A Variant of GJD2, Encoding for Connexin 36, Alters the Function of Insulin Producing β-Cells

Signalling through gap junctions contributes to control insulin secretion and, thus, blood glucose levels. Gap junctions of the insulin-producing β-cells are made of connexin 36 (Cx36), which is encoded by the GJD2 gene. Cx36-null mice feature alterations mimicking those observed in type 2 diabetes (T2D). GJD2 is also expressed in neurons, which share a number of common features with pancreatic β-cells. Given that a synonymous exonic single nucleotide polymorphism of human Cx36 (SNP rs3743123) associates with altered function of central neurons in a subset of epileptic patients, we investigated whether this SNP also caused alterations of β-cell function. Transfection of rs3743123 cDNA in connexin-lacking HeLa cells resulted in altered formation of gap junction plaques and cell coupling, as compared to those induced by wild type (WT) GJD2 cDNA. Transgenic mice expressing the very same cDNAs under an insulin promoter revealed that SNP rs3743123 expression consistently lead to a post-natal reduction of islet Cx36 levels and β-cell survival, resulting in hyperglycemia in selected lines. These changes were not observed in sex- and age-matched controls expressing WT hCx36. The variant GJD2 only marginally associated to heterogeneous populations of diabetic patients. The data document that a silent polymorphism of GJD2 is associated with altered β-cell function, presumably contributing to T2D pathogenesis.


Introduction
Gap junctional channels are composed of connexin (Cx) proteins, and allow for the communication between adjacent cells through the diffusion of cytosolic ions and small molecules [1,2]. Cx36 is the main connexin isoform expressed in neurons and pancreatic β cells [3][4][5][6][7][8], and previous studies have provided evidence that alterations of Cx36 signalling profoundly affects the function and survival of these two cell types [9,10]. Thus, deletion of Cx36 results in loss of gap junctions between fast-spiking interneurons of hippocampus and cortex, and interferes with their oscillatory activity [11,12]. This deletion also impairs the coupling of amacrine and bipolar neurons of retina, resulting in vision alterations [13,14] and increased retinal vulnerability [15]. In pancreatic islets, loss of Cx36 alters the regular Ca 2+ oscillations which are induced in β cells during glucose stimulation, as well as basal, first and second phases of insulin release [16], resulting in glucose intolerance [17]. The absence of Cx36 also leads to increased apoptosis of β cells after exposure to cytotoxic drugs and cytokines [18,19], and to decreased transcriptional regulation of the insulin gene [4]. Several of these alterations mimic signs of type 2 diabetes (T2D) [20].
A single-nucleotide polymorphism (SNP rs3743123) in the coding sequence of the GJD2 gene, which encodes for human Cx36 (hCx36), has been associated with juvenile myoclonic epilepsy [21,22]. Alike type 2 diabetes, this form of epilepsy has a complex inheritance pattern [23].
Given the numerous similarities between neurons and β cells [24], we investigated whether the same GJD2 polymorphism may alter the function of the insulin-producing β cells, sufficiently to cause an abnormal regulation of glycaemia. By generating novel lines of HeLa cells stably expressing either the WT or the SNP rs3743123 variant of hCx36, we found that the latter reduced the gap junction-mediated coupling of β cells and altered the packing of Cx36 channels in the cell membrane. By generating novel lines of transgenic mice, we further observed that the variant form of hCx36 decreased after birth, consistently resulting in loss of β cells which, in some lines, lead to sustained hyperglycemia. By investigating a population of Caucasian individuals, we show that the variant GJD2 is marginally associated to type 2 diabetics.

Culture and transfection of HeLa cells
HeLa cells (American Type Culture Collection-LGC Promochem, Teddington, Middlesex, UK) were grown in DMEM without glutamax (Gibco 61965), containing 10% (v/v) fetal calf serum (INVITROGEN 10270098), and a 1% penicillin/streptomycin mix (GIBCO 15140). Cells were cultured in 75 cm 2 culture flasks, and incubated in a 5% CO 2 humidified environment at 37 C. Once confluent, cells were trypsinized and seeded in 12-well culture plates (5×10 4 cells per well). Cells were incubated to reach 70% confluence and then transfected with an empty pcDNA3.1 (3.4 μg/μl vector) or with a pcDNA3.1 construct containing 3.8 μg/μl cDNA encoding for either hCx36 WT or hCx36 SNP rs3743123, using Lipofectamine 2000 (GIBCO 11668-030) according to the manufacturer's instructions. One day later, the cells were collected and cultured in a medium containing 750 μg/mL G418 (GIBCO 11811-031), which was changed every 2 days. Surviving cells were passed at one week intervals, and plated under limiting dilution conditions (1 cell/well) in 96 well plates, to select individual clones which, thereafter, were cultured for a 3 year period under the continuous pressure selection provided by G418. Three clones, which were shown by immunofluorescence staining and western blot analysis of total proteins to express similar and stable levels of either the WT or the rs3743123 form of hCx36, were selected for the experiments.

Predicted folding of Cx36 mRNAs
The most recent annotated Cx36 mRNA sequence (NM_020660.2) of 1096 bp, covering the complete coding region of Cx36, was downloaded from the NCBI. ClustalW [25] implemented in Jalview [26] was used to generate the sequence alignment of WT Cx36 mRNA (681C) and of two allelic variants: variant 681C>T, previously known as 588C>T, and variant 462C>T, previously known as 369C>T. Visual Gene Developer 1.7 program [27] was used to calculate the mRNA structure by employing the "mRNA structure (slow)" tool.

Generation of transgenic mice
The experiments were carried out in accordance with the animal protection law of the State of Geneva. All animals were housed and cared for according to the guidelines of the Direction Générale de la Santé du Canton de Genève. This study was reviewed and approved by the Commission cantonale pour les expériences sur les animaux and the Direction Générale de la Santé du Canton de Geneva. Mice were euthanized by rapid cervical dislocation.
cDNAs encoding either hCx36 WT or hCx36 SNP rs3743123 were subcloned into a plasmid containing a 0.7 kb-long fragment of the rat insulin II promoter, and a 1.6 kb-long sequence containing an intron and the polyA signal of the rabbit β-globin gene. After testing the actual expression of the transgenic proteins by transient transfection of the 2 constructs in the RIN cell line [4,28], the transgenes were excised from the plasmids and injected into the zygotic pronuclei of B6D2/JIcoF1 hybrid mice (C57BL/6J x DBA/2J), which were implanted into pseudo-pregnant NMRI females [29]. Nine and six independent founders (F 0 ) were generated using the hCx36 WT and the hCx36 SNP rs3743123 construct, respectively. Expression of either hCx36 WT or hCx36 SNP rs3743123 was detected in three and two lines of mice, respectively. Transgenic female mice positive for the transgenes, and heterozygous for mCx36, were then crossed with Cx36-null male mice [16] to obtain litters whose β cells only expressed either the WT (hereafter referred to as RIP-hCx36WT mice) or the rs3743123 form of hCx36 (hereafter referred to as RIP-hCx36rs3743123 mice). Mice were then bred to maintain the transgenes at the heterozygous state in all animals, and to avoid homozygous loss of function. We generated three independent lines of RIP-hCx36WT mice and two independent lines of RIP-hCx36rs3743123 mice (lines A and B), expressing comparable levels of hCx36. The genotype of littermates was determined by PCR amplification of ear DNA [30]. Experiments were initiated with mice of the F2 generation and repeated with mice of the F6 generation. Both males and females were used for the experiments.

Electron Microscopy
Cells were fixed for 60 min in 2.5% glutaraldehyde in 0.1 M phosphate buffer at room temperature, and processed for freeze-fracture, as previously described [31,32].

Western Blot
For preparation of total protein extracts, transfected HeLa cells were sonicated 3 times during 10 sec in a 0.1 M Tris-HCl lysis buffer containing 5% SDS, 5 mM EDTA and a mix of protease inhibitors (Roche Applied Science).
For preparation of membrane proteins, HeLa cells were sonicated in a 0.1 M Tris-HCl lysis buffer, pH 7.4, containing 20 mM EDTA and a mix of protease inhibitors. The homogenates were centrifuged at 4000 g for 10 min at 4°C. Supernatants were collected and centrifuged for 90 min at 260'000 g and 4°C. The membrane pellet was suspended in 0.1 M Tris-HCl buffer, pH 7.4, supplemented with 5% SDS and 5 mM EDTA. Membrane proteins were incubated at 95°C for 10 min and sonicated a second time. Protein content was determined by the DC protein assay reagent kit (Bio-Rad). Proteins were heated at 50°C in a loading buffer, separated by electrophoresis in a 10% polyacrylamide gel, and transferred for 60 min onto immobilon polyvinylidene difluoride membranes (Millipore), at a constant voltage of 100 V. Membranes were washed 4 times 15 min in TBS-Tween20 0.1% and then incubated for 30 min at room temperature in TBS containing 5% milk and 0.1% Tween20 (blocking buffer). Then, membranes were incubated overnight at 4°C with an antibody against Cx36, diluted 1:150 or actin (Sigma), diluted 1:250 in blocking buffer. Membranes were washed and incubated with secondary antibodies for 1 hour at room temperature, and antigen-antibody complexes were detected with ECL. In these experiments, negative and positive controls included extracts of wild-type HeLa and MIN6 cells, respectively. Quantifications were performed using the ChemiDoc™hemiDoccat (Biorad, Cressier, Switzerland) and the Quantity One software.

Dye injection
Three day-old cultures of HeLa cells were transferred onto the heated (37°C) stage of an inverted Zeiss ICM35 microscope, and individual cells were microinjected with either 4% Lucifer Yellow (LY) or 4% ethidium bromide (EB) in 150 mM LiCl buffered with 10 mM Hepes-buffered (pH 7.2), as previously reported [34]. Three independent clones of each type of transfected cell were tested, and data pooled for each cell type. Cell coupling extent was calculated after each injection by scoring the number of cells containing one of the two injected tracers, including the injected cell. Cell coupling incidence was determined by calculating the percentage of injections resulting in the cell-to-cell transfer (i.e. more than one cell stained) of one of the two tracers. From these data, we calculated a coupling index for either the LY or the EB tracers, given by the product of mean coupling extent and coupling incidence, and a total coupling index given by the product of the coupling index of LY and that of EB.

In vitro and in vivo data analysis
Data are expressed as means + SE of the indicated number of experiments. Statistical analysis was performed using the Statistical Package for Social Science (SPSS 15.0, SPSS inc.). For normally distributed values, differences between means were assessed by analysis of variance, using the post hoc Bonferroni test. Coupling extent data were compared using the median test. Coupling indices were compared using the Chi square test. Statistical analysis of data from transgenic mice was performed using GraphPad Prism 6.00 software (GraphPad, San Diego, CA). Differences were considered significant when p<0.05.

eQTLs of human pancreatic islets
Islets from cadaver organ donors were provided by the Nordic Islet Transplantation Program (www.nordicislets.org), courtesy of Prof. Olle Korsgren, Uppsala University, Sweden. All procedures were approved by the ethics committees of the Uppsala and Lund Universities, and informed written consent obtained from donors or their relatives. The microarray experiments (Human Gene 1.0 ST whole transcript) were performed on islets isolated from 81 normoglycemic individuals, (aged 56.3 ± 1.3 years, and featuring a BMI 25.7 ± 0.4 kg/m 2 , and a HbA1 c 5.5 ± 0.04%), and 47 hyperglycemic patients (aged 60.3 ± 1.2 years, and featuring a BMI 27.8 ±0.6 kg/m 2 , impaired glucose tolerance, and a HbA1 c 6.6 ± 0.1%). RNA products were fragmented and hybridized to the GeneChip Human HG U 133A Array (Affymetrix, Santa Clara, CA, USA) [35]. Statistical analyses of expression data were performed using two-tailed Spearman's t-test.

CoLaus study
The CoLaus cohort [36] consists of a random sample of 5435 Caucasian women and men, genotyped using the 500 K Affymetrix chip technology. In this cohort, patients were defined as T2D when featuring a fasting plasma glucose ! 7.0 mmol/L or receiving an oral hypoglycaemic or insulin treatment. The study was approved by the Institutional Ethics Committee of the University of Lausanne (Commission d'Ethique de la recherche clinique, Sous-Commission I). All participants received an information letter about the study and signed informed consent.
Out of this cohort, we initially analyzed a group of 299 T2D patients and 500 unrelated normoglycaemic subjects (the clinical characteristics of the 2 groups are given in S1 Table), predicted to provide a 70% power of detecting a SNP associated to T2D, assuming that the relative risk conferred by this SNP was about 1.5, i.e. similar to that of previously reported loci. Each SNP was amplified with 10 ng total genomic DNA, using the primers and probes reported in Mas et al. 2004 [22] and a jump start red taq ready mix (Sigma). Amplicons were analysed by the Pyrosequencing™ technology (Biotage, Uppsala, Sweden). All amplification reactions were carried out under identical conditions. 26 individuals were genotyped in duplicate to assess genotyping accuracy. All SNPs gave a genotyping concordance rate of 100%. Allele and genotype frequencies were tested for Hardy-Weinberg equilibrium by a Chi-square test. Differences in allele and genotype distributions between cases and controls were compared using Pearson's chi square. Odds ratios, with 95% CIs and p values, were determined using a Chi-square test. For all quantitative analyses, data were log transformed when appropriate, and a p value less than 0.05 was considered significant. Statistics were performed using Minitab and SPSS (windows version 14.0). Haploview software version 3.32 [37] was used to determine the pairwise linkage disequilibrium and haplotype structure of GJD2. The haplotype reconstruction was carried out using the PHASE software [38]. Power calculations were performed using the Genetic Power Calculator [39], assuming a co-dominant model, 5% prevalence and a genotype relative risk of 1.36.

SNP rs3743123 alters Cx36 packing and function, but not half-life in vitro
To investigate the effect of SNP rs3743123, we transfected HeLa cells, which lack connexin expression ( [34], S1 Fig and Table 1), with a cDNA fragment encoding either the WT or the rs3743123 variant of human GJD2. For each of these 2 constructs, we selected 3 stable clones expressing comparable levels of transfected hCx36 (S1 Fig). All clones showed the membrane insertion of the transfected proteins, as assessed by immunoblotting of membrane proteins (S1 Fig), and by immunofluorescence staining of cells (Fig 1A, left panel). The latter approach further revealed that whereas most WT hCx36 featured a spotted distribution at small membrane domains, rs3743123 hCx36 was often more broadly distributed along the cell membrane ( Fig  1A, right panel). Freeze-fracture electron microscopy further revealed polygonal, linear or arrayed gap junction plaques within the membranes of all stably transfected HeLa cell clones (Fig 1B and 1C). While the distribution of these gap junction types differed (p < 0.004) in the cells transfected for WT and variant hCx36, gap junction plaques contained on average a comparable number of connexons in the two cell types (Fig 1D). Microinjections of ethidium bromide and lucifer yellow, showed a sizable coupling of the transfected cells which, as expected for channels made by Cx36 [34], was larger in all clones when tested with ethidium bromide than with lucifer yellow (Table 1). However, the estimates of coupling extent and incidence were lower in the cells that expressed the variant form of hCx36 than in those which were coupled by WT hCx36 ( Table 1).
Exposure of HeLa cells to the transcription inhibitor actinomycin D, revealed that the transcript levels of both WT and variant hCx36 decayed with a similar time-course (T½~about 3 h, Fig 2).
These data show that that SNP rs3743123 does not interfere with the intracellular trafficking of hCx36, its insertion into the cell membrane and its packaging into functional gap junction plaques. However, it affects gap junction distribution and reduces the extent of intercellular coupling, without altering the native half-life of hCx36 mRNA. These mice were crossed with Cx36-null male mice [16], whose β cells lack endogenous mCx36, to allow for evaluation of the effects solely dependent on either WT or variant hCx36.
Immunofluorescence showed that hCx36 was similarly expressed in the β cells of 1 monthold RIP-hCx36WT and RIP-hCx36rs3743123 mice (Fig 3) at levels significantly higher than those of native mCx36 of non-transgenic animals (S5B- S5E Fig), consistent with the strong activity of the insulin promoter used to generate the transgenic animals. All 1 month-old mice featured comparable islet architecture, with somatostatin-and glucagon-containing cells located as a mantle at the islet periphery, and surrounding a core of insulin-producing β-cells (S6A and S6B Fig top rows and Fig 3 top row). At this stage, morphometry revealed a comparable number of β-cells in the islets of the two mouse types (Fig 3B).
Islet structure and proper control of blood glucose levels were not altered with aging in mice expressing the WT form of hCx36 (Fig 3). In contrast, a progressive loss of β-cells (Fig 3A bottom row and Fig 3B), altering islet structure (S6A and S6B Fig bottom rows) and resulting in hyperglycemia (Fig 3C and 3D), was observed with time in one of the two lines (line A) expressing the variant form of hCx36. These alterations, which were observed in male and female mice, and across multiple animal generations, were paralleled by a reduction of hCx36 expression (Fig 4A-4C). Five months after birth, the second line expressing the variant hCx36 (line B), and which was generated independently of line A, also featured a statistically significant reduction in the number of β cells and of immunolabelled hCx36, as compared to mice expressing the WT form of hCx36 (S7A, S7B, S7E- S7H Fig). However, these alterations were substantially milder than those observed in line A. Accordingly, mice of line B remained normoglycemic throughout the entire duration of the experiment (S7C and S7D Fig).
The data show that the overexpression of WT and variant hCx36 did not affect the structure of the endocrine pancreatic islets of young mice, and that the variant connexin later impaired both islet structure and function.
SNP rs3743123 reduces GJD2 expression in human pancreatic islets, but marginally associates to T2D patients Comparison of the expression of quantitative trait loci (eQTL) in human islets of normoglycaemic and hyperglycaemic donors showed that the expression of hCx36 transcript was significantly decreased (p<0.03) in pancreatic islets of hyperglycemic organ donors, and specifically in those expressing SNP rs3743123 than in those expressing the WT form of the gene. (S2 Table).
To test whether SNP rs3743123 associates to T2D, we investigated the CoLaus cohort ( [36], S1 Table) for several SNPs which lie in the haplotype block of rs3743123, with pair-wise linkage coefficients D'> 0.98 [22]. Five common haplotypes, accounting for 99% of control chromosomes were identified, whose distribution was not significantly different in control and T2D individuals (S3 Table). Comparison of the genotype and allele frequencies of the 4 SNPs we investigated revealed that SNPs rs651724, rs35174018 and rs34964522 did not associate to T2D in the CoLaus population (S4 Table). In contrast, the synonymous SNP rs3743123 (S196S) was nominally associated to the disease, at both allele (p = 0.03; OR = 1.27 [1.02-1.82]) and genotype levels, as assessed per a recessive model (p = 0.03; OR = 1.36 [1.02-1.59]), although this association did not reach statistical significance after correction for multiple testing (S4 Table). The data show that SNP rs3743123 reduces the islet expression of hGJD2, but marginally associates to T2D, in a heterogeneous population of patients.

Discussion
Type 2 diabetes (T2D) refers to a set of pathogenically distinct disorders which are usually identified by a persistent hyperglycemia, often due to a variable loss of the insulin-producing β cells of pancreas, and to a selective insensitivity to glucose of the residual β cells. These alterations are believed to be caused via a complex interplay of multiple genetic, cellular and environmental factors [40,41]. Previous studies have indicated that Cx36, a protein of the connexin family which forms membrane channels for the electrical and metabolic coupling of β cells [42], contributes to control glucose-stimulated insulin secretion and the resistance of β cells to cytotoxic conditions [18,42,43]. Strikingly, the pharmacological, siRNA and genetic interference with the expression and function of Cx36 results in alterations of murine β cells [16,18,44], which mimic the major alterations observed in T2D [45].
In humans and rodents, the GJD2 gene which codes for Cx36 (http://www.genenames.org/ genefamily/gj.php) is solely expressed in pancreatic β cells, neurons, and neuron-related endocrines [46]. Previous studies have shown that a specific SNP (rs3743123) in the exon 2 of GJD2, is associated with juvenile myoclonic epilepsy [21,22]. Since neurons and β cells share a number of common features [24], in spite of a rather different embryological origin, we investigated whether the same SNP also causes alterations of β-cell function, possibly involved in the development of T2D. Stable transfection experiments of human cells which lack native connexin expression, demonstrated that the variant cDNA containing SNP rs3743123 did not alter the expected half-life of the hCx36 transcript, nor prevent the quantitative biosynthesis of the cognate protein, its transport to and insertion within the cell membrane, and its aggregation into bona fide gap junction plaques. Still, and in spite of a normal electrophoretic mobility and preservation of the expected immunoreactivity at the C terminus, the hCx36 protein encoded by the variant mRNA formed channels less permeable to two gap junction-permeant tracers, distributed differently within the cell membrane, and aggregated into distinct patterns of gap junction plaques. These observations suggest that the form of hCx36 carrying SNP rs3743123 is processed somewhat differently than the wild type form. Our computing analysis confirmed that the synonymous SNP rs3743123 alters the predicted structure of hCx36 mRNA, to an extent which is not induced by other SNPs located in the same exon of GJD2. Other synonymous SNPs, have been shown to affect the splicing [47], stability [48], and secondary structure of messenger RNAs [49][50][51], as well as the levels and function of the cognate proteins [52][53][54][55]. For example, differences in the translation rate due long ribosomal pause along mRNAs featuring a SNP can result in major alterations in the co-translational protein folding [53][54][55], leading to altered protein conformation. Our data now document that, in the case of GJD2, the synonymous SNP rs3743123 did not affect the translation of hCx36, but somehow altered the packing of the protein in the cell membrane, and decreased the permeability of the cognate cell-to-cell channels. Whether the latter change is due to the modified aggregation pattern of connexons and it Variant of Connexin 36 and β-Cells Function occurs also in vivo remains to be validated. However, based on previous studies, indicating that the experimental modifications of Cx36-dependent coupling induced in cell lines consistently mimicked those found in primary mouse islets exposed to the same conditions [16,19,28,34], the observed decrease in cell-to-cell coupling would be expected to decrease both the secretion and survival of β cells [16,18,44].
To validate this possibility, we generated the first lines of transgenic mice expressing in β cells solely the wild type or the variant form of human Cx36. Comparison of these lines showed that they all exhibited normal islet structure and were normoglycemic at birth. However, mice of the two lines expressing the variant form of hCx36 developed a significant reduction in the number of β cells and of Cx36 immuno-labeling within the first five months of life, which persisted in both genders and across many generations and were paralleled by hyperglycemia in one of the lines. Given the independent generation of these two lines, and the hemizyogous genotype of all the mice we used (which was purposely planned to decrease the risk of a positional loss of function), it is very unlikely that the phenotype observed resulted from a random, non-specific, positional effect of the transgene. Rather, the data strengthen the alternative view that this phenotype was specifically due to the expression of the hCx36 variant. However, as sustained hyperglycemia does decrease the β-cell population in many models of diabetic mice [56], and may reduce Cx36 expression [57], the possibility that the altered islet and Cx36 phenotypes we observed were induced by the elevated circulating levels of glucose should also be considered. Two observations do not support this possibility: first, islets of mice expressing rs3743123-hCx36 of the A line, which were hyperglycemic, did not show the large increase in αand δ-cell numbers, which consistently characterizes the abnormal islet architecture in most models of diabetic mice [56]; second, a loss of β-cells was also observed in the islets of line B, which did not featured elevated circulating levels of glucose. Thus, our experiments suggest that the expression of variant hCx36 decreased Cx36 signaling, leading first to a post-natal loss of β cells that, when sufficient, resulted, in turn, in altered homeostasis of blood glucose. This sequence also fits with the finding that the altered islet and Cx36 phenotypes were more intense in mice expressing rs3743123-hCx36 of line A, which eventually developed hyperglycemia, than in those of line B, which remained normoglycemic throughout the duration of the experiment. Most likely, this difference can be accounted for by a different level of expression of the hCx36 transgene between the two transgenic lines, which may have been influenced by its site of insertion (due to a different euchromatin environment) and number of copies (due to tandem repeats). Thus, in animals of the A line the lresidual levels of hCx36 may not have suffice to maintain the β-cell mass and, therefore, normal glucose homeostasis, whereas the higher levels of hCx36 expressed in the mice of line B, may have been adequate to sustain both functions. This is in agreement with the previous observations that Cx36 is dispensable for the development and function of pancreatic islets, till more than 50% of the protein is lost [58].
An obvious question is whether our mouse findings apply to humans. In this perspective, it is striking that the islets of cadaveric donors expressing a GJD2 with SNP rs3743123, featured a lower expression of Cx36 mRNA than those of individuals expressing the WT form of the gene. Accordingly, our analysis of the CoLaus cohort revealed a nominal, if marginal association of SNP rs3743123 to T2D patients. However, investigating the DIAGRAM and MAGIC meta-analyses consortia, we failed to detect a significant association of SNP rs3743123 in other populations of T2D patients (data not shown). Because T2D is a heterogeneous disease, this negative finding does not rule out a relevant contribution of the GJD2 gene in subpopulations of T2D patients, specifically those who feature the lowest residual insulin secretion in response to glucose stimulation [59], or other phenotypic traits. The validation of this tentative hypothesis awaits the further screening of other patients and transgenic mice populations. At any rate, our data extend to a different and much large human cohort the preliminary findings that hCx36 levels are decreased in some, but not all T2D patients [4], and provide the very first evidence for an in vivo pathogenic role of a connexin variant in the function of pancreatic islets.
Supporting Information S1 Fig. Expression of hCx36 is induced in HeLa cells after transfection of either the WT or the SNP rs3743123 form of Cx36. A-B, Representative western blots of total and membrane protein extracts. hCx36 is induced in several independent clones of HeLa cells stably transfected with either the WT (clones WT#1-2-3) or the SNP rs3743123 form of hCx36 (clones SNP#1-2-3). C-D, Densitometric quantification of Cx36 signal in western blots of total (C) and membrane proteins (D). The hCx36 signal was normalized to the actin signal. SNP rs3743123 does not alter the membrane insertion of Cx36. Data are mean + SD values of three independent experiments. Student's t test with Welch's correction. Ã P 0.05 ÃÃ P 0.01 ÃÃÃ P 0.001 ÃÃÃÃ P 0.0001 compared to non-transfected HeLa cells, § P 0.05 § § P 0.01 § § § P 0.001 § § § § P 0.0001 compared to Min6 cells.