Molecular Vision
2010; 16:713-719 <http://www.molvis.org/molvis/v16/a81> Received 10 March 2010 | Accepted 15 April 2010 | Published 21 April 2010
Molecular Vision
2010; 16:713-719 <http://www.molvis.org/molvis/v16/a81>
Received 10 March 2010 | Accepted 15 April 2010 | Published 21 April
2010
Zhou Zhou,1 Shanshan Hu,1 Binbin Wang,2 Nan Zhou,1 Shiyi Zhou,2 Xu Ma,2 Yanhua Qi1
The first two authors contributed equally to this work
1Department of Ophthalmology, The Second Affiliated Hospital of Harbin Medical University, Harbin, China; 2Department of Genetics, National Research Institute for Family Planning, Beijing, China
Correspondence to: Yanhua Qi, The Second Affiliated Hospital of Harbin Medical University, Department of Ophthalmology, 246 Xuefu Road, Harbin, Heilongjiang Province 150086, China; Phone: 086-451-86605643; FAX: 086-451-86605116; email: QI_yanhua@yahoo.com
Purpose: To identify the genetic defects in a three-generation Chinese family with congenital nuclear cataract.
Methods: Four patients and three healthy members from the family underwent complete physical and ophthalmic examinations. Genomic DNA was extracted from peripheral blood leukocytes of the family members as well as from 100 healthy normal controls. Polymerase chain reaction (PCR) amplification and direct sequencing of all coding exons of candidate genes were performed. The functional consequences of the mutation were analyzed with biology softwares.
Results: A novel mutation (c.130G>A) was identified in the connexin 46 gene (GJA3), which resulted in the substitution of valine by methionine at the highly conserved codon 44 of connexin 46. This mutation co-segregated among the affected members of the family and was not observed in either unaffected members or the 100 normal controls.
Conclusions: This is a novel missense mutation identified in the first extracellular loop of connexin 46; this expands the mutation spectrum of GJA3 in association with congenital cataract.
Congenital cataract is a significant cause of poor vision or blindness in children worldwide and is responsible for 10.7%–14.0% of the children who are blind [1]. It is a clinically and genetically heterogeneous lens disorder, with autosomal dominant inheritance being most common. Currently, more than 22 genes have been identified to be associated with various forms of congenital cataract, including ten crystalline genes (CRYAA [2], CRYAB [3], CRYBA1/A3 [4], CRYBA4 [5], CRYBB1 [6], CRYBB2 [7], CRYBB3 [8], CRYGC [9], CRYGD [10], and CRYGS [11]), three transcription factor genes (HSF4 [12], PITX3 [13], and MAF [14]), two cytoskeletal protein genes (BFSP1 [15] and BFSP2 [16]), four membrane transport protein genes (MIP [17], GJA8 [18], GJA3 [19], and LIM2 [20]), glucosaminyl (N-acetyl) transferase 2 (GCNT2) [21], chromatin-modifying protein-4B (CHMP4B) [22], and transmembrane protein 114 (TMEM114) [23]. Knowledge of the structure and function of these candidate genes as well as the pathophysiological effect of their disease-associated mutations on their functions will aid in understanding the mechanisms of cataractogenesis.
Here, we report a heterozygous 130G>A transition in the connexin 46 gene (GJA3) associated with congenital nuclear cataract in a Chinese family, while it co-segregated completely with the disease phenotype. This is a novel mutation and has not been reported previously with congenital cataract.
A three-generation Chinese Han family (Figure 1) with congenital nuclear cataract was recruited from the Second Affiliated Hospital of Harbin Medical University, Harbin, China. Seven members of the pedigree were involved in this study, including four affected individuals (II:3, II:5, III:2, and III:3) and three unaffected ones (II:4, II:6, and III:4). All participants underwent full physical and ophthalmic examinations. Phenotype was documented by slit-lamp photography (Figure 2). One hundred subjects without diagnostic features of congenital cataract were recruited from the Chinese Han population to serve as normal controls. After informed consent, 5 ml venous blood from family members and controls was collected in a BD Vacutainer (BD, San Jose, CA) containing EDTA. Genomic DNA was extracted by QIAamp DNA Blood Mini Kits (QIAGEN Science, Germantown, MD). The research was approved by the Institutional Review Board of Harbin Medical University and followed the clauses of the Declaration of Helsinki.
All coding exons and their flanking regions of the known candidate genes associated with autosomal dominant congenital nuclear cataract, such as CRYAA, CRYAB, CRYBA1, CRYBB2, CRYGC, CRYGD, CRYGS, GJA3, and GJA8, were amplified by PCR with primers listed in Table 1. The PCR products were sequenced from both directions with the ABI3730 Automated Sequencer (PE Biosystems, Foster City, CA). The sequencing results were analyzed using Chromas (version 2.3) and compared with the reference sequences in the NCBI database.
The wild-type and mutant connexin 46 (Cx46) protein sequences were analyzed with computer assistance for better understanding the effects of the mutation on its biochemical properties. We used PolyPhen (polymorphism phenotyping), which is based on the position-specific independent counts score derived from multiple sequence alignments of observations [24], to predict whether the amino acid substitution affects protein function. An online bio-software program Misc Protein Analysis was used to compute the hydrophilicity of the wild-type and mutant Cx46.
There were five affected people in 13 members of this family (Figure 1). The proband (III:2) was a 5-year-old girl whose grandmother (I:1), mother (II:3), aunt (II:5), and male cousin (III:3) also had poor vision in their childhood. Among them, one (I:1) passed away and two (II:3, II:5) had had cataract extractions before examination. The other subjects had had no operations and showed bilateral cataract characterized as a central nuclear opacity involving embryonic and fetal nucleus with punctate cortical opacities (Figure 2). There was no history of other ocular or systemic abnormalities in the family. To date, all of the affected individuals have had cataract surgery.
Direct sequencing of candidate genes revealed a heterozygous G>A transition in GJA3 at position 130 that led to the replacement of the highly conserved valine with methionine at codon 44 (Figure 3). This mutation was detected in all affected members but was not observed in either the unaffected family members or the normal controls. There was no noticeable nucleotide polymorphism in other candidate genes.
The GJA3 gene, coding a 435-amino acid protein, was first reported by Willecke et al. [25] in 1990 and is located on chromosome 13q11. Cx46, which is encoded by GJA3, is mainly expressed in lens fiber cells. Like others connexins, Cx46 has four transmembrane domains (M1, M2, M3, and M4), two extracellular loops (E1 and E2), an intracellular loop (CL), and intracellular NH2 and COOH termini. Cx46 functions as a gap junction that mediates the intercellular transport of small molecules (<1 kDa), including ions, metabolites, and second messengers between elongated fiber cells [26]. Since the lens is an avascular structure and lens fiber cells lose all intracellular organelles during development, the fiber cells are highly dependent on intercellular communication for their survival [27]. The intercellular communication network is formed mainly by the gap junctions. This extensive network is vital since it maintains osmotic and metabolic homeostasis in lens fiber cells and ultimately maintains lens transparency [28].
However, extracellular domains of connexins that contain two extracellular loops (E1 and E2) play a key role in both mediating hemichannel docking [29,30] and regulating voltage gating of the channel [31]. The two extracellular loops are the most conserved domains among connexins and are the sites that provide the strong interaction between the two hemichannels that enable the formation of an intercellular channel with no leakage of current and molecules to the extracellular environment [32]. Furthermore, the first extracellular loop (E1) has been proven to be a major determinant of charge selectivity in Cx46 channels [33].
In this study we identified a new mutation (130G>A) in GJA3. This variation seems to be disease causative as it segregated with the phenotype and was absent in both unaffected pedigrees and the 100 unrelated controls from a similar ethnic background. This substitution resulted in the replacement of valine to methionine at codon 44 (V44M), localized in the first extracellular loop (E1) of Cx46. A multiple amino acid sequence alignment showed that valine at position 44 is phylogenetically conserved in different species and gap junctions (Figure 5), and Polyphen predicted the mutation to be possibly damaging. These results suggest that valine may be functionally important and the mutation may lead to damaging interference with conformation and function of Cx46. The decline of hydrophilicity in the mutant (Figure 4) might alter the charge on the surface of the extracellular loop, thereby affecting hemichannel docking [34]. The mutation may also affect the charge selectivity in Cx46 channels, disturbing the charge balance inside the lens fiber cells [33]. These changes would disorder intercellular homeostasis in the lens fiber cells and result in lens nucleus opacity.
To date, 15 mutations in GJA3 have been reported to be associated with congenital cataract in humans (Table 2) [35-45]. Most of these are described as nuclear or zonular pulverulent types and share genotype–phenotype similarities to some extent. In this study the phenotype also shows a conspicuous nuclear cataract but one that is surrounded with punctate opacities. The difference in the cataract phenotypes associated with GJA3 may be attributed to the action of modifier genes or environmental factors that could affect the expression of GJA3 and thus resulting cataract types.
In summary, we described a novel missense mutation (V44M) in GJA3 that causes congenital cataract in a three-generation Chinese family. This study further confirms that Cx46 plays a vital role in the maintenance of human lens transparency and expands the mutation spectrum of GJA3 in association with congenital cataract.
The authors are grateful to all patients, the family, and normal volunteers for their participation in this investigation. This study was supported by the National Science & Technology Pillar Program of China (No.2008BAH24B05) and the National Infrastructure Program of Chinese Genetic Resources (2006DKA21300). Professors Xu Ma genetics@263.net.cn and Yanhua Qi contributed equally to the research project and can be considered co-corresponding authors.