Vision 2011; 17:2380-2385
Received 9 May 2011 | Accepted 28 August 2011 | Published 1 September 2011
Department of Ophthalmology, Eye and ENT hospital of Fudan University, Shanghai, China
Correspondence to: Dr. Yi Lu, Department of Ophthalmology, Eye and ENT hospital of Fudan University, Shanghai, China; Phone: (086)-(021) 6437-7134; FAX: (086)-(021) 6437-7151; email: email@example.com
Purpose: To identify the pathogenic gene mutation in a Chinese family with autosomal dominant inherited nuclear cataract.
Methods: After obtained informed consent, detailed ophthalmic examinations were performed, genomic DNAs were obtained from eighteen family members in a four-generation Chinese family with five affected. All exons of candidate genes were amplified by polymerase chain reaction (PCR) and were sequenced performed by bidirectional sequencing. The stability of mutation was predicted with Prediction of Protein Mutant Stability changes (PoPMuSiC). The structure homology modeling of the mutant protein was based on Swiss-Model Serve, and its structure was displayed and compared with human connexin26 using the RasMol software.
Results: By sequencing the encoding regions of the candidate genes, a missence mutation (c.139G>A) was detected in gap junction protein alpha 8 (GJA8) gene, which resulted in the substitution of highly conserved aspartic acid by asparagine at codon 47 (p.D47N). The mutation co-segregated with all patients and was absent in 100 normal Chinese controls. PoPMuSiC analysis showed the change in folding free energy upon mutation (ΔΔG) is 0.31 kcal/mol and the mutation p.D47N is destabilizing. The homology modeling showed that the structure of the mutant protein was different with that of human connexin26.
Conclusions: The study identified a missence mutation (c.139G>A) in GJA8 gene associated with autosomal dominant congenital cataract in a Chinese family. It gave further evidence for GJA8 associated with congenital cataract.
The lens is an avascular organ, which is composed of a monolayer of cuboidal epithelial cells covering the anterior surface of elongated fibers, which transmits and focuses light images onto the retina. Interior fiber cells, including both primary and secondary fiber cells, undergo a maturation process to eliminate all intracellular organelles, such as the nucleus, mitochondria, endoplasmic reticulum, Golgi apparatus, etc., thereby minimizing light scattering and ensuring lens transparency . The interior mature fibers have an extremely low metabolic activity and depend mainly on the epithelium and peripheral differential fibers for maintenance. Therefore, the lens has developed as a syncytium and a sophisticated cell-cell communication network, which facilitates both an active metabolism and the transport of small metabolites, such as ions, water and secondary messengers . Intercellular gap junction channels provide pathways for metabolic and electrical coupling between cells in the lens. Gap junction channels consist of connexin protein subunits. To date, many connexin (Cx) genes have been found in the mouse genome and the human genome . Mutations in connexin have been identified with various inherited diseases , including Cx32 mutation in X-linked Charcot Marie tooth disease, Cx26 and Cx30 mutations in deafness and skin diseases, Cx46 and Cx50 mutations in hereditary cataracts and Cx31 mutation in erythrokeratodermia variabilis (EKV) and hearing impairment with/without peripheral neuropathy.
In our study, we found a missense mutation – the substitution of aspartic acid toasparagine of the codon 47 (p.D47N) in gap junction protein alpha 8 (GJA8) associated with autosomal dominant nuclear cataract in a Chinese family.
A four-generation family with autosomal dominant congenital cataract was ascertained (Figure 1). After explanation of the nature and possible consequences of the study, eleven individuals participated in the study. The study was performed with informed consent and following all the guidelines for experimental investigations required by the Institutional Review Board of Eye and EENT Hospital of Fudan University, Shanghai, China. The ophthalmologic examinations, including visual function and dilated slit-lamp examination, were performed by ophthalmologists. Blood samples were collected and leukocyte genomic DNA was extracted.
All the exons of candidate genes which associated with autosomal dominant congenital nuclear cataract were amplified by PCR method. The primers used are listed in Appendix 1. The PCR products were sequenced on both directions with an ABI 3130XL Genetic Analyzer (Applied Biosystems, Foster City, CA). The results were analyzed using Chromas (version 2.23) software and compared with the reference sequences in the NCBI gene bank.
The stability of the mutant GJA8 protein sequences were predicted by Prediction of Protein Mutant Stability changes (PoPMuSiC)  with the change in folding free energy upon mutation (ΔΔG). The ΔΔG values are given in kcal/mol. A negative sign corresponds to a mutation predicted as stabilizing. The structure homology modeling of the mutant protein was modeled by Swiss-Model Serve , and its structure was displayed and compared with native Cx26 using RasMol software. The structure of native human Cx26 (2zw3) was obtained from the PDB database.
There were five affected members in this four-generation family (Figure 1). Cataract characterized as bilateral central nuclear cataract with punctiform opacities (Figure 2). There were no other ocular or systemic abnormalities. The affected individuals have had cataract surgery. Autosomal dominant inheritance mode of the cataract was supported by the presence of affected individuals in each of the four generations, and male-to-male transmission.
By bidirectional sequencing of amplified exons of the candidate genes, we found a heterozygous missense mutation, G>A at position 139 in GJA8 (NM_005267) in affected individuals, but not in unaffected individuals. This change led to the substitution of aspartic acid by asparagine at position 47 (p.D47N; Figure 3). This mutation was not found in 100 unrelated control individuals. No other sequence variant was found.
In a Chinese family with congenital nuclear cataract, we identified a missense mutation c.139G>A in GJA8, leading to the substitution of aspartic acid byasparagine (p.D47N). This mutation co-segregated with the phenotype and was not found in 100 unrelated control individuals.
Congenital cataracts are one of the common eye disorders leading to visual impairment or blindness in children worldwide. Congenital cataract may be inherited or familial, either as an isolated form or as a part of a syndrome, such as Nance-Horan syndrome. Along with the development of molecular genetics, more than 20 genes have been identified to be involved in isolated cataract formation, including crystallins, such as αA-crystallin (CRYAA), αB-crystallin (CRYAB), βA1/A3-crystallin (CRYBA1/A3), βA4-crystallin (CRYBA4), βB1-crystallin (CRYBB1), βB2-crystallin (CRYBB2), βB3-crystallin (CRYBB3), γC-crystallin (CRYGC), γD-crystallin (CRYGD), and γS-crystallin (CRYGS); membrane transport and channel proteins,such as gap junction protein, alpha 3 (GJA3), gap junction protein, alpha 8 (GJA8)，intrinsic member protein (LIM2), and major intrinsic protein (MIP); cytoskeletal proteins, such as beaded filament structural protein 1 (BFSP1), beaded filament structural protein 2 (BFSP2); transcription factors, such as paired-like homeodomain 3 (PITX3), heat shock transcription factor 4 (HSF4), Maf-like protein gene (MAF), and paired box gene 6 (PAX6); others, such as chromatin modifying protein 4B (CHMP4B) and Eph-receptor type-A2 (EPHA2) [7-12].
Intercellular gap junction channels provide pathways for metabolic and electrical coupling between cells in different tissues. Gap junction channels consist of connexin protein subunits. Connexin proteins have four transmembrane domains with three intracellular regions (the NH2-terminus, a cytoplasmic loop and the COOH-terminus) and two extracellular loops (E1 and E2). Six connexin protein subunits oligomerize to form one connexon. A gap junction channel is formed by the docking of extracellular loops of two opposing connexons (hemichannels) in the plasma membrane.
Three isoforms of the connexin gene family are expressed abundantly in the vertebrate lens: GJA1 (Cx43), GJA3 (Cx46) and GJA8 (Cx50) [13-15]. GJA1 is restrictively expressed in the lens epithelial cells. GJA3 and GJA8 are two connexin isoforms in the plasma membrane of fiber cells [16,17]. Many mutations of Cx43 and Cx46 have been reported to be associated with congenital catatact with different phenotype. To date, 19 mutations in the different domain of Cx50 have been identified to contribute to human inherited cataracts (Appendix 2).
Animal models of different connexin knockout and knockin and genetic studies showed GJA3 and GJA8 are essential for maintaining lens transparency, and GJA8 is required for proper fiber cell maturation and control of lens size . Cx46 cannot substitute for Cx50 in lens growth but can prevent lens opacity caused by a lack of Cx50 .Electrophysiological studies of intact lenses confirm that Cx46 is essential for the coupling of interior fiber cells while Cx50 is needed for the coupling of both peripheral and interior fiber cells [20-22]. Moreover, Cx50 is clearly necessary for pH-mediated gating of gap junction channels in the differentiating fibers. Mutated Connexins could alter electrical properties of gap junction channels. In No2 mice with dominant cataract, D47A mutant protein of Cx50 was unable to form functional channels and did not inhibit wild type Cx46 or Cx50 junctional conductance in paired Xenopus oocytes . A similar point mutation D47N related to human dominant nuclear pulverulent cataracts affect the channel properties in the similiar way , D47A and D47N mutants were loss-of-function mutants.
We identified a missense mutation (D47N) in GJA8 associated with autosomal dominant nuclear cataract in a Chinese family. This finding gives further evidence for GJA8 in association with congenital cataract. To date, studies of D47N mutant focus on the cellular level, the activity of D47N mutation needs to be further certificated in animal mode.
We are grateful to the family for their participation and all the people which helped us in this study. This project is supported by the financial support of the Scientific Research Foundation for Young Core from Shanghai medical college of Fudan University (EENT-2009–07).