- Open Access
Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns
Orphanet Journal of Rare Diseases volume 7, Article number: 56 (2012)
Inherited malabsorption of cobalamin (Cbl) causes hematological and neurological abnormalities that can be fatal. Three genes have been implicated in Cbl malabsorption; yet, only about 10% of ~400-500 reported cases have been molecularly studied to date. Recessive mutations in CUBN or AMN cause Imerslund-Gräsbeck Syndrome (IGS), while recessive mutations in GIF cause Intrinsic Factor Deficiency (IFD). IGS and IFD differ in that IGS usually presents with proteinuria, which is not observed in IFD. The genetic heterogeneity and numerous differential diagnoses make clinical assessment difficult.
We present a large genetic screening study of 154 families or patients with suspected hereditary Cbl malabsorption. Patients and their families have been accrued over a period spanning >12 years. Systematic genetic testing of the three genes CUBN, AMN, and GIF was accomplished using a combination of single strand conformation polymorphism and DNA and RNA sequencing. In addition, six genes that were contenders for a role in inherited Cbl malabsorption were studied in a subset of these patients.
Our results revealed population-specific mutations, mutational hotspots, and functionally distinct regions in the three causal genes. We identified mutations in 126/154 unrelated cases (82%). Fifty-three of 126 cases (42%) were mutated in CUBN, 45/126 (36%) were mutated in AMN, and 28/126 (22%) had mutations in GIF. We found 26 undescribed mutations in CUBN, 19 in AMN, and 7 in GIF for a total of 52 novel defects described herein. We excluded six other candidate genes as culprits and concluded that additional genes might be involved.
Cbl malabsorption is found worldwide and genetically complex. However, our results indicate that population-specific founder mutations are quite common. Consequently, targeted genetic testing has become feasible if ethnic ancestry is considered. These results will facilitate clinical and molecular genetic testing of Cbl malabsorption. Early diagnosis improves the lifelong care required by these patients and prevents potential neurological long-term complications. This study provides the first comprehensive overview of the genetics that underlies the inherited Cbl malabsorption phenotype.
The metabolic pathway of vitamin B12 (Cobalamin, Cbl) was elucidated by studying rare disorders in children [1, 2]. Deficiency of vitamin B12 (Cobalamin, Cbl) in childhood is usually caused by chronic malnutrition, parasitic infections, or genetic defects. With the advent of modern agriculture and medicine, the first two causes have largely disappeared, although they may persist in less developed regions of the world or among individuals who practice unbalanced dietary habits . Genetic defects in Cbl absorption, serum transport, and intracellular metabolism are found worldwide [1, 4, 5]. Clinical symptoms may be present at birth for intracellular defects (complementation groups cblA OMIM251100; cblB OMIM251110; cblC OMIM277400; cblD OMIM277410; cblE OMIM236270; cblF OMIM277380; cblG OMIM 250940) and transcobalamin 2 deficiency (OMIM275350). However, in the case of intestinal Cbl malabsorption, obvious signs emerge usually only after several months or even years, when the fetal supply stored in the liver has been exhausted , and some adolescent cases have been noted [7, 8]. The signs of Cbl malabsorption are general weakness, slow growth, developmental delays and learning difficulties, dementia, psychological problems, neurodegeneration of the spinal cord, increased rate of infections due to neutropenia, thrombocytopenia, and megaloblastic anemia with lethal consequences if not treated . Clinical diagnostic markers include low serum Cbl, elevated homocysteine and methylmalonic acid in serum or urine, and exclusion of antibodies against parietal cells and gastric intrinsic factor (IF), whose presence would indicate pernicious anemia. But none of these tests is specific for Cbl malabsorption . The Schilling test , measuring the absorption of radio-labeled Cbl, was prematurely retired without an adequate replacement . Ultimately, the final diagnosis is reached by exclusion of many differential diagnoses and can only be confirmed by genetic testing. On the other hand, treatment is often administered via parenteral Cbl supplementation without confirming the diagnosis .
The knowledge of the genetic basis of hereditary Cbl malabsorption has much improved over the past decade, with three genes now implicated in its etiology. In 1999, the gene CUBN encoding cubilin was found mutated in a series of Finnish patients with selective malabsorption of Cbl and proteinuria , followed by the gene AMN that encodes amnionless, which was found mutated in several Norwegian and Jewish patients [14, 15]. Recessive mutations in either of these two genes cause the disease known as Imerslund-Gräsbeck syndrome (IGS, megaloblastic anemia 1; OMIM261100) or selective vitamin B12 malabsorption with proteinuria [16–19]. Cubilin and amnionless form the cubam dimer, which functions as the ileal receptor for the gastric intrinsic factor and Cbl complex (IF-B12) that is responsible for uptake of the essential food-born vitamin [20, 21]. A clinically similar disease without proteinuria is gastric intrinsic factor deficiency (IFD, OMIM261000 ) due to recessive mutations in GIF[23–25]. The two-stage Schilling test  distinguishes IGS from IFD by the addition of IF in the second assay step, which corrects the malabsorption of Cbl in IFD but not in IGS. However, this test is rarely used today  and for clinical purposes the differentiation is usually not possible.
With the implication of these three genes, the majority of IGS and IFD can be reliably diagnosed by genetic testing. However, the diagnostic work is daunting given the genetic heterogeneity and therefore many differential diagnoses have to be excluded before one embarks on genetic testing. In addition, the size of CUBN, which consists of 67 exons, and AMN, which has proved difficult to analyze, complicate the task. Not surprisingly, of about 400–500 patients reported since 1960, only some 10% were genetically tested and many reports include only a few patients [8, 26–36]. This situation has resulted in an incomplete genetic picture of intestinal Cbl malabsorption and hampers not only patient care but future research as well.
We present the results of systematic genetic testing in hereditary intestinal Cbl malabsorption among 154 consecutively recruited sibships or patients. We report 52 previously undescribed mutations in CUBN, AMN, and GIF and discuss the mutational spectrum in various regions of the world, the genetic testing strategy, functional consequences, and suggest that not all responsible genes have been identified yet.
Subjects and methods
We studied patients from all over the world. Both parents were available for study in 90 cases, one parent each in 15 cases, and none in 49 cases (Table 1 and Additional file 1). The diagnosis of hereditary deficiency of vitamin B12 absorption was made based on established criteria [6, 16, 19], usually but not always in tertiary level hospitals. Patients were typically in the range of 6 months to 5 years of age when first diagnosed with Cbl deficiency, however, several patients were over 5 years old before they displayed chronic health problems. Clinical and laboratory details on work-up, exclusion of differential diagnoses, symptom management, and therapy varied widely according to country and treatment center. Low serum Cbl (<200 pg/ml) was the most commonly used marker of Cbl deficiency, sometimes combined with proteinuria, after exclusion of intestinal parasites and nutritional deficiencies. Only very few cases ever had a Schilling test (Additional file 1).
Blood samples for DNA or RNA isolation were obtained after informed consent with prior Institutional Review Board approval (OSU protocol 2005 H0201) according to the Declaration of Helsinki. DNA isolation was performed by standard proteinase K digest, phenol-chloroform extraction and EtOH precipitation at the Ohio State University or locally using commercially available DNA isolation kits from various companies. Total RNA was isolated using the Trizol protocol according to the manufacturer’s instructions (Invitrogen, Carlsbad, CA).
Mutation screening and genetic analyses
We amplified individual exons of CUBN (GenBank RefSeq: NM001081.2), AMN (GenBank RefSeq: NM030943.1), and GIF (GenBank accession NM005142.2) from genomic DNA by PCR and analyzed the PCR amplicons by single strand conformation polymorphism (SSCP, ) and direct DNA sequencing. Sequencing was performed on an ABI PRISM® 3730 DNA analyzer (Applied Biosystems, Foster City, CA). PCR and SSCP conditions and primer sequences are available under a collaborative agreement. All nucleotide numbering is relative to the adenine in the first ATG start codon of the three genes, while the amino acid residue numbering is relative to the first methionine deduced from these cDNA sequences according to standard mutation nomenclature . All exons were sequenced in at least 100 anonymized controls from various ethnic backgrounds (89% Caucasian, 10% African-American, 1% other; . Missense changes were studied for conservation using HomoloGene (Additional file 2) and the PolyPhen-2 program . The genes TCN1 TCN2 FUT2 CD320 LMBRD1, and ABCC1 were screened by DNA sequencing in a selected group of patients (Additional file 1).
Suspected splice site changes were studied by comparing them to consensus sequences in spliceDB . If RNA was available, first-strand cDNA was produced from 0.5-1 μg total RNA using the AMV cDNA Synthesis Kit (Roche Applied Science, Indianapolis, IN) according to the instructions with a poly dT24-primer. Subsequent reverse-transcription-PCR was performed with assorted cDNA primers covering the desired regions within CUBN (GenBank RefSeq: NM001081.2), AMN (GenBank RefSeq: NM030943.1), or GIF (GenBank accession NM005142.2). DNA sequencing was performed as above.
Nature and frequency of the mutations
We have identified mutations in 126 of 154 (82%) cases or families that were ostensibly unrelated (Table 1 and Figure 1; Additional files 1 & 2). Of these 126 cases, 53 (42%) were mutated in CUBN, 45 (36%) were mutated in AMN, and 28 (22%) had mutations in GIF. We analyzed both parents in 75 cases and one parent in eight cases and positive carrier status in all parents was established, excluding any de novo mutations. Parental samples were unavailable for 43 cases. In nine cases only one mutation was identified (see missing mutations). One case (MGA9) was initially classified as IGS, based on a false-positive Schilling test, but later turned out to be mutated in the gene LMBRD1 coding for a lysosomal Cbl exporter (cblF defect; patient 9 in ). Twenty-seven cases (18%) remain unresolved and sequencing of TCN1 TCN2 FUT2 CD320 LMBRD1, and ABCC1 in selected cases identified no additional mutations (Additional file 1).
Several intronic and suspected silent changes caused splicing defects (AMN c.514-34G>A and c.1006+34_48del15bp; CUBN c.489G>A and c.1530G>A) and thus predictions of mRNA processing based on sequence changes might deviate from reality (Table 1). Consequently, mutations which seemingly caused a frameshift were described as to where the frameshift occurred rather than when the next stop codon was predicted, unless the consequences on the mRNA level were studied.
Mutations in CUBN
We have identified 30 CUBN point mutations and three large deletions (Table 1 and Additional file 1) in 53 cases or families. Of these 33 different gene defects, seven were previously reported, while 26 novel changes are presented here.
The most common CUBN mutation was missense change c.3890C>T; p.Pro1297Leu, a Finnish founder mutation in exon 27 [13, 43]. It occurred mostly in homozygous state but its relatively high incidence among the Finns (>25 families or cases) also unraveled two other rare CUBN mutations c.1838delG; p.Gly613fs in MGA34 and c.1230+1G>A .
Our results showed that several other ethnicity-specific mutations exist in CUBN. Two Saudi Bedouin families shared missense change c.434G>A; p.Gly145Glu (Fam SA in  and ZX-1). Missense mutation c.1010C>T; p.Pro337Leu was found three times in combination with other defects in cases of German (MGA53 with p.Gln297* and MGA20 with a large deletion) and Western European origin (case MGA1 with p.Cys891*), suggesting that p.Pro337Leu is a Germanic mutation. Intronic mutation c.3330-439C>G is Swedish in origin (homozygous in patient MGA7 and case FM2 in ; compound in MGA 11 with p.Ile690Val). Furthermore, Ashkenazi frameshift mutation c.2614_2615delGA (cases 4655–2590 and MGA78) and Turkish missense mutation c.4115C>G; p.Thr1372Arg (families KA95 and MGA2) were found twice each homozygously. However, patients from multi-ethnic Turkey carried several different IGS and IFD mutations (Table 1 and Additional file 1).
Missense change c.2594G>A; p.Ser865Asn occurred in Albania (family MGA3, homozygous), Turkey (case MT2 with p.Ser1250Phe), and in a Scottish case in whom the second mutation is still undetected (MGA43). This is the only IGS or IFD mutation we have encountered in one anonymized control individual. However, p.Ser865Asn was heterozygous in that individual, who had no other suspicious changes. Missense change p.Ser865Asn was found at low frequency in the NIH Exome Sequencing Project (rs138083522, A-allele frequency 0.014). Ser865 is not 100% conserved among mammals and p.Ser865Asn was considered a benign amino acid change (PolyPhen-2 score = 0.007). Thus, its functional relevance is unknown. However, it was seen in four patients, homozygously in two siblings of family MGA3 and once in combination with the damaging mutation p.Ser1250Phe, which suggests that missense p.Ser865Asn is a pathogenic IGS mutation or at least in linkage disequilibrium with an undetected CUBN mutation.
Of the remaining 20 CUBN mutations, 15 are clearly deleterious: two large deletions, seven nonsense, one splice site, and three frameshift mutations. The two alleged silent mutations in individual MGA57 each affected the last nucleotide in exons 5 and 13, respectively. Reverse-transcription-PCR revealed that c.489G>A (exon 5) caused retention of part of intron 5 (137 bp) and c.1530G>A (exon 13) led to the skipping of exon 13 (113 bp), causing a frameshift in both alleles (p.Gly164fs and p.Val473fs).
Of the 5 remaining missense changes, p.Gly1390Ser occurred in combination with a frameshift mutation in family MGA76. Similarly, p.Cys225Ser (patient Norge 1) and p.Trp1193Gly (patient RL02) targeted residues that are 100% conserved from humans to C. elegans and were considered damaging by PolyPhen-2, supporting their pathogenic role. The other two missense mutations p.Arg651Gly (family Taiwan 1) and p.Ser829Leu (MGA66) are discussed further below.
Mutations in AMN
In total we have detected 27 different AMN mutations of which 19 were previously undescribed (Table 1 and Additional file 1). The most frequent mutation is c.208-2A>G, which causes an out-of-frame loss of exon 4 in the mRNA . This ancient founder mutation is about 13,600 years old  and causes some 15% of IGS cases worldwide and more than 50% among Turks, Jordanians, and Sephardim combined, many of them expatriates. It accounted for 16 of the 45 AMN-mutated sibships in our cohort. A second acceptor splice site mutation in intron 3 (c.208-1G>C) affected the neighboring nucleotide in family FT.
The second most common mutation is a 15-bp deletion in intron 9 (c.1006+34_48del15bp) that was found in 5 sibships, in two of them combined with other mutations (MGA37: c.468_469insT, and MGA13: c.1314_1315delCA). At first, we assumed that the 15-bp deletion was a polymorphism. However, non-Mendelian inheritance patterns of flanking markers indicated that in the presence of this mutation, the wildtype allele in heterozygotes failed to amplify. After designing deletion-specific PCR primers, we were able to show that for example in MGA8 both parents were heterozygous and the patient was homozygous for c.1006+34_48del15bp. Follow-up reverse-transcription-PCR analysis and DNA sequencing showed that this particular deletion caused the complete loss of exon 9 (163 bp), leading to a frameshift in the resulting mRNA. The mutation occurred in Southwestern Europe (France and Spain) but was also found in Sudan (family Sudan 1) and in the USA (patient MGA82). The differing flanking haplotypes in the European, American, and Sudanese cases and the fact that two similar 15-bp deletions occurred in patients MGA86 (homozygous c.1006+16_30del15bp) from Yemen and Belgium 1 (compound heterozygous c.1006+36_50del15bp and c.1253_1254insA; ) from Europe pointed to a mutational hotspot. Four additional insertion-deletion mutations in the same region accounted for four more cases from Europe (MGA51: c.1118_1119insCGCT with missense c.122C>T; Thr41Ile and MGA19: c.967_(1169+15)del296bp and c.977_978insCCCG) and Central America (MGA38 and MGA73: homozygous c.1014_1021delCCTCGGCG). Moreover, the heterozygous change c.1170-6C>T in intron 10 (patient MGA81) and a homozygous change (c.1257+10C>T, patient MGA74) in intron 11 might affect mRNA processing as seen with other intronic changes in this region but RNA was not available to study them further. The repetitive and GC-rich region extending from intron 8 to intron 11 (838 bp with 75% G+C-content) includes the transmembrane domain in exon 10 (aa ~360-380; ).
The remaining 12 AMN mutations were private events in individual families or cases, with the exception of c.1314_1315delCA, which was seen in MGA13 and homozygously in MGA68. Case MGA12 carried a donor splice site and a missense mutation as detailed previously . Patient MGA88 was compound heterozygous for a splice site and a frameshift mutation, while the remaining seven sibships were homozygous for the respective mutation: MGA5, MGA77, MGA22, MGA83, Fam AK , PT, and BT with intronic point mutation c.514-34G>A. This ostensibly harmless change activated a cryptic splice site that caused the misincorporation of 32 bp in the mRNA (c.513_514ins32bp; p.Thr172fs).
Mutations in GIF
In our cohort 28/126 (22%) carried mutations in GIF. A total of 18 different mutations were identified of which 11 were previously reported and 7 are documented here (Table 1 and Additional file 1). The most numerous was splice site mutation c.79+1G>A in intron 1 that was found in seven sibships. Three times it was found homozygously (France 1, MGA4, and MGA25) and four times in combination with other defects: with a 3’-terminal deletion in MGA49 (see below) and with three different missense mutations in MGA79, MGA67, and MGA64, respectively. In patient MGA79 from Siberia it was missense mutation c.137C>T; p.Ser46Leu that was also found in two families from Turkey (IT and NT). Mutation p.Ser46Leu might be a Central Asian founder event but we lack sufficient information to prove that. In patient MGA67, we detected missense change c.290T>C; p.Met97Thr, which was described previously  and also occurred in a case from Finland (MGA35). In MGA64, the splice site mutation was compound heterozygous with missense mutation c.673A>C; p.Ser225Arg. Splice site mutation c.79+1G>A is apparently a Western Caucasian founder mutation, as we have not observed variation on the flanking haplotype.
Two more founder mutations were detected in GIF: c.183_186delGAAT; p.Met61fs, which is African in origin  and Chaldean splice site mutation c.1073+5G>A . While the latter was only found in homozygosity, p.Met61fs once occurred in a mixed African-Caucasian patient (MGA39) together with missense mutation c.659T>C; p.Ile220Thr . Residue Ile220 is conserved among mammals and the mutation scored damaging (PolyPhen-2 score 0.998). This missense change was also found in a second case (MGA27) together with a splice site mutation c.256+2 T>G .
Kuwaiti acceptor splice site mutation c.80-1G>A and two private insertion-deletion mutations c.161delA (case LT) and c.1175_1176insT (case AT) were described previously  and missense change c.1222G>A; p.Glu408Lys in case MGA61  affected a conserved residue. All these mutations were homozygous.
Families HT from Turkey and MGA36 from Lebanon shared the missense mutation c.685G>A; p.Ala229Thr. MGA54 carried two private frameshift mutations: c.431_438delAGAAGAAC and c.974_975insG and may have had a false positive Schilling test. Families MGA48 and D2914 are described below.
Large deletions in CUBN and GIF
Large gene deletions were discovered via incompatible Mendelian inheritance patterns of sequence polymorphisms or microsatellite markers. All four identified deletions were compound heterozygous with point mutations found on the other allele (Table 1 and Additional file 1). Three large deletions were detected in the CUBN gene, two removed the complete gene (MGA20 and MGA29), while one deletion removed the 5’-half of the gene up to exon 28 (MGA47). In GIF, a partial gene deletion extended from intron 8 past the 3’-end in the two siblings of MGA49. Because of the large physical distances involved we were unable to identify the exact deletion breakpoints via PCR but we have used markers flanking the genes in order to demarcate the deletions.
In nine cases, we have found only one likely mutation (one in AMN; five in CUBN, and three in GIF; Table 1 and Additional file 1). Four cases had recurrent mutations seen in other IGS or IFD cases or they were clearly deleterious (MGA43, MGA26, MGA65, and MGA35). The remaining five cases (Taiwan 1, MGA66, MGA81, MGA48, and D2914) carried heterozygous changes that were not encountered among controls or dbSNP with the exception of CUBN c.1951C>G; p.Arg651Gly (SNP rs182512508, without frequency information), which was detected in two siblings of family Taiwan 1. The two affected brothers shared the same CUBN genotype, while residue Arg651 is 100% conserved among vertebrates and considered detrimental by PolyPhen-2 (score = 1.0). Thus, p.Arg651Gly is likely a pathogenic change. In patient MGA66, the observed missense change CUBN c.2486C>T; p.Ser829Leu likewise affected a highly conserved residue which was considered damaging by PolyPhen-2 (score = 1.0). Thus, we concluded that p.Ser829Leu is an IGS mutation.
The change in intron 10 of AMN (c.1170-6C>T) in patient MGA81 was found in the aforementioned unstable GC-rich region of AMN. It is therefore possible that this change disturbed the mRNA processing as seen with several other intronic changes in this region but RNA was not available to study it further.
In patient MGA48, only GIF c.469T>C; p.Phe157Leu was detected as a candidate mutation. The IF residue Phe157Leu is conserved among vertebrates with the exception of the dog, which has a leucine residue in place of phenylalanine, thus its exact functional consequences remain to be studied (PolyPhen-2 score = 0.003). However, it was never detected in any other individual or control other than the older sister of the patient, who is healthy and has a different GIF genotype. Thus, p.Phe157Leu is a likely culprit in this Lebanese girl with Cbl deficiency since the other two genes were excluded. Finally, in patient D2914, missense change GIF c.938C>T; p.Thr313Ile is likely pathogenic (100% conserved among vertebrates and PolyPhen-2 score = 0.999).
Genetic defects in intestinal malabsorption
The spectrum of mutations in the three genes CUBN, AMN, and GIF includes nonsense, missense, insertion-deletion, splice site, and intronic mutations, as well as large deletions first reported herein (Table 1 and Additional file 1).
Given that many mutations appear to be private or restricted to a specific ethnicity or population, estimates of the population frequency of IGS or IFD and their underlying mutations are difficult to make and cannot be extrapolated across populations. Thus, we purposely avoided estimating the frequency of IGS or IFD as we believe it will not be sufficiently accurate to be useful. However, many mutations affect specific ethnic groups; as a result, ancestry was demonstrated to facilitate genetic testing [23, 44, 46]. The genetic heterogeneity led us to develop an ethnicity-focused screening strategy that targets founder mutations first (Figure 2).
Our analyses of 53 families or cases with 33 CUBN mutations show that no IGS mutation was found beyond exon 28 and one of the deletions (case MGA47) covered the same region. This observation is of clinical utility because it suggests that defects beyond exon 28 have no impact on the absorption of Cbl, as long as the protein is stable. In fact, it was shown that a homozygous frameshift mutation in exon 53 of CUBN (c.8355delA; p.Ser2785fs) only caused proteinuria . Moreover, a missense variant in exon 57 (c.8950A>G; p.Ile2984Val) was associated with albuminuria . Thus, mutations in CUBN cause IGS apparently only when they affect the cubilin-amnionless interaction domain (amino-terminal third of cubilin, exons ~1-20; ) or the IF-Cbl binding site (CUB domains 5–8, exons 21–29; ; Figure 1). It is possible that genomic deletions in CUBN are more common and could account for some of the missing mutations and unresolved cases. In individual patients however, deletions can be difficult to detect unless the deletion is homozygous. It is therefore prudent to include parents and siblings in the genetic analysis since the genetic information (heritable SNPs and other variants) might expose genomic deletions. Technically, multiplex ligation-dependent probe amplification (MLPA) or next-generation sequencing should detect deletions but an MLPA kit for CUBN is currently not available and whole-genome sequencing for routine diagnostics is still in its infancy.
Mutations in AMN are dominated by founder events and a mutational hotspot in the region of introns 8–11 that includes the transmembrane domain in exon 10 . Its analysis was technically challenging because of a highly repetitive GC-content and required high-quality genomic DNA. Moreover, in individuals heterozygous for AMN c.1006+34_48del15bp the wildtype allele dropped-out during PCR; thus in cases that show seemingly non-Mendelian inheritance of rare changes, a detailed molecular follow-up by RT-PCR or various PCR primer combinations is advisable.
A single IFD patient with a homozygous 4-bp deletion in GIF was first described in 2004 . The finding of additional mutations in GIF was the result of a genome-wide search among patients with suspected IGS that were previously excluded for defects in CUBN and AMN.
While IF is conserved among Amniota (mammals, birds, and reptiles) the level of conservation among lower vertebrates is less clear. This analysis is complicated by the fact that the genes for transcobalamin 2 (TCN2) and haptocorrin (transcobalamin 1; TCN1) are similar as a result of ancient gene duplication events . The three genes share the same genomic structure with 9 exons and a Cbl binding domain, pointing to a common ancestral gene [49, 50]. Despite the coding and structural similarities, PCR-based analysis of three genes, GIF TCN1, and TCN2 has not caused technical problems. Conversely, transcript analysis of GIF using RNA derived from blood cells has proved difficult because the gene is not expressed in that tissue. Even successive rounds of PCR with nested primers and have not succeeded in amplifying the GIF mRNA. This is not particularly surprising since haptocorrin and transcobalamin are the specific Cbl-transporters in the blood , and haptocorrin is also found in saliva . Thus, transcript studies of GIF will likely require gastric sampling to obtain the parietal cells that produce IF.
Because of the limited clinical details that were available from some patients and the fact that many mutations were private, meaningful phenotype-genotype correlations in IGS and IFD were limited. The course of therapy and the health care environment varied widely, as did the age of onset of the symptoms. The most obvious clinical sign, megaloblastic anemia, was not always present and is not unique to IGS or IFD . On the other hand, early hematological and neurological signs can go unnoticed for many months or years. Generally, clinical diagnosis was based on excluding various differential diagnoses, so many patients were only referred for genetic testing several months after acute problems began. However, treatment with parenteral Cbl was often initiated before a firm diagnosis could be made. Thus, the necessary information to predict the age of onset, the degree of manifestations, and the course of the disease depending on the type of mutation is lacking.
Proteinuria is found in many IGS cases  but has rarely been seen in IFD except in two cases from our series, MGA67 and MGA79. We suspect that these two cases had proteinuria unrelated to their IFD defects. The root cause of the proteinuria in IGS is due to the fact that mutations in CUBN or AMN not only prevent the intestinal uptake of Cbl but may also impair the renal reabsorption of proteins [21, 52]. Since amnionless is required to localize cubilin to the luminal membrane in the intestines and kidneys [34, 53], deleterious mutations in AMN often cause simultaneous Cbl deficiency and proteinuria since the cubam complex is no longer able to mediate uptake of its many ligands . In CUBN, mutations in the cubilin-amnionless interaction domain (amino-terminal third of cubilin, exons ~1-20; ) or total loss of the protein may similarly lead to concurrent Cbl deficiency and proteinuria, while mutations in the IF-Cbl binding site (CUB domains 5–8, exons 21–29; ) can cause Cbl deficiency without proteinuria . The finding of mono-symptomatic proteinuria due to mutations in CUBN (c.8355delA; p.Ser2785fs;  and c.8950A>G; p.Ile2984Val; ) pointed to the fact that not all mutations in this gene have the same physiological consequences. Thus, defects in cubilin have pleiotropic effects, e.g. for kidney function .
Lack of Cbl not only causes anemia but also impairs neurological function . In young infants, hypotonia, seizures, developmental delay, and brain atrophy often occur during the first six months . In severe cases, the patients can perish during early childhood. In older children, movement disorders, dementia, delirium, or psychosis were observed . One IGS case (MGA12) with mutations in AMN showed severe psychosis, which only responded to high-dose Cbl therapy . It was suggested that an active Cbl transport mechanism at the blood–brain barrier exists, and that amnionless may be part of this mechanism. Consequently, it is possible that certain mutations in CUBN or AMN affect the neurological presentation differently.
Mouse models deficient in CUBN or AMN have been developed and proved embryonic lethal. Given the deleterious nature of many CUBN and AMN mutations in humans, it has become clear that the role of cubilin and amnionless in rodent development is distinct from the role that these proteins play in humans. Thus far, it is not obvious what functions cubilin and amnionless have in primate embryogenesis . IGS was also observed in dogs with two different mutations in the canine AMN gene and the phenotype was similar to that observed in humans . In an attempt to define the differences between rodents and higher mammals regarding AMN, we created Amn knock-in mice with three different human IGS mutations (data not shown). The high degree of sequence conservation between human and mouse permitted the identical recreation of the human IGS mutations in the mouse. Two of these mutations (Amn c.14delG; p.Gly5fs and Amn c.683_730del48; p.Gln228_Leu243del) were homozygously lethal, since we never observed any homozygous pups among over 100 offspring in each case (data not shown). On the other hand, the Norwegian missense mutation Amn c.122C>T; p.Thr41Ile was viable in the homozygous mouse and without any apparent phenotype (data not shown). Recently, conditional Cubn knock-out mice were created , which should permit a better definition of the essential role of cubilin in mouse embryogenesis and renal function.
Other candidate genes
We have screened 27 cases or sibships (18%) for mutations in CUBN AMN, and GIF without detecting any pathogenic mutations (Table 1). For seven families the involvement of some or all of the genes was genetically excluded based on different genotypes in two affected siblings (JCA1, MGA40, MGA41, MGA46, MGA85, MGA89, and MGA90). Among the 20 remaining single patients, patients MGA62 and MGA91 were thought to suffer from a defect in the TCN1 gene that encodes haptocorrin. Patient MGA91 carried a novel heterozygous change in intron 5 (TCN1 c.747+3A>C) that was suspect but no RNA was available to study potential splicing aberrations. So far, two truncating mutations have been described in TCN1 but to what degree haptocorrin deficiency plays a role in Cbl deficiency remains to be studied.
It is conceivable that we have missed some mutations. These could be located in introns or regulatory sequences distant from the exons. However, many cases carried two distinct alleles of the IGS/IFD genes, thus we would have expected two different disease mutations, which would be less likely to be missed. Overall, we have achieved a sensitivity of 82% in our mutation screening strategy (Figure 2).
Based on their role in transport of Cbl, alternative candidate genes FUT2[61–63], CD320[64, 65], LMBRD1, and ABCC1 were screened by DNA sequencing in a selected group of unresolved cases but no mutations were found (Additional file 1 and ).
Deficiency of transcobalamin 2 (TC2; OMIM275350) with mutations in TCN2[68, 69] represents an alternative diagnosis. Symptoms include megaloblastic anemia, diarrhea, vomiting, failure to thrive, recurring infections, and mental retardation. Thus, many clinical features overlap with IGS and IFD, although mental retardation is not usually associated with IGS and IFD. We sequenced a few atypical cases for mutations in TCN2 (MGA6, MGA23, and MGA62) but found no mutation. In general, TC2 deficiency manifests rapidly in the first 1–2 months after birth and was excluded in most cases before referral for IGS/IFD mutation screening.
Accordingly, Cbl pathway genes yet to be identified might explain some of these remaining cases of inherited Cbl deficiency. Based on the documented Cbl uptake pathway (Figure 3), a likely location for failure could be the loading of TC2 with Cbl in the enterocyte to form holo-TC2 or the export of holo-TC2 from of the enterocyte. This particular part of the Cbl transport is not well understood but similarities to the intracellular cblF defect (OMIM277380) that affects the lysosomal membrane transport  could be postulated.
Prospective screening recommendations and future prospects
With the gathered information on ethnicity-specific mutations, it has become feasible to perform targeted screening for common or local founder mutations (Figure 2 and Additional file 1). However, human migrations change the genetic make-up of populations and it is important to trace ethnic ancestry cautiously.
The observation that mutations in CUBN are limited to the first 28 exons has simplified the genetic analysis (Figure 1) but the need to screen three genes remains unchallenged for now because clinical tests cannot reliably distinguish IGS and IFD. Parallel, whole-exome or whole-genome sequencing using next generation technology might permit concurrent screening of the three genes. However, clinical laboratory regulations and ethical concerns about the additional sequence data produced will delay the routine introduction of the technology. Consequently, Sanger-based exon-by-exon sequencing will remain the method of choice for the coming years to confirm IGS and IFD.
For clinical diagnostics, a new non-radioactive Cbl absorption test may eventually replace the Schilling test . The patient is given a dose of cyano-Cbl, which enters the blood unchanged via the intestine in healthy people but not in cases with IGS or IFD. Then the fraction of transcobalamin-bound cyano-Cbl is measured, which reflects the degree of Cbl absorption. In IGS or IFD, the rate of cyano-Cbl loading of the holo-transcobalamin will be lower. As with the Schilling test, it is conceivable that the addition of IF in a second test step could distinguish IGS from IFD, as the added IF should restore the Cbl absorption in IFD only. This test promises to be more specific than serum levels of total Cbl, methylmalonic acid, or homocysteine . However, questions of sensitivity remain to be answered but such a test would streamline clinical diagnostics.
Elucidating the genetic basis of inherited Cbl malabsorption has provided the tools to verify the diagnosis in over 80% of the cases on the molecular level. In addition, studying this rare phenotype has elucidated the mechanisms and pathway of Cbl uptake in great detail. Our study triples the number of Cbl malabsorption cases molecularly analyzed and provides a comprehensive overview of the genetic patterns that cause this genetically heterogenous disease. The mutational patterns we have identified should simplify genetic diagnostics.
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We thank the families and their clinicians and genetic counselors for supporting our research over many years (Additional file 1). We are grateful to Ralph Gräsbeck, John C. Fyfe, David S. Rosenblatt, Harald Broch, Søren K. Moestrup, and Ralph Green for their advice. We thank Ryan Bisson, Zhongyuan Li, James D. Perko, Cameron M. Beech, Andrea E. Ament, Ceren Acar, Nidhi P. Shah, Ann-Kathrin Eisfeld, and particularly Jan C. Lockman for assistance in the laboratory. This work was supported by grant CA16058 from the National Cancer Institute, USA.
The authors have no competing financial interests.
SMT conceived and designed the study, coordinated the research, and wrote the manuscript. ACS and ECB coordinated DNA sample collection and performed genetic counseling. SL helped to draft the manuscript. AdlC commented on the manuscript draft. All authors read and approved the final manuscript.
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Tanner, S.M., Sturm, A.C., Baack, E.C. et al. Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns. Orphanet J Rare Dis 7, 56 (2012). https://doi.org/10.1186/1750-1172-7-56
- Vitamin B12
- Hereditary cobalamin malabsorption
- Gastric intrinsic factor
- Genetic testing
- Founder mutation
- Genetic heterogeneity