The SLC30A8 gene encodes the zinc transporter ZnT-8, which provides zinc for insulin-hexamer formation. Genome-wide association studies have shown that a polymorphic variant in SLC30A8 is associated with altered susceptibility to Type 2 diabetes and we recently reported that glucose-stimulated insulin secretion is decreased in islets isolated from Slc30a8-knockout mice. The present study examines the molecular basis for the islet-specific expression of Slc30a8. VISTA analyses identified two conserved regions in Slc30a8 introns 2 and 3, designated enhancers A and B respectively. Transfection experiments demonstrated that enhancer B confers elevated fusion gene expression in both βTC-3 cells and αTC-6 cells. In contrast, enhancer A confers elevated fusion gene expression selectively in βTC-3 and not αTC-6 cells. These data suggest that enhancer A is an islet β-cell-specific enhancer and that the mechanisms controlling Slc30a8 expression in α- and β-cells are overlapping, but distinct. Gel retardation and ChIP (chromatin immunoprecipitation) assays revealed that the islet-enriched transcription factor Pdx-1 binds enhancer A in vitro and in situ respectively. Mutation of two Pdx-1-binding sites in enhancer A markedly reduces fusion gene expression suggesting that this factor contributes to Slc30a8 expression in β-cells, a conclusion consistent with developmental studies showing that restriction of Pdx-1 to pancreatic islet β-cells correlates with the induction of Slc30a8 gene expression and ZnT-8 protein expression in vivo.
Since the derivation of insulin-secreting β-cells from stem cells represents a potential cure for Type 1 diabetes, significant efforts have been made to understand the mechanisms controlling islet β-cell differentiation. Growth factors have been identified that drive the conversion of stem cells towards a β-cell fate  and multiple transcription factors, including Pdx-1, Isl-1, Pax-4, Pax-6, Nkx2.2, Nkx6.1, BETA2/NeuroD1 and MafA/B , have been shown to be important for islet-specific gene expression. Many of these transcription factors were identified through the analysis of key cis-acting elements in promoters and enhancers of genes whose expression are islet-specific or islet-enriched, including those encoding insulin, glucagon, islet amyloid polypeptide, glucokinase, somatostatin and GLUT2 (glucose transporter 2) . None of these transcription factors are islet-specific, rather islet-specific expression appears to be conferred by the particular combination of transcription factors bound to a given promoter or enhancer, with islet-enriched transcription factors playing a major role . Several of these islet-enriched factors have been shown to be not only important for islet-specific gene expression in the adult, but also for pancreas and islet development , underscoring how the study of islet-specific gene transcription can provide insight into islet physiology and development, in addition to the mechanisms of tissue-specific gene expression.
One of the most important islet-enriched transcription factors is Pdx-1, a homeodomain protein that, in adults, is primarily expressed in pancreatic β-cells and at low levels in pancreatic exocrine cells, islet δ-cells and the duodenum . Pdx-1 has been shown to regulate expression of a number of genes in islets, including those encoding insulin  and G6pc2, also known as IGRP . Although not sufficient by itself to mediate transcriptional activation, Pdx-1 is critical for insulin and G6pc2 promoter activity and most likely functions in a higher order complex containing other islet-enriched factors [4,5].
The studies described in the present paper were initiated with the goal of using the Slc30a8 gene, which encodes ZnT-8 (zinc transporter-8), to supplement previous studies on islet-specific gene transcription. ZnT-8 belongs to a group of zinc transporters that, along with metallothioneins, are involved in intracellular zinc trafficking and storage so as to tightly maintain intracellular zinc homoeostasis . ZnT-8 is predominantly expressed in pancreatic α- and β-cells [7–9], with much lower levels of expression in testis and submaxillary glands . ZnT-8 localizes to insulin secretory granules within β-cells  and it is thought to be important for providing zinc to allow for proper maturation, storage and secretion of insulin .
Consistent with an important role for ZnT-8 in the β-cell, genome-wide association studies have linked a single nucleotide polymorphism in amino acid 325 of human ZnT-8 to increased susceptibility to Type 2 diabetes [12–15], gestational diabetes , impaired proinsulin into insulin conversion  and reduced first-phase insulin secretion . Interestingly, this same variant is also associated with auto-antibody epitope specificity changes in human Type 1 diabetes . Also consistent with an important role for ZnT-8 in insulin secretion, we have recently shown that, in mice lacking ZnT-8, pancreatic islet zinc content and fasting plasma insulin concentrations are markedly reduced . In addition, glucose-stimulated insulin secretion is impaired in islets isolated from ZnT-8-knockout mice, although glucose metabolism is surprisingly unaffected . Related data from other groups suggest that the phenotype may vary depending on the genetic background [19,20] and whether mice lack ZnT-8 globally or only in β-cells .
The studies described in the present paper identify key regulatory sequences driving expression of the Slc30a8 gene. We identify two conserved intronic enhancers in Slc30a8, designated enhancer A and B, each of which contains multiple cis-acting elements that are critical for enhancer activity. Enhancer B is active in both α- and β-cells, whereas enhancer A is an islet β-cell-specific enhancer. We also show that two elements in enhancer A bind Pdx-1 in vitro and that Pdx-1 binds enhancer A in βTC-3 cells in situ, indicating that Pdx-1 plays an important role in the regulation of Slc30a8 gene expression in β-cells, as it does with other genes whose expression are islet β-cell-enriched.
Fusion gene plasmid construction
For details on the generation of fusion gene plasmids please see the Supplementary material at http://www.BiochemJ.org/bj/433/bj4330095add.htm.
Cell culture, transfection and luciferase assays
Mouse islet β-cell-derived βTC-3 cells and α-cell-derived αTC-6 cells were grown in DMEM (Dulbecco's modified Eagle's medium) containing 10% (v/v) FBS (fetal bovine serum), whereas human cervix-derived HeLa cells were grown in DMEM containing 10% (v/v) bovine serum. For transient transfections, cells were transfected with 0.5 μg of an expression vector encoding SV40 (Simian virus 40)–Renilla luciferase (Promega) and 2 μg of a firefly luciferase pGL3 fusion gene plasmid using the Lipofectamine™ reagent (GibcoBRL) as described previously . Following overnight incubation in serum-containing medium, cells were harvested by trypsin digestion and then solubilized in passive lysis buffer (Promega). After two cycles of freeze/thawing, firefly and Renilla luciferase activities were assayed using the Promega Dual-Luciferase Reporter Assay System according to the manufacturer's instructions. To correct for variations in transfection efficiency, the results are expressed as the ratio of firefly/Renilla luciferase activity. In addition, three independent preparations of each fusion gene plasmid construct were analysed in triplicate.
Complementary sense and anti-sense oligonucleotides with overhanging GATC ends were synthesized, annealed and labelled with [α-32P]dATP using the Klenow fragment of Escherichia coli DNA Polymerase I to a specific activity of approx. 2.5 μCi/pmol . [α-32P]dATP (>3000 Ci·mmol−1) was obtained from PerkinElmer.
Low-salt nuclear extract preparation
Low-salt βTC-3, αTC-6, HeLa and H4IIE nuclear extracts were prepared as described previously , except that the nuclear pellet was extracted with 20 mM Hepes (pH 7.8), 0.75 mM spermidine, 0.15 mM spermine, 0.2 mM EDTA, 2 mM EGTA, 2 mM DTT (dithiothreitol) and 25% glycerol containing 200 mM NaCl, instead of 0.4 M ammonium sulfate, and the supernatant was used directly in gel-retardation assays. The protein concentration of the nuclear extracts was determined using the Bio-Rad assay and was typically ~1 μg·μl−1.
Approx. 14 fmol of radiolabelled probe (~30000 c.p.m.) was incubated with 4 μg of βTC-3, αTC-6, HeLa or H4IIE nuclear extract in a 20 μl reaction volume containing 20 mM Hepes (pH 7.9), 0.1 mM EDTA, 1 mM EGTA, 0.375 mM spermidine, 0.075 mM spermine, 12.5% (v/v) glycerol, 1 mM DTT, 1 μg of poly(dI-dC)·poly(dI-dC) and 50 mM NaCl. After incubation at room temperature (22 °C) for 10 min the reactions were loaded on to a 6% polyacrylamide gel containing 1× TGE buffer (25 mM Tris Base, 190 mM glycine and 1 mM EDTA) and 2.5% (v/v) glycerol. Samples were electrophoresed for 1.5 h at 150 V in 1× TGE buffer before the gel was dried and exposed to Kodak XB film with intensifying screens.
Competition experiments and gel supershifts
For competition experiments, unlabelled competitor DNA was mixed with the radiolabelled oligomer at the molar excess indicated prior to addition of nuclear extract. For supershift experiments, specific antisera (1 μl) were pre-incubated with βTC-3 nuclear extract for 10 min at room temperature prior to the addition of the labelled oligonucleotide probe and incubation for an additional 10 min at room temperature. All subsequent steps were carried out as described above. An antiserum specific to Pdx-1 was a gift from Professor Chris Wright (Vanderbilt University, Nashville, TN, U.S.A.) , whereas an antiserum specific to USF-1 (upstream stimulatory factor-1) (sc-229) was purchased from Santa Cruz Biotechnology.
ChIP (chromatin immunoprecipitation) assays
βTC-3 cells [(0.5–1.0)×108] were formaldehyde cross-linked, and sonicated chromatin–DNA complexes were prepared as described previously . The size of DNA fragments that were subjected to ChIP was ~500 bp. Aliquots (20 μg) of sheared chromatin were immunoprecipitated with either 5 μl of rabbit anti-MafA antibody (Bethyl Laboratory), 2 μl of rabbit anti-Pdx-1 antibody (a gift from Professor Chris Wright, Vanderbilt University, Nashville, TN, U.S.A.) or normal rabbit IgG for 16 h at 4 °C. The resulting chromatin–antibody complexes were isolated with Protein A/G–agarose (Upstate Biotechnology). PCR was performed on one-tenth of the purified immunoprecipitated DNA using Ready-to-Go PCR beads (GE Healthcare) using 15 pmol of each of the following mouse primer pairs: Pck1, −434 (5′-GAGTGACACCTCACAGCTGTGG-3′) to −96 (5′-GGCAGGCCTTTGGATCATAGCC-3′); Slc30a8, +20153 (5′-CCCCATCATTCATGGCTAAA-3′) to +20467 (5′-TCATTGCAATAATCCCCACA-3′). The amplified PCR products were resolved by electrophoresis on 1.4% agarose gels.
The animal housing and surgical facilities used for the mice in the present studies meet the American Association for the Accreditation of Laboratory Animal Care standards. All animal protocols were approved by the University of Colorado Denver Animal Care and Use Committee. Mice were maintained on standard rodent chow with food and water provided ad libitum. CD1 mice were procured from The Jackson Laboratories. Embryonic pancreata were harvested from time-mated mice at e12.5, e15.5 and e17.5 (e is embryonic day) and immediately fixed for histological studies or pooled and stored in RNAlater® (Ambion) at 4 °C for subsequent expression analyses.
Mouse pancreata fixed in 4% paraformaldehyde were sectioned (6 μm) after embedding in OCT™ (Tissue Tek, Sakura Finetek). For immunofluorescence microscopy, sections were incubated for 1 h at room temperature with blocking buffer (TSA system; Zymed, Invitrogen) and then overnight in a humid chamber with four primary antibodies: guinea pig anti-insulin (1:50 dilution) (Sigma), rabbit anti-β-catenin (1:200 dilution) (Neomarkers), mouse anti-ZnT-8 (1:20 dilution) (Professor John Hutton, University of Colorado, Denver, CO, U.S.A.) and goat anti-Pdx-1 (1:10000 dilution). Sections were washed three times for 5 min in PBS before secondary antibodies (1:250 dilution) conjugated to AMCA (7-amino-4-methylcoumarin-3-acetic acid), Cy2 (carbocyanine), Cy3 (indocarbocyanine) and Cy5 (indodicarbocyanine) fluorophores (Jackson Immunoresearch Laboratories) were applied and incubated at room temperature for 60 min. The sections were rinsed in PBS and mounted in a glycerol-based medium. Image panels were acquired using Intelligent Imaging System software in conjunction with a Nikon Microphot FXA inverted microscope equipped with a Photometrics CoolSnap cooled monochromatic CCD (charge-coupled device) camera. The images were later pseudo-coloured for illustration: red (Pdx-1), white (β-catenin) and green (insulin and ZnT-8).
RNA extraction and quantitative RT (reverse transcription)–PCR
Total RNA was extracted from pooled fetal pancreata using TRIzol® (Invitrogen) and purified using RNeasy columns (Qiagen), with RNA quality verified by capillary electrophoresis (Agilent-2100 Bioanalyzer). cDNA was prepared from total RNA (1 μg) using the iScript cDNA synthesis kit (Bio-Rad Laboratories). cDNA samples (5 ng) served as the templates for amplification in a 5′-nuclease-assay-based system using FAM (6-carboxyfluorescein) dye-labelled Taqman MGB probes (Applied Biosystems) and a 96-well ABI 7000 PCR instrument. The Gapdh (glyceraldehyde-3-phosphate dehydrogenase) gene was used for sample normalization. The CT (cycle threshold) values were determined in triplicate, and the samples were normalized relative to the CT values obtained using embryonic pancreatic samples from e12.5.
The transfection data were analysed for differences from the control values, as specified in the Figure legends. Statistical comparisons were calculated using an unpaired Student's t test. The level of significance was P< 0.05 (as determined using a two-sided test).
A conserved islet β-cell-specific enhancer is located in the second intron of the Slc30a8 gene
Intronic enhancers have previously been identified in several genes whose expression are enriched in islets including those encoding glucagon , islet amyloid polypeptide  and G6pc2 . To determine whether intronic enhancers may also exist in the human SLC30A8 and mouse Slc30a8 genes, a sequence alignment was performed using the VISTA program  focusing on the region between the translation start site and the last exon . This analysis identified two conserved intronic regions, located between +20125 and +20745 in intron 2 and between +25228 and +25704 in intron 3 in the mouse Slc30a8 gene (Figure 1). These regions are found in similar locations in the human SLC30A8 gene (results not shown).
We hypothesized that these regions might represent transcriptional enhancers. To address this hypothesis these regions, designated intronic enhancers A and B respectively, were isolated using PCR and ligated 5′ of a heterologous TK (thymidine kinase)–luciferase fusion gene containing TK genomic sequence between −105 and +51, relative to the transcription start site . Luciferase expression directed by these fusion genes was then analysed by transient transfection of βTC-3 cells, an islet β-cell-derived line , αTC-6 cells, an islet α-cell-derived line [32,33] and HeLa cells, a cervix-derived cell line . Figure 2 shows that in βTC-3 cells, but not αTC-6 or HeLa cells, intronic enhancer A elevated reporter gene expression beyond that driven by the TK–luciferase fusion gene alone, indicating that this region is an islet β-cell-specific enhancer. In contrast, intronic enhancer B had no effect on fusion gene expression in any of the cell lines (Figure 2).
To address the possibility that intronic enhancer B is an enhancer, but that this activity is not manifest in the context of the TK promoter, intronic enhancer B, as well as enhancer A, were ligated 5′ of a heterologous G6PC2–luciferase fusion gene containing the proximal human G6PC2 promoter sequence between −150 and +3 relative to the transcription start site. Luciferase expression directed by these fusion genes was then analysed by transient transfection of βTC-3 and αTC-6 cells. Figure 3(A) shows that, in βTC-3 cells, in the context of the G6PC2 promoter, intronic enhancer B elevated reporter gene expression beyond that driven by the −150/+3 G6PC2–luciferase fusion gene alone. Figure 3(A) also shows that, in βTC-3 cells, intronic enhancer A markedly elevated reporter gene expression beyond that driven by the −150/+3 G6PC2–luciferase fusion gene alone, and to a much greater degree than enhancer B. In addition, this effect was independent of orientation (Figure 3A), consistent with the strict definition of an enhancer , and much greater in magnitude than seen in the context of the TK promoter (Figure 2). Strikingly, Figure 3(A) shows that, in αTC-6 cells, intronic enhancer B but not enhancer A elevated reporter gene expression beyond that driven by the −150/+3 G6PC2–luciferase fusion gene alone. These data demonstrate that enhancer B is active in both α- and β-cells and, in contrast, again indicate that enhancer A is an islet β-cell-specific enhancer. Overall these data suggest that the mechanisms controlling Slc30a8 expression in α- and β-cells are overlapping, but distinct. Because intronic enhancer B only enhanced reporter gene expression driven by the islet-specific G6PC2 promoter and not the ubiquitously active TK promoter, further studies will be needed to determine whether this enhancer is active in other cell lines or instead is an islet-specific enhancer.
Since enhancer A is a much stronger enhancer than enhancer B, subsequent studies focused mainly on enhancer A. To delineate the precise region of enhancer A that was primarily responsible for increasing fusion gene expression, enhancer A (+20125 to +20745) was arbitrarily divided into three regions, +20125 to +20324, +20325 to +20524, and +20525 to +20745, designated regions 1–3. Each region was then ligated 5′ of the −150/+3 G6PC2–luciferase fusion gene described above and reporter gene expression was again assessed following transient transfection of βTC-3 cells. Figure 3(B) shows that enhancer A region 2 markedly elevated reporter gene expression beyond that driven by the −150/+3 G6PC2–luciferase fusion gene alone and to a greater extent than regions 1 or 3. The effect of region 2 was also independent of orientation (Figure 3B). This result suggests that region 2 represents the key region within enhancer A.
Alignment of mouse enhancer A region 2 using MacVector7.0 with the human, rat, dog and chicken sequences indicated that this region is highly conserved between species with 87%, 96%, 89% and 70% identity with the human, rat, dog and chicken sequences respectively (Figure 4). Interestingly, this conservation exceeds the conservation observed with the −350 to −90 region of the mouse and human insulin promoters . The conservation of enhancer B sequence across species was much lower (Supplementary Figure S1 at http://www.BiochemJ.org/bj/433/bj4330095add.htm). Owing to the highly conserved nature of enhancer A region 2 and the presence of many putative transcription-factor-binding sites (Supplementary Figure S2 at http://www.BiochemJ.org/bj/433/bj4330095add.htm), a scanning mutation approach was employed to identify functionally important sites. Site-directed mutagenesis was used to introduce 5-bp block mutations across region 2 (Figure 4) in the context of the enhancer A region 2 −150/+3 G6PC2–luciferase fusion gene described above. Reporter gene expression directed by the resulting fusion genes was again assessed following transient transfection of βTC-3 cells. The results show that multiple sites within region 2 were sensitive to mutation (Figure 5), particularly those targeted by mutations 1, 7 and 8, 16, and 18 (Figure 4). A similar functional analysis was performed with enhancer B. The results show that mutation of two conserved elements in enhancer B, that sequence analyses suggest have the potential to bind Pdx-1 and another islet-enriched transcription factor, namely Foxa2 (Supplementary Figure S1), reduce the activity of this enhancer (Supplementary Figure S3 at http://www.BiochemJ.org/bj/433/bj4330095add.htm).
Pdx-1 binds to Slc30a8 enhancer A in vitro
Mutations 1 and 8 in enhancer A region 2 disrupt TAAT-containing motifs that are conserved across multiple species, including humans (Figure 4). This motif represents the core binding site recognized not only by Pdx-1, but also many other homeodomain proteins . Given the numerous reports demonstrating a role for Pdx-1 in the expression of β-cell-specific or -enriched proteins we next sought to determine whether Pdx-1 interacts with these motifs.
The potential of these motifs to interact with Pdx-1 was first examined using gel-retardation assays. When a labelled oligonucleotide, representing the Slc30a8 region between +20325 and +20339 that encompasses the TAAT motif disrupted by mutation 1 (Figure 6A), was incubated with nuclear extract prepared from βTC-3 cells, a single major protein–DNA complex was formed (Figure 6B; see arrow). The specificity of this protein–DNA interaction was investigated by including various cold (non-radioactive) competitors in the gel-retardation assay. Figure 6(B) shows that the WT (wild-type) unlabelled +20325/+20339 oligonucleotide competed for formation of the major protein–DNA complex, whereas an oligonucleotide containing just two point mutations in the TAAT motif (Figure 6A), rather than the more extensive block mutation used in the fusion gene experiments (Figure 4), did not compete, suggesting that the complex represents a specific protein–DNA interaction whose formation is dependent on the TAAT motif and correlates with the gene expression data (Figure 5).
Figure 6(C) shows that this complex is only detected using nuclear extract prepared from βTC-3 cells and not αTC-6, H4IIE or HeLa cells, indicating that the factor present in the complex is β-cell-specific or -enriched. To assess the presence of Pdx-1 in the major protein–DNA complex, nuclear extract was pre-incubated with antisera raised against the N-terminus of Pdx-1  or, as a negative control, against USF-1. As can be seen in Figure 6(D), the USF-1 antiserum had no appreciable effect on formation of the TAAT-specific complex. In contrast, pre-incubation with the Pdx-1 antisera resulted in the disappearance of the TAAT-specific complex and the appearance of a lower mobility, or supershifted, complex, suggesting that the major complex detected represents Pdx-1 binding. Finally, gel-retardation analyses using Pdx-1 synthesized by in vitro transcription and translation directly demonstrated that Pdx-1 can bind to the +20325/+20339 region of enhancer A (Figure 6E).
Similar analyses were performed using a labelled oligonucleotide, representing the Slc30a8 region between +20380 and +20409 that encompasses the TAAT motif disrupted by mutation 8 (Supplementary Figure 4A at http://www.BiochemJ.org/bj/433/bj4330095add.htm). The results show specific protein binding to this region (Supplementary Figure 4B) by a β-cell-specific factor (Supplementary Figure 4C) that cross-reacts with Pdx-1 antisera (Supplementary Figure 4D) and also that Pdx-1 produced by in vitro transcription and translation can directly bind to this element (Supplementary Figure 4E). Interestingly, in contrast with the +20325/+20339 element, the +20380/+20409 element forms two complexes with βTC-3 nuclear extract that both cross-react with the Pdx-1 antiserum (Supplementary Figures 4B and 4D). Previous studies have shown that Pdx-1 can bind certain elements either alone or in a complex with other factors .
Pdx-1 binds to Slc30a8 enhancer A in situ
To complement the results of the in vitro gel-retardation analyses, ChIP assays were performed to assess Pdx-1 binding to Slc30a8 enhancer A region 2 within intact cells. Fragmented chromatin from formaldehyde cross-linked βTC-3 cells was subjected to immunoprecipitation with antibodies against either MafA or Pdx-1. The presence of region 2 in the immunoprecipitates was then analysed by PCR using primers that recognize the Slc30a8 gene sequence between +20153 and +20467. As can be seen in Figure 7, region 2 was enriched in the Pdx-1 immunoprecipitates compared with the MafA immunoprecipitates and IgG control. To test the specificity of the antibody–protein interactions, these immunoprecipitates were also analysed for the presence of the Pck1 gene, which is not expressed in these cells , using PCR primers that recognize the Pck1 promoter sequence between −434 and −96. As expected, no enrichment of the Pck1 promoter was detected in the Pdx-1 immunoprecipitate compared with the IgG control (Figure 7). The low signal in the experimental lanes cannot be explained by the lack of Pck1 promoter in the starting material as a signal of the expected size was obtained when the PCR was performed using the chromatin input prior to immunoprecipitation. These results demonstrate that Pdx-1 binds to Slc30a8 enhancer A region 2 within intact cells.
The restriction of Pdx-1 to pancreatic islet β-cells correlates with the induction of Slc30a8 gene and ZnT-8 protein expression
Pdx-1 is expressed throughout the pancreatic epithelium in the multipotent pancreatic progenitor cells beginning as early as e8.5 . It becomes down-regulated in acinar and duct cells around e15.5 and greatly up-regulated in insulin-positive cells beginning around e16.5–17.5 [40,41]. To determine whether Pdx-1 might contribute to the induction of Slc30a8 gene expression during pancreatic islet development, we compared the time course for the appearance of Slc30a8 mRNA and ZnT-8 protein in embryonic mouse pancreas relative to Pdx-1. Figure 8(A) confirms that between e12.5 and e15.5 Pdx-1 becomes restricted to pancreatic islet β-cells, as reported previously [40,41]. This correlates with the initial induction of Slc30a8 gene expression (Figure 8B), whereas ZnT-8 protein levels were still below the limit of detection (Figure 8A). A marked increase in Slc30a8 gene expression and the appearance of ZnT-8 protein was observed between e15.5 and e17.5 (Figure 8B), which correlates with the previously reported up-regulation of Pdx-1 in insulin-positive cells (Figure 8A) . Little change in pancreatic Pdx-1 gene expression was observed in whole pancreata between e12.5 and e17.5 (Figure 8B), consistent with the reciprocal increase in β-cell expression and decrease in acinar and ductal cell expression (Figure 8A).
Many islet-specific promoters and enhancers utilize a similar mechanism to achieve tissue-specific expression, specifically a complex interaction between islet-enriched and ubiquitous factors . We have been interested in expanding the current understanding of the molecular mechanisms driving islet-specific expression using Slc30a8 as a model. By analysing uncharacterized islet-specific promoters and enhancers, it may be possible to identify novel factors that are important for selective gene expression within islets. In the present study we have identified two conserved intronic regions, designated enhancers A and B, that are capable of enhancing fusion gene expression in transient transfections (Figures 1–3). Enhancer A is an islet β-cell-specific enhancer whereas enhancer B is active in both α- and β-cells. Additional studies showed that Pdx-1 regulates Slc30a8 gene expression through binding two sites in intronic enhancer A (Figures 4–7), although gel-retardation and ChIP assays cannot distinguish whether one or both of these two sites binds Pdx-1 in vivo.
The insulin gene promoter has been extensively characterized and contains multiple cis-acting elements that are required for high promoter activity, most importantly elements designated as the A, C and E boxes, which have been shown to bind Pdx-1 , MafA  and NeuroD/BETA2  respectively. Several other genes whose expression are islet-specific or -enriched are regulated by the same three factors . Since we have demonstrated that Slc30a8 gene expression is regulated by Pdx-1 this raises the question as to whether MafA and NeuroD are also required for islet-specific Slc30a8 gene expression. Future experiments will address this question. Interestingly, the induction of both Slc30a8 and G6pc2 gene expression between e13.5 and e17.5 parallels the induction of MafA expression (Figure 8B) [44,45] and the restriction of Pdx-1 to β-cells (Figure 8A). Previous promoter analyses have shown that G6pc2 expression is regulated by both Pdx-1 and MafA , whereas recent microarray analyses demonstrate that Slc30a8 and G6pc2 gene expression are markedly reduced in islets lacking MafA , suggesting that MafA might also contribute to the induction of Slc30a8 and G6pc2 gene expression.
Pdx-1, MafA and NeuroD have also been shown to play major roles in the glucose responsiveness of the insulin gene . Pdx-1 is the primary regulator of glucose-stimulated insulin gene expression and it is thought to modulate transcription via phosphorylation-dependent changes in subcellular localization and interactions with co-regulators . Although our results show that Pdx-1 also regulates Slc30a8 gene expression, studies in INS-1E cells surprisingly demonstrated that glucose decreases Slc30a8 gene expression . Whether this negative effect is also mediated through Pdx-1 remains to be determined.
Pdx-1 is not only critical for proper pancreas development (Pdx-1-null mice are apancreatic and die soon after birth ), but it is also important for proper islet function in the adult. Heterozygous mutations in the Pdx-1 gene in humans have been shown to result in MODY-4 (Maturity Onset Diabetes of the Young type 4), a rare monogenic form of diabetes characterized by a loss of insulin production . Our results suggest that a reduction in Pdx-1 levels will result in a reduction in Slc30a8 gene expression, which may contribute to the phenotype observed in individuals with MODY-4.
It has been suggested that ZnT-8 is responsible for providing zinc to allow for proper insulin maturation, storage and secretion . This concept is supported by the observed reduction in fasting plasma insulin in mice lacking ZnT-8 as well as glucose-stimulated insulin secretion in islets isolated from those mice . Surprisingly, however, mice in which the Slc30a8 gene was globally deleted have normal glucose tolerance [9,19,20] and mice with a β-cell-specific Slc30a8 gene deletion have only mildly impaired glucose tolerance . The observations made in mice in which the Slc30a8 gene was globally deleted raise two key questions. First, how do these knockout mice maintain normal glucose tolerance despite impaired insulin secretion? And secondly, how do polymorphisms in the SLC30A8 gene confer increased susceptibility to the development of Type 2 diabetes if glucose tolerance is not affected by the absence of ZnT-8? Future studies with these Slc30a8-knockout mice will no doubt address both of these questions.
Lynley Pound performed most of the gel-retardation and fusion gene studies and wrote parts of the manuscript. Yan Hang performed the ChIP assay studies and wrote parts of the manuscript. Suparna Sarkar designed the developmental islet gene expression studies and wrote parts of the manuscript. Yingda Wang assisted with the fusion gene expression studies. Laurel Milam assisted with the fusion gene expression studies. James Oeser assisted with the fusion gene expression studies. Richard Printz assisted with the fusion gene expression studies. Catherine Lee assisted with the developmental islet gene expression studies. Roland Stein was the primary investigator for the ChIP studies and wrote parts of the manuscript. John Hutton was the primary investigator for the developmental islet gene expression studies and wrote parts of the manuscript. Richard O'Brien was the primary investigator for the gel-retardation and fusion gene studies and wrote parts of the manuscript.
Research in the laboratory of R.O'B. was supported by the National Institutes of Health [grant numbers DK76027, P60 DK20593], the latter supports the Vanderbilt Diabetes Center Core Laboratory. Research in the laboratory of R.S. was supported by the National Institutes of Health [grant numbers P01 DK42502, DK50203] and by the American Diabetes Association [grant number 7-04-RA-116]. Research in the laboratory of J.C.H. was supported by a Juvenile Diabetes Research Foundation Autoimmunity Prevention Center grant, the National Institutes of Health [grant number DK076027], and the Barbara Davis Center Diabetes and Endocrinology Research Center [grant number P30 DK57516]. L.D.P. was supported by the Vanderbilt Molecular Endocrinology Training Program [grant number 5T32 DK07563]. S.A.S. was supported by the National Institute of Diabetes and Digestive and Kidney Diseases [grant number K01DK080193], and the Juvenile Diabetes Research Foundation [grant number 1-2008-1021].
We thank Dr Maureen Gannon (Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, TN, U.S.A.) for useful comments on pancreatic islet development and Dr Shimon Efrat (Department of Human Molecular Genetics and Biochemistry, Sackler School of Medicine, Tel Aviv University, Ramat Aviv, Tel Aviv, Israel) for providing the βTC-3 and αTC-6 cell lines.
Abbreviations: AMCA, 7-amino-4-methylcoumarin-3-acetic acid; ChIP, chromatin immunoprecipitation; CT, cycle threshold; Cy2, carbocyanine; Cy3, indocarbocyanine; Cy5, indodicarbocyanine; DMEM, Dulbecco's modified Eagle's medium; DTT, dithiothreitol; e, embryonic day; Gapdh, glyceraldehyde-3-phosphate dehydrogenase; MODY-4, Maturity Onset Diabetes of the Young type 4; RT, reverse transcription; TGE buffer, Tris Base, glycine and EDTA buffer; TK, thymidine kinase; USF-1, upstream stimulatory factor-1; WT, wild-type; ZnT-8, zinc transporter-8
- © The Authors Journal compilation © 2011 Biochemical Society