A frameshift mutation in the CHM gene causes choroideremia with acute angle‑closure glaucoma

  • Authors:
    • Pingbo Ouyang
    • Yun Li
    • Feng Zhang
    • Chengzhang Zhu
    • Beiji Zou
    • Jianlan Le
    • Lusi Zhang
  • View Affiliations

  • Published online on: April 5, 2018     https://doi.org/10.3892/mmr.2018.8851
  • Pages: 7918-7924
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Abstract

Choroideremia is an X‑linked recessive chorioretinal degenerative disease that is characterized by progressive centripetal loss of the photoreceptor, retinal pigment epithelium (RPE), and choriocapillaris layers. The CHM gene [choroideremia (Rab escort protein 1)] has been identified as the pathogenic gene in choroideremia. The aim of the present study was to describe the clinical and genetic characteristics of a family with choroideremia family. In the present study, a family with choroideremia presenting with serious chorioretinal atrophy and pigment proliferation, shallow anterior chambers, angle closure and high intraocular pressure (IOP) were recruited. The affected family members underwent a complete ophthalmologic examination. DNA samples obtained from the proband II:1 and the patient II:2 were used for targeted exome sequencing of the CHM gene. PCR amplification and Sanger sequencing were used to validate the variations exhibited in family members and controls. A novel frameshift mutation c.280delA (p.Thr94LeufsTer32), in CHM was identified in the male proband, the normal carrier I:2 and the phenotyped carrier II:2, which was absent in the normal individual II:3 as well as in 200 normal controls. Comparing the amino acid sequences of CHM between multiple species through Clustal Omega indicated conserved amino acids in these mutant sites. Additionally, an X‑chromosome inactivation (XCI) assay was performed in the female carriers in the family, in which DNA of the abnormal carrier II:2 and normal carrier I:2 showed a random XCI pattern. To conclude, the present findings strongly indicate that the c.280delA mutation is a disease‑causing mutation in our choroideremia pedigree with acute angle‑closure glaucoma.

Introduction

Choroideremia (OMIM: 303100) is an X-linked recessive chorioretinal disorder characterized by progressive degeneration of photoreceptors, retinal pigment epithelium (RPE) and the choroid, with an estimated incidence estimated of 1 in 50,000 to 1 in 100,000 in men (1). Affected hemizygous males usually develop progressive vision loss beginning with night blindness in the first or second decade of their lives, that progresses to reduced function of the peripheral visual fields, and eventually complete blindness later in life (1). Female carriers are often asymptomatic or experience mild symptoms due to X-inactivation (2). However, occasional female carriers can also be fully affected by choroideremia (3).

The molecular basis of choroideremia involves mutation in the CHM gene (MIM: 300390) on chromosome Xq21.2. The CHM gene contains 15 exons spanning approximately 150 Kb of genomic DNA that encodes a ubiquitously expressed protein, Rab escort protein-1 (REP-1). Until recently, about 300 pathogenic variations of the CHM gene have been identified in choroideremia patients (LOVD Retinal and Hearing Impairment Genetic Mutation Database; http://www.lovd.nl/CHM), including small deletions, duplication, nonsense mutations, missense mutations, frameshifts, splice site defects, substitution in the promoter, retrotransposon insertion, and deletion of the entire CHM gene (46). REP-1 is an essential component of the catalytic Rab geranyl-geranyl transferase (GGTase) II complex, in which it is involved in post-translational isoprenyl modification (7) and intracellular vesicular trafficking (8). REP-1 loss-of-function mutations can be compensated by REP-2 in most tissues; however, REP-2 exhibits less effective geranylgeranylation of Rab27 (9), which plays an important and unique role in regulating vesicular transport in RPE and choriocapillaris cells (10,11). Moreover, REP-1 is particularly crucial for the physical function of RPE and photoreceptors (12,13).

In this study, we conducted a detailed clinical investigation and targeted exome sequencing in a Chinese choroideremia pedigree. A frameshift mutation c.280delA (p.Thr94LeufsTer32) in CHM was detected in the male patients as well as a female carrier. This mutation was absent in the unaffected parents and 200 ethnicity-matched healthy controls. Our findings indicate that this mutation might be an etiological factor of the current pedigree, thus expanding the genetic variation spectrum of choroideremia.

Subjects and methods

Subjects

A choroideremia pedigree from Hunan Province, China, consisting of five members (two males and three females) from two generations (Fig. 1) was recruited by the Second Xiangya Hospital, Central South University (Changsha, China). Ocular examinations, including a slit lamp examination, intraocular pressure (IOP) test, fundus photography (FP), best corrected visual acuity (BCVA) test, A/B-scan ultrasonography, ultrasound biomicroscopy (UBM), optical coherence tomography (OCT), infrared reflectance (IR) imaging, fundus autofluorescence (FAF), and fundus fluorescein angiography (FFA), were performed on these patients. A group of 200 unrelated normal controls who were ethnically matched with the patients were recruited mainly from the hospital and as additional volunteers. This study was approved by the Second Xiangya Hospital Ethics Committee. All of the pedigree members and controls gave their written informed consent complying with the Declaration of Helsinki principles (as revised in Brazil 2013).

Targeted exome sequencing

DNA samples obtained from the proband II:1 and the patient II:2 were used for targeted exome sequencing of the CHM gene. Library construction was performed with the custom NimbleGen SeqCap EZ System (Roche NimbleGen, Madison, WI, USA), and 90-cycles paired-end sequencing was performed on Illumina HiSeq2500 Analyzers (Illumina, Inc., San Diego, CA, USA). Illumina Pipeline software (version 1.3.4) was used to perform base-calling and the calculation of quality values for every base.

Reads were aligned to the human reference genome hg19 using Burrows-Wheeler Aligner (BWA, http://bio-bwa.sourceforge.net/). Single nucleotide variation (SNV) and insertion and deletion (indel) identification was performed with SOAPsnp (http://soap.genomics.org.cn/soapsnp.html) and SAMtools (http://samtools.sourceforge.net/). SNVs and indels with read depth ≥8X and Phred score quality ≥30 were reserved and annotated by Annotate Variation (ANNOVAR; http://annovar.openbioinformatics.org/en/latest/user-guide/download/). Multiple sequence alignment was conducted through Clustal Omega (https://www.ebi.ac.uk/Tools/msa/clustalo/) to compare the amino acid sequences of CHM between multiple species.

Sanger sequencing

PCR amplification and Sanger sequencing were used to validate the presence of variation. The primer sequences used were as follows: Forward primer, 5′-cat gtt tca cac tgc cca ct-3′, and reverse primer, 5′-aaa ttc gga ggc gtt aag gt-3′. PCR was performed in a 10-µl reaction mixture containing 5 µl 2X TaKaRa Taq™ HS Perfect Mix (Takara Biotechnology Co., Ltd., Dalian, China), 30 ng of each primer, and 30 ng of genomic DNA. The amplification conditions consisted of denaturation at 94°C for 30 sec, followed by 33 cycles of denaturation at 94°C for 5 sec, annealing at 60°C for 20 sec and extension at 72°C for 20 sec. Final extension was performed at 72°C for 7 min. Sanger sequencing was performed on ABI 3730 DNA Analyzer (Thermo Fisher Scientific, Inc., Waltham, MA, USA).

X-chromosome inactivation (XCI) assay

Human androgen receptor gene (NM_000044) and ZNF261 gene (DXS6673E) were chosen to perform XCI analysis on methylated HpaII and/or HhaI sites as described previously (1415). The primers sequences are as follows: NM_000044 forward primer, 5′-GCTGTGAAGGTTGCTGTTCCTCAT-3′, and reverse primer, 5′-TCCAGAATCTGTTCCAGAGCGTGC-3′; DXS6673E forward primer, 5′-ATGCTAAGGACCATCCAGGA-3′, and reverse primer, 5′-GGAGTTTTCCTCCCTCACCA-3′. The two forward primers were labeled with hexachlorofluorescein fluorescent dye. DNA (2 µg) was digested with 20 units of HpaII or HhaI, respectively. Reactions were performed in a 25-µl total volume including 2.5 µl 10X buffer. All incubations were performed for 12 h at 37°C and then for 20 min at 65°C. For the PCR reaction, 100 ng DNA was added to a 20-µl PCR reaction mixture containing 0.1 µl ABI Gold Taqase (Applied Biosystems; Thermo Fisher Scientific, Inc.), 2 µl 10X PCR Buffer, 2 µl 25 mM MgCl2, 0.4 µl 10 mM dNTP, 1 µl forward primer, and 1 µl reverse primer. Samples were amplified using a Bio-Rad T100 thermocycler (Bio-Rad Laboratories, Inc., Hercules, CA, USA) for 32 cycles (45 sec at 95°C, 30 sec at 60°C, and 30 sec at 72°C), with initial denaturation at 95°C for 5 min. The PCR products were separated by capillary electrophoresis on an ABI 3100 DNA analyzer (Applied Biosystems; Thermo Fisher Scientific, Inc.), and were analyzed with GeneMarker® HID software (SoftGenetics, LLC., State College, PA, USA; https://www.softgenetics.com/GeneMarkerHID.php).

Results

Clinical findings

In this family, the proband II:1 was a 46-year-old man who reported having sudden ocular pain and decreased vision in his left eye for one day before he came to our hospital. He also complained of headache and nausea. The BCVA was hand motion in both eyes. The Goldmann IOP of the right eye was 16 mmHg and of the left eye was 42 mmHg. The slit-lamp examination identified a shallow anterior chamber and peripheral chambers of <1/4 cornea thickness (CT) in both eyes, and conjunctival congestion and corneal edema in the left eye. The fundus examination results were indicated in Fig. 2. Fundus examination (Fig. 2A and B) identified a cup-to-disc ratio of 0.4 in the right eye and 0.8 in the left eye, pink optic nerves in both eyes, vessel narrowing in both eyes, dimming of the color and lustre of the macular in both eyes, severe chorioretinal atrophy with exposure of the sclera in both eyes, and pigment proliferation in the posterior polar and peripheral fundus in both eyes. The A-scan showed that the axial lengths of the right and left eye were 23.11 and 23.10 mm, respectively. The B-scan showed vitreous opacity in both eyes. UBM of the right eye showed that the anterior chamber depth (ACD) was shallow (Fig. 3A), and also that the anterior chamber angles were narrow at the superior side, the temporal side, the inferior side and the nasal side (Fig. 3B-E). The ACD of the left eye was shallow (Fig. 3F), and was closed at the superior side, the temporal side, and the inferior side (Fig. 3G-I). The angles of the left eye were narrow at the nasal side (Fig. 3J). OCT imaging (Fig. 4) of both eyes indicated widespread disappearance of the choroid and the outer retinal layer, which was accompanied with pigment hyperplasia, though a small part of the choroid was retained in the central macula. In the left fovea, the outer nuclear layer, external limiting membrane, and photoreceptor layer were still present. IR imaging (Fig. 2C and D) demonstrated hyperreflective lesions corresponding to the area of serious chorioretinal atrophy and hyporeflective lesions corresponding to the area of pigment proliferation. FAF (Fig. 2E and F) of both eyes showed an isolated area of hyperautofluorescence in the foveal area. Part of the transparent sclera was also observed as hyperreflective in FAF image. FFA (Fig. 2G and H) of both eyes showed an absence of the choriocapillaris in the regions of pigment accumulation. The retinal vessels were normal in FFA. According to the above information, the patient's clinical diagnosis was choroideremia in both eyes and angle-closure glaucoma (preclinical stage in the right eye, acute attack stage in the left eye).

The proband's sister, II:2, did not report any vision problems, and the anterior segments of both of her eyes were normal. However, the fundus examination identified darkened color and lustre of the retina, and a crystal-like appearance in the retina of both eyes (Fig. 5). The proband's parents, I:1 and I:2, showed no clinical manifestation.

Targeted exome sequencing and sanger validation

We selected the proband II:1 and the patient II:2 for targeted exome sequencing, which was designed to isolate a 1,962-bp DNA region of the CHM gene. In our sequencing results, 96.00 and 95.82% of the qualified bases for II:1 and II:2 were mapped to the targeted sequence, with mean read depths of approximately 210.32- and 208.61-fold for II:1 and II:2 (Table I). The exon coverage rates were 99.75 and 99.26% for the patient and female carrier samples, respectively, which was sufficient to pass our thresholds for calling SNVs and indels (Table I). After alignment and variation calling, a total of 12 variations in the CHM gene were identified among the two family members, including 2 exonic variations, 9 intronic variations, and 1 in the 3′-UTR (Table II). However, only 1 frameshift variation, c.280delA (p.Thr94LeufsTer32), in CHM was found in II:1 and II:2, that had not been reported either in the dbSNP database or in the 1,000 Genomes database, which was predicted to produce a truncated REP-1 protein. Comparing the amino acid sequences of CHM between multiple species demonstrated asterisks and codons among the amino acids 94 to 126 (Fig. 6A), which indicated conserved amino acids on these sites.

Table I.

Summary of the targeted exome sequencing results.

Table I.

Summary of the targeted exome sequencing results.

SampleTargeted geneTargeted region (bp)Targeted region mapped (%)Targeted exon coverage (%)Mean depth (x)Mean depth >30× (%)
II-1CHM196296.0099.75210.3298.45
II-2 95.8299.26208.6195.87

Table II.

Variations detected in CHM gene (NM_000325) in the pedigree by targeted exome sequencing.

Table II.

Variations detected in CHM gene (NM_000325) in the pedigree by targeted exome sequencing.

PositionSNP no.Variation typeLocationNucleotide changeAmino acid changeAllele frequency in 1,000 genomeAffected member
chrX:85281760rs1015148Hemi, HetIntron 2c.116+80C>TNone0.2024II-1, II-2
chrX:85281760rs5923428HomoIntron 2c.116+735A>GNone0.065II-2
chrX:85261183rs62607865HomoIntron 2 c.116+21312C>ANone0.0137II-2
chrX:85236825 HetIntron 2c.117-12delTNone0II-2
chrX:85219021rs10217950HetExon 5c.351A>Gp.A117A0.1401II-2
chrX:85233805 Hemi, HetExon 4c.280 delAp.T94LfsTer320II-1, II-2
chrX:85215758rs7880234HomoIntron 5 c.703-1776G>ANone0.0183II-2
chrX:85212717 HetIntron 7 c.940+143C>ANone0II-1
chrX:85166221~85166222 HetIntron 9 c.1244+44_+45insATATNone0II-2
chrX:85155596 HemiIntron 11 c.1413+55G>TNone0II-1
chrX:85145586 HomoIntron 12c.1510+3607 A>GNone0II-2
chrX:85119508 Hemi3-UTRc.*127T>CNone0II-1

[i] Homo, homozygous; Het, heterozygous; Hemi, hemizygous.

We used Sanger sequencing to validate the c.280delA variation and analyze the co-segregating status of the variant in all family members. Hemizygous c.280delA variation was found in II:1, and heterozygous c.280delA variations were found in I:2 and II:2, respectively, while the variation was not detected in II:3 (Fig. 6B). The variation was completely cosegregated with the phenotype in all family members except for carrier II:2. In addition, the variation was not identified in the 200 unrelated normal controls. Thus, our results indicate that the variation c.280delA (p.Thr94LeufsTer32) in the CHM gene is a genetic etiological factor of the current choroideremia pedigree. Our phenotype and variation data in this study have been submitted to ClinVar (accession no. SCV000600017).

XCI

Given that the carrier II:2 exhibited disease-related phenotypes, we determined the XCI profile of the female family members. The DNA of the carrier II:2 and normal female I:2 showed 48 and 43% inactivated X chromosome, respectively, indicating that both the female carrier and normal female had a random XCI pattern. Thus, no correlation between phenotypic status and X-inactivation pattern was established in these females.

Discussion

Choroideremia is an X-linked, recessive, chorioretinal degenerative disease characterized by progressive centripetal loss of the photoreceptor, retinal RPE and choroid layers. Our initial patient (II:1) revealed exhibited choroideremia with acute angle-closure glaucoma. Subsequently, in our female carrier II:2, we identified darkening of the color and lustre of the retina, along with a crystal-like appearance of the retina was observed, which was likely due to hypopigmentation of the RPE. These clinical manifestations were similar to phenotypes reported in other studies (16,17) with the exception of the presentation of acute angle-closure glaucoma. II:2 also exhibited narrow or closed anterior chamber angles in both eyes, which may lead to high IOP and acute angle-closure glaucoma in the future.

A novel frameshift variant, c.280delA (p.Thr94LeufsTer32), was identified in the CHM gene through targeted exome sequencing in our pedigree, and was validated by Sanger sequencing. The variant was detected in the mother I:2, and in the offspring II:1 and II:2, and thus the proband and the female carrier inherited the variant from their carrier mother rather than acquiring it from a de novo germline mutation. As with phenotyped carriers reported in other studies (17,18), our variant was completely cosegregated with the phenotypes. Moreover, our data revealed that both a normal female and a carrier had random XCI patterns, which suggested that there is no preferential XCI of the mutant X chromosome allele. This result is consistent with a previous study of XCI detection in 13 heterozygous females from two families (19).

Other previous studies have suggested that the molecular basis of choroideremia may involve selective underprenylation of Rab protein due to the absence of REP-1 (20). Our frameshift mutation was predicted to create a premature stop codon and to thus lead to a lack of full-length REP-1. In turn, this would likely lead to a deficiency of GGTase function, with the insufficient transfer of geranylgeranylpyrophosphate groups onto Rab proteins potentially resulting in abnormal protein function, preventing their participation in intracellular vesicular transport (21). This would ultimately cause several ocular defects as observed in our patients.

In conclusion, our results suggest that c.280delA (p.Thr94LeufsTer32) in CHM was a pathogenic mutation in the present choroideremia family as determined by captured exome sequencing. Such targeted exome sequencing technology may provide a promising tool for genetics testing and counseling among families with choroideremia. Further functional and animal studies on the mutant protein will be required to interpret its role in the pathogenesis of the disease.

Acknowledgements

Not applicable.

Funding

This study was supported by the Natural Science Foundation of Hunan Province Project (grant no. 14JJ3041), the National Natural Science Foundation of China (grant nos. 81700837, 81300798, and 61573380), and Department of Science and Technology, Hunan (grant no. 2015TP2007).

Availability of data and materials

Our phenotype and variation data in this study are available from ClinVar (https://www.ncbi.nlm.nih.gov/clinvar/; accession no. SCV000600017). Other datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Authors' contributions

PO, FZ, CZ, and BZ performed the genetic studies, participated in the sequence alignment and analyzed the data. YL and JL participated in the sample collection and clinical examination. LZ designed and supervised the study. LZ and PO wrote the manuscript. All authors read and approved the final manuscript.

Ethical approval and Informed consent

All procedures performed in studies involving human participants were in accordance with the ethical standards of the Second Xiangya Hospital Ethics Committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. Informed consent was obtained from all individuals participants included in the study.

Consent for publication

The patient, the family members and the normal control subjects provided their written informed consents for the publication of any associated data and accompanying images.

Competing interests

All authors declare that they have no competing interests.

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Ouyang P, Li Y, Zhang F, Zhu C, Zou B, Le J and Zhang L: A frameshift mutation in the CHM gene causes choroideremia with acute angle‑closure glaucoma. Mol Med Rep 17: 7918-7924, 2018
APA
Ouyang, P., Li, Y., Zhang, F., Zhu, C., Zou, B., Le, J., & Zhang, L. (2018). A frameshift mutation in the CHM gene causes choroideremia with acute angle‑closure glaucoma. Molecular Medicine Reports, 17, 7918-7924. https://doi.org/10.3892/mmr.2018.8851
MLA
Ouyang, P., Li, Y., Zhang, F., Zhu, C., Zou, B., Le, J., Zhang, L."A frameshift mutation in the CHM gene causes choroideremia with acute angle‑closure glaucoma". Molecular Medicine Reports 17.6 (2018): 7918-7924.
Chicago
Ouyang, P., Li, Y., Zhang, F., Zhu, C., Zou, B., Le, J., Zhang, L."A frameshift mutation in the CHM gene causes choroideremia with acute angle‑closure glaucoma". Molecular Medicine Reports 17, no. 6 (2018): 7918-7924. https://doi.org/10.3892/mmr.2018.8851