSM510 microscope (20X objective) and the images were pseudo-colored using Adobe Photoshop (Adobe Systems, Inc., San Jose, CA). To genotype, we collected each embryo in 10 μl of 100 μg/ml Proteinase K solution, incubated the embryos at 55°C for 10 minutes, and then heat inactivated at 95°C for 5 minutes. We used these lysates to genotype each embryo by two rounds of PCR using primers that flanked an insertion/deletion in exon 8.
Quantative RT-PCR (qRT-PCR) by TaqMan
RNA isolated from embryos separated by genotype (mutant vs. wild-type) and stage (morula, full blastocyst and hatched blastocyst) was reverse transcribed individually following the protocol by Tang and Colleagues . Following a 1:1 addition of 100% ethanol, RNA was concentrated with a SpeedVac for 15 mins, resuspended in 4.5 μl lysis buffer and reverse transcribed. We performed a two-step linear amplification process using barcoded primers as described . Products from the first and second rounds were purified using Zymo DNA concentration kits (Zymo Research, Irvine, CA) and eluted in 30 μl of 1 X T10E0.1. Eed expression was used to check the cDNA quality following the first linear amplification step (primers listed in Table 1). cDNA was quantified using a Bio-Rad SmartSpec™ Plus Spectrophotometer. Ten ng of cDNA was used as a template for qRT-PCR in combination with TaqMan® Gene Expression Master Mix (PN#4369514; Life Technologies, Grand Island, NY) and Taqman Gene-specific probes (Life Technologies, Grand Island, NY) on a Prism 7000HT Sequence Detection System (Life Technologies, Grand Island, NY). We assayed a minimum of three biological replicates for each group. Cycling reactions were performed in duplicate or triplicate. The relative expression of each gene was calculated based on the ΔΔCt value, where the results were normalized to the average Ct value of Gapdh. Samples that failed to generate a signal above threshold at the end of the reaction were given a Ct value of 40.
SAB PCR Array Study. These data can be thought of as a complex nested block design: Plate is nested within Pool and Pool is nested within Genotype (Plate and Pool are both blocks). Transcript is nested within biological Role (each transcript was assigned one biological Role), and transcript and role are crossed with each level of nesting (i.e. each transcript is measured on each plate). The data were analyzed in a GLM, blocked by Plate nested within Pool, and Pool nested within Genotype. Transcript was nested within Role; and Role and Transcript crossed with the blocking factors Plate and Pool, and with the experimental factor Genotype. Each Plate and Pool acted as its own control. The relationship of Plates as technical replicates from the same Pools is recognized. Transcript describes the overall expression profile, while Role describes the overall Functional Profile, and their interactions with Genotype test (respectively) whether particular Transcripts differ from the average for the Role between Genotypes, and whether particular Roles differ as a whole between Genotypes. We partitioned out between-plate error and used this as the error term for analyses for two reasons: 1) the plate reader software controls within plate error and 2) the use of between-plate error is conceptually equivalent to (the source of error in a traditional ANOVA approach testing each gene independently. By using ΔCt values, the analysis directly calculates ΔΔCt.
qRT-PCR study by TaqMan analysis. We adopted a similar GLM approach to individually test and calculate the ΔΔCt values from Cdkn1a and Trp53 gene expression studies. Since we used the –ΔCt for each individual as raw data, genotype interactions figures and tests a ΔΔCt value. We also tested for common changes in gene expression in different stages of pre-implantation development and used the full pairwise comparisons table to generate the individual ΔΔCt values and standard errors.
Phenotypic analysis of l11Jus1 andl11Jus4
We screened a cohort of 59 lethal mutants (45 of which were embryonic lethal) that were generated by ENU mutagenesis , and identified an allelic series of two mutants (l11Jus1 and l11Jus4) mapping to mouse chromosome 11 that failed to gastrulate. Histological sections performed at embryonic day (E) 7.5 show completely resorbing implantation sites compared to control littermates (Figure 2). In contrast, animals inheriting two copies of the 34 Mb inversion, In(11Trp53;11Wnt3)8Brd, are homozygous mutant for Wnt3 and display a distinct, much less severe phenotype during the gastrulation stage (Table 2) [3, 4]. Complementation studies revealed that the phenotype of the l11Jus1/l11Jus4 double heterozygotes is identical to either single homozygous mutant (data not shown), thereby placing l11Jus1 and l11Jus4 in the same complementation group.
Penetrance of l11Jus1 (L1) (Table 2A): We genotyped a total of 34 l11Jus1 (L1/L1) homozygotes (32 normal and 2 abnormal blastocysts), 117 heterozygotes (L1/Inv) and 49 animals homozygous for the inversion (Inv/Inv). We failed to genotype 98 embryos due to lack of DNA from normal (n = 40) and abnormal (n = 2) embryos; resorption sites (n = 38) and lost embryos (n = 18) accounted for the remainder of non-genotyped embryos. At E6.5, we detected 0 homozygous mutant embryos out of 62 total embryos. X2 analysis indicates that these numbers are statistically significant, with p < 0.0001 (Table 3). At the blastocyst stage (E3.5), we detected normal Mendelian ratios, indicating that the time of death occurs between E3.5 and E6.5.
Penetrance of l11Jus4 (L4) (Table 2B). We genotyped a total of 28 l11Jus4 (L4/L4) homozygotes (all normal), 153 heterozygotes (L4/Inv) and 49 animals homozygous for the inversion (Inv/Inv). We failed to genotype 58 embryos due to lack of DNA from normal (n = 9) and abnormal (n = 2) embryos; resorption sites (n = 46) and lost embryos (n = 1) accounted for the remainder of non-genotyped embryos. At E6.5, we detected 0 homozygous mutant embryos out of 32 total embryos. X2 analysis indicates that these numbers are statistically significant, with a p-value of 0.004 (Table 3). At the blastocyst stage (E3.5), we detected all genotypes, but saw an unexpectedly high number of heterozygotes (p = 0.014). Together, these data indicate that l11Jus1 homozygotes and l11Jus4 homozygotes both die in utero prior to E6.5.
Positional cloning of l11Jus1 andl11Jus4
Since L1 and L4 homozygotes failed at the implantation stage, meiotic mapping would be difficult, at best, using traditional methods that rely on haplotype analysis in phenotypically mutant animals. To circumvent this obstacle, we narrowed the critical interval by exclusion mapping (Figure 1A). Exclusion mapping involves haplotype analysis of all progeny at weaning for several markers across the candidate interval (i.e. from Trp53 to Wnt3 on Mmu 11). Since homozygous mutants are embryonic lethal, any marker that is homozygous for the mutant allele (i.e. C57BL/6J) will effectively ‘exclude’ this marker from the candidate interval. Parents were heterozygous for the l11Jus1 mutation and for the dominant coat color marker, Rex. Throughout the 34 Mb critical interval, l11Jus1 is on a C57BL/6J background, while Rex is on a 129S6/SvEvTac background. Since the balancer chromosome is not present in the F1 generation, it is possible to obtain animals that have recombination events on one or both parental alleles. These recombination events were visualized by haplotype analysis in the F2 generation (Figure 1B). We genotyped 487 progeny (974 individual meiotic events), and narrowed the critical region to a 4.4 Mb domain flanked by Wsb1 and D11Mit120 (Figure 1B, C).
Of the 75 genes in this interval, 16 top candidates were selected based on microarray expression data and mutant phenotype. We sequenced 8 of these genes in the process of identifying the l11Jus1 and l11Jus4 mutations: adaptor-related protein complex 2, beta1 subunit (Ap2b1); chaperonin containing Tcp1, subunit 6b (zeta) (Cct6b); suppressor of zest 12 homolog (Suz12); fringe isoform 1 (Rffl); ecotropic viral integration site 2a (Evi2a); proteasome (prosome, macropain) 26S subunit non-ATPase 11 (Psmd11); TAF15 RNA polymerase II, TATA box binding protein (TBP)-associated factor (Taf15); and Notchless homolog 1 (Drosophila) (Nle1).
We found no non-synonymous mutations in our first 7 candidates (Ap2b1, Cct6b, Suz12, Rffl, Evi2a, Psmd11 or Taf15) . However, we identified a T 1184 G transversion (I 395 S missense mutation) in l11Jus1 heterozygotes in exon 10 of Nle1 (Figure 1D). This non-conservative substitution replaces an aliphatic, hydrophobic amino acid with a polar residue, which likely disrupts functionality . Subsequent mutation detection efforts resulted in the identification of a second missense mutation (T 484 C transition; S 162 P missense mutation) in exon 5 of Nle1 for the l11Jus4 allele (Figure 1D). This non-conservative amino acid substitution has a high probability to alter protein function, as serines easily form hydrogen bonds with polar substrates, while prolines are rarely found in active sites . In addition, we detected an endogenous C57BL/6J non-synonymous SNV (A 535 G transition; I 179 V) in exon 6 (Figure 1D). This well-documented SNV (rs2820949) leads to a very conservative amino acid substitution . Both mutants share the endogenous mutation (Figure 1D, 1F), indicating that l11Jus1 and l11Jus4 homozygotes harbor two coding changes in Nle1–an ENU-induced allele and an endogenous C57BL/6J missense mutation.
Sequence variations within the Nle1 locus
We identified 21 new polymorphisms and compiled a list of all of the polymorphisms found to date within the Nle1 locus (MGI dbSNP Build 128) (Additional file 1: Table S1) . Nle1 is transcribed from the Crick strand, and variances are ordered in reference to Nle1, not the chromosome. The nucleotide position is noted in column one (NCBI Build 37) and the location within Nle1 in column two. Variances detected within exons are designated as synonymous (S) or non-synonymous (N). Variances reported in the MGI database, but not found in our sequencing studies are depicted by gray cells, and dbSNP IDs for previously identified changes are noted.
We included known variants in the reference strain (C57BL/6J), as well as those found in the 129S1/SvImJ, C3H/HeJ, NOD and CzechII strains, and the strains that we sequenced (l11Jus1, l11Jus4, C57BL/6J, 129S6/SvEvTac, and C3HeB/FeJ). In total, there are 73 variances across the Nle1 locus, including 5’ and 3’ UTR sequences. We saw no discordance between the C57BL/6J sequences and the reference sequence. We discovered 10 new indels; 129S6/SvEvTac and C3HeB/FeJ had identical sequences across these regions, while C57BL/6J, l11Jus1 and l11Jus4 segregated together. cDNA comparison studies also indicate that the NOD allele (Genbank Accession # AK170853.1) has a single nucleotide deletion in the 3’UTR sequence . All polymorphisms identified in the 129S6/SvEvTac and C3HeB/FeJ strains are new. We identified five new expressed SNVs across the gene and one expressed indel in the 3’UTR. One previously reported expressed SNV (rs28209059) is a missense mutation (C 912 G; Additional file 1; Table S1) in the 129S1/SvImJ and C3J/HeJ strains. This results in a neutral amino acid substitution (N 291 K)  within exon 8, which does not encode for any type of functional domain.
The Nle1 locus
BLAT analysis of the mouse RefSeq cDNA (Accession # NM_15431) at the UCSC genome browser , reveals that the Nle1 locus contains 13 exons and spans 7628 bp of genomic DNA. cDNA and EST sequences indicate the potential for generating several alternatively-spliced transcripts. The RefSeq cDNA is predicted to encode a 485 amino acid protein that has an NLE1 domain at the N-terminus and 8 WD40-like repeats (Figure 1F). NLE1 is highly conserved, with orthologues in multiple species, even yeast and plants; it is over 91% identical among mouse, rat, human and cow (Figure 3). In addition, it is highly conserved in yeast (42%), fruit fly (55%) and potato (58%) (data not shown).
Expression analysis of the Notch pathway in mutant embryos
Since Nle1l11Jus1/l11Jus1 embryos die shortly after implantation, while disruption of NOTCH signaling by multiple methods (i.e. targeted deletion of Notch receptors and ligands, [11–21], γ secretase or Pofut1[25, 26]) in mice leads to embryonic lethality after mid-gestation, we hypothesized that Nle1l11Jus1/l11Jus1 and Nle1l11Ju41/l11Jus4 mutants had defects in multiple signaling pathways. To test for defects in NOTCH signaling, we analyzed Notch pathway gene expression in homozygous mutant (i.e. Nle1l11Jus1/l11Jus1) blastocysts using the PAMM-059 Notch Pathway SAB PCR Array (SABiosciences/Qiagen, Frederick, MD). We compared expression levels of 84 Notch pathway genes in Nle1l11Jus1/l11Jus1 pre-implantation embryos to Nle+/+ control littermates.
We eliminated 19 genes, including 8 Notch downstream targets (Cflar, Ifng, Il2ra, Pparγ, Cd44, Dtx1, Krt1 and Ptcra) and the Notch ligand, Dll1, due to lack of expression (i.e. had a Ct value ≥ 29.5). This left 65 genes for statistical analysis, including the Notch receptors (Notch1-4), Jagged ligands (Jag1-2) and receptor processing and modifying enzymes (i.e. the γ-secretase complex and protein O-fucosyltransferase genes: Adam10, Adam17, Psen1, Psen2, Psenen and Pofut1).
Notch target genes include Cdkn1a (a marker of cell cycle arrest), Hes1, Hey1, Stat6, Nr4a2, Nfkb1 and Pparg (transcriptional regulators), Ccnd1 (cell cycle), as well as Chuk, Il17b and Krt1 (downstream targets with unspecified functions in the NOTCH pathway). In addition, the PCR array contains several members of the Wnt (Aes, Axin1, Lrp5, Fzd1-7 and Wnt11) and Hedgehog signaling pathways (Gli1, Gsk3b, Shh, Smo and Sufu). To ensure biological significance, genes with less than a 1.5 fold change were included in the statistical analyses, but not considered differentially expressed.
We analyzed the data using a GLM blocked by plate (technical replicate) nested within pool (biological replicate) and pool nested within genotype. Transcript levels were nested within biological function/pathway (role). Role and transcript were crossed with the blocking factors plate and pool, and with the experimental factor genotype. Therefore, testing for genotype X transcript interactions will identify single genes that are statistically upregulated or downregulated in mutant embryos, while testing for genotype X role interactions identifies groups of genes with similar biological functions (i.e. Wnt pathway, transcriptional regulation, etc.) that are as a whole misregulated in mutant embryos compared to wild-type controls. The role (GLM: F7,84 = 248.3; P < 0.0001) and transcript (F7,84 = 224.0; P < 0.0001) effects were significant, indicating the presence of consistent functional and expression profiles in both genotypes.
The genotype X transcript interaction was significant (F57,684 = 1.5490; P = 0.0073), indicating that at least one transcript differed from the overall mean of transcripts within the same role. Of the 16 Notch target genes detected in this study, 6 were overexpressed by at least 1.5 fold (Cdkn1a, Nfkb1, Hes1, Erbb2 (Esr2), Il17b, Map2k7). However only Cdkn1a, which was upregulated by 4.7 fold in mutant samples (Figure 4) (p = 1.94X10-8), was statistically significant using post hoc tests corrected for multiple comparisons (accepting p < 0.000769); none of the other genes approached significance, even at an uncorrected threshold of p < 0.05.
Seven genes demonstrated a more than 1.5 fold reduction in expression in Nle1l11Jus1/l11Jus1 embryos: Lrp5, Fzd7, Fzd4 and Wnt11, which are members of the Wnt signaling pathway, and Chuk, Nr4a2 and Stat6. However, none of these met the rigorous criteria (p < 0.000769) that accounts for the multiple comparison analysis. Setting aside Bonferroni corrections for false positive detection rate, and accepting a false discovery rate (FDR) of 5% leads to the inclusion of Fzd7 (p = 0.00168), Nr4a2 (p = 0.00422), Fzd4 (p = 0.00461) and Chuk (p = 0.02492); using an FDR of 10% leads to the inclusion of Wnt11 (p = 0.02679) (Figure 4). This analysis indicates that multiple members of the Wnt pathway are downregulated in Nle1 mutant embryos.
Confirmation of Cdkn1a in different stages of pre-implantation development
The SAB PCR array study was performed on three pools (n = 15) of E3.5 embryos at different stages (i.e. a mix of morula, blastocysts and hatched blastocysts). This could have introduced biased expression or masked subtle alterations in stage-specific gene expression due to pooling of embryos from different stages. To control for these possibilities and confirm the PCR array results, we analyzed expression of Cdkn1a between wild-type and mutant embryos at multiple embryonic stages (morula, full blastocyst and hatched blastocyst) in single embryos using TaqMan assays. Expression of each gene was normalized relative to expression of Gapdh and compared to the stage-matched wild-type controls. Wild-type expression was set at a value of one.
We used a multivariate GLM model to calculate ΔΔCt and fold change and to properly control and test for differences between the mutant alleles and stages of development. Using a least squares mean, which corrected for all of the variables in the analysis (line, genotype, stage of development), we did not detect differences in Cdkn1a expression between mutants compared to control embryos as a function of stage (morula, blastocyst and hatched blastocyst; F2,32 = 0.2701; P = 0.7650), line (Nle1l11Jus1 and Nle1l11Jus4; F1,32 = 1.293; P = 0.2640) or stage and line (F2,32 = 0.0574; P = 0.9444), indicating that we did not detect differences in expression due to developmental stage or mutant line. However, overall, Cdkn1a was expressed at 4.69 fold (95% CI: 1.02 - 21.5 fold) higher levels both in Nle1l11Jus1/l11Jus1 and Nle1l11Jus4/l11Jus4 mutant embryos compared to wild-type controls at all stages (GLM: F1,32 = 4.2561; P = 0.0473). These data are consistent with our PCR array findings for l11Jus1 mutant embryos, show that there are no significant differences in expression of Cdkn1a at the different stages tested in the PCR array, and demonstrate that the phenotypes associated with l11Jus1 and l11Jus4 do not differ at the molecular level.
Apoptosis occurs at E4.5 in Nle1l11Jus1/l11Jus1and Nle1l11Jus4/l11Jus4mutants
These Cdkn1a expression findings are intriguing, as targeted disruption of Nle1 in mice indicated that mutant embryos started to undergo apoptosis at E3.5 plus 1 day in culture, which is approximately equivalent to E4.5 embryos (i.e. hatched blastocysts) . If our mutant embryos were also undergoing apoptosis, we would expect that they would not show high levels of Cdkn1a, as Cdkn1a expression is most often an indication that cells have exited the cell cycle following a DNA damage response or other type of cellular stress event [43, 44]. However the function of CDKN1A in cell cycle arrest and apoptosis is still unclear, as other studies have shown that Cdkn1a expression levels can be upregulated in cells undergoing apoptosis . Given that Cdkn1a was expressed at much higher levels in Nle1 mutants compared to wild-type embryos, we hypothesized that animals expressing high levels of Cdkn1a would be protected from apoptosis at E3.5, but would ultimately become apoptotic by E4.5, which would be consistent with previous studies .
Therefore, we analyzed caspase 3 activity at E3.5 and E4.5 (Figure 5; Table 4). We tested these data in a single logistic multiple regression. We detected caspase 3 activity solely in homozygous mutants (Likelihood Ratio χ2 = 21.75, p < 0.0001) at E4.5 (LR χ2 = 15.11; p < 0.0001). Strain had no effect (LR χ2 < 0.0001; p > 0.9999). We did not find any evidence for an interaction between genotype and stage (LR χ2 < 0.0001; p > 0.9999). Overall, these data indicate that apoptosis appears at E4.5, but not at E3.5, that apoptosis is only seen in homozygous mutants and that these two effects are independent and additive in both alleles.
qRT-PCR analysis of Trp53 in mutant embryos
We then asked whether the apoptotic phenotype is Trp53-dependent. Taqman assays were conducted to compare Trp53 expression between wild-type and mutant embryos. Identical GLM models were used to calculate fold change and test significance, with additional planned contrasts performed to test differences at different embryonic stages. Trp53 expression did not differ between control and mutant embryos overall (GLM: F1,33 = 0.5316; P = 0.4711), by line (F1,33 = 0.0057; P = 0.9404), by embryonic stage (F2,33 = 0.0994; P = 0.9056), or the interaction of line and stage (F2,33 = 0.1782; P = 0.8376).
Together, the gene expression and caspase 3 data indicate that Nle1l11Jus1/l11Jus1 and Nle1l11Jus4/l11Jus4 homozygotes undergo caspase 3-mediated apoptosis at the hatched blastocyst stage. This is not mediated by alterations in mRNA levels of Trp53, and apoptosis does not correlate with upregulation of Cdkn1a expression in homozygous mutant embryos, as upregulation of Cdnk1a occurs from the morula through the hatched blastocyst stage, even though apoptosis only is observed at the latest stages. Furthermore, we demonstrate that several members of the Wnt pathway are downregulated in mutant embryos, suggesting that NLE1 interacts with the WNT pathway during pre-implantation development.
We present evidence that the l11Jus1 and l11Jus4 mutant phenotypes are caused by non-conservative missense mutations in the Nle1 gene. Gene targeting studies indicate that l11Jus1 and l11Jus4 phenocopy the null allele . These ENU mutants were created on a C57BL/6J background, which also contains a conservative missense mutation in Nle1. Therefore, l11Jus1 and l11Jus4 homozygotes harbor two mutations within predicted functional domains of NLE1. Previous studies in Drosophila and Xenopus indicate that NLE1 is a member of the NOTCH pathway [5, 6]. NOTCH signaling facilitates short-range cell-cell communication during diverse cellular processes, in multiple tissues and at a multitude of developmental stages. Loss of function or gain of function mutations in various factors that are fundamental to canonical NOTCH signaling are often associated with developmental disorders, adult-onset diseases and a variety of cancers in humans .
However, the function of NLE1 in NOTCH signaling remains elusive. Initial studies in Drosophila show that NLE1 function is context and dosage dependent. NLE1 was identified as a dominant suppressor of the viable mutant allele, notchoid. Notchoid mutants have characteristic wing notches; in the notchoid mutant background, Nle1 heterozygosity (i.e. Nle1/+) rescued the notchoid phenotype, while simultaneously causing shortened and thickened wing veins . Interestingly, overexpression of wingless, the Drosophila Wnt orthologue, in the notchoid background also rescues the notchoid phenotype [46, 47], while overexpression of Notch leads to shortened, thickened wing veins . Since NLE1 can bind the NOTCH intracellular domain (NICD), these experiments suggest that NLE1 is a negative regulator of NOTCH, and that NLE1 functions by blocking the ability of the NICD to regulate expression of downstream targets. Studies in Xenopus come to the opposite conclusion, as overexpression of Murine or a combination of Xenopus and DrosophilaNle1 mRNAs into single blastomeres at the 4-cell or 2-cell stage, respectively, lead to decreased numbers of primary neurons at the early neurula stage. These results indicate that NOTCH activity was upregulated following injection of Nle1 mRNAs, suggesting that NLE1 positively regulates NOTCH signaling.
These studies indicate that NLE1 acts as both a positive and negative regulator of NOTCH signaling. If NLE1 acts as a general positive regulator of NOTCH signaling during murine pre-implantation development, then elimination of NLE1 could lead to compensatory over-expression of the Notch receptors, ligands and protease family members, but reduced expression of downstream target genes. In contrast, if NLE1 functions as a negative regulator of NOTCH signaling, we would predict that disruption of NLE1 would lead to increased expression of Notch target genes. To our surprise, we saw no generalized misregulation of Notch target genes in the PCR array study. In addition, the Notch receptors, ligands and other family members were not significantly altered. At a false discovery rate of 5%, the only genes that are misregulated in the PCR array study were: Cdkn1a, Nr4a2, Fzd7, Fzd4 and Chuk. Cdkn1a, Nr4a2 and Chuk are downstream targets of NOTCH signaling, while Fzd7 and Fzd4 encode receptors in the WNT pathway. To tease out the gene expression changes that occurred during specific pre-implantation stages, we analyzed expression of Cdkn1a on individual staged embryos (morulae, full blastocysts and hatched blastocysts). Cdkn1a was significantly upregulated in Nle1l11Jus1/l11Jus1and Nle1l11Jus4/l11Jus4 animals at all three stages. These studies indicate that mutations in Nle1 do not significantly affect the NOTCH pathway during pre-implantation development.
CDKN1A is a powerful cyclin-dependent kinase inhibitor that functions in several developmental pathways and negatively regulates the cell cycle at G1 via a TRP53-mediated response to DNA damage . This can happen directly by competing with DNA polymerase δ for PCNA binding sites at the replication fork, leading to decreased DNA synthesis . Alternatively, CDKN1A can inhibit CDK2, which leads to suppression of E2F-dependent transcripts, downregulation of components of the DNA synthesis machinery and reduced firing at origins of replication . In addition, CDKN1A can act as a negative regulator of caspase-mediated apoptosis . Gene targeting studies demonstrated that the inner cell mass of Nle1−/− embryos was undergoing apoptosis via a caspase-dependent mechanism in E3.5 blastocysts that were cultured for 24 hours . We analyzed caspase 3 activity in blastocysts and hatched blastocysts at E3.5 and E4.5. Consistent with the results of Cormier and colleagues (2006), we demonstrate that l11Jus1 and l11Jus4 show evidence of apoptosis only in hatched blastocysts.
Although we show upregulation of Cdkn1a and downregulation of several members of the Wnt pathway, how these two networks work together to regulate pre-implantation development is still unknown. One attractive possibility is via the TRP53-mediated stress response pathway, which is upstream of CDKN1A. We predicted that if our Nle1 mutations were causing severe cellular damage, the cell would not be able to recover during cell cycle arrest (at E3.5), which would then force the cell to undergo apoptosis (at E4.5). If this were true, we would expect to see increased expression of Trp53, as the cells proceeded through apoptosis. However, we did not detect altered expression of Trp53 by qRT-PCR studies in our mutants at any stage. In retrospect, this result is not that surprising, as TRP53-mediated apoptosis (via Cdkn1a upregulation) is not necessarily correlated with mRNA expression of Trp53, but is instead associated with upregulation of the active, acetylated form of the TRP53 protein . Alternately, it is possible that the expression changes in Trp53 were too subtle to detect, or apoptosis could be occurring via non-TRP53 mediated pathways .
Our results refute the possibility that NLE1 functions as a negative regulator of NOTCH signaling during mammalian pre-implantation development, as mutation of Nle1 does not lead to increased expression of key Notch downstream target genes. In addition, our PCR array studies indicate that most downstream targets of NOTCH are unaffected by Nle1 mutations. Much to our surprise, instead of confirming the role of NLE1 in the NOTCH pathway, our data implicate NLE1 in WNT signaling and cell cycle arrest and/or apoptosis via Cdkn1a during pre-implantation development. Although NOTCH signaling is dispensable in mice prior to gastrulation, WNT signaling is not. Deletion of Wnt3 leads to failure prior to primitive streak formation , and multiple Wnt ligands and Fzd receptors are detected at the blastocyst stage [55, 56], as well as in the uterus during peri-implantation [57–59]. We provide evidence that NLE1 is co-opted by the WNT and CDKN1A pathways in mammals, while in lower vertebrates, several studies indicate that NLE1 acts in the NOTCH pathway, and reports in yeast and plants (which lack NOTCH signaling) demonstrate a role for NLE1 in ribosomal biogenesis [60–64]. Therefore, NLE1 may perform widely varied functions in a species and stage-dependent context, and out studies suggest that NLE1 may co-opt different signaling pathways during different stages of development.
ACL initiated this project while a postdoctoral fellow under the supervision of MJJ at Baylor College of Medicine. All gene expression studies were conducted under the direction of ACL at Purdue University.
General linear model
Complementary deoxyribonucleic acid
Expressed sequence tag
Quantitative reverse transcription PCR
Notchless homologue 1 (Drosophila)
Transformation related protein 53
Cyclin dependent kinase inhibitor 1a (p21)
BLAST like alignment tool
Threshold cycle; the relative measure of the target in a quantitative PCR reaction
Boles MK, Wilkinson BM, Wilming LG, Liu B, Probst FJ, Harrow J, Grafham D, Hentges KE, Woodward LP, Maxwell A, et al: Discovery of candidate disease genes in ENU-induced mouse mutants by large-scale sequencing, including a splice-site mutation in nucleoredoxin. PLoS Genet. 2009, 5 (12): e1000759-10.1371/journal.pgen.1000759.
Hentges KE, Pollock DD, Liu B, Justice MJ: Regional variation in the density of essential genes in mice. PLoS Genet. 2007, 3 (5): e72-10.1371/journal.pgen.0030072.
Hentges KE, Nakamura H, Furuta Y, Yu Y, Thompson DM, O'Brien W, Bradley A, Justice MJ: Novel lethal mouse mutants produced in balancer chromosome screens. Gene Expr Pattern: GEP. 2006, 6 (6): 653-665. 10.1016/j.modgep.2005.11.015.
Kile BT, Hentges KE, Clark AT, Nakamura H, Salinger AP, Liu B, Box N, Stockton DW, Johnson RL, Behringer RR, et al: Functional genetic analysis of mouse chromosome 11. Nature. 2003, 425 (6953): 81-86. 10.1038/nature01865.
Cormier S, Le Bras S, Souilhol C, Vandormael-Pournin S, Durand B, Babinet C, Baldacci P, Cohen-Tannoudji M: The murine ortholog of notchless, a direct regulator of the notch pathway in Drosophila melanogaster, is essential for survival of inner cell mass cells. Mol Cell Biol. 2006, 26 (9): 3541-3549. 10.1128/MCB.26.9.3541-3549.2006.
Royet J, Bouwmeester T, Cohen SM: Notchless encodes a novel WD40-repeat-containing protein that modulates Notch signaling activity. EMBO J. 1998, 17 (24): 7351-7360. 10.1093/emboj/17.24.7351.
Good K, Ciosk R, Nance J, Neves A, Hill RJ, Priess JR: The T-box transcription factors TBX-37 and TBX-38 link GLP-1/Notch signaling to mesoderm induction in C. elegans embryos. Development. 2004, 131 (9): 1967-1978. 10.1242/dev.01088.
Sherwood DR, McClay DR: LvNotch signaling mediates secondary mesenchyme specification in the sea urchin embryo. Development. 1999, 126 (8): 1703-1713.
Sherwood DR, McClay DR: LvNotch signaling plays a dual role in regulating the position of the ectoderm-endoderm boundary in the sea urchin embryo. Development. 2001, 128 (12): 2221-2232.
Contakos SP, Gaydos CM, Pfeil EC, McLaughlin KA: Subdividing the embryo: a role for Notch signaling during germ layer patterning in Xenopus laevis. Dev Biol. 2005, 288 (1): 294-307. 10.1016/j.ydbio.2005.09.015.
Conlon RA, Reaume AG, Rossant J: Notch1 is required for the coordinate segmentation of somites. Development. 1995, 121 (5): 1533-1545.
Hamada Y, Kadokawa Y, Okabe M, Ikawa M, Coleman JR, Tsujimoto Y: Mutation in ankyrin repeats of the mouse Notch2 gene induces early embryonic lethality. Development. 1999, 126 (15): 3415-3424.
Krebs LT, Xue Y, Norton CR, Sundberg JP, Beatus P, Lendahl U, Joutel A, Gridley T: Characterization of Notch3-deficient mice: normal embryonic development and absence of genetic interactions with a Notch1 mutation. Genesis. 2003, 37 (3): 139-143. 10.1002/gene.10241.
McCright B, Gao X, Shen L, Lozier J, Lan Y, Maguire M, Herzlinger D, Weinmaster G, Jiang R, Gridley T: Defects in development of the kidney, heart and eye vasculature in mice homozygous for a hypomorphic Notch2 mutation. Development. 2001, 128 (4): 491-502.
Swiatek PJ, Lindsell CE, del Amo FF, Weinmaster G, Gridley T: Notch1 is essential for postimplantation development in mice. Genes Dev. 1994, 8 (6): 707-719. 10.1101/gad.8.6.707.
Hrabe de Angelis M, McIntyre J, Gossler A: Maintenance of somite borders in mice requires the Delta homologue DII1. Nature. 1997, 386 (6626): 717-721. 10.1038/386717a0.
Krebs LT, Shutter JR, Tanigaki K, Honjo T, Stark KL, Gridley T: Haploinsufficient lethality and formation of arteriovenous malformations in Notch pathway mutants. Genes Dev. 2004, 18 (20): 2469-2473. 10.1101/gad.1239204.
Krebs LT, Xue Y, Norton CR, Shutter JR, Maguire M, Sundberg JP, Gallahan D, Closson V, Kitajewski J, Callahan R, et al: Notch signaling is essential for vascular morphogenesis in mice. Genes Dev. 2000, 14 (11): 1343-1352.
Dunwoodie SL, Clements M, Sparrow DB, Sa X, Conlon RA, Beddington RS: Axial skeletal defects caused by mutation in the spondylocostal dysplasia/pudgy gene Dll3 are associated with disruption of the segmentation clock within the presomitic mesoderm. Development. 2002, 129 (7): 1795-1806.
Jiang R, Lan Y, Chapman HD, Shawber C, Norton CR, Serreze DV, Weinmaster G, Gridley T: Defects in limb, craniofacial, and thymic development in Jagged2 mutant mice. Genes Dev. 1998, 12 (7): 1046-1057. 10.1101/gad.12.7.1046.
Jiang YJ, Smithers L, Lewis J: Vertebrate segmentation: the clock is linked to Notch signalling. Curr Biol: CB. 1998, 8 (24): R868-R871. 10.1016/S0960-9822(07)00547-7.
Kopan R, Ilagan MXG: The canonical Notch signaling pathway: unfolding the activation mechanism. Cell. 2009, 137 (2): 216-233. 10.1016/j.cell.2009.03.045.
Schwanbeck R, Martini S, Bernoth K, Just U: The Notch signaling pathway: Molecular basis of cell context dependency. Eur J Cell Biol. 2011, 90 (6–7): 572-581.
Shi S, Stanley P: Evolutionary origins of Notch signaling in early development. Cell Cycle. 2006, 5 (3): 274-278. 10.4161/cc.5.3.2396.
Shi S, Stahl M, Lu L, Stanley P: Canonical Notch signaling is dispensable for early cell fate specifications in mammals. Mol Cell Biol. 2005, 25 (21): 9503-9508. 10.1128/MCB.25.21.9503-9508.2005.
Shi S, Stanley P: Protein O-fucosyltransferase 1 is an essential component of Notch signaling pathways. Proc Natl Acad Sci USA. 2003, 100 (9): 5234-5239. 10.1073/pnas.0831126100.
Donoviel DB, Hadjantonakis AK, Ikeda M, Zheng H, Hyslop PS, Bernstein A: Mice lacking both presenilin genes exhibit early embryonic patterning defects. Genes Dev. 1999, 13 (21): 2801-2810. 10.1101/gad.13.21.2801.
Oka C, Nakano T, Wakeham A, de la Pompa JL, Mori C, Sakai T, Okazaki S, Kawaichi M, Shiota K, Mak TW, et al: Disruption of the mouse RBP-J kappa gene results in early embryonic death. Development. 1995, 121 (10): 3291-3301.
Souilhol C, Cormier S, Tanigaki K, Babinet C, Cohen-Tannoudji M: RBP-Jkappa-dependent notch signaling is dispensable for mouse early embryonic development. Mol Cell Biol. 2006, 26 (13): 4769-4774. 10.1128/MCB.00319-06.
Cormier S, Vandormael-Pournin S, Babinet C, Cohen-Tannoudji M: Developmental expression of the Notch signaling pathway genes during mouse preimplantation development. Gene Expr Patterns. 2004, 4 (6): 713-717. 10.1016/j.modgep.2004.04.003.
Zheng B, Sage M, Cai WW, Thompson DM, Tavsanli BC, Cheah YC, Bradley A: Engineering a balancer chromosome in the mouse. Nat Genet. 1999, 22 (4): 375-378. 10.1038/11949.
Hentges KE, Justice MJ: Checks and balancers: balancer chromosomes to facilitate genome annotation. Trends Genet. 2004, 20 (6): 252-259. 10.1016/j.tig.2004.04.004.
Noveroske JK, Lai L, Gaussin V, Northrop JL, Nakamura H, Hirschi KK, Justice MJ: Quaking is essential for blood vessel development. Genesis. 2002, 32 (3): 218-230. 10.1002/gene.10060.
Livak KJ, Schmittgen TD: Analysis of relative gene expression data using real-time quantitative PCR and the 2(−Delta Delta C(T)) Method. Methods. 2001, 25 (4): 402-408. 10.1006/meth.2001.1262.
Slee EA, Adrain C, Martin SJ: Serial killers: ordering caspase activation events in apoptosis. Cell Death Differ. 1999, 6 (11): 1067-1074. 10.1038/sj.cdd.4400601.
Bedner E, Smolewski P, Amstad P, Darzynkiewicz Z: Activation of caspases measured in situ by binding of fluorochrome-labeled inhibitors of caspases (FLICA): correlation with DNA fragmentation. Exp Cell Res. 2000, 259 (1): 308-313. 10.1006/excr.2000.4955.
Tang F, Barbacioru C, Nordman E, Li B, Xu N, Bashkirov VI, Lao K, Surani MA: RNA-Seq analysis to capture the transcriptome landscape of a single cell. Nat Protoc. 2010, 5 (3): 516-535. 10.1038/nprot.2009.236.
Lo C-L, Shen F, Baumgarner K, Cramer MJ, Lossie AC: Identification of 129S6/SvEvTac-Specific polymorphisms on mouse chromosome 11. DNA Cell Biol. 2012, 31 (3): 402-414. 10.1089/dna.2011.1353.
Livingstone CD, Barton GJ: Protein sequence alignments: a strategy for the hierarchical analysis of residue conservation. Comput Appl Biosci. 1993, 9 (6): 745-756.
Blake JA, Bult CJ, Kadin JA, Richardson JE, Eppig JT: The Mouse Genome Database (MGD): premier model organism resource for mammalian genomics and genetics. Nucleic Acids Res. 2011, 39 (Database issue): D842-D848.
Carninci P, Hayashizaki Y: High-efficiency full-length cDNA cloning. Methods Enzymol. 1999, 303: 19-44.
Kent WJ: BLAT–the BLAST-like alignment tool. Genome Res. 2002, 12 (4): 656-664.
Brugarolas J, Chandrasekaran C, Gordon JI, Beach D, Jacks T, Hannon GJ: Radiation-induced cell cycle arrest compromised by p21 deficiency. Nature. 1995, 377 (6549): 552-557. 10.1038/377552a0.
Deng C, Zhang P, Harper JW, Elledge SJ, Leder P: Mice lacking p21CIP1/WAF1 undergo normal development, but are defective in G1 checkpoint control. Cell. 1995, 82 (4): 675-684. 10.1016/0092-8674(95)90039-X.
Gartel AL: The conflicting roles of the cdk inhibitor p21(CIP1/WAF1) in apoptosis. Leuk Res. 2005, 29 (11): 1237-1238. 10.1016/j.leukres.2005.04.023.
Couso JP, Martinez Arias A: Notch is required for wingless signaling in the epidermis of Drosophila. Cell. 1994, 79 (2): 259-272. 10.1016/0092-8674(94)90195-3.
Hing HK, Sun X, Artavanis-Tsakonas S: Modulation of wingless signaling by Notch in Drosophila. Mech Dev. 1994, 47 (3): 261-268. 10.1016/0925-4773(94)90044-2.
Matsuno K, Diederich RJ, Go MJ, Blaumueller CM, Artavanis-Tsakonas S: Deltex acts as a positive regulator of Notch signaling through interactions with the Notch ankyrin repeats. Development. 1995, 121 (8): 2633-2644.
Abbas T, Dutta A: p21 in cancer: intricate networks and multiple activities. Nat Rev Cancer. 2009, 9 (6): 400-414. 10.1038/nrc2657.
Moldovan GL, Pfander B, Jentsch S: PCNA, the maestro of the replication fork. Cell. 2007, 129 (4): 665-679. 10.1016/j.cell.2007.05.003.
Zhu W, Abbas T, Dutta A: DNA replication and genomic instability. Adv Exp Med Biol. 2005, 570: 249-279. 10.1007/1-4020-3764-3_9.
Yamakuchi M, Lowenstein CJ: MiR-34, SIRT1 and p53: the feedback loop. Cell Cycle. 2009, 8 (5): 712-715. 10.4161/cc.8.5.7753.
Gurley KE, Moser R, Gu Y, Hasty P, Kemp CJ: DNA-PK suppresses a p53-independent apoptotic response to DNA damage. EMBO Rep. 2009, 10 (1): 87-93. 10.1038/embor.2008.214.
Barrow JR, Howell WD, Rule M, Hayashi S, Thomas KR, Capecchi MR, McMahon AP: Wnt3 signaling in the epiblast is required for proper orientation of the anteroposterior axis. Dev Biol. 2007, 312 (1): 312-320. 10.1016/j.ydbio.2007.09.030.
Kemp C, Willems E, Abdo S, Lambiv L, Leyns L: Expression of all Wnt genes and their secreted antagonists during mouse blastocyst and postimplantation development. Dev Dyn. 2005, 233 (3): 1064-1075. 10.1002/dvdy.20408.
Kemp CR, Willems E, Wawrzak D, Hendrickx M, Agbor Agbor T, Leyns L: Expression of Frizzled5, Frizzled7, and Frizzled10 during early mouse development and interactions with canonical Wnt signaling. Dev Dyn. 2007, 236 (7): 2011-2019. 10.1002/dvdy.21198.
Hayashi K, Burghardt RC, Bazer FW, Spencer TE: WNTs in the ovine uterus: potential regulation of periimplantation ovine conceptus development. Endocrinology. 2007, 148 (7): 3496-3506. 10.1210/en.2007-0283.
Hayashi K, Erikson DW, Tilford SA, Bany BM, Maclean JA, Rucker EB, Johnson GA, Spencer TE: Wnt genes in the mouse uterus: potential regulation of implantation. Biol Reprod. 2009, 80 (5): 989-1000. 10.1095/biolreprod.108.075416.
Miller C, Sassoon DA: Wnt-7a maintains appropriate uterine patterning during the development of the mouse female reproductive tract. Development. 1998, 125 (16): 3201-3211.
Chantha S-C, Tebbji F, Matton DP: From the notch signaling pathway to ribosome biogenesis. Plant Signal Behav. 2007, 2 (3): 168-170. 10.4161/psb.2.3.3724.
Chantha SC, Emerald BS, Matton DP: Characterization of the plant Notchless homolog, a WD repeat protein involved in seed development. Plant Mol Biol. 2006, 62 (6): 897-912. 10.1007/s11103-006-9064-4.
Chantha SC, Matton DP: Underexpression of the plant NOTCHLESS gene, encoding a WD-repeat protein, causes pleitropic phenotype during plant development. Planta. 2007, 225 (5): 1107-1120. 10.1007/s00425-006-0420-z.
de la Cruz J, Sanz-Martínez E, Remacha M: The essential WD-repeat protein Rsa4p is required for rRNA processing and intra-nuclear transport of 60S ribosomal subunits. Nucleic Acids Res. 2005, 33 (18): 5728-5739. 10.1093/nar/gki887.
Strain E, Hass B, Banks JA: Characterization of mutations that feminize gametophytes of the fern Ceratopteris. Genetics. 2001, 159 (3): 1271-1281.
We thank Temenit Asgedom, Chia-Li Shih, Lei Xing, Marianne Luu, Rebecca Zaremba, and Jeremy Sherrill for expert technical assistance; Drs. Susan Mendrysa, Shihuan Kuang and Yuk Fai Leung for critical reading of this manuscript; and Jason Fields for expert animal care. Funding for this project was provided by grants from the NIH-5F32HD44407 to ACL, NIH-U01HD39372 to MJJ and the Purdue Research Foundation, as well as generous startup funds from Department of Animal Sciences, Purdue University (protocol # 06–068).
The authors acknowledge no competing interests.
ACL conceived of and participated in the design of the study; conducted the meiotic mapping and haplotype studies; identified the critical interval; supervised C-LL, KMB and MJC; and drafted the manuscript. C-LL participated in the design of the study, conducted the qRT-PCR studies and caspase 3 analysis and drafted corresponding parts of the manuscript. KMB participated in the design of the study, identified the Nle1l11Jus4 mutation, conducted the PCR array study and drafted corresponding parts of the manuscript. MJC participated in the design of the study, found the Nle1l11Jus1 mutation and edited the manuscript. JPG conducted the statistical analysis for the SAB PCR arrays, TaqMan assays and caspase 3 studies and edited the manuscript. MJJ conceived of the study, participated in the design and edited the manuscript. All authors read and approved the final manuscript.
Electronic supplementary material
Authors’ original submitted files for images
About this article
Cite this article
Lossie, A.C., Lo, C., Baumgarner, K.M. et al. ENU mutagenesis reveals that Notchless homolog 1 (Drosophila) affects Cdkn1a and several members of the Wnt pathway during murine pre-implantation development. BMC Genet 13, 106 (2012) doi:10.1186/1471-2156-13-106
- Notchless homolog 1 (Drosophila)
- ENU mutagenesis
- Pre-implantation development
- Embryonic lethal