Pleiotropic effect of a novel mutation in GCNT2 causing congenital cataract and a rare adult i blood group phenotype

Mutations in GCNT2 have been associated with the rare adult i blood group phenotype with or without congenital cataract. We report a novel homozygous frameshift mutation c.1163_1166delATCA, p.(Asn388Argfs*20) as the cause of congenital cataract in two affected siblings. Blood group typing confirmed that both affected males have the rare adult i phenotype, supporting the hypothesis that the partial association of I/i phenotype and congenital cataract is due to the differential expression of GCNT2 isoforms.

to the study ( Figure 1a). Patient (II:2), now age 40 years, was noted in early infancy to have reduced vision. Examination under anesthesia was performed at the age of 4 months, which identified pendular nystagmus and bilateral lamellar cataracts. Initial management was with pupil dilatation using guttae atropine 0.5% in each eye. At 10 months of age, cataract surgery was performed with lens aspiration, which left him aphakic. Contact lens refractive correction was subsequently used. Further treatment included two left lens surgical capsulotomies at the age of 2 and 17 years, right occlusion therapy for left amblyopia and squint surgery for left esotropia at the age of 2 years. At the age of 3 years, the first recorded uniocular visual acuity was 6/24 Snellen (right eye, RE), and 4/60 (left eye, LE). At last review, at 40 years old, visual acuity was 6/60 (RE), and 6/24 (LE) with refractive correction of +13.25/ − 2.25 × 105 (RE), +14.75/ − 1.25 × 170 (LE). Patient (II:3), now age 39 years, was noted at 2 months of age by his mother to have nystagmus and a white reflex. Central lens opacities were found with abnormal posterior curvature of the lens, and normal fundi. Lens aspiration was performed in the left eye at 7 months of age, and in the right eye at 10 months of age with soft contact lens refractive correction afterwards. Further procedures included left needle capsulotomy at 8 months of age, left laser capsulotomy at the age of 15 years, secondary sulcus intraocular lens in the right eye at the age of 19 years and in the left eye at 29 years of age. Axial lengths on B scan ultrasound prior to lens insertion demonstrated long axial lengths of 27.88 mm (RE), 29.31 mm (LE) and refractive errors of +10.50/ − 1.00 × 10 (RE), and +10.00/ − 2.00 × 15 (LE). At the age of 29 years, Snellen visual acuity was 6/36 in both eyes. Fundus examinations and electroretinogram were normal in both siblings and there was no evidence of anterior segment dysgeneses or glaucoma.
Both parents were examined. Their mother (I:2) had subtle lamellar lens opacities at the age of 61 years. However, given her age and prevalence of cataracts in the general population at that age, these findings could be age-related. Their deceased father (I:1) was unilaterally aphakic (trauma-related), the other lens was clear. Both affected siblings had uncomplicated births and were 1  Mutations in GCNT2 causing CC and rare adult i blood group phenotype S-S Cheong et al well with normal development. All investigations were conducted in accordance with the principles of the Declaration of Helsinki. The study was approved by the local ethics committees at Moorfields Eye Hospital, UK. After written informed consent was obtained from all subjects, blood samples were donated and genomic DNA was extracted from peripheral blood lymphocytes using conventional methodologies. Patients were clinically assessed by experienced ophthalmologists. Inheritance of CC was consistent with recessive disease (Figure 1a). WES was performed for individual II:3 using Nimblegen sequence capture (v2) and a HiSeq2000 sequencer (Illumina, San Diego, CA, USA). Reads were aligned to the hg19 human reference sequence using Novoalign (Novocraft, www.novocraft.com) version 2.05. The ANNOVAR tool (OpenBioinformatics, www.open bioinformatics.org/annovar/) was used to annotate sequence variants. Filtering was performed to identify variants with a minor allele frequency ⩽ 0.005 in 1000 Genomes Project (www.1000gen omes.org/), the National Heart, Lung, and Blood Institute Exome Sequencing Project Exome Variant Server (http://evs.gs.washing ton.edu/EVS/), Exome Aggregation Consortium database (http:// exac.broadinstitute.org/) and our internal University College London exomes consortium database comprising of 1,980 exomes. Variants were then cross-referenced with CatMap (http://cat-map.wustl.edu/) for variants in known cataract genes. WES data were also analyzed by ExomeDepth 20 to identify any potential causative exonic copy number variations. The GCNT2 variant in exon 3 was tested for segregation in the affected males (II:2 and II:3), their mother (I:2) and the children of individual II:2 (III:1 and III:2) by direct sequencing. Primer sequences are available on request. GCNT2 cDNA is numbered in accordance with Ensembl transcript ID ENST00000316170, with +1 corresponding to the A of the ATG translation initiation codon.
WES analysis of individual II:3 identified a unique homozygous 4-bp deletion in GCNT2 (Figure 1b), predicted to cause a frameshift mutation, c.1163_1166delATCA, p.(Asn388Argfs*20). Copy number variation analysis of this WES data did not identify any potential exonic copy number variations in any genes associated with CC, and excluded copy number variations at the GCNT2 locus. Direct Nucleotide sequences and corresponding amino acid residues are shown below the exome data tracks. (c) Sequence electropherograms demonstrate segregation of the GCNT2 mutation. The proband (II:3) and his affected brother (II:2) are homozygous for the 4-bp deletion. Their mother (I:2) and the children of II:2 (III:1 and III:2) are carriers for the mutation. Control sequence electropherogram is shown above I:2 sequence. The exon 3 mutation is predicted to cause a frameshift [c.1163_1166delATCA, p.(Asn388Argfs* 20)]. GCNT2 cDNA is numbered in accordance with Ensembl transcript ID ENST00000316170, with +1 corresponding to the A of the ATG translation initiation codon.
sequencing of GCNT2 exon 3 confirmed that both affected males are homozygous for the frameshift mutation, whereas their mother (I:2) and two children (III:1 and III:2) of affected male II:2 are carriers (Figure 1c).
GCNT2 has three isoforms, GCNT2-A, GCNT2-B and GCNT2-C, which are alternatively spliced with a different exon 1 (refs 10,16) ( Figure 2). These isoforms are differentially expressed, with only transcript GCNT2-B expressed in lens epithelial cells and GCNT2-C in reticulocytes. Differential expression of GCNT2 isoforms has been proposed as a potential mechanism for the absence of CC in some patients with an adult i blood group. 10 The mutation identified in this family is located in exon 3, and is therefore present in all three GCNT2 isoforms (Figure 2), suggesting these individuals may also have an adult i blood group. Blood samples were collected in EDTA tubes for I/i blood group typing for individuals II:2 (age 40 years) and II:3 (age 39 years). Monoclonal anti-I (HIRO-245) from the Japanese Red Cross, and polyclonal anti-i (P.E.) from the in-house reference collection were tested by standard direct agglutination tube technique and scored according to Marsh. 21 Expression of i antigen was assessed by titration, using a base dilution of 1:40 and then doubling dilutions. An example of adult cells with normal I expression (L2325-8) and adult i cells (074-214RF) from the in-house reference collection were included as controls.
Our finding confirmed that both affected individuals have the adult i phenotype, thereby establishing the association of the homozygous GCNT2 frameshift mutation p.(Asn388Argfs*20) with CC and the adult i phenotype in this family.
Thus, in this study, we describe the first report of the association of GCNT2 mutation with CC and rare adult i phenotype in the Caucasian population, and our data support the hypothesis that differentially expressed GCNT2 isoforms account for the partial association of the adult i phenotype with CC, irrespective of ethnicity.

HGV DATABASE
The relevant data from this Data Report are hosted at the Human Genome Variation Database at http://dx.doi.org/10.6084/m9. fig  share.hgv.952.