Abstract
C16orf35 is a conserved and widely expressed gene lying adjacent to the human α-globin cluster in all vertebrate species. In-depth sequence analysis shows that C16orf35 (now called NPRL3) is an orthologue of the yeast gene Npr3 (nitrogen permease regulator 3) and, furthermore, is a paralogue of its protein partner Npr2. The yeast Npr2/3 dimeric protein complex senses amino acid starvation and appropriately adjusts cell metabolism via the TOR pathway. Here we have analysed a mouse model in which expression of Nprl3 has been abolished using homologous recombination. The predominant effect on RNA expression appears to involve genes that regulate protein synthesis and cell cycle, consistent with perturbation of the mTOR pathway. Embryos homozygous for this mutation die towards the end of gestation with a range of cardiovascular defects, including outflow tract abnormalities and ventriculoseptal defects consistent with previous observations, showing that perturbation of the mTOR pathway may affect development of the myocardium. NPRL3 is a candidate gene for harbouring mutations in individuals with developmental abnormalities of the cardiovascular system.
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Introduction
Of the ~22,000 genes currently annotated in the human genome (GRCh37, 59.37d, Ensembl), the true function is known for only a fraction. Identifying the role played by uncharacterized genes and the proteins they encode is still an important task for fully annotating the functional genome. C16orf35 is a highly conserved gene that lies upstream of the human α-globin cluster in all vertebrates tested (Hughes et al. 2005). Interestingly, this gene contains within its introns three highly conserved regulatory elements (R1–R3) that are required to express the α-globin genes at high levels late in erythroid differentiation. Presumably, these embedded regulatory elements have ensured the close linkage (conserved synteny) between C16orf35 and the α-globin genes throughout vertebrate evolution (Hughes et al. 2005). The C16orf35 gene is widely expressed throughout development, predominantly from a housekeeping promoter that in many species is associated with a classical, unmethylated CpG island. However, we have also noted that expression of the C16orf35 gene is very highly induced in erythroid cells when the α-globin genes are fully activated (Kowalczyk et al. 2012; Lower et al. 2009).
The C16orf35 protein is well conserved across the metazoa with 87, 79, and 36 % amino acid identity of the human protein with its chicken, zebrafish, and Drosophila orthologues, respectively (Lunardi et al. 2009). Upon initial inspection, we and others (Lunardi et al. 2009; Neklesa and Davis 2009) could not identify any recognizable sequence features or domains associated with these proteins or any recognizable paralogues. However, more recently others have identified C16orf35 as a homologue of yeast Npr3 (nitrogen permease regulator 3). Npr3 plays a role in sensing amino acid starvation and mediating changes in cellular metabolism via the TOR (target of rapamycin) pathway. Npr3 has been shown to form a dimer with Npr2 (Neklesa and Davis 2009), yet no homology between these subunits has been described. The human protein corresponding to C16orf35 has thus been annotated as NPRL3 (Nitrogen Permease Regulator-Like 3) and it too forms a dimer with NPRL2 (the orthologue of Npr2) in human cells (Neklesa and Davis 2009). This suggests that NPRL2 and NPRL3 form an evolutionarily conserved complex, although its implied role in mTOR (mammalian target of rapamycin) signaling has not been established in human.
To analyse the role of NPRL3 (C16orf35), we analysed in further detail a previously described mouse model in which expression of the Nprl3 protein has been ablated by removal of its constitutive promoter (Kowalczyk et al. 2012). This model has enabled us to examine the effects of a null phenotype in mice in which both alleles have been inactivated. These mice die late in gestation with a range of cardiac defects, including outflow tract abnormalities and ventricular-septal defects.
Materials and methods
Protein sequence alignments
Initial sequence similarity searches were performed with BLAST (Altschul et al. 1997) against the nonredundant protein sequence databases Uniref50 and Uniref90 (Wu et al. 2006). Multiple sequence alignments of homologous protein sequences were generated with the program T-Coffee and HMMer (Eddy 1996; Notredame et al. 2000) using default parameters, slightly refined manually and visualized with the Belvu program (Sonnhammer and Hollich 2005). Profiles of the alignment as global hidden Markov models (HMMs) were generated using HMMer (Eddy 1996). Profile-based sequence searches were performed against Uniref50 (Wu et al. 2006) using HMMsearch (Eddy 1996). Fold recognition analyses were performed using profile-to-profile comparisons with HHpred software (Soding et al. 2005). Secondary structure predictions were acquired using PsiPred (Jones 1999). The NPR2/NPR3 dendrogram in Fig. 1 was generated by the neighbour-joining method (Saitou and Nei 1987) using ClustalW (Higgins et al. 1996) and edited with Treetool (Maciukenas 1994).
More specifically, iterative similarity searches using profile hidden Markov models (HMMer) (Eddy 1996) against the nonredundant protein sequence databases Uniref50 (Wu et al. 2006), with C16orf35 (SwissProt: CP035_HUMAN) N-terminal conserved region (amino acids 66-168) as the query identified remote homologues in the NPR2 family with statistically significant E values (inclusion threshold < 0.005). Reciprocally, iterative similarity searches with the NPRL2 (SwissProt: TUSC4_HUMAN) N-terminal conserved region (amino acids 37–124) as the query produced convergent results. Hidden Markov models of the yeast Npr3 domains alignment and those for Npr2 were compared using HHpred (Soding et al. 2005) and found to be highly significant (E < 10−5). A protein-domains hunting strategy, based on profile–profile comparisons (HHpred), identified both Npr3 and NPRL2 protein families as having three HTH (helix-turn-helix) domains located at their C termini. Moreover, two high-performing methods of protein structure prediction (Zhang 2008), HHpred and I-TASSER (Soding et al. 2005; Zhang 2008), independently yielded consistent results.
Fetal liver cell culture
Erythroid cells were grown from foetal livers following a published protocol (Dolznig et al. 2001).
RNA sequencing
Total RNA was prepared using Trizol reagent (Sigma) and was DnaseI-treated (Ambion). Poly(A)+ mRNA was isolated from total RNA using the PolyA selection kit (Promega) according to the manufacturer’s protocol. Poly(A)+ mRNA from erythroid cells was depleted of globin transcripts using GlobinClear (Ambion). cDNA libraries were prepared from poly(A)+ mRNA from Nprl3 extended knockout and wild-type cultured foetal liver cells using the mRNA-Seq pair-end kit (Illumina) and then sequenced using massively parallel sequencing (Illumina, GAII) with 50-bp end reads. A total of 67 and 37 million reads were generated from Nprl3 extended knockout (ΔP6-R3 −/−) and wild type, respectively. Reads were mapped to the mm9 mouse genome build using TopHat 1.1.1b (Trapnell et al. 2009). Transcript abundances and differential expression were tested using Cufflinks and Cuffdiff (Mortazavi et al. 2008) with current Ensembl transcript ID and Refseq gene annotation. Gene ontology analysis was performed using DAVID (da Huang et al. 2009). RNA-Seq data has been submitted to NCBI Gene Expression Omnibus (GSE26877).
Animal work
All animal work was carried out according to UK Home Office regulations under the appropriate project licenses. Mice were killed by cervical dislocation and dissections performed immediately. To obtain staged mouse embryos, the morning on which a vaginal plug was noted was taken as embryonic day 0.5. Embryos were dissected from the uterus and placenta as described in Nagy et al. (2003).
Histology
Embryos were fixed overnight at 4 °C in 4 % PFA, washed twice in PBT (PBS + 0.1 % Tween 20), and dehydrated by sequential washing in 25, 50, and 75 % ethanol in PBT and finally by two washes in 100 % ethanol. For embedding in paraffin wax, embryos were washed twice in Histoclear II (National Diagnostics) and immersed in Paraplast compound (Sigma) at 60 °C for 3–6 h prior to embedding. Six-micron sections were cut and mounted on Superfrost®Plus microscope slides (VWR International). Tissue sections were deparaffinised by incubation in Histoclear II for 8 min, rehydrated by sequential washing in 100, 95, and 70 % ethanol, stained with Ehrlich’s hematoxylin (RA Lamb) for 1 min, and washed with tap water for 2 min. Sections were stained with 0.1 % eosin (RA Lamb) for 1 min. Stained sections were washed in tap water for 2 min, hydrated in ascending ethanol solutions (70, 95, and twice in 100 %), washed twice in Histoclear II, and allowed to dry for 10 min. Subsequently, stained sections were mounted using glass coverslips (BDH) and Histomount (RA Lamb). Tissue sections were examined using a Leica light microscope and photographs taken using OpenLab software (Improvision).
Skeletal preps
Embryos for skeletal staining were dissected as described above and fixed in 95 % ethanol for 1–3 days. They were immersed in Alcian blue stain (Sigma) (75 % ethanol, 20 % acetic acid, 3 mg/ml Alcian blue) for 21–28 days at 37 °C. They were differentiated in 95 % ethanol, macerated in 1 % KOH for 1–5 days, and stained in 0.1 % aqueous Alizarin red (Sigma) for 24 h. Embryos were washed in tap water and cleared in 0.8 % KOH and 20 % glycerol, sequentially dehydrated, and stored in 50 % ethanol/50 % glycerol.
Magnetic resonance imaging
Single- and multiembryo imaging and data reconstruction and analysis were performed as described previously (Szumska et al. 2008).
Patients
DNA from 67 patients with dilated cardiomyopathy and/or left ventricular noncompaction and ventriculoseptal defects (VSD) that was collected in the Department of Cardiology of Children’s Hospital Boston and the Department of Cardiovascular Medicine at the University of Oxford and that of 37 normal controls was used to survey the coding regions of the Nprl3 gene. Patients from the UK were ascertained through the Department for Cardiovascular Medicine clinical practice or the practice of referring physicians and evaluated by physical examination, echocardiography, and/or cardiac MRI and ECG, allowing the diagnosis of Left Ventricular Non Compaction (LVNC) to be made. All participants gave informed consent and local research ethical approval (ref. 09/H0605/3) was obtained. Patients from US were ascertained at Children’s Hospital Boston. The diagnoses were made on the basis of echocardiographic images interpreted by board-certified cardiologists. DNA samples and phenotypic information were collected under research projects approved by the Internal Review Board of Children’s Hospital Boston with informed consent.
Sequencing
Amplicons over the coding regions of the human NPRL3 gene were amplified with FastTaq (Roche). Sequencing was performed using Big Dye chemistry on Applied Biosystems PRISM 3730 Genetic Analyzer. All sequences were analysed using Mutation Surveyor software (SoftGenetics LCC).
Results
Computational sequence analysis of the NPRL3 family
Consistent with previous reports (Jordan et al. 2007; Lunardi et al. 2009; Neklesa and Davis 2009), we identified NPRL3 as a likely orthologue of yeast Npr3. Sequence similarity between yeast Npr3 and human NPRL3 proteins was statistically highly significant (E < 10−5). Moreover, database searches using Npr3 also identified it to be a remote homologue of a second family of proteins (Fig. 1a, b), namely, the NPR2 family (Pfam family: NPR2). Iterative interrogation of protein sequence databases using HMMer, a profile-to-sequence comparison method (Eddy 1996), with the N-terminal region of human NPRL3 (UniProt:Q12980; amino acids 66–168) as the query, identified remote homologues in the NPR2 family (Fig. 1a, b) with statistically significant E values (inclusion threshold E < 0.005). A similar, but reciprocal, search using human NPRL2 (UniProt:Q8WTW4; amino acids 37–124) as the query corroborated the evolutionary relationship of Npr3 and Npr2 families. Consequently, members of the NPR2 and NPR3 families are also homologous and thus share a common ancient ancestry. These results are in agreement with those recently generated automatically by PFAM (Clan:NPR/CL0435) (Finn et al. 2010).
Multiple alignment of NPR2 and NPR3 sequences reveals evolutionarily conserved regions shared between both families (Fig. 1b). The proteins’ N-terminal regions contain the most conserved sequence between these families (shown in orange in Fig. 1a), whilst their C-terminal regions contain three homologous sequences (green, purple, and blue ovals in Fig. 1a) present in all NPR2 and NPR3 protein family members. A protein domain hunting strategy, based on profile–profile comparisons and protein structure prediction using HHpred (Soding et al. 2005), demonstrated that these regions contain consecutive helix-turn-helix domains (indicated in green, purple, and blue in Fig. 1a, b; HHpred probability >94 %; E = 0.021) that point to their potential roles in binding nucleic acid (RNA or DNA) rather than protein molecules (Aravind et al. 2005; Yoshizawa et al. 2005), although we do not rule out the latter. These sequence similarities were all highly significant, thereby indicating homologies (Supplementary Fig. 1). Sequence conservation between the two families is illustrated in Fig. 1b.
These findings therefore show that not only is human NPRL3 a yeast Npr3 orthologue, it is also a paralogue of NPRL2, with which it heterodimerises (Neklesa and Davis 2009). Yeast Npr2 and Npr3 are known to bind proteins in common, including Cdc45 (Tong et al. 2004), Csm3 (Pan et al. 2006), and Hsp82 (McClellan et al. 2007). These observations are consistent with Npr2 and Npr3 being subunits of a heterodimer, since paralogues often possess common interaction partners (Baudot et al. 2004; Musso et al. 2007).
Transcriptome analysis
We previously generated two mouse models in which the Nprl3 promoter sequence was deleted by homologous recombination (ΔP6 −/− and ΔP6-R3 −/−) (Kowalczyk et al., 2012) (see schematic diagram in Supplementary Fig. 2). Both models abolished Nprl3 transcription in all tissues tested apart from erythroid cells. We have recently shown that transcription of Nprl3-related RNAs in erythroid cells originates from intragenic, erythroid-specific enhancers embedded in the Nprl3 gene which produce noncoding RNAs (so-called meRNAs). Importantly, the subtle 2.3-kb promoter deletion (ΔP6) abolished expression of the Nprl3-encoded protein in all tissues (Kowalczyk et al. 2012).
To assess the general consequences of Nprl3 inactivation, we next analysed the transcriptomes of erythroid cells derived from either wild-type or homozygous mutant (ΔP6-R3 −/−) mice previously generated by our laboratory (Kowalczyk et al. 2012). Although either mouse model could have been analysed for this purpose, we chose to analyse ΔP6-R3 −/− mice. As expected, in the absence of the promoter, we observed only multiexonic RNA transcripts (meRNAs) originating from the remaining intragenic enhancers within the Nprl3 locus. Since these meRNA transcripts have low coding potential, as expected, no NPRL3-associated protein was detected (Kowalczyk et al. 2012).
RNA transcripts from wild-type and mutant (ΔP6-R3 −/−) cells were assembled and gene expression levels inferred (as FPKM values: fragments per kilobase of exon model per million mapped fragments) using TopHat and Cufflinks (Trapnell et al. 2009, 2010) and current RefSeq and Ensembl gene models, including mitochondrial genome genes. Considering only expressed genes (FPKM >10) in either mutant or wild-type samples, 4,513 significantly differentially expressed genes were identified using Cuffdiff (Trapnell et al. 2010). To investigate whether these differentially expressed genes are randomly distributed throughout Gene Ontology (GO) annotations (Gene Ontology Consortium 2010), we used DAVID (da Huang et al. 2009) to apply the one-tail Fisher’s exact test followed by Benjamini’s false discovery rate correction on the full set of GO terms.
The transcriptome of ΔP6-R3 −/− mice differed substantially from that of wild-type mice, with 101 and 51 GO terms being significantly (p < 0.1) enriched among genes up- and downregulated, respectively, in the mutant mice. The most significant annotation cluster enriched in upregulated genes contained five GO terms related to ribosomal biogenesis (Table 1). The most significant annotation cluster enriched in downregulated genes contained ten GO terms related to cell cycle (Table 1). A more stringent analysis identified the most significantly enriched GO terms that were consistent with the cluster analysis and further confirmed involvement in ribosomal biogenesis and cell cycle (Supplementary Table 1). These findings are consistent with a role for Nprl3 in regulating the well-documented pathway by which mTOR controls ribosomal biogenesis, protein synthesis, and the cell cycle (Wang and Proud 2006). This analysis was performed in erythroid cells, and, therefore, given the widespread pattern of Nprl3 expression, it will be important in the future to examine other cell types.
Phenotype of Nprl3 mutant
Male and female ΔP6 +/− mice grew and bred normally indicating that loss of one functional allele resulted in no major detectable phenotypic effects. ΔP6 +/− × ΔP6 +/− matings resulted in variable-sized litters. Genomic analysis of tail DNA taken at day 14 after birth revealed no ΔP6 −/− mice among 128 weaned offspring of these intercrosses (Table 2). Both WT and heterozygote offspring were born with the expected Mendelian ratio (χ2 test, p = 0.059). This indicated either embryonic or perinatal lethality of ΔP6 −/− mice.
To determine the developmental stage at which ΔP6 −/− embryos were lost, embryos from timed matings of ΔP6 +/− were retrieved on various days post-coitum (dpc). In total, 175 embryos between 10.5 and 15.5 dpc were examined and as a cohort the expected Mendelian distribution for all three genotypes (WT, ΔP6 +/−, and ΔP6 −/−) was observed (Table 2). Most of the ΔP6 −/− embryos were found dead prior to delivery (18.5 dpc). These results suggest that mutant mice die between 15.5 dpc and birth.
To determine the causes of this embryonic and/or perinatal lethality, embryos derived at various time points of development were examined to detect gross phenotypic abnormalities. Embryos were inspected in detail at four different stages of mid- to late gestation (10.5, 12.5, 14.5, and 15.5 dpc). ΔP6 −/− embryos from 10.5 dpc appeared normal and similar to the WT and ΔP6 +/− littermates. In general, ΔP6 −/− embryos could be morphologically distinguished from their WT littermates as early as 12.5 dpc and defects became more obvious at late gestation. The ΔP6 −/− embryos dissected at 15.5 dpc appeared slightly smaller and pale in comparison with their normal littermates.
Gross examination also showed that many ΔP6 −/− embryos had some defect of body wall closure producing small to large forms of umbilical hernia (liver hernia, Fig. 2a–f). In some embryos there was a complete failure to close the ventral body wall and thoracic cavity (Supplementary Fig. 3a, b). In the latter case, abdominal and thoracic organs (heart and intestines) were exposed through an open rib cage. At 15.5 dpc, it was rare that ΔP6 −/− embryos in utero were already dead as judged by the absence of heartbeat.
Most ΔP6 −/− embryos had hemorrhages and fragmented vasculature. Generalised oedema was frequently seen and in some cases nuchal translucency was also present (Fig. 2f). The development of such oedema is frequently associated with cardiovascular defects (Haak et al. 2002).
The Nprl3 knockout exerts a major effect on cardiovascular development
To determine the cause of perinatal lethality in more detail, we examined the structure of the internal organs of ΔP6 −/− mice. Two such embryos were sectioned (coronally and sagitally) and their tissues stained with hematoxylin and eosin (H&E). The histological examination and comparison of ΔP6 −/− and WT littermates showed that most major internal organs were present and generally of similar, normal appearance.
The major abnormalities in mutant homozygote embryos were detected in the heart and great vessels. By this stage of development, WT hearts are four-chambered (Fig. 3a, b) and all major structures are fully developed. The ventricular muscle is dense and the trabeculi are organised on the inner side of the thick compact zone (Fig. 3a, b). By contrast, hearts of ΔP6 −/− embryos were dramatically enlarged (Fig. 3c, d) compared to those of WT littermates (Fig. 3a, b). Nprl3-deficient hearts contained all four chambers (Fig. 3c, d), separated as expected and with mitral and tricuspid valves. However, the ventricles were dilated and abnormally structured (Fig. 3c, d). Detailed analysis showed prominent clear passage between the ventricles (ventricular septal defect, VSD) in both ΔP6 −/− embryos initially examined (Fig. 3d). Moreover, in Nprl3-deficient hearts the ventricles were severely hypoplastic and their compact muscle layer was almost absent (Fig. 3c, d). The trabeculi of the left ventricle were hypertrophic with deep intertrabecular recesses (Fig. 3c, d). The myocardium of the right ventricle was similarly disorganised (Fig. 3c, d). This demonstrates that Nprl3-deficient hearts have disrupted condensation of the myocardium.
In addition to these studies we examined several ΔP6 −/− embryos using magnetic resonance imaging (MRI), which was previously reported to allow identification of congenital malformations with high spatial resolution (Schneider et al. 2004) and which had been used to analyse subtle cardiac and visceral malformations in late gestation mouse embryos (Szumska et al. 2008). Analysis was performed on 10 ΔP6 −/− embryos, 14 ΔP6 +/− embryos, and 8 WT embryos from ΔP6 +/− intercrosses retrieved at 14.5 and 15.5 dpc. While there was no evidence of cardiac abnormalities in WT (Fig. 4a, b) or ΔP6 +/−, ΔP6 −/− mice showed severe cardiac malformations, including ventricular septal defects, right-sided aortic arch and pulmonary artery (Fig. 4c, d), a right-sided pulmonary artery forming a vascular ring with normally localised aortic arch, and an interrupted aortic arch. Moreover, in one case there was a double-outlet right ventricle (DORV) or a form of overriding aorta, where the aorta is positioned directly over a VSD and not over the left ventricle. In three other ΔP6 −/− embryos the hearts were contracted precluding further analysis. The details of MRI-based malformations in ΔP6 −/− mice are summarised in Table 3.
In addition to these multiple cardiac malformations, there were other signs consistent with failure of blood perfusion and/or general heart failure, including general oedema together with pericardial oedema (Fig. 5a), dilated hepatic veins (data not shown), and large bilateral cysts in jugular lymphatic sacs (Fig. 5b). Additionally, in a subset of ΔP6 −/− embryos, some internal organs (e.g., lungs, thymus, kidneys, and adrenals) appeared to be smaller as judged by eye. Liver hernia was frequently seen. Similarly, cleft palate was observed (Fig. 5c, d). The body size of some Nprl3-deficient embryos was noted to be decreased.
Using the multiembryo MRI technique, a wider range of malformations was observed in ΔP6 −/− embryos at 14.5 dpc than was detected by standard histological analysis. Importantly, ΔP6 +/− mice did not show any of the features described in ΔP6 −/− mice except for one which had a large cleft palate. The remaining embryos did not differ significantly from WT littermates. Finally, we examined skeletal morphology which showed no abnormalities (data not shown).
In summary, these findings showed that mice in which the promoter of the Nprl3 gene had been deleted died in late gestation, often with severe cardiac defects.
Analysis of individuals hemizygous for NPRL3
Although heterozygous mice appeared to survive normally, it was of interest to determine whether human heterozygotes, with long life spans and potential exposure to environmental stresses, display any evidence for abnormal myocardial structure or function or any other late-developing congenital abnormalities. Two previously reported individuals with α-thalassaemia due to deletions that also inactivate NPRL3 (Hatton et al. 1990; Wilkie et al. 1990) were investigated. Neither had any symptoms or signs attributable to cardiac dysfunction and MRI scans of their hearts revealed no significant abnormalities (data not shown). Furthermore, we also investigated 12 patients previously diagnosed with left ventricular noncompaction (resembling the myocardial defect seen in ΔP6 −/− mice) to determine whether they had associated α-thalassaemia (due to removal of NRPL3 gene and the α-globin regulatory elements) but found no such instance.
Finally, we performed a pilot study in a cohort of patients with various types of cardiomyopathy and/or left ventricular noncompaction and ventricular septal defects (VSD) to look for possible disease-causing mutations within the NPRL3 gene. We screened coding regions of NPRL3 in 67 patients and 37 normal controls by direct sequencing. We identified three well-described single nucleotide polymorphisms (SNPs) and one polymorphism not found in current SNP databases (Table 4). Despite these searches no disease-causing mutations were found in the patients studied here.
Discussion
Evolutionary studies have shown that the prototypical globin cluster has been located adjacent to a widely expressed gene (NPRL3) in all species since the evolution of jawed vertebrates more than 450 million years ago (Hughes et al. 2005). Key cis-acting regulatory elements that control expression of the α-globin genes lie within the introns of this gene. This may account for the conserved synteny between C16orf35 and the α-globin cluster. We previously noted that many deletions that cause α-thalassaemia in humans also inactivate C16orf35, and heterozygotes for such mutations appear to be phenotypically normal. The role of this highly conserved gene remained unknown.
Here we have confirmed that NPRL3 is the orthologue of the yeast protein Npr3 (nitrogen permease regulator 3) (Neklesa and Davis 2009), whose name originates from the observation that the yeast protein acts as part of a complex (with Npr2) which senses amino acid starvation. The Npr2/Npr3 complex influences cell metabolism via the mTOR pathway (Neklesa and Davis 2009). By separating the protein structure into smaller domains we were able to show for the first time that Npr3 and its interacting partner Npr2 are, in fact, paralogues, as are their human and mouse counterparts (NPRL3 and NPRL2). Although it has been shown that NPRL2 and NPRL3 physically interact with each other (Neklesa and Davis 2009), it remains to be seen whether, like their yeast orthologues, they act via the mTOR pathway. The wide phylogenetic distributions of NPR2 and NPR3 orthologues, which are highly conserved in sequence and domain architecture from yeast to human, certainly suggest that they perform fundamental cellular roles.
Of interest, we found that inactivation of the mouse Nprl3 gene leads to a substantial increase in expression of many ribosomal protein genes and reduction of cell cycle-associated genes. Since disruption of yeast Npr2 or Npr3 is also known to result in a large (~2.5-fold) increase in ribosomal protein subunit gene expression and causes a severe proliferation defect (Neklesa and Davis 2009), transcriptional coupling of Npr3, ribosomal protein genes, and cell cycle is clearly a conserved feature of both yeast and mammals. Yeast Npr2 and Npr3 act as regulators of the TOR complex 1 (TORC1), and loss of TOR results in inhibition of ribosomal protein gene transcription (Hardwick et al. 1999; Powers and Walter 1999). Consequently, it appears that both yeast Npr3 and mouse Nprl3 may act by suppressing TOR-dependent transcription of ribosomal protein genes and affect the cell cycle. Further investigation of mammalian Nprl3 may elucidate how it affects mTOR signaling and how this controls protein synthesis and the cell cycle.
Analysis of ΔP6 −/− embryos showed that the Nprl3 protein is essential for normal mouse development. Consistent with its widespread pattern of expression (Mitiku and Baker 2007), we noted a variety of developmental abnormalities affecting many different organs when the Nprl3 gene is deleted. Nevertheless, the most consistent and dramatic effects are seen in heart development. These findings suggest that failure of normal cardiovascular development may, at least in part, be responsible for the observed embryonic/perinatal lethality. Although it is not known if NPRL2 and NPRL3 interact with the human mTOR pathway, it is interesting that mouse knockouts of the mTOR pathway components similarly lead to embryonic lethality (Guertin et al. 2006). Furthermore, in a wide range of studies (Shioi et al. 2002, 2003), including a conditional knockout model (Zhang et al. 2010), it has been shown that this pathway is important for the survival and normal function of cardiac cells.
Other malformations observed in ΔP6 −/− embryos, such as small internal organs and cleft palate, could be secondary to a compromised cardiovascular system, which may lead to insufficient blood flow to sustain rapid growth of developing embryos. Of course, given its ubiquitous pattern of expression, it is also possible that Nprl3 may play a cell autonomous role in the proper development of other organs besides the heart. Again, these effects could be mediated by the mTOR pathway since many mutations of regulators lying upstream and downstream of this pathway have been associated with acquired and inherited genetic disorders in mice and humans (Inoki et al. 2005).
In summary, we have demonstrated that in a mouse model, disruption of Nprl3 results in developmental defects (particularly in the cardiovascular system) leading to embryonic lethality late in gestation. Its wide conservation, widespread expression, and potential involvement in important general mechanisms and pathways suggest that NPRL3 underpins important cellular functions throughout development. Although the precise molecular functions of NPRL3 remain to be determined, the work presented here should focus future work on the normal role of NPRL3 and how mutations within it may give rise to human genetic disease.
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Acknowledgments
This work was supported by Marie Curie RTN EUrythron (MRTN-CT-2004-005499 to MSK), European Molecular Biology Organisation (ALT 325-2008 to LSP), Medical Research Council [Chris P. Ponting (C.P.P.) laboratory and Douglas R. Higgs (D.R.H.) laboratory], and the National Institute of Health Biomedical Research Centre Programme (D.R.H.) laboratory. We thank Dr. Taavi Neklesa for critically reading the manuscript. Thanks to Liz Ormondroyd from the Department of Cardiovascular Medicine (John Radcliffe Hospital, Oxford, UK) for collecting patients for the study. We also thank Pik-Shan Li, Christina Rode, and Sue Butler for assistance with transgenic lines production, breeding, and genotyping. We thank the patients for participation in this study.
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The authors have no conflicts of interests to declare.
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Kowalczyk, M.S., Hughes, J.R., Babbs, C. et al. Nprl3 is required for normal development of the cardiovascular system. Mamm Genome 23, 404–415 (2012). https://doi.org/10.1007/s00335-012-9398-y
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DOI: https://doi.org/10.1007/s00335-012-9398-y