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Biallelic Mutations in NBAS Cause Recurrent Acute Liver Failure with Onset in Infancy
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abstract
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Acute liver failure (ALF) in infancy and childhood is a life-threatening emergency. Few conditions are known to cause recurrent acute liver failure (RALF), and in about 50% of cases, the underlying molecular cause remains unresolved. Exome sequencing in five unrelated individuals with fever-dependent RALF revealed biallelic mutations in NBAS. Subsequent Sanger sequencing of NBAS in 15 additional unrelated individuals with RALF or ALF identified compound heterozygous mutations in an additional six individuals from five families. Immunoblot analysis of mutant fibroblasts showed reduced protein levels of NBAS and its proposed interaction partner p31, both involved in retrograde transport between endoplasmic reticulum and Golgi. We recommend NBAS analysis in individuals with acute infantile liver failure, especially if triggered by fever.
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Acute liver failure (ALF) in infancy and childhood is a life-threatening emergency. Few conditions are known to cause recurrent acute liver failure (RALF), and in about 50% of cases, the underlying molecular cause remains unresolved. Exome sequencing in five unrelated individuals with fever-dependent RALF revealed biallelic mutations in NBAS. Subsequent Sanger sequencing of NBAS in 15 additional unrelated individuals with RALF or ALF identified compound heterozygous mutations in an additional six individuals from five families. Immunoblot analysis of mutant fibroblasts showed reduced protein levels of NBAS and its proposed interaction partner p31, both involved in retrograde transport between endoplasmic reticulum and Golgi. We recommend NBAS analysis in individuals with acute infantile liver failure, especially if triggered by fever.
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Main Text
Acute liver failure (ALF) is a very severe, life-threatening event which can result from toxin exposure, inherited metabolic disease, autoimmune disease, infectious disease, shock, and other rare causes. The exact incidence of pediatric ALF is unknown, and in about 50% of cases the underlying cause remains obscure.1,2 Prognosis is guarded and emergency liver transplantation is often the only therapeutic option. Known causes of recurrent acute liver failure (RALF) with clinical and biochemical hepatic recovery in the interval include fulminant viral hepatitis, autoimmune hepatitis, disorders of long-chain fatty acid oxidation and the carnitine cycle, dihydrolipoamide dehydrogenase (E3) deficiency (MIM: 246900), and Wolcott-Rallison syndrome (MIM: 226980).3–7 Here we report the identification of homozygous or compound heterozygous mutations in NBAS (neuroblastoma amplified sequence) in 11 individuals with RALF starting in infancy.
A group of four unrelated German individuals with previously unclassified early-onset RALF (according to the definition of the Pediatric Acute Liver Failure Study Group)1 was recruited in one clinical center (University Hospital Heidelberg) and jointly analyzed. Clinical and genetic findings are summarized in Table 1. Informed consent to participate in the study was obtained from all affected individuals (or their parents, in the case of minor study participants). The study was approved by the ethical committees of the University Hospital Heidelberg and of the Technische Universität München. Whole exome sequencing was performed on genomic DNA from four unrelated affected individuals as described previously.8 Using a frequency filter of minor allele frequency < 0.1% in our in-house database and public databases, we identified six, seven, three, and nine compound heterozygous or homozygous variants in individuals F1:II.1, F2:II.1, F3:II.1, and F4:II.3, respectively. NBAS (GenBank: NM_015909.3, MIM: 608025) is the only gene where biallelic mutations were identified in all affected individuals (Figure 1). In individual F5:II.2, presumably disease-causing mutations in NBAS had been identified in a preceding exome sequence analysis but the relevance of this finding had remained unclear. The analysis of exome sequencing data from approximately 4,000 individuals with unrelated phenotypes (all subjects were sequenced in the Institute of Human Genetics, Helmholtz Zentrum München, and their data stored in an in-house database) identified only one additional sample with two rare variants in NBAS potentially compatible with a recessive disease. However, parental samples were not available and a compound heterozygous state of the two variants has not been confirmed. We subsequently studied 15 additional unrelated individuals with unresolved RALF and ALF from four additional clinical centers by Sanger sequencing. Primer sequences and PCR conditions for Sanger sequencing of NBAS are available on request. This resulted in the identification of six additional individuals from five families with compound heterozygous mutations in NBAS (Figure 1). All 11 individuals carry at least one missense mutation on one allele. All missense mutations change evolutionarily conserved amino acid residues (Figure 2) and are accordingly predicted to be damaging (PolyPhen-2 and SIFT). Carrier testing showed that each parent analyzed was heterozygous for one allele; the mother of individual F4:II.3 had died before the study was performed so testing was impossible and parental samples of individuals F8:II.2, F9:II.2, and F10:II.1 were not available. Remarkably, in two families, F8 and F9, the oldest siblings had died in early infancy due to acute liver failure, aged 14 and 11 months, respectively; however, no material was available to genetically confirm their clinical diagnosis of NBAS deficiency.
Notably, all mutations, which are not predicted to cause a loss of function, are clustered in two regions in the first half of the gene, exons 8–12 and exons 21–28. The mutations in the latter region affect the secretory pathway sec39 domain of NBAS (Figure 2). Individual F2:II.1 carries a homozygous missense variant and individual F3:II.1 an in-frame deletion of one amino acid compound heterozygous with a missense mutation. All other affected individuals are compound heterozygotes for one out of seven different predicted loss-of-function mutations (three stop mutations, two frameshift, and two splice site mutations) plus a missense mutation or a deletion of a single amino acid. None of the NBAS missense mutations is present in >120,000 alleles from the Exome Aggregation Consortium (ExAC) Server (12/2014). Three of the loss-of-function mutations, c.686dup (p.Ser230Glnfs∗4), c.2827G>T (p.Glu943∗), and c.3010C>T (p.Arg1004∗), are listed in the heterozygous state 59×, 8×, and 1×, respectively (MAF < 0.04%). Although we have no indication for a shared haplotype for the c.3164T>C variant identified heterozygous in three families, the exome data suggests a common founder c.2708T>G mutation in German families 2 and 4.
Next, the functional consequences of NBAS mutations on the protein level were investigated. In eukaryotic cells, soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) tethering factors mediate the docking and fusion of transport vesicles with target membranes. Fusion of membranes is mediated by membrane-bound proteins on the transport vesicles (v-SNARE) and target membrane (t-SNARE). NBAS is thought to function as a component of an ER tethering complex that interacts with the t-SNAREs p31, BNIP1, and STX18 at the ER and the v-SNARE Sec22b. This tethering complex also includes ZW10, RINT1, and Sly1 (see Figure S1).9,10 Mutant and control fibroblasts were cultivated in D-MEM media supplemented with 10% FBS, 1% penicillin-streptomycin, and 200 μM uridine at 37°C and 5% CO2. For immunoblots, cells were collected, washed in PBS, and resolved in RIPA buffer.11 10 μg of protein of every sample were separated on a 4%–12% acrylamide gradient gel (LONZA). Primary antibodies (all Sigma-Aldrich) against NBAS (1:2,000), p31 (USE-1) (1:250), and β-actin (1:15,000) were incubated overnight. Enhanced chemiluminescence of proteins was detected with a Vilberscan Fusion FX7. Protein levels were quantified with the software Bio-1D. Testing of individual F1:II.1 fibroblasts showed a significant decrease in NBAS steady-state levels (p = 0.03; two-tailed unpaired t test). Extending the quantification of NBAS protein to affected individuals from families 2–5 and 7 showed a reduction of NBAS levels to 18%–36% in comparison to controls, indicating a substantial impairment of protein translation and/or stability in all seven affected individuals investigated (Figure 3 shows representative findings for individuals from families 1–5). Moreover, the reduction of NBAS was concomitant with a reduction of its proposed interaction partner p31, supporting an important function of NBAS within the syntaxin 18 complex (Figure S1). None of the additional components have been associated with a human disorder. Mouse models of deleted p31 and RINT1 were shown to be embryonic lethal.12,13
Next, we investigated whether an assumed defect in the assembly of the ER tethering complex impairs glycosylation and/or results in increased ER stress. Isoelectric focusing of transferrin, alpha-1-antitrypsin, and apolipoprotein CIII followed by in-gel immunodetection was performed in sera of a control subject, a COG6-CDG individual, and five individuals with NBAS mutations. Although the observed patterns indicated a clear deficiency in N-/O-glycosylation in the CDG individual, no differences were observed for the NBAS-mutant individuals compared to controls (Figure S2). These findings suggest that under the investigated conditions NBAS deficiency does not disturb retrograde transport between ER and Golgi to the extent that obvious changes in glycosylation patterns can be observed.
We next performed expression profiling in NBAS-mutant fibroblast to test for alterations suggestive for ER stress. Total cellular RNA was isolated from fibroblasts of three NBAS-affected individuals (F1:II.1, F2:II.1, F5:II.2) and 12 healthy controls. The quality of the RNA isolated from whole-cell lysates was determined with the Agilent 2100 BioAnalyzer (RNA 6000 Nano Kit, Agilent). All samples had a RNA integrity number (RIN) value greater than 8. RNA libraries were sequenced as 100 bp paired-end runs on an Illumina HiSeq2500 platform as described.14 In order to get expression measurements, we counted reads with HTSeq-count using the intersection-strict option on 20,345 protein coding genes from the Gencode database (GRCh37, p13, 19.07.2013).15 Read counts were normalized with size factors computed by DESeq2 to account for differences in sequencing depth per sample.16 We discarded genes with an average normalized expression below 10 over all samples and performed all consecutive analysis on the remaining 13,392 genes. Although there was no global change in gene expression, we did observe a significant increase in the expression of genes involved in ER stress response in NBAS-mutant fibroblasts compared to controls (Figure 4).
Together, our genetic and experimental findings provide evidence that mutations affecting functionally conserved domains in NBAS resulting in severely decreased NBAS levels cause RALF in infancy. Although no changes in glycosylation patterns were observed in the conditions investigated, expression profiles in NBAS mutant fibroblasts are suggestive for ER stress. RALF due to mutated NBAS is a presumably relatively frequent inherited cause of RALF, because NBAS screening of 15 individuals with RALF or acute infantile liver failure resulted in the discovery of six affected individuals from five additional families. The pivotal feature of this disease is RALF precipitated by intercurrent febrile illnesses during infancy and childhood. Intriguingly, with conservative management, liver function recovered completely and was normal in the interval. Crises are heralded by vomiting and lethargy and start rather uniformly with massively elevated ASAT and ALAT (range of maximum ALAT 4,001–17,700 U/l; normal < 50 U/l), followed by coagulopathy requiring FFP substitution (maximum INR 10; normal < 1.2) and mild to moderate jaundice (range of maximum total bilirubin 46.8–207.4 μmol/l; normal < 20.4 μmol/l). In some cases, significant hypoglycemia, hyperammonemia (maximum 209 μmol/l; normal < 53 μmol/l), and hepatic encephalopathy developed, which we consider to be secondary to ALF. Several affected individuals suffered from a range of comorbidities including cardiomyopathy, autoimmune gastrointestinal diseases, and neurological phenotypes such as epilepsy. However, none of those conditions is present in two individuals (Table 1).
Mutations in NBAS have not been linked to liver disease before, but a homozygous missense mutation c.5741G>A (p.Arg1914His) in the C-terminal domain of unknown function of NBAS has been associated with a syndrome of short stature, cone and optic nerve atrophy, and Pelger-Huët anomaly in Yakuts (SOPH syndrome [MIM: 614800]).17 RALF-causing NBAS deficiency and SOPH syndrome are clearly different clinical entities. Importantly, individuals with SOPH syndrome were not reported to have ALF or any hepatic disease manifestation and the impact of the SOPH-associated mutation on NBAS protein function is unknown.
None of the individuals with NBAS-induced (R)ALF carried two loss-of-function mutations in NBAS. However, NBAS mutations led to low levels of the gene product of about 25% NBAS protein (compared to healthy probands). The affected individuals recovered completely in the intervals between the crises and otherwise presented a rather mild phenotype, so reduced NBAS protein levels due to the mutations appear to be sufficient for normal function of most tissues including liver under afebrile conditions.
The physiologic function of NBAS is not yet understood. In yeast, sec39 is involved in retrograde transport between ER and Golgi.9 Aoki et al.9 provided evidence for a similar function of NBAS in humans where it is interacting with p31. Together with other SNARE proteins, they are forming the syntaxin 18 complex implicated in ER membrane fusion. Concomitant with reduced NBAS levels, p31 levels were also decreased, providing additional evidence that both proteins are subunits of the same SNARE complex. Similar findings were observed after targeted knockdown in HeLa cells.9 The exact mechanism of ALF due to NBAS deficiency remains unclear. We reason that a catabolic state with high energy demand during febrile infections or the raised temperature itself might be the starting points of the derailment, speculatively via a thermal susceptibility of the syntaxin 18 complex.
In contrast to acute infantile liver failure resulting from mutations in TRMU (MIM: 613070), MARS (MIM: 615486), or LARS (MIM: 615438), NBAS deficiency was not associated with increased serum lactate or muscular hypotonia. In about 50% of cases of acute infantile liver failure, the underlying cause remains undetermined. Some of these children might have an underlying genetic disorder or predisposition. The detection rate of NBAS mutations in random individuals with (recurrent) acute infantile liver failure was very high (6 out of 15 screened individuals), so NBAS deficiency might be a frequent cause of not only RALF but also isolated ALF at least in children. The differing genetic origins of affected individuals and variety of mutations suggest that this autosomal-recessive disease is not a regional phenomenon.
In conclusion, mutations in NBAS are delineated as a previously unknown cause of acute liver failure with onset in childhood triggered by febrile infections. It is possible that the affected individuals reported in this study present the severe end of the phenotypic spectrum. Notably, in families F8 and F9, two older siblings had died from acute liver failure, aged 14 and 11 months. Unfortunately, no material was available for diagnostics from the deceased individuals. However, the finding of NBAS mutations in their siblings suggests NBAS-induced ALF. Hence, these individuals might provide examples for a lethal course of NBAS deficiency. We recommended sequencing NBAS in cases of ALF in infancy and childhood of unknown cause, especially in individuals with fever-associated ALF and/or RALF.
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Main Text
Acute liver failure (ALF) is a very severe, life-threatening event which can result from toxin exposure, inherited metabolic disease, autoimmune disease, infectious disease, shock, and other rare causes. The exact incidence of pediatric ALF is unknown, and in about 50% of cases the underlying cause remains obscure.1,2 Prognosis is guarded and emergency liver transplantation is often the only therapeutic option. Known causes of recurrent acute liver failure (RALF) with clinical and biochemical hepatic recovery in the interval include fulminant viral hepatitis, autoimmune hepatitis, disorders of long-chain fatty acid oxidation and the carnitine cycle, dihydrolipoamide dehydrogenase (E3) deficiency (MIM: 246900), and Wolcott-Rallison syndrome (MIM: 226980).3–7 Here we report the identification of homozygous or compound heterozygous mutations in NBAS (neuroblastoma amplified sequence) in 11 individuals with RALF starting in infancy.
A group of four unrelated German individuals with previously unclassified early-onset RALF (according to the definition of the Pediatric Acute Liver Failure Study Group)1 was recruited in one clinical center (University Hospital Heidelberg) and jointly analyzed. Clinical and genetic findings are summarized in Table 1. Informed consent to participate in the study was obtained from all affected individuals (or their parents, in the case of minor study participants). The study was approved by the ethical committees of the University Hospital Heidelberg and of the Technische Universität München. Whole exome sequencing was performed on genomic DNA from four unrelated affected individuals as described previously.8 Using a frequency filter of minor allele frequency < 0.1% in our in-house database and public databases, we identified six, seven, three, and nine compound heterozygous or homozygous variants in individuals F1:II.1, F2:II.1, F3:II.1, and F4:II.3, respectively. NBAS (GenBank: NM_015909.3, MIM: 608025) is the only gene where biallelic mutations were identified in all affected individuals (Figure 1). In individual F5:II.2, presumably disease-causing mutations in NBAS had been identified in a preceding exome sequence analysis but the relevance of this finding had remained unclear. The analysis of exome sequencing data from approximately 4,000 individuals with unrelated phenotypes (all subjects were sequenced in the Institute of Human Genetics, Helmholtz Zentrum München, and their data stored in an in-house database) identified only one additional sample with two rare variants in NBAS potentially compatible with a recessive disease. However, parental samples were not available and a compound heterozygous state of the two variants has not been confirmed. We subsequently studied 15 additional unrelated individuals with unresolved RALF and ALF from four additional clinical centers by Sanger sequencing. Primer sequences and PCR conditions for Sanger sequencing of NBAS are available on request. This resulted in the identification of six additional individuals from five families with compound heterozygous mutations in NBAS (Figure 1). All 11 individuals carry at least one missense mutation on one allele. All missense mutations change evolutionarily conserved amino acid residues (Figure 2) and are accordingly predicted to be damaging (PolyPhen-2 and SIFT). Carrier testing showed that each parent analyzed was heterozygous for one allele; the mother of individual F4:II.3 had died before the study was performed so testing was impossible and parental samples of individuals F8:II.2, F9:II.2, and F10:II.1 were not available. Remarkably, in two families, F8 and F9, the oldest siblings had died in early infancy due to acute liver failure, aged 14 and 11 months, respectively; however, no material was available to genetically confirm their clinical diagnosis of NBAS deficiency.
Notably, all mutations, which are not predicted to cause a loss of function, are clustered in two regions in the first half of the gene, exons 8–12 and exons 21–28. The mutations in the latter region affect the secretory pathway sec39 domain of NBAS (Figure 2). Individual F2:II.1 carries a homozygous missense variant and individual F3:II.1 an in-frame deletion of one amino acid compound heterozygous with a missense mutation. All other affected individuals are compound heterozygotes for one out of seven different predicted loss-of-function mutations (three stop mutations, two frameshift, and two splice site mutations) plus a missense mutation or a deletion of a single amino acid. None of the NBAS missense mutations is present in >120,000 alleles from the Exome Aggregation Consortium (ExAC) Server (12/2014). Three of the loss-of-function mutations, c.686dup (p.Ser230Glnfs∗4), c.2827G>T (p.Glu943∗), and c.3010C>T (p.Arg1004∗), are listed in the heterozygous state 59×, 8×, and 1×, respectively (MAF < 0.04%). Although we have no indication for a shared haplotype for the c.3164T>C variant identified heterozygous in three families, the exome data suggests a common founder c.2708T>G mutation in German families 2 and 4.
Next, the functional consequences of NBAS mutations on the protein level were investigated. In eukaryotic cells, soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) tethering factors mediate the docking and fusion of transport vesicles with target membranes. Fusion of membranes is mediated by membrane-bound proteins on the transport vesicles (v-SNARE) and target membrane (t-SNARE). NBAS is thought to function as a component of an ER tethering complex that interacts with the t-SNAREs p31, BNIP1, and STX18 at the ER and the v-SNARE Sec22b. This tethering complex also includes ZW10, RINT1, and Sly1 (see Figure S1).9,10 Mutant and control fibroblasts were cultivated in D-MEM media supplemented with 10% FBS, 1% penicillin-streptomycin, and 200 μM uridine at 37°C and 5% CO2. For immunoblots, cells were collected, washed in PBS, and resolved in RIPA buffer.11 10 μg of protein of every sample were separated on a 4%–12% acrylamide gradient gel (LONZA). Primary antibodies (all Sigma-Aldrich) against NBAS (1:2,000), p31 (USE-1) (1:250), and β-actin (1:15,000) were incubated overnight. Enhanced chemiluminescence of proteins was detected with a Vilberscan Fusion FX7. Protein levels were quantified with the software Bio-1D. Testing of individual F1:II.1 fibroblasts showed a significant decrease in NBAS steady-state levels (p = 0.03; two-tailed unpaired t test). Extending the quantification of NBAS protein to affected individuals from families 2–5 and 7 showed a reduction of NBAS levels to 18%–36% in comparison to controls, indicating a substantial impairment of protein translation and/or stability in all seven affected individuals investigated (Figure 3 shows representative findings for individuals from families 1–5). Moreover, the reduction of NBAS was concomitant with a reduction of its proposed interaction partner p31, supporting an important function of NBAS within the syntaxin 18 complex (Figure S1). None of the additional components have been associated with a human disorder. Mouse models of deleted p31 and RINT1 were shown to be embryonic lethal.12,13
Next, we investigated whether an assumed defect in the assembly of the ER tethering complex impairs glycosylation and/or results in increased ER stress. Isoelectric focusing of transferrin, alpha-1-antitrypsin, and apolipoprotein CIII followed by in-gel immunodetection was performed in sera of a control subject, a COG6-CDG individual, and five individuals with NBAS mutations. Although the observed patterns indicated a clear deficiency in N-/O-glycosylation in the CDG individual, no differences were observed for the NBAS-mutant individuals compared to controls (Figure S2). These findings suggest that under the investigated conditions NBAS deficiency does not disturb retrograde transport between ER and Golgi to the extent that obvious changes in glycosylation patterns can be observed.
We next performed expression profiling in NBAS-mutant fibroblast to test for alterations suggestive for ER stress. Total cellular RNA was isolated from fibroblasts of three NBAS-affected individuals (F1:II.1, F2:II.1, F5:II.2) and 12 healthy controls. The quality of the RNA isolated from whole-cell lysates was determined with the Agilent 2100 BioAnalyzer (RNA 6000 Nano Kit, Agilent). All samples had a RNA integrity number (RIN) value greater than 8. RNA libraries were sequenced as 100 bp paired-end runs on an Illumina HiSeq2500 platform as described.14 In order to get expression measurements, we counted reads with HTSeq-count using the intersection-strict option on 20,345 protein coding genes from the Gencode database (GRCh37, p13, 19.07.2013).15 Read counts were normalized with size factors computed by DESeq2 to account for differences in sequencing depth per sample.16 We discarded genes with an average normalized expression below 10 over all samples and performed all consecutive analysis on the remaining 13,392 genes. Although there was no global change in gene expression, we did observe a significant increase in the expression of genes involved in ER stress response in NBAS-mutant fibroblasts compared to controls (Figure 4).
Together, our genetic and experimental findings provide evidence that mutations affecting functionally conserved domains in NBAS resulting in severely decreased NBAS levels cause RALF in infancy. Although no changes in glycosylation patterns were observed in the conditions investigated, expression profiles in NBAS mutant fibroblasts are suggestive for ER stress. RALF due to mutated NBAS is a presumably relatively frequent inherited cause of RALF, because NBAS screening of 15 individuals with RALF or acute infantile liver failure resulted in the discovery of six affected individuals from five additional families. The pivotal feature of this disease is RALF precipitated by intercurrent febrile illnesses during infancy and childhood. Intriguingly, with conservative management, liver function recovered completely and was normal in the interval. Crises are heralded by vomiting and lethargy and start rather uniformly with massively elevated ASAT and ALAT (range of maximum ALAT 4,001–17,700 U/l; normal < 50 U/l), followed by coagulopathy requiring FFP substitution (maximum INR 10; normal < 1.2) and mild to moderate jaundice (range of maximum total bilirubin 46.8–207.4 μmol/l; normal < 20.4 μmol/l). In some cases, significant hypoglycemia, hyperammonemia (maximum 209 μmol/l; normal < 53 μmol/l), and hepatic encephalopathy developed, which we consider to be secondary to ALF. Several affected individuals suffered from a range of comorbidities including cardiomyopathy, autoimmune gastrointestinal diseases, and neurological phenotypes such as epilepsy. However, none of those conditions is present in two individuals (Table 1).
Mutations in NBAS have not been linked to liver disease before, but a homozygous missense mutation c.5741G>A (p.Arg1914His) in the C-terminal domain of unknown function of NBAS has been associated with a syndrome of short stature, cone and optic nerve atrophy, and Pelger-Huët anomaly in Yakuts (SOPH syndrome [MIM: 614800]).17 RALF-causing NBAS deficiency and SOPH syndrome are clearly different clinical entities. Importantly, individuals with SOPH syndrome were not reported to have ALF or any hepatic disease manifestation and the impact of the SOPH-associated mutation on NBAS protein function is unknown.
None of the individuals with NBAS-induced (R)ALF carried two loss-of-function mutations in NBAS. However, NBAS mutations led to low levels of the gene product of about 25% NBAS protein (compared to healthy probands). The affected individuals recovered completely in the intervals between the crises and otherwise presented a rather mild phenotype, so reduced NBAS protein levels due to the mutations appear to be sufficient for normal function of most tissues including liver under afebrile conditions.
The physiologic function of NBAS is not yet understood. In yeast, sec39 is involved in retrograde transport between ER and Golgi.9 Aoki et al.9 provided evidence for a similar function of NBAS in humans where it is interacting with p31. Together with other SNARE proteins, they are forming the syntaxin 18 complex implicated in ER membrane fusion. Concomitant with reduced NBAS levels, p31 levels were also decreased, providing additional evidence that both proteins are subunits of the same SNARE complex. Similar findings were observed after targeted knockdown in HeLa cells.9 The exact mechanism of ALF due to NBAS deficiency remains unclear. We reason that a catabolic state with high energy demand during febrile infections or the raised temperature itself might be the starting points of the derailment, speculatively via a thermal susceptibility of the syntaxin 18 complex.
In contrast to acute infantile liver failure resulting from mutations in TRMU (MIM: 613070), MARS (MIM: 615486), or LARS (MIM: 615438), NBAS deficiency was not associated with increased serum lactate or muscular hypotonia. In about 50% of cases of acute infantile liver failure, the underlying cause remains undetermined. Some of these children might have an underlying genetic disorder or predisposition. The detection rate of NBAS mutations in random individuals with (recurrent) acute infantile liver failure was very high (6 out of 15 screened individuals), so NBAS deficiency might be a frequent cause of not only RALF but also isolated ALF at least in children. The differing genetic origins of affected individuals and variety of mutations suggest that this autosomal-recessive disease is not a regional phenomenon.
In conclusion, mutations in NBAS are delineated as a previously unknown cause of acute liver failure with onset in childhood triggered by febrile infections. It is possible that the affected individuals reported in this study present the severe end of the phenotypic spectrum. Notably, in families F8 and F9, two older siblings had died from acute liver failure, aged 14 and 11 months. Unfortunately, no material was available for diagnostics from the deceased individuals. However, the finding of NBAS mutations in their siblings suggests NBAS-induced ALF. Hence, these individuals might provide examples for a lethal course of NBAS deficiency. We recommended sequencing NBAS in cases of ALF in infancy and childhood of unknown cause, especially in individuals with fever-associated ALF and/or RALF.
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Acute liver failure (ALF) is a very severe, life-threatening event which can result from toxin exposure, inherited metabolic disease, autoimmune disease, infectious disease, shock, and other rare causes. The exact incidence of pediatric ALF is unknown, and in about 50% of cases the underlying cause remains obscure.1,2 Prognosis is guarded and emergency liver transplantation is often the only therapeutic option. Known causes of recurrent acute liver failure (RALF) with clinical and biochemical hepatic recovery in the interval include fulminant viral hepatitis, autoimmune hepatitis, disorders of long-chain fatty acid oxidation and the carnitine cycle, dihydrolipoamide dehydrogenase (E3) deficiency (MIM: 246900), and Wolcott-Rallison syndrome (MIM: 226980).3–7 Here we report the identification of homozygous or compound heterozygous mutations in NBAS (neuroblastoma amplified sequence) in 11 individuals with RALF starting in infancy.
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A group of four unrelated German individuals with previously unclassified early-onset RALF (according to the definition of the Pediatric Acute Liver Failure Study Group)1 was recruited in one clinical center (University Hospital Heidelberg) and jointly analyzed. Clinical and genetic findings are summarized in Table 1. Informed consent to participate in the study was obtained from all affected individuals (or their parents, in the case of minor study participants). The study was approved by the ethical committees of the University Hospital Heidelberg and of the Technische Universität München. Whole exome sequencing was performed on genomic DNA from four unrelated affected individuals as described previously.8 Using a frequency filter of minor allele frequency < 0.1% in our in-house database and public databases, we identified six, seven, three, and nine compound heterozygous or homozygous variants in individuals F1:II.1, F2:II.1, F3:II.1, and F4:II.3, respectively. NBAS (GenBank: NM_015909.3, MIM: 608025) is the only gene where biallelic mutations were identified in all affected individuals (Figure 1). In individual F5:II.2, presumably disease-causing mutations in NBAS had been identified in a preceding exome sequence analysis but the relevance of this finding had remained unclear. The analysis of exome sequencing data from approximately 4,000 individuals with unrelated phenotypes (all subjects were sequenced in the Institute of Human Genetics, Helmholtz Zentrum München, and their data stored in an in-house database) identified only one additional sample with two rare variants in NBAS potentially compatible with a recessive disease. However, parental samples were not available and a compound heterozygous state of the two variants has not been confirmed. We subsequently studied 15 additional unrelated individuals with unresolved RALF and ALF from four additional clinical centers by Sanger sequencing. Primer sequences and PCR conditions for Sanger sequencing of NBAS are available on request. This resulted in the identification of six additional individuals from five families with compound heterozygous mutations in NBAS (Figure 1). All 11 individuals carry at least one missense mutation on one allele. All missense mutations change evolutionarily conserved amino acid residues (Figure 2) and are accordingly predicted to be damaging (PolyPhen-2 and SIFT). Carrier testing showed that each parent analyzed was heterozygous for one allele; the mother of individual F4:II.3 had died before the study was performed so testing was impossible and parental samples of individuals F8:II.2, F9:II.2, and F10:II.1 were not available. Remarkably, in two families, F8 and F9, the oldest siblings had died in early infancy due to acute liver failure, aged 14 and 11 months, respectively; however, no material was available to genetically confirm their clinical diagnosis of NBAS deficiency.
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Notably, all mutations, which are not predicted to cause a loss of function, are clustered in two regions in the first half of the gene, exons 8–12 and exons 21–28. The mutations in the latter region affect the secretory pathway sec39 domain of NBAS (Figure 2). Individual F2:II.1 carries a homozygous missense variant and individual F3:II.1 an in-frame deletion of one amino acid compound heterozygous with a missense mutation. All other affected individuals are compound heterozygotes for one out of seven different predicted loss-of-function mutations (three stop mutations, two frameshift, and two splice site mutations) plus a missense mutation or a deletion of a single amino acid. None of the NBAS missense mutations is present in >120,000 alleles from the Exome Aggregation Consortium (ExAC) Server (12/2014). Three of the loss-of-function mutations, c.686dup (p.Ser230Glnfs∗4), c.2827G>T (p.Glu943∗), and c.3010C>T (p.Arg1004∗), are listed in the heterozygous state 59×, 8×, and 1×, respectively (MAF < 0.04%). Although we have no indication for a shared haplotype for the c.3164T>C variant identified heterozygous in three families, the exome data suggests a common founder c.2708T>G mutation in German families 2 and 4.
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Next, the functional consequences of NBAS mutations on the protein level were investigated. In eukaryotic cells, soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) tethering factors mediate the docking and fusion of transport vesicles with target membranes. Fusion of membranes is mediated by membrane-bound proteins on the transport vesicles (v-SNARE) and target membrane (t-SNARE). NBAS is thought to function as a component of an ER tethering complex that interacts with the t-SNAREs p31, BNIP1, and STX18 at the ER and the v-SNARE Sec22b. This tethering complex also includes ZW10, RINT1, and Sly1 (see Figure S1).9,10 Mutant and control fibroblasts were cultivated in D-MEM media supplemented with 10% FBS, 1% penicillin-streptomycin, and 200 μM uridine at 37°C and 5% CO2. For immunoblots, cells were collected, washed in PBS, and resolved in RIPA buffer.11 10 μg of protein of every sample were separated on a 4%–12% acrylamide gradient gel (LONZA). Primary antibodies (all Sigma-Aldrich) against NBAS (1:2,000), p31 (USE-1) (1:250), and β-actin (1:15,000) were incubated overnight. Enhanced chemiluminescence of proteins was detected with a Vilberscan Fusion FX7. Protein levels were quantified with the software Bio-1D. Testing of individual F1:II.1 fibroblasts showed a significant decrease in NBAS steady-state levels (p = 0.03; two-tailed unpaired t test). Extending the quantification of NBAS protein to affected individuals from families 2–5 and 7 showed a reduction of NBAS levels to 18%–36% in comparison to controls, indicating a substantial impairment of protein translation and/or stability in all seven affected individuals investigated (Figure 3 shows representative findings for individuals from families 1–5). Moreover, the reduction of NBAS was concomitant with a reduction of its proposed interaction partner p31, supporting an important function of NBAS within the syntaxin 18 complex (Figure S1). None of the additional components have been associated with a human disorder. Mouse models of deleted p31 and RINT1 were shown to be embryonic lethal.12,13
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Next, we investigated whether an assumed defect in the assembly of the ER tethering complex impairs glycosylation and/or results in increased ER stress. Isoelectric focusing of transferrin, alpha-1-antitrypsin, and apolipoprotein CIII followed by in-gel immunodetection was performed in sera of a control subject, a COG6-CDG individual, and five individuals with NBAS mutations. Although the observed patterns indicated a clear deficiency in N-/O-glycosylation in the CDG individual, no differences were observed for the NBAS-mutant individuals compared to controls (Figure S2). These findings suggest that under the investigated conditions NBAS deficiency does not disturb retrograde transport between ER and Golgi to the extent that obvious changes in glycosylation patterns can be observed.
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We next performed expression profiling in NBAS-mutant fibroblast to test for alterations suggestive for ER stress. Total cellular RNA was isolated from fibroblasts of three NBAS-affected individuals (F1:II.1, F2:II.1, F5:II.2) and 12 healthy controls. The quality of the RNA isolated from whole-cell lysates was determined with the Agilent 2100 BioAnalyzer (RNA 6000 Nano Kit, Agilent). All samples had a RNA integrity number (RIN) value greater than 8. RNA libraries were sequenced as 100 bp paired-end runs on an Illumina HiSeq2500 platform as described.14 In order to get expression measurements, we counted reads with HTSeq-count using the intersection-strict option on 20,345 protein coding genes from the Gencode database (GRCh37, p13, 19.07.2013).15 Read counts were normalized with size factors computed by DESeq2 to account for differences in sequencing depth per sample.16 We discarded genes with an average normalized expression below 10 over all samples and performed all consecutive analysis on the remaining 13,392 genes. Although there was no global change in gene expression, we did observe a significant increase in the expression of genes involved in ER stress response in NBAS-mutant fibroblasts compared to controls (Figure 4).
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Together, our genetic and experimental findings provide evidence that mutations affecting functionally conserved domains in NBAS resulting in severely decreased NBAS levels cause RALF in infancy. Although no changes in glycosylation patterns were observed in the conditions investigated, expression profiles in NBAS mutant fibroblasts are suggestive for ER stress. RALF due to mutated NBAS is a presumably relatively frequent inherited cause of RALF, because NBAS screening of 15 individuals with RALF or acute infantile liver failure resulted in the discovery of six affected individuals from five additional families. The pivotal feature of this disease is RALF precipitated by intercurrent febrile illnesses during infancy and childhood. Intriguingly, with conservative management, liver function recovered completely and was normal in the interval. Crises are heralded by vomiting and lethargy and start rather uniformly with massively elevated ASAT and ALAT (range of maximum ALAT 4,001–17,700 U/l; normal < 50 U/l), followed by coagulopathy requiring FFP substitution (maximum INR 10; normal < 1.2) and mild to moderate jaundice (range of maximum total bilirubin 46.8–207.4 μmol/l; normal < 20.4 μmol/l). In some cases, significant hypoglycemia, hyperammonemia (maximum 209 μmol/l; normal < 53 μmol/l), and hepatic encephalopathy developed, which we consider to be secondary to ALF. Several affected individuals suffered from a range of comorbidities including cardiomyopathy, autoimmune gastrointestinal diseases, and neurological phenotypes such as epilepsy. However, none of those conditions is present in two individuals (Table 1).
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Mutations in NBAS have not been linked to liver disease before, but a homozygous missense mutation c.5741G>A (p.Arg1914His) in the C-terminal domain of unknown function of NBAS has been associated with a syndrome of short stature, cone and optic nerve atrophy, and Pelger-Huët anomaly in Yakuts (SOPH syndrome [MIM: 614800]).17 RALF-causing NBAS deficiency and SOPH syndrome are clearly different clinical entities. Importantly, individuals with SOPH syndrome were not reported to have ALF or any hepatic disease manifestation and the impact of the SOPH-associated mutation on NBAS protein function is unknown.
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None of the individuals with NBAS-induced (R)ALF carried two loss-of-function mutations in NBAS. However, NBAS mutations led to low levels of the gene product of about 25% NBAS protein (compared to healthy probands). The affected individuals recovered completely in the intervals between the crises and otherwise presented a rather mild phenotype, so reduced NBAS protein levels due to the mutations appear to be sufficient for normal function of most tissues including liver under afebrile conditions.
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The physiologic function of NBAS is not yet understood. In yeast, sec39 is involved in retrograde transport between ER and Golgi.9 Aoki et al.9 provided evidence for a similar function of NBAS in humans where it is interacting with p31. Together with other SNARE proteins, they are forming the syntaxin 18 complex implicated in ER membrane fusion. Concomitant with reduced NBAS levels, p31 levels were also decreased, providing additional evidence that both proteins are subunits of the same SNARE complex. Similar findings were observed after targeted knockdown in HeLa cells.9 The exact mechanism of ALF due to NBAS deficiency remains unclear. We reason that a catabolic state with high energy demand during febrile infections or the raised temperature itself might be the starting points of the derailment, speculatively via a thermal susceptibility of the syntaxin 18 complex.
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In contrast to acute infantile liver failure resulting from mutations in TRMU (MIM: 613070), MARS (MIM: 615486), or LARS (MIM: 615438), NBAS deficiency was not associated with increased serum lactate or muscular hypotonia. In about 50% of cases of acute infantile liver failure, the underlying cause remains undetermined. Some of these children might have an underlying genetic disorder or predisposition. The detection rate of NBAS mutations in random individuals with (recurrent) acute infantile liver failure was very high (6 out of 15 screened individuals), so NBAS deficiency might be a frequent cause of not only RALF but also isolated ALF at least in children. The differing genetic origins of affected individuals and variety of mutations suggest that this autosomal-recessive disease is not a regional phenomenon.
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In conclusion, mutations in NBAS are delineated as a previously unknown cause of acute liver failure with onset in childhood triggered by febrile infections. It is possible that the affected individuals reported in this study present the severe end of the phenotypic spectrum. Notably, in families F8 and F9, two older siblings had died from acute liver failure, aged 14 and 11 months. Unfortunately, no material was available for diagnostics from the deceased individuals. However, the finding of NBAS mutations in their siblings suggests NBAS-induced ALF. Hence, these individuals might provide examples for a lethal course of NBAS deficiency. We recommended sequencing NBAS in cases of ALF in infancy and childhood of unknown cause, especially in individuals with fever-associated ALF and/or RALF.
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back
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Web Resources
The URLs for the data presented herein are as follows:ExAC Browser, http://exac.broadinstitute.org/
MutationTaster, http://www.mutationtaster.org/
OMIM, http://www.omim.org/
Supplemental Data
Document S1. Figures S1 and S2
Document S2. Article plus Supplemental Data
Acknowledgments
The authors thank Lena Pawella, Elisabeth Specht-Delius, Eva Eiteneuer, Marion Hahne, Zlata Antoni, Lena Protzmann, and Sabine Schäfer for excellent technical assistance. Human control tissues were provided by the Tissue Bank of the National Center for Tumor Diseases (NCT, Heidelberg, Germany) in accordance with the ethics committee of the University of Heidelberg. We thank Dr. Ronald J.A. Wanders, Department of Medical Biochemistry, Academic Medical Centre, University of Amsterdam, the Netherlands, who excluded fatty acid oxidation disorders in individuals from families 1, 2, 3, 5, and 7. This study was supported by the German Bundesministerium für Bildung und Forschung (BMBF) through the German Network for mitochondrial disorders (mitoNET, 01GM1113C to T.M. and H.P.) and through the E-Rare project GENOMIT (01GM1207 for T.M. and H.P.). T.B.H. and J.G. were supported by the BMBF through the Juniorverbund in der Systemmedizin “mitOmics” (FKZ 01ZX1405C and 01ZX1405A). R.W.T was supported by a Wellcome Trust Strategic Award (096919/Z/11/Z) and the UK NHS Highly Specialised “Rare Mitochondrial Disorders of Adults and Children” Service. B.K.S. was supported by grants of the DFG (STR 1160/1-1 and 1-2). D.M.B. was supported by a DFG Fellowship through the Graduate School of Quantitative Biosciences Munich (QBM). This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
Supplemental Data include two figures and can be found with this article online at http://dx.doi.org/10.1016/j.ajhg.2015.05.009.
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Web Resources
The URLs for the data presented herein are as follows:ExAC Browser, http://exac.broadinstitute.org/
MutationTaster, http://www.mutationtaster.org/
OMIM, http://www.omim.org/
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The URLs for the data presented herein are as follows:ExAC Browser, http://exac.broadinstitute.org/
MutationTaster, http://www.mutationtaster.org/
OMIM, http://www.omim.org/
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ExAC Browser, http://exac.broadinstitute.org/
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Document S1. Figures S1 and S2
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Acknowledgments
The authors thank Lena Pawella, Elisabeth Specht-Delius, Eva Eiteneuer, Marion Hahne, Zlata Antoni, Lena Protzmann, and Sabine Schäfer for excellent technical assistance. Human control tissues were provided by the Tissue Bank of the National Center for Tumor Diseases (NCT, Heidelberg, Germany) in accordance with the ethics committee of the University of Heidelberg. We thank Dr. Ronald J.A. Wanders, Department of Medical Biochemistry, Academic Medical Centre, University of Amsterdam, the Netherlands, who excluded fatty acid oxidation disorders in individuals from families 1, 2, 3, 5, and 7. This study was supported by the German Bundesministerium für Bildung und Forschung (BMBF) through the German Network for mitochondrial disorders (mitoNET, 01GM1113C to T.M. and H.P.) and through the E-Rare project GENOMIT (01GM1207 for T.M. and H.P.). T.B.H. and J.G. were supported by the BMBF through the Juniorverbund in der Systemmedizin “mitOmics” (FKZ 01ZX1405C and 01ZX1405A). R.W.T was supported by a Wellcome Trust Strategic Award (096919/Z/11/Z) and the UK NHS Highly Specialised “Rare Mitochondrial Disorders of Adults and Children” Service. B.K.S. was supported by grants of the DFG (STR 1160/1-1 and 1-2). D.M.B. was supported by a DFG Fellowship through the Graduate School of Quantitative Biosciences Munich (QBM).
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The authors thank Lena Pawella, Elisabeth Specht-Delius, Eva Eiteneuer, Marion Hahne, Zlata Antoni, Lena Protzmann, and Sabine Schäfer for excellent technical assistance. Human control tissues were provided by the Tissue Bank of the National Center for Tumor Diseases (NCT, Heidelberg, Germany) in accordance with the ethics committee of the University of Heidelberg. We thank Dr. Ronald J.A. Wanders, Department of Medical Biochemistry, Academic Medical Centre, University of Amsterdam, the Netherlands, who excluded fatty acid oxidation disorders in individuals from families 1, 2, 3, 5, and 7. This study was supported by the German Bundesministerium für Bildung und Forschung (BMBF) through the German Network for mitochondrial disorders (mitoNET, 01GM1113C to T.M. and H.P.) and through the E-Rare project GENOMIT (01GM1207 for T.M. and H.P.). T.B.H. and J.G. were supported by the BMBF through the Juniorverbund in der Systemmedizin “mitOmics” (FKZ 01ZX1405C and 01ZX1405A). R.W.T was supported by a Wellcome Trust Strategic Award (096919/Z/11/Z) and the UK NHS Highly Specialised “Rare Mitochondrial Disorders of Adults and Children” Service. B.K.S. was supported by grants of the DFG (STR 1160/1-1 and 1-2). D.M.B. was supported by a DFG Fellowship through the Graduate School of Quantitative Biosciences Munich (QBM).
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This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
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This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
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Supplemental Data include two figures and can be found with this article online at http://dx.doi.org/10.1016/j.ajhg.2015.05.009.
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Supplemental Data include two figures and can be found with this article online at http://dx.doi.org/10.1016/j.ajhg.2015.05.009.
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Figure 1 Pedigrees of Investigated Families
Pedigrees of ten families affected by RALF and mutations in NBAS. Mutation status of affected (closed symbols) and healthy (open symbols) family members.
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Figure 1
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Pedigrees of Investigated Families
Pedigrees of ten families affected by RALF and mutations in NBAS. Mutation status of affected (closed symbols) and healthy (open symbols) family members.
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Pedigrees of Investigated Families
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Pedigrees of ten families affected by RALF and mutations in NBAS. Mutation status of affected (closed symbols) and healthy (open symbols) family members.
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Figure 2 NBAS Structure and Conservation of Identified Mutations
Gene structure of NBAS with known protein domains of the gene product and localization and conservation of amino acid residues affected by mutations. Mutation c.5741G>A (p.Arg1914His) in exon 45 in the C-terminal domain of unknown function is associated with SOPH syndrome.17 Amino acids 90–371 form a quinoprotein aminedehydrogenase, beta chain like domain (IPR011044) and amino acids 725–1,376 form a secretory pathway sec39 domain (IPR013244). Intronic regions are not drawn to scale.
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Figure 2
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NBAS Structure and Conservation of Identified Mutations
Gene structure of NBAS with known protein domains of the gene product and localization and conservation of amino acid residues affected by mutations. Mutation c.5741G>A (p.Arg1914His) in exon 45 in the C-terminal domain of unknown function is associated with SOPH syndrome.17 Amino acids 90–371 form a quinoprotein aminedehydrogenase, beta chain like domain (IPR011044) and amino acids 725–1,376 form a secretory pathway sec39 domain (IPR013244). Intronic regions are not drawn to scale.
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NBAS Structure and Conservation of Identified Mutations
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Gene structure of NBAS with known protein domains of the gene product and localization and conservation of amino acid residues affected by mutations. Mutation c.5741G>A (p.Arg1914His) in exon 45 in the C-terminal domain of unknown function is associated with SOPH syndrome.17 Amino acids 90–371 form a quinoprotein aminedehydrogenase, beta chain like domain (IPR011044) and amino acids 725–1,376 form a secretory pathway sec39 domain (IPR013244). Intronic regions are not drawn to scale.
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Figure 3 Quantification of NBAS and p31 Protein Levels
Mutant and control fibroblast cell lines were cultivated at 37°C. 10 μg protein of collected cells were separated on a 4%–12% acrylamide gradient gel, transferred to a PVDF membrane, and immunodecorated with antibodies against NBAS, p31, and β-actin. The antibody for NBAS was detecting a single protein band at approximately 270 kDa corresponding to the predicted molecular weight of NBAS. β-actin was used as a loading control. The quantified protein levels are based on three independent experiments and expressed as percentages of a control cell line, corrected for β-actin. Five of the eight investigated subject cell lines are shown. NBAS and p31 protein levels were severely reduced in fibroblast cell lines of RALF-affected individuals to 21% and 33% of control subjects, respectively. Error bar indicates 1 SD. Protein amount in control 1 was set as 100%.
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Figure 3
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Quantification of NBAS and p31 Protein Levels
Mutant and control fibroblast cell lines were cultivated at 37°C. 10 μg protein of collected cells were separated on a 4%–12% acrylamide gradient gel, transferred to a PVDF membrane, and immunodecorated with antibodies against NBAS, p31, and β-actin. The antibody for NBAS was detecting a single protein band at approximately 270 kDa corresponding to the predicted molecular weight of NBAS. β-actin was used as a loading control. The quantified protein levels are based on three independent experiments and expressed as percentages of a control cell line, corrected for β-actin. Five of the eight investigated subject cell lines are shown. NBAS and p31 protein levels were severely reduced in fibroblast cell lines of RALF-affected individuals to 21% and 33% of control subjects, respectively. Error bar indicates 1 SD. Protein amount in control 1 was set as 100%.
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Quantification of NBAS and p31 Protein Levels
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Mutant and control fibroblast cell lines were cultivated at 37°C. 10 μg protein of collected cells were separated on a 4%–12% acrylamide gradient gel, transferred to a PVDF membrane, and immunodecorated with antibodies against NBAS, p31, and β-actin. The antibody for NBAS was detecting a single protein band at approximately 270 kDa corresponding to the predicted molecular weight of NBAS. β-actin was used as a loading control. The quantified protein levels are based on three independent experiments and expressed as percentages of a control cell line, corrected for β-actin. Five of the eight investigated subject cell lines are shown. NBAS and p31 protein levels were severely reduced in fibroblast cell lines of RALF-affected individuals to 21% and 33% of control subjects, respectively. Error bar indicates 1 SD. Protein amount in control 1 was set as 100%.
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Figure 4 Increased Expression of ER Stress Response Genes
Quartiles (boxes) and 1.5 times the interquartile range (whiskers) of the fold change of normalized RNA-seq read counts from fibroblasts are displayed. Three individuals with pathogenic variants in NBAS (F1:II.1, F2:II.1, and F5:II.2) are compared against the median per gene over 12 control samples. We obtained interaction partners of the NBAS protein from the BioGrid database (v.3.3).18 The genes associated with the corresponding gene ontology terms were downloaded from UniProt (accessed March 2015).19 For every box, we computed a two-sided Wilcoxon test whether it is symmetric about 1. Single data points are shown for boxes with less than 50 genes. Gene ontology (GO) terms: GO 0034976, response to endoplasmic reticulum stress; GO 0001889, liver development; GO 0006259, DNA metabolic process; GO 0006119, oxidative phosphorylation. ns, p > 0.1.
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Figure 4
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Increased Expression of ER Stress Response Genes
Quartiles (boxes) and 1.5 times the interquartile range (whiskers) of the fold change of normalized RNA-seq read counts from fibroblasts are displayed. Three individuals with pathogenic variants in NBAS (F1:II.1, F2:II.1, and F5:II.2) are compared against the median per gene over 12 control samples. We obtained interaction partners of the NBAS protein from the BioGrid database (v.3.3).18 The genes associated with the corresponding gene ontology terms were downloaded from UniProt (accessed March 2015).19 For every box, we computed a two-sided Wilcoxon test whether it is symmetric about 1. Single data points are shown for boxes with less than 50 genes. Gene ontology (GO) terms: GO 0034976, response to endoplasmic reticulum stress; GO 0001889, liver development; GO 0006259, DNA metabolic process; GO 0006119, oxidative phosphorylation. ns, p > 0.1.
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Increased Expression of ER Stress Response Genes
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Quartiles (boxes) and 1.5 times the interquartile range (whiskers) of the fold change of normalized RNA-seq read counts from fibroblasts are displayed. Three individuals with pathogenic variants in NBAS (F1:II.1, F2:II.1, and F5:II.2) are compared against the median per gene over 12 control samples. We obtained interaction partners of the NBAS protein from the BioGrid database (v.3.3).18 The genes associated with the corresponding gene ontology terms were downloaded from UniProt (accessed March 2015).19 For every box, we computed a two-sided Wilcoxon test whether it is symmetric about 1. Single data points are shown for boxes with less than 50 genes. Gene ontology (GO) terms: GO 0034976, response to endoplasmic reticulum stress; GO 0001889, liver development; GO 0006259, DNA metabolic process; GO 0006119, oxidative phosphorylation. ns, p > 0.1.
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Table 1 Genetic and Clinical Findings in Individuals with NBAS Mutations
ID Sex NBAS Mutations Protein Levels Fibroblasts Clinical Features
cDNA (NM_015909.3), Protein (NP_056993.2) NBAS p31 AO Age Last Crisis Number of ALF Age Last Visit Other Clinical Findings
F1:II.1 F c.[558_560del];[686dup], p.[Ile187del];[Ser230Glnfs∗4] 21% 27% 21 14 9/12 years 2 18 years none reported
F2:II.1 F c.[2708T>G];[2708T>G], p.[Leu903Arg];[Leu903Arg] 22% 30% 7 21 1/12 years 7 22 years acute renal failure, epilepsy
F3:II.1 F c.[603_605del];[3164T>C], p.[Leu202del];[Leu1055Pro] 20% 38% 10 11 7/12 years 5 18 years celiac disease
F4:II.3 F c.[2708T>G];[2827G>T], p.[Leu903Arg];[Glu943∗] 26% 38% 8 ND ND 37 years none reported
F5:II.2 M c.[3010C>T];[3164T>C], p.[Arg1004∗];[Leu1055Pro]; 18% 33% 7 9 10/12 years 10 14 years cardiomyopathy
F6:II.1 M c.1533_1545del];[2951T>G], p.[Ile512Thrfs∗4];[Ile984Ser] ND ND 18 3 11/12 years 5 3 years none reported
F7:II.1 F c.[1042C>T];[2203−3C>G], p.[Pro348Ser];[?] 32% ND 11 6 7/12 years 4 9 years none reported
F7:II.2 F c.[1042C>T];[2203−3C>G], p.[Pro348Ser];[?] 36% ND 6 8/12 years 6 8/12 years 1 11 years erythema nodosum, Crohn’s disease
F8:II.2 M c.[1187G>A];[2330C>A], p.[Trp396∗];[Pro777His] ND ND 21 3 years 1 8 years none reported
F9:II.2 F c.[118−2A>G];[2524G>T], p.[?(;)Val842Phe] ND ND 18 2 2/12 years 3 4 years none reported
F10:II.1 F c.[686dup];[3164T>C], p.[Ser230Glnfs∗4];[Leu1055Pro] ND ND 4 5 10/12 years 5 18 years ND
NBAS and p31 protein levels are normalized to β-actin and are given in percent of a control cell line. Abbreviations are as follows: AO, age of onset (in months if not stated otherwise); M, male; F, female; ND, not determined.
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Table 1
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Genetic and Clinical Findings in Individuals with NBAS Mutations
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Genetic and Clinical Findings in Individuals with NBAS Mutations
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table
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ID Sex NBAS Mutations Protein Levels Fibroblasts Clinical Features
cDNA (NM_015909.3), Protein (NP_056993.2) NBAS p31 AO Age Last Crisis Number of ALF Age Last Visit Other Clinical Findings
F1:II.1 F c.[558_560del];[686dup], p.[Ile187del];[Ser230Glnfs∗4] 21% 27% 21 14 9/12 years 2 18 years none reported
F2:II.1 F c.[2708T>G];[2708T>G], p.[Leu903Arg];[Leu903Arg] 22% 30% 7 21 1/12 years 7 22 years acute renal failure, epilepsy
F3:II.1 F c.[603_605del];[3164T>C], p.[Leu202del];[Leu1055Pro] 20% 38% 10 11 7/12 years 5 18 years celiac disease
F4:II.3 F c.[2708T>G];[2827G>T], p.[Leu903Arg];[Glu943∗] 26% 38% 8 ND ND 37 years none reported
F5:II.2 M c.[3010C>T];[3164T>C], p.[Arg1004∗];[Leu1055Pro]; 18% 33% 7 9 10/12 years 10 14 years cardiomyopathy
F6:II.1 M c.1533_1545del];[2951T>G], p.[Ile512Thrfs∗4];[Ile984Ser] ND ND 18 3 11/12 years 5 3 years none reported
F7:II.1 F c.[1042C>T];[2203−3C>G], p.[Pro348Ser];[?] 32% ND 11 6 7/12 years 4 9 years none reported
F7:II.2 F c.[1042C>T];[2203−3C>G], p.[Pro348Ser];[?] 36% ND 6 8/12 years 6 8/12 years 1 11 years erythema nodosum, Crohn’s disease
F8:II.2 M c.[1187G>A];[2330C>A], p.[Trp396∗];[Pro777His] ND ND 21 3 years 1 8 years none reported
F9:II.2 F c.[118−2A>G];[2524G>T], p.[?(;)Val842Phe] ND ND 18 2 2/12 years 3 4 years none reported
F10:II.1 F c.[686dup];[3164T>C], p.[Ser230Glnfs∗4];[Leu1055Pro] ND ND 4 5 10/12 years 5 18 years ND
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ID Sex NBAS Mutations Protein Levels Fibroblasts Clinical Features
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th
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ID
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Sex
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th
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NBAS Mutations
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th
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Protein Levels Fibroblasts
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th
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Clinical Features
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tr
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cDNA (NM_015909.3), Protein (NP_056993.2) NBAS p31 AO Age Last Crisis Number of ALF Age Last Visit Other Clinical Findings
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th
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cDNA (NM_015909.3), Protein (NP_056993.2)
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th
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NBAS
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th
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p31
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th
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AO
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th
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Age Last Crisis
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th
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Number of ALF
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th
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Age Last Visit
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th
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Other Clinical Findings
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tr
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F1:II.1 F c.[558_560del];[686dup], p.[Ile187del];[Ser230Glnfs∗4] 21% 27% 21 14 9/12 years 2 18 years none reported
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td
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F1:II.1
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td
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F
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td
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c.[558_560del];[686dup], p.[Ile187del];[Ser230Glnfs∗4]
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td
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21%
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td
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27%
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td
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21
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td
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14 9/12 years
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td
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2
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td
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18 years
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none reported
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F2:II.1 F c.[2708T>G];[2708T>G], p.[Leu903Arg];[Leu903Arg] 22% 30% 7 21 1/12 years 7 22 years acute renal failure, epilepsy
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td
|
F2:II.1
|
|
td
|
F
|
|
td
|
c.[2708T>G];[2708T>G], p.[Leu903Arg];[Leu903Arg]
|
|
td
|
22%
|
|
td
|
30%
|
|
td
|
7
|
|
td
|
21 1/12 years
|
|
td
|
7
|
|
td
|
22 years
|
|
td
|
acute renal failure, epilepsy
|
|
tr
|
F3:II.1 F c.[603_605del];[3164T>C], p.[Leu202del];[Leu1055Pro] 20% 38% 10 11 7/12 years 5 18 years celiac disease
|
|
td
|
F3:II.1
|
|
td
|
F
|
|
td
|
c.[603_605del];[3164T>C], p.[Leu202del];[Leu1055Pro]
|
|
td
|
20%
|
|
td
|
38%
|
|
td
|
10
|
|
td
|
11 7/12 years
|
|
td
|
5
|
|
td
|
18 years
|
|
td
|
celiac disease
|
|
tr
|
F4:II.3 F c.[2708T>G];[2827G>T], p.[Leu903Arg];[Glu943∗] 26% 38% 8 ND ND 37 years none reported
|
|
td
|
F4:II.3
|
|
td
|
F
|
|
td
|
c.[2708T>G];[2827G>T], p.[Leu903Arg];[Glu943∗]
|
|
td
|
26%
|
|
td
|
38%
|
|
td
|
8
|
|
td
|
ND
|
|
td
|
ND
|
|
td
|
37 years
|
|
td
|
none reported
|
|
tr
|
F5:II.2 M c.[3010C>T];[3164T>C], p.[Arg1004∗];[Leu1055Pro]; 18% 33% 7 9 10/12 years 10 14 years cardiomyopathy
|
|
td
|
F5:II.2
|
|
td
|
M
|
|
td
|
c.[3010C>T];[3164T>C], p.[Arg1004∗];[Leu1055Pro];
|
|
td
|
18%
|
|
td
|
33%
|
|
td
|
7
|
|
td
|
9 10/12 years
|
|
td
|
10
|
|
td
|
14 years
|
|
td
|
cardiomyopathy
|
|
tr
|
F6:II.1 M c.1533_1545del];[2951T>G], p.[Ile512Thrfs∗4];[Ile984Ser] ND ND 18 3 11/12 years 5 3 years none reported
|
|
td
|
F6:II.1
|
|
td
|
M
|
|
td
|
c.1533_1545del];[2951T>G], p.[Ile512Thrfs∗4];[Ile984Ser]
|
|
td
|
ND
|
|
td
|
ND
|
|
td
|
18
|
|
td
|
3 11/12 years
|
|
td
|
5
|
|
td
|
3 years
|
|
td
|
none reported
|
|
tr
|
F7:II.1 F c.[1042C>T];[2203−3C>G], p.[Pro348Ser];[?] 32% ND 11 6 7/12 years 4 9 years none reported
|
|
td
|
F7:II.1
|
|
td
|
F
|
|
td
|
c.[1042C>T];[2203−3C>G], p.[Pro348Ser];[?]
|
|
td
|
32%
|
|
td
|
ND
|
|
td
|
11
|
|
td
|
6 7/12 years
|
|
td
|
4
|
|
td
|
9 years
|
|
td
|
none reported
|
|
tr
|
F7:II.2 F c.[1042C>T];[2203−3C>G], p.[Pro348Ser];[?] 36% ND 6 8/12 years 6 8/12 years 1 11 years erythema nodosum, Crohn’s disease
|
|
td
|
F7:II.2
|
|
td
|
F
|
|
td
|
c.[1042C>T];[2203−3C>G], p.[Pro348Ser];[?]
|
|
td
|
36%
|
|
td
|
ND
|
|
td
|
6 8/12 years
|
|
td
|
6 8/12 years
|
|
td
|
1
|
|
td
|
11 years
|
|
td
|
erythema nodosum, Crohn’s disease
|
|
tr
|
F8:II.2 M c.[1187G>A];[2330C>A], p.[Trp396∗];[Pro777His] ND ND 21 3 years 1 8 years none reported
|
|
td
|
F8:II.2
|
|
td
|
M
|
|
td
|
c.[1187G>A];[2330C>A], p.[Trp396∗];[Pro777His]
|
|
td
|
ND
|
|
td
|
ND
|
|
td
|
21
|
|
td
|
3 years
|
|
td
|
1
|
|
td
|
8 years
|
|
td
|
none reported
|
|
tr
|
F9:II.2 F c.[118−2A>G];[2524G>T], p.[?(;)Val842Phe] ND ND 18 2 2/12 years 3 4 years none reported
|
|
td
|
F9:II.2
|
|
td
|
F
|
|
td
|
c.[118−2A>G];[2524G>T], p.[?(;)Val842Phe]
|
|
td
|
ND
|
|
td
|
ND
|
|
td
|
18
|
|
td
|
2 2/12 years
|
|
td
|
3
|
|
td
|
4 years
|
|
td
|
none reported
|
|
tr
|
F10:II.1 F c.[686dup];[3164T>C], p.[Ser230Glnfs∗4];[Leu1055Pro] ND ND 4 5 10/12 years 5 18 years ND
|
|
td
|
F10:II.1
|
|
td
|
F
|
|
td
|
c.[686dup];[3164T>C], p.[Ser230Glnfs∗4];[Leu1055Pro]
|
|
td
|
ND
|
|
td
|
ND
|
|
td
|
4
|
|
td
|
5 10/12 years
|
|
td
|
5
|
|
td
|
18 years
|
|
td
|
ND
|
|
table-wrap-foot
|
NBAS and p31 protein levels are normalized to β-actin and are given in percent of a control cell line. Abbreviations are as follows: AO, age of onset (in months if not stated otherwise); M, male; F, female; ND, not determined.
|
|
footnote
|
NBAS and p31 protein levels are normalized to β-actin and are given in percent of a control cell line. Abbreviations are as follows: AO, age of onset (in months if not stated otherwise); M, male; F, female; ND, not determined.
|
|
p
|
NBAS and p31 protein levels are normalized to β-actin and are given in percent of a control cell line. Abbreviations are as follows: AO, age of onset (in months if not stated otherwise); M, male; F, female; ND, not determined.
|
