Nine affected individuals with isolated anophthalmia/microphthalmia from a large Muslim-inbred kindred were investigated. Assuming autosomal-recessive mode of inheritance, whole-genome linkage analysis, on DNA samples from four affected individuals, was undertaken. Homozygosity mapping techniques were employed and a 1.5-Mbp region, homozygous in all affected individuals, was delineated. The region contained nine genes, one of which, aldehyde dehydrogenase 1 (ALDH1A3), was a clear candidate. This gene seems to encode a key enzyme in the formation of a retinoic-acid gradient along the dorsoventral axis during an early eye development and the development of the olfactory system. Sanger sequence analysis revealed a missense mutation, causing a substitution of valine (Val) to methionine (Met) at position 71. Analyzing the p.Val71Met missense mutation using standard open access software (MutationTaster online, PolyPhen, SIFT/PROVEAN) predicts this variant to be damaging. Enzymatic activity, studied in vitro, showed no changes between the mutated and the wild-type ALDH1A3 protein.
Anophthalmia and microphthalmia (A/M) are rare developmental anomalies resulting in absent or small ocular globes, respectively. Anophthalmia refers to complete absence of the ocular globe in the presence of adnexa (eyelids, conjunctiva and lacrimal apparatus). Microphthalmia is defined as such when the total axial length of the globe is at least two SD below the mean for age; this typically correlates to an axial length below 21 mm in adult eyes.1, 2
A/M is a heterogenous condition. A/M may affect one or both eyes and present as either an isolated or syndromic disorder.1, 2 Both genetic and environmental factors, such as fetal alcohol syndrome and vitamin A excess or deficiency, contribute to congenital eye defects.3, 4, 5, 6, 7 All types of Mendelian inheritance have been reported for A/M. The majority of genes known to be involved in the pathogenesis of A/M are transcription factors or homeobox genes.8
We have previously described a highly inbred Muslim kindred, from Northern Israel, with isolated A/M.9 Nine affected individuals had isolated bilateral microphthalmia and no light perception. All showed normal intelligence, displayed no other anomalies and were otherwise healthy. Responses on electroretinogram or visually evoked potentials were consistently absent in all cases. Computed tomography scans disclosed small congenital cystic globes, with rudimentary optic nerves and extraocular muscles. This study aimed to unravel the genetic basis underlying A/M in our family.
Patients and families
Four highly inbred nuclear families of Muslim origin displaying autosomal-recessive, isolated A/M were studied. Thirteen healthy parents and siblings and nine affected individuals were clinically investigated. Blood samples were drawn from all participants. Skin biopsy was obtained from one affected individual. The study was approved by the institutional review board at Rambam Health Care Campus, Haifa. Signed informed consent (self and parental) was obtained.
Using linkage analyses, known A/M causative genes such as VSX2 (MIM:610093), RAX (MIM:611038), SOX2 (MIM:206900) and PAX6 (OMIM: 607108) were excluded. Genomic DNA of four affected individuals (VI_2, VI_6, VI_12 and VI_13) was genotyped using the Affimetrix GeneChip Human Mapping 250 K Nsp microarray (Santa Clara, CA, USA). Homozygosity-by-descent analysis was carried out manually, exploring identical homozygous intervals in all affected individuals. Linkage analysis, of a candidate homozygous locus on chromosome 15, was expanded to include additional family members, using two microsatellite markers designed by us: GT22 at chr15: 101094111-101094103 (marker_1:F_5′-IndexTermTGT CAA CCA CGA GCA GTT TC-3′; R_5′-IndexTermGCC CTC AGC ATC CTG ATA TT-3′) and TG24 at chr15:102147332-102147378 (marker_2:F_5′-IndexTermGTG GTG GGC TGA TAA ATG CT; R_5′-IndexTermAAC AAA GGC ATT CTG TGA GGA-3′). Haplotypes of family members were manually constructed and analyzed with SUPERLINK online under the assumption of autosomal-recessive inheritance and disease allele frequency of 0.01. One candidate gene, aldehyde dehydrogenase 1 (ALDH1A3), within the homozygous region was sequenced using genomic DNA from one affected individual. Sanger sequencing of coding regions and flanking intron–exon boundaries was undertaken (primer sequences are available on request). Once the causative mutation was detected (c.211 G>A), a PCR-RFLP assay was developed using primers designed by us: exon3_F:5′-IndexTermCAG TCT CTC TCT GTT GTT CTG G-3′ and exon3_R:5′-IndexTermGAG AGC CGT GTC TCA GAG GA-3′. The G to A substitution abolishes an HpyCH4IV restriction-native site, generating cleavage-differential products for the wild-type (277 bp, 35 bp) and the mutated (312 bp) alleles.
Total RNA was extracted from cultured epidermal fibroblasts using the RNeasy Mini Kit (Qiagen, Hilden, Germany) and reverse transcribed into cDNA by the QuantiTect reverse transcription kit (Qiagen) using RT primer mix according to the manufacturer’s protocol. cDNA of ALDH1A3 was sequenced using primers devised by us: cDNA_exon2_F: 5′-IndexTermGCA ACC TGG AGG TCA AGT TC-3′ and cDNA_exon5_R: 5′-IndexTermCAG CTT CCA CAC CAG CAT C-3′.
Kinetic studies of the p.Val71Met mutation
ALDH1A3 cDNA was subcloned into the pET-30 Xa/LIC (Novagen, Bloemfontein, South Africa) expression vector, coding for an N-terminal (His)6 tag, by using two primers containing ligation-independent cloning overhangs, as indicated by the manufacturer (EMD Biosciences, Darmstadt, Germany). All reactions were performed in a DNA thermal cycler with Phusion High-Fidelity DNA Polymerase (Thermo Scientific, Waltham, MA, USA). Two mutagenic primers, 5′-IndexTermGGA GAT AAG CCC GAC ATG GAC AAG GCT GTG GAG GCT GC-3′ and 5′-IndexTermCTC CAC AGC CTT GTC CAT GTC GGG CTT ATC TCC TTC TTC-3′, were designed to introduce the p.71Met mutation, using the wild-type ALDH1A3 cDNA cloned into pET-30 Xa/LIC as a template. Mutated nucleotides are underlined. The procedure was based on the QuikChange Site-Directed Mutagenesis Kit method (Stratagene, Leicester, UK). The mutagenic strands were sequence verified and then transformed into Escherichia coli BL21 cells, in which recombinant ALDH1A3 was expressed at 24 °C and purified, as previously described10 and as follows: cells were lysed by sonication and the homogenate was applied onto a nickel-charged chelating Sepharose Fast Flow (GE Healthcare, Little Chalfont, UK) column (5 ml). After washing with 60 mM imidazole in 20 mM Tris-HCl, 0.5 M NaCl, pH 8.0, the enzyme was eluted with 250 mM imidazole in the same buffer. Protein fractions were concentrated and imidazole was removed with an Amicon ultra device (Millipore, Little Chalfont, UK). Protein concentration was determined by a dye-binding assay using bovine serum albumin as a standard.11 Enzymatic activity of ALDH1A3 was determined in 50 mM HEPES, 50 mM magnesium chloride, 5 mM dithiothreitol, pH 8.5, at 37 °C, and in the presence of a saturating concentration of cofactor NAD+. The activity with 4-nitrobenzaldehyde was measured in a Cary 400 Bio (Varian, Palo Alto, CA, USA) spectrophotometer, as described.12 Activity with retinoids was analyzed by HPLC; after extraction, retinoids were separated by chromatography on a Nova-Pak Silica column in n-hexane:methyl-tert-butyl ether:isopropanol:acetic acid (95.9:4:0.075:0.025, v/v) mobile phase, at a flow rate of 2 ml/min, and separation of retinaldehyde, retinoic acid and retinol was achieved in a single step, with retention times of 6.76, 8.72 and 29.45 min, respectively, based on previously described protocols.12, 13 An Mr of 244 000 was used to calculate the kcat values. The kinetic constants were expressed as the mean±SEM of two determinations. In addition to HPLC-based kinetics with retinoids, UV–vis spectrophotometric determination of 4-nitrobenzaldehyde oxidation, in which NAD+ reduction was measured at 340 nm, was undertaken.
Whole-genome homozygosity mapping defined a single homozygous segment on chromosome 15q26.3 spanning 1 340 206 bp between rs1552101 and rs6598484 shared by four affected individuals. We thereafter developed and genotyped two microsatellite markers in this interval; all affected individuals (n=9) shared the same homozygote haplotype for marker_1, all parents (n=8) were heterozygote for the linked haplotype and healthy siblings (n=5) were either heterozygote or noncarriers of the linked haplotype (Figure 1a). A two-point LOD score of 7.9 was calculated. The region encompassed nine genes, one of which, ALDH1A3 (NM_000693.2 (MIM600463)), a key enzyme in the formation of a retinoic-acid gradient along the dorsoventral axis during an early eye development, was sequenced. Sanger sequencing revealed a homozygous missense mutation c.211G>A (p.Val71Met) in an affected individual (Figure 1b). Using PCR-RFLP analyses, the mutation was tested in all parents and healthy siblings from our four related families and was found to cosegregate with the disease; all affected individuals were homozygous for the mutation (n=9; probability for a random amino-acid exchange 3.3147E-06). Unaffected siblings were either heterozygous or noncarriers (n=5), and all parents were heterozygotes (n=8). The mutation was tested and not observed in 100 individuals from the same ethnic origin.
The mutation was not recorded in the dbSNP databases or the Exome Variant Server. MutationTaster online predicts p.Val71Met to be disease causing (probability score: 0.92). SIFT/PROVEAN (San Diego, CA, USA) and PolyPhen2 predict the mutation to be damaging. ALDH1A3 consists of 13 exons that encode retinaldehyde dehydrogenase, a protein of 512 amino-acid residues involved in retinoic-acid synthesis. Residue 71 is positioned in exon 3, within a DXXDXD motif, between two strictly conserved Asp residues.
The mutation is located at position +7 of exon 3 and does not overlap with the consensus splicing sequence. We, however, have excluded an eventual splicing effect by sequencing the corresponding cDNA from an affected individual. No aberration was identified other than the homozygote G>A substitution.
Wild-type and p.71Met-mutant ALDH1A3 were expressed as soluble proteins in E. coli. Comparable expression levels were observed for the wild-type and p.71Met-mutant ALDH1A3, as assessed from the SDS-PAGE analysis of E. coli lysates (Figure 2). Similar purification yields and activity loss over time were obtained for the mutant and wild-type protein. Under the purification and storage conditions used, both proteins displayed low stability, and precipitation over time was equivalent. No evidence of misfolding or increased instability was observed for the p.71Met mutant.
Kinetic constants were determined using freshly prepared protein. Both wild-type and p.71Met mutant showed comparable enzymatic activity using NAD+ as a cofactor. Kinetic analysis revealed that wild-type and mutant protein display similar Km (0.083±0.01 vs 0.085±0.01 μ M) and kcat (0.79±0.02 vs 0.62±0.02 per min) values for all-trans-retinaldehyde. Very small differences in the Km values for NAD+ (7.9±1.7 vs 4±0.3 μ M) were observed between the wild-type and the mutant enzymes.
UV–vis spectrophotometric determination yielded Vmax values for wild-type and p.71Met-mutant ALDH1A3 of 0.23 and 0.13 μmols per min per mg, respectively.
Nine individuals, from one inbred kindred, segregating isolated A/M with orbital cysts were homozygous for a missense mutation in the gene encoding the A3 isoform of the ALDH1A3. The probability for this being a random association stands at 3.8 × 10−6. ALDH1A3 is a key enzyme in the formation of a retinoic-acid gradient along the dorsoventral axis during an early eye development.3, 6, 7 Fares-Taie et al14 have recently shown that mutations in ALDH1A3 cause A/M. Two missense mutations and one splice mutation, namely, p.Arg89Cys, p.Ala493Pro and c.475+1G->T, were reported to segregate in three consanguineous families with A/M. Here, we report on yet another ALDH1A3 missense mutation, namely, p.Val71Met that causes A/M. Although the role of retinoic-acid signaling in the eye development is well established, the results provided by Fares-Taie et al14 and that of ours ascertain the genetic linkage between retinoic-acid synthesis dysfunction and an early eye development anomalies, namely, A/M, in humans.
The mutation described here affects an amino-acid residue that is fairly well conserved in the ALDH1A1 gene orthologs, as well as in the ALDH1A2 and ALDH1A3 gene paralogs. Otherwise, valine (Val) is replaced by another apolar residue (Ile) in most instances. Thr, an isosteric residue, has also been observed to substitute Val (Figure 3). After assessing the highly similar 3D structures of sheep ALDH1A1 (PDB code 1BXS) and rat ALDH1A2 (PDB code 1BI9), we conclude that residue 71 is located at the beginning of an α-helix in the NAD+-binding domain near the protein surface. Apparently, the p.Val71Met substitution should not greatly disturb protein stability or enzymatic function. Methionine (Met) is a rather rare amino acid in proteins, moderately hydrophobic, that similar to Val tends to stabilize α-helices. Unlike residues 89 and 493, reported by Fares-Taie et al,14 Val71 is not involved in subunit–subunit interactions.
Our kinetic assays delivered comparable expression and activity levels for the wild-type and mutant ALDH1A3 proteins. To our knowledge, this report is the first to provide kinetic constants of human ALDH1A3 and retinaldehyde. It has been reported that oxidative stress may render Met susceptible to oxidation, in the process yielding hydrophilic Met sulfoxide and Met sulfone, which can destabilize α-helices. Solvent-exposed Met residues are much more susceptible to oxidation than buried ones, and this may lead to protein misfolding, lower thermal stability or altered activity.15 It is conceivable that the reductive environment of the E. coli cytosol and the low growth temperature in vitro prevented the oxidation and subsequent instability of the recombinant enzyme. It is also likely that conditions used during the purification and enzymatic assay protected Met from being oxidized. Thus, enhanced sensitivity of the p.71Met mutant to oxidation, if the case, might have passed undetected in our assays. Val to Met substitutions were indeed reported to increase temperature sensitivity in other proteins.16, 17 Likewise, a p.Thr49Met mutation in retinol dehydrogenase 12, which reduces retinaldehyde to retinol, was reported to cause severe retinal degeneration.18 This protein, which retained significant catalytic activity in vitro, demonstrated higher instability linked to proteosome degradation in the cell.18
The dynamics of the p.Val71Met mutation remain elusive at this stage. It is plausible that the Met to Val substitution at codon 71 may constitute a secondary initiation for translation mechanisms, or alternately the mutation may cause abnormal protein folding. Further studies on thermal stability, protease sensitivity or in vivo turnover rate of the p.71Met mutant could provide additional information.
Microphthalmia, a strong manifestation within the fetal alcohol spectrum disorder,19 is attributed to a competitive effect of ethanol, or its metabolite acetaldehyde, for retinaldehyde dehydrogenase.20, 21 We could assume that A/M, caused by defects in ALDH1A3, is the genetic alternative of this disorder.
Thus far, the mutations described have been associated with nonsyndromic A/M. The families reported by Fares-Taie et al14 have inconsistently demonstrated additional features (autism and heart anomalies), which may be mutation related or incidental. Fares-Taie et al14 question the validity of these additional signs. In our families, all affected cases had isolated A/M and normal intelligence. Recently, homozygosity for two nonsense mutations in ALDH1A3, namely, c.568A>G (p.Lys190*) and c.1165A>T (p.Lys389*), that predict nonsense-mediated decay and complete loss of function were linked to anophthalmia and hypoplasia of the optic nerve and optic chiasma. With this in mind it remains speculative whether missense mutations are preferentially associated with microphthalmia, whereas nonsense and frameshift mutations are linked to anophtalmia.22
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We are grateful to all family members for their participation in this study. We thank Gregg Duester who provided the ALDH1A3 cDNA clone. Affymetrix GeneChip Human Mapping 250K Nsp microarray was carried out in the Biological Services Unit at the Weizmann Institute. This work was supported in part by the Spanish Ministerio de Economía y Competitividad (BFU2011-24176) and Generalitat de Catalunya (2009 SGR 795).
The authors declare no conflict of interest.
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Mory, A., Ruiz, F., Dagan, E. et al. A missense mutation in ALDH1A3 causes isolated microphthalmia/anophthalmia in nine individuals from an inbred Muslim kindred. Eur J Hum Genet 22, 419–422 (2014). https://doi.org/10.1038/ejhg.2013.157
- ALDH1A3 gene
- homozogosity mapping
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