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The murine surfactant-associated protein B (Sftpb) gene promoter, spanning nucleotides −653 to +42, is composed of functionally distinct proximal and distal regions. Although both regions contain consensus/putative activator protein 1 (AP-1) sites, the distal, but not the proximal, region mediates the inhibition by jun proto-oncogene (JUN) of Sftpb promoter activity. In transient cotransfection assays, JUN inhibited the luciferase reporter activity of plasmid constructs containing Sftpb promoter fragments that lacked the distal putative AP-1 site, indicating that another regulatory motif mediates JUN-dependent inhibition. Electrophoretic mobility shift assays and in silico analyses identified a DNA target sequence (Sftpb nucleotides −339 to −316) and transcription factors that regulate Sftpb promoter activity. The identified sequence contains a CCAAT/enhancer-binding protein (C/EBP) consensus recognition element. Mutation of the site reduced Sftpb promoter activity and sensitivity to inhibition by JUN. Purified recombinant JUN, which did not recognize the −339 to −316 target sequence when added alone, supershifted the mobility of in vitro translated C/EBP-α and C/EBP-β proteins complexed with the identified cis-regulatory element. These findings support the idea that heterodimerization between JUN and C/EBP-α and/or C/EBP-β targets JUN to the Sftpb promoter, thereby mediating its inhibitory regulatory role.
One of the key events in acute lung injury is the loss of functional surfactant. Thus, surfactant has long been investigated in the treatment of acute lung injury. However, surfactant replacement has yet to be demonstrated as an effective therapy for acute lung injury. An alternative strategy may involve the development of treatments that maintain or restore the production of endogenous surfactant. We analyzed the core surfactant-associated protein B (Sftpb) promoter to identify transcription factors and recognition sites that contribute to the inhibition of SFTPB.
The Sftpb gene product (SFTPB) is one of the protein components of pulmonary surfactant. The other protein components include SFTPA, SFTPC, and SFTPD. These proteins represent a small fraction (~ 10%) of surfactant, and were initially considered contaminants (1). SFTPB and SFTPC constitute approximately 1% of the total surfactant mass (2). However, the surfactant-associated proteins, and in particular SFTPB, are essential for normal lung function and survival. Because SFTPB is essential for surfactant function, lamellar body formation, and the processing of SFTPC, SFTPB deficiency causes congential alveolar proteinosis and respiratory failure (3–6).
The expression levels of SFTPB may be reduced because of genetic disorders or during acute lung injury after exposure to toxicants. Recently, we reported that the maintenance of SFTPB expression is critical to survival during nickel-induced lung injury in mice (7). Nickel increased jun proto-oncogene (JUN) transcripts in murine lung and alveolar type II epithelial cells (MLE-15), and the induction of JUN inhibited Sftpb gene promoter activity. Studies aimed at understanding the molecular basis of SFTPB inhibition may thus advance our ability to develop strategies that reverse the loss of SFTPB during lung injury.
The 5′-flanking region of the murine Sftpb gene contains functionally important proximal (nucleotides −132 to −1) and distal (nucleotides −382 to −283) promoter regions (8). Both promoter regions contain a number of transcription factor recognition sites, including activator protein 1 (AP-1) recognition sequences. JUN-related proteins bind to and activate AP-1 regulatory elements in the promoter and enhancer regions of several mammalian genes (9). Despite the presence of a consensus AP-1 site in the Sftpb proximal promoter region and a putative AP-1 site in the distal promoter region, we found that the distal, but not the proximal, Sftpb promoter region mediated the JUN-dependent inhibition of promoter activity (7). The mechanism of the JUN-mediated inhibition of Sftpb transcription is unclear.
The transcription factor JUN participates in regulating a variety of biological processes, including cell proliferation, survival, apoptosis, tumorigenesis, tissue remodeling, and development (10–16). JUN controls these diverse processes through its ability to regulate the transcription and activity of numerous target genes and gene products. JUN, which was originally identified as AP-1 (17–19), belongs to a large family of proteins known as bZIP. These bZIP proteins are functionally related proteins with homologous sequences containing a basic DNA-binding domain and a leucine zipper region. JUN interacts with more than 50 related bZIP proteins and with structurally unrelated transcription factors, forming homodimeric and heterodimeric protein complexes (20, 21). The multiplicity of combinatorial JUN–protein interactions and the sequence compositions of DNA recognition sites determine target-gene specificity and regulatory selectivity in a cell type–dependent manner.
Another group within the bZIP transcription factor family is the CCAAT/enhancer-binding protein (C/EBP) subfamily. C/EBP subfamily members (α, β, and δ), in addition to C/EBP-γ and C/EBP-ζ, are expressed and play important roles in lung development, gene regulation, and acute lung injury (22–26). The deletion of C/EBP-α is perinatally lethal, in part because of lung abnormalities attributable to the hyperproliferation of alveolar type II cells (27). C/EBP-α–deficient newborn mice also exhibited increased surfactant associated protein A, B, and C mRNA, indicating a role for C/EBP-α in the control of alveolar cell proliferation/differentiation and the regulation of lung-specific target genes (28). In contrast, a deficiency of C/EBP-β and C/EBP-δ did not lead to lung abnormalities (29). However, the expression levels of C/EBP-β, C/EBP-δ, and C/EBP-regulated inflammatory mediators are increased in LPS-induced, bleomycin-induced, and oxidative stress–induced acute lung injury (26). Here, we investigated the role of C/EBP proteins in the inhibition by JUN of Sftpb promoter activity.
To analyze Sftpb promoter regulation, the region spanning nucleotides −653 to +42 (numbering according to Bruno and colleagues (8)) and its mutant variants were inserted into the luciferase reporter pGL4–10 (catalogue number E6651; Promega, Madison, WI). The plasmids pCMV6-XL4 and pCMV-Jun (pJun; Origene Technologies, Inc., Rockville, MD) and the luciferase reporters were transfected into MLE-15 cells (a gift of Dr. Jeffrey Whitsett) (30). The efficiency of transfection was normalized using pCMV-β–Gal. To determine promoter luciferase reporter activity, cells were lysed using Glolysis buffer, assayed in 96-well plates using the Bright-Glo luciferase or Beta-Glo systems (catalogue numbers E2610 and E4720, respectively; Promega), and luminescence was measured (Fusion α; Packard Bioscience/Perkin Elmer Life and Analytical Science, Waltham, MA) (see the online supplement for additional details).
To investigate protein–promoter binding, biotinylated oligonucleotides were used for electrophoretic mobility shift assays (EMSAs). A probe containing a binding site for AP-1 JUN homodimer and JUN/FOS heterodimeric complexes (5′-CGCTTGATGACTCAGCCGGAA-3′ annealed with 3′-GCGAACTACTGAGTCGGCCTT-5′) served as a positive control for purified recombinant JUN binding. Nuclear protein extracts (2.5 μg) were incubated with biotinylated probes and competitors, and were analyzed (see the online supplement for additional details).
To examine whether the bZIP proteins D site albumin promoter binding protein (DBP), C/EBP-α, and C/EBP-β bind to the endogenous Sftpb promoter, chromatin immunoprecipitation (ChIP) was performed with MLE-15 chromatin (ChIP-IT Express, catalogue number 53008; Active Motif, Inc., Carlsbad, CA) (see the online supplement for additional details) and control rabbit IgG (sc-2027), anti–C/EBP-α (sc-61), anti–C/EBP-β (sc-150), or anti-DBP (sc-98411) antibodies (Santa Cruz Biotechnology, Inc., Santa Cruz, CA). The immunoprecipitated chromatin, after repeated washings, was eluted, reverse cross-linked, and treated with proteinase K. The supernatant and eluate fractions were analyzed by PCR amplification for the Sftpb promoter region −159 to −541, using the primer pair forward 5′-CCACAGGGGACACAGAAATC-3′ and reverse 5′-CGATGTCGGTTCCTAGTCCT-3′ (31).
C/EBP-α and C/EBP-β cDNA expression constructs (plasmids 12550 and 12557, respectively; Addgene, Cambridge, MA) and negative control pSP72 (catalogue number P2191; Promega) were linearized to produce in vitro translated proteins (catalogue number L4610; Promega). In addition, full-length Dbp (catalogue number 4195116), NKX2–1 (catalogue number 3941576), POU2F1 (catalogue number 2966289), and Jund (catalogue number 4456297) cDNAs (Open Biosystems/Thermo Scientific, Huntsville, AL) were subcloned into pSP72 for coupled in vitro transcription/translation. The reactions were incubated for 90 minutes at 30°C. For EMSA analysis, 1 μl of the transcription/translation product that had been diluted 4-fold or 8-fold was used.
Groups were compared by one-way ANOVA with the Holm-Sidak all pairwise multiple comparison procedure (SigmaStat Program; SPSS, Inc., Chicago, IL). Relative luciferase activity units of each Sftpb promoter reporter construct are expressed as folds of the vector pGL4–10-ΔBgl II/Hind III or percentages of control values. Transient reporter assays were performed at least three times each, in triplicate or more. Results are expressed as means ± SE, and P < 0.05 was considered significantly different from the appropriate control.
Previous studies reported that the distal Sftpb promoter region mediated the inhibition by JUN of Sftpb promoter activity (34). We further demonstrated that JUN inhibited the distal, but not the proximal, promoter region (7). Because the Sftpb distal promoter region contains a putative AP-1 site, whereas the proximal region contains a consensus recognition site (nucleotide sequences −370 to −364 and −16 to −10, respectively), the mechanism underlying JUN's regulatory selectivity for the distal region was not known. To investigate the mechanism of JUN's inhibition of Sftpb promoter activity, luciferase reporter constructs under the control of the Sftpb promoter region, encompassing nucleotides −653 to +42 and mutant variants (Figure 1A), were analyzed. The enzyme reporter activity of the distal promoter region −653 to −194 was greater than the activity of the proximal promoter region −198 to +42 (4.6-fold versus 1.4-fold, respectively) compared with the control vector (Figure 1B). Upon subsequent deletion of the −653 to −194 promoter fragment, the reporter activity of the −400 to −275 was enhanced (4.6-fold versus 7.2-fold, respectively), whereas reporter activity of the promoter fragments −653 to −401 and −274 to −194 was reduced compared with the −653 to −194 fragment. These results indicate the presence of inhibitory cis-acting regulatory sequences in the −653 to −401 or −274 to −194 promoter regions. In contrast to the −653 to −194 fragment, deletion of the −198 to +42 promoter region reduced reporter activity. These results demonstrate that both the proximal and distal Sftpb promoter regions are functionally active and distinguishable, enabling further investigation of the molecular basis of the inhibition by JUN of Sftpb promoter activity.
A previous study suggested that the distal promoter region contained an AP-1 element that is part of a composite binding site wherein AP-1, the cyclic AMP response element binding protein (CREB), thyroid transcription factor–1 (also known as NKX2–1), and nuclear factor I (NF1) (Figure 1C) interact (34). The nucleotide sequence of the Sftpb distal putative AP-1 site (TGCGTCA) differs from that of the proximal AP-1 site (TGACTCA) in the third and fourth nucleotides, raising the possibility that this property may underlie the selective JUN inhibition on the distal compared with the proximal promoter region. To investigate the contribution of the distal putative AP-1 site to JUN's inhibition of Sftpb promoter activity, a reporter construct with point mutations in the distal AP-1 site was generated. Dose-dependently, JUN inhibited both the wild-type and the AP-1 mutant −400 to −275 promoter reporters (pGL4−400/−275, pGL4−400/−275AP-1m), but not the proximal promoter reporter (pGL4−102/+42) (Figure 1D).
The protein JUN represses glucocorticoid-receptor and retinoic acid receptor gene regulatory activities by direct protein–protein interaction (35, 36). In a recent study (37), interactions of the TGF-β signaling protein SMAD3 with NKX2–1 and FOXA1 reduced binding to cognate DNA sites, leading to Sftpb gene repression by TGF-β. Retinoic acid and NKX2–1 recognition elements play important roles in Sftpb gene regulation (38–40). One of the NKX2–1 consensus core sites in the distal Sftpb promoter region overlaps the putative AP-1 site and retinoic acid receptor sites. To investigate the contribution of NKX2–1 recognition sites to JUN inhibition, a reporter with point mutations in the NKX2–1 sites (pGL4−400/−275 NKX2–1m; Figure 2A) was constructed. The mutant construct exhibited reduced reporter activity. The treatment of transfected MLE-15 cells with all trans-retinoic acid stimulated wild-type and mutant reporter activity, which was inhibited by JUN (Figure 2B).
To rule out the possibility that point mutations neither abolished the binding of an inhibitory AP-1 complex nor interfered with protein–protein interactions, rendering mutant reporter activity sensitive to JUN inhibition, we generated deletion mutants lacking the AP-1 and upstream NKX2–1 consensus core sites. Further deletion of the distal reporter pGL4−400/−275 reduced reporter activity. Moreover, despite the lack of a putative AP-1 site, the deletion reporters remained responsive to inhibition by JUN (Figures 3A and 3B). These results suggest that JUN exerts its inhibitory effect either through Sftpb promoter sites independent of the targeted putative AP-1 recognition sequence, or through protein–protein interactions.
After finding that the Sftpb distal putative AP-1 and NKX2–1 recognition sites may not be critical for JUN inhibition, we sought to determine whether JUN directly or indirectly influenced the formation of DNA–protein complexes. Oligonucleotide probes (24-mer) spanning the Sftpb promoter region −375 to −275 were incubated in the absence or presence of recombinant JUN, with or without MLE-15 cell nuclear extracts, and were analyzed by EMSAs (Figure 4A). All probes formed DNA–protein complexes. The recombinant JUN, when used alone, interacted with an AP-1 consensus oligonucleotide probe included as a positive control (Figure 4A, lane 16), whereas no interaction was evident with Sftpb promoter–derived oligonucleotides (Figure 4A, lanes 1, 4, 7, 10, and 13). However, the presence of recombinant JUN increased the intensity of the probe–protein complexes formed by incubating the Sftpb oligonucleotide probe −339/−316 with MLE-15 nuclear protein extract (in particular, the slow-migrating complex) (Figure 4A, lane 9, arrow).
To identify potential transcription factor binding sites in Sftpb promoter region −339 to −316, in silico analysis was performed using TESS (32) and JASPAR (33). Several transcription factor recognition sites were predicted (ABF1, DBP, POU1F1a, EFII, HOXA5, GAL4, DDIT3C/EBP-α, BRCA1, NFIL3, HLF, POU5F1, C/EBP-α, FOXL1, SOX2, GATA2, HLTF, TBP, NKX2–5, FOXC1, EN1, ZNF354C, MZF1_1–4, SPIB, and ETS1). To locate regions within the 24-mer oligonucleotide that may be critical to the formation of DNA–protein complexes, mutations were introduced in the −339/−316 oligonucleotide and designated m4,7,8, m12,13, and m20,21 (Figure 4B). To test the effects of the mutations on the formation of DNA–protein complexes, a 100-fold molar excess of unlabeled wild-type and mutant oligonucleotide competitors was used. The formation of faster and slower migrating complexes was inhibited by wild-type and m20,21 oligonucleotide −339/−316 (Figure 4B, lanes 3 and 6). In contrast, oligonucleotides −339/−316 m4,7,8 and m12,13 inhibited the formation of complexes differentially. Whereas −339/−316 m4,7,8 inhibited the faster migrating complex, −339/−316 m12,13 inhibited the slower migrating complex (Figure 4B, lanes 4 and 5). These results suggested the presence of multiple protein species with partial selectivity to subregions of the −339/−316 region of the Sftpb promoter and the presence of exogenously added recombinant JUN modulated DNA–protein interactions.
The Sftpb promoter region −339 to −316 contained nucleotide sequences that highly matched the consensus recognition site for the D-site albumin promoter binding protein (DBP, a member of the proline-rich and acid-rich bZIP [PAR-bZIP] protein subfamily) and C/EBP-α transcription factor (a member of the C/EBP subfamily) (Figure 5A) (41, 42). The putative DBP and C/EBP recognition elements were selected for further analysis because both DBP and the C/EBP proteins belong to the bZIP protein family, of which JUN is a member. Members of different bZIP protein subfamilies homodimerize and heterodimerize, expanding the repertoire of target sites recognized by bZIP proteins.
To examine the role of the putative DBP and C/EBP site in the Sftpb promoter, we generated a reporter construct containing point mutations (pGL4−653/+42 C/EBPm; Figure 5A). The mutations introduced were intended to target the two halves of the recognition site, and are different from the mutations used in the competitive EMSA (Figure 4B). The wild-type and mutant reporter constructs were transfected into MLE-15 cells in the presence or absence of the JUN expression plasmid pJun (Figure 5B). Mutagenesis of the putative DBP and C/EBP site reduced Sftpb promoter activity by 4.5-fold, indicating that this region plays a critical role in regulating Sftpb promoter activity. Further, the pGL4−653/+42 C/EBPm reporter was less sensitive to JUN-mediated inhibition (Figure 5B). These results suggested that JUN forms complexes with Sftpb gene transactivators or repressors.
To examine whether the bZIP proteins DBP, C/EBP-α, and C/EBP-β bind to the endogenous Sftpb promoter, ChIP was used. The DNA–protein complex immunoprecipitated using anti–C/EBP-α and anti–C/EBP-β antibodies was enriched compared with either control IgG or anti-DBP antibodies, as determined by PCR analysis (Figure 6). These results suggest that C/EBP-α and C/EBP-β proteins bind to the murine Sftpb promoter.
Because of the DNA fragment sizes of the chromatin sonicate used as a template for PCR analysis (100 to 1,000 bp) in the ChIP assay and the presence of multiple putative C/EBP sites in the Sftpb promoter, the exact location of the region mediating C/EBP binding could not be determined using ChIP. EMSA was used to demonstrate direct C/EBP protein binding to the Sftpb −339/−316 region in which C/EBP-α and C/EBP-β proteins were expressed, using a rabbit reticulocyte lysate system, and incubated with biotinylated probe −339/−316. The presence of C/EBP-α or C/EBP-β translation products shifted probe mobility (Figure 7A, lanes 3 and 5), and complex formation was competed by 100-fold excess unbiotinylated −339/−316 oligonucleotide (Figure 7A, lanes 4 and 6). In contrast, the nonspecific complex formation detected in the negative control sample was not competed by the addition of unbiotinylated oligonucleotide (Figure 7A, lane 2).
To test whether C/EBP binding to the promoter region −339/−316 mediated JUN binding, the in vitro translation products were preincubated with purified recombinant JUN. The presence of recombinant JUN supershifted the mobility of the C/EBP-DNA complex (Figure 7B, lanes 4 and 6). These results, in combination with the effect of recombinant JUN on EMSAs of nuclear proteins (Figure 4), suggest that C/EBP-α and/or C/EBP-β proteins bind to the identified Sftpb promoter region, and JUN binding is mediated through the formation of heteromeric complexes.
In addition, DBP, NKX2–1, POU2F1, and JUND binding to the Sftpb −339/−316 probe was examined by EMSA, because one of the putative NKX2–1 sites overlaps the C/EBP site, and JUND and POU2F1 (also known as OCT1) regulate Sftpb and Clara cell secretory protein genes, respectively (34, 43). DBP, NKX2–1, POU2F1, and JUND translation products were incubated with the Sftpb −339/−316 region and analyzed by EMSA. DBP, but not NKX2.1, POU2F1, or JUND, bound the −339/−316 oligonucleotide (Figure 7C).
To examine DBP binding further, the formation of DBP–DNA complexes in the absence or presence of JUN was compared. The migration pattern of the DBP-biotinylated oligonucleotide complex remained similar in the absence or presence of JUN (Figure 7D). The ability of DBP, in addition to C/EBP-α and C/EBP-β, to interact with the Sftpb −339/−316 region raises the possibility that other transcription factors or bZIP family members could bind to the same site.
SFTPB is critical in maintaining lung function, because SFTPB-deficient mice die of respiratory failure shortly after birth (3–6). One of the key events in acute lung injury is the loss of functional surfactant. Thus, surfactant has long been investigated as a treatment for acute lung injury. Surfactant replacement, however, has yet to be demonstrated as an effective therapy for acute lung injury because of immense hurdles in its administration (44). An alternative strategy may involve the development of treatments that maintain or restore endogenous surfactant production. We previously reported that in a murine model of acute lung injury, the induction of JUN was associated with a diminution of SFTPB expression (7). SFTPB expression was maintained in resistant, compared with sensitive, murine strains, and inducible SFTPB expression increased the survival of mice (7). The present work focused on analyses of the core Sftpb promoter, to identify transcription factor recognition sites that contribute to the JUN-mediated inhibition of SFTPB.
The murine Sftpb promoter, spanning nucleotides −653 to +42, contains two functionally distinguishable proximal (−132 to −1) and distal (−382 to −283) promoter regions (8). The distal promoter region can be transcriptionally active in the absence of the proximal promoter region. The distal promoter region contains a putative initiator sequence (CATTCTG) at nucleotides −286 to −280. This initiator element, which was originally identified in the TATA-less murine terminal deoxynucleotidyl transferase gene, encompasses the transcription start site and can direct basal transcription (45). As determined by primer extension (8) and expressed-sequence Tag (EST) database analyses, the SFTPB mRNA 5′ untranslated region contains ≤14–16 nucleotides. However, basal promoter activity was lost with the deletion of promoter sequences from −415 to −353 (34), demonstrating the critical role of the distal promoter region. Although the occurrence of an alternative SFTPB transcriptional initiation site is unknown, the functionality of the distal region as a promoter provided a useful tool for analyzing the role of its putative transcription factor recognition sites, independent of those in the proximal region.
The Sftpb promoter contains AP-1, NKX2–1, trans-acting transcription factors 1 and 3 (SP1, SP3), hepatocyte nuclear factor 3 (HNF3), retinoic acid receptor, and other recognition elements (8, 34, 38, 40, 46). Although JUN can activate numerous genes by binding to AP-1 recognition elements, it can also inhibit the induction of other genes by a different mechanism. JUN inhibits the induction of the bone γ-carboxyglutamate protein (osteocalcin) gene by retinoic acid and vitamin D3 (35) and the induction of the kallikrein-related peptidase 3 (prostate-specific antigen) gene by androgen (47). Direct interactions between JUN and the receptors for vitamin D3 or androgen inhibit the induction of target genes.
The Sftpb proximal and distal promoter regions contain putative AP-1 sites. The proximal AP-1 site is identical to the optimal consensus AP-1 site (TGACTCA), whereas the distal AP-1 site (TGCGTCA) differs by two nucleotides. In addition, the distal CREB site differs from the consensus CREB site (TGACGTCA). However, these nucleotide sequence differences could not explain JUN's ability to inhibit the distal, but not the proximal, promoter region. The patterns of JUN inhibition of the distal AP-1 wild-type and point mutant reporters were comparable. To rule out the possibility that the introduced mutations may not have sufficiently altered the mode of protein–DNA interactions, we investigated the effects of JUN co-expression on reporter constructs that lacked the distal putative AP-1 site. Despite the absence of the putative AP-1 site, JUN inhibited reporter activity. These results suggest that the presence of the putative AP-1 site in the distal promoter region is not required for the inhibition by JUN of Sftpb promoter activity, raising the possibility of protein–protein interactions as a mediator of JUN's inhibitory effect.
Our conclusion about the role of the Sftpb AP-1 sites contrasts with those of previous studies (34). Sever-Chroneos and colleagues (34) observed that mutation in the distal AP-1 binding site increased basal promoter activity fivefold in MLE-15 cells. In addition, they concluded that the distal AP-1 element is involved in, but is not sufficient for, the inhibition by JUN of promoter activity. In our analysis, although deletion of the distal element containing the overlapping AP1/NKX2–1 recognition sites reduced promoter activity, mutation of the AP-1 site did not induce basal promoter activity or reverse JUN inhibition. It is unclear whether the use of the luciferase reporter (half-life of approximately 0.84 hours) (48) versus the CAT reporter (half-life of approximately 16 hours) (49) and other experimental variations (e.g., the use of different promoter fragments) contributed to the discrepancies observed. In support of our observations, a genome-wide analysis of the frequency and distribution of AP-1 sites indicated that the number of AP-1–regulated genes identified is far smaller than the number of genes containing potential AP-1 sites, and that not all AP-1 sites are activated in a given cell under a given condition (50, 51).
In addition, the interaction of JUN with NKX2–1 appears unlikely to inhibit Sftpb promoter activity. Point mutations at the NKX2–1 sites in the distal promoter reduced reporter activity, but the mutants remained sensitive to inhibition by JUN, suggesting that other recognition sites or regulatory factors mediated the JUN-mediated inhibition of Sftpb.
Mobility shift assays indicated that JUN may target the Sftpb promoter by binding to a site within the −339/−316 region. Nucleotide sequence analysis for potential transcription factor binding sites in the −339/−316 Sftpb promoter region predicted recognition sites for DBP and C/EBP. This was a pertinent finding because DBP and the C/EBPs, like JUN, belong to the bZIP protein family. The contribution of the identified site to the regulation of Sftpb promoter activity was demonstrated in MLE-15 cells transfected with pGL4−653/+42 wild-type and mutant reporters. Mutagenesis of the putative recognition site reduced Sftpb promoter activity and sensitivity to JUN-mediated inhibition.
Endogenous DBP or C/EBP binding to the Sftpb promoter was investigated by chromatin immunoprecipitation. Immunoprecipitation of MLE-15 chromatin sonicate with anti-DBP antibodies did not enrich the Sftpb promoter PCR amplification product, suggesting that DBP does not associate with Sftpb promoter in vivo, or that the abundance of DBP–Sftpb promoter complexes formed in vivo does not permit detection by this method. In contrast, C/EBP-α and C/EBP-β binding to the Sftpb promoter was evidenced by the enrichment of chromatin immunoprecipitation.
JUN modulates gene transcription by forming homodimeric or heterodimeric complexes (52, 53). Our results indicate that JUN may not inhibit Sftpb promoter activity by forming homodimers. The recombinant JUN protein formed a complex with the consensus AP-1 oligonucleotide, but with none of the Sftpb-derived oligonucleotides spanning the Sftpb promoter region −375 to −275. However, in the presence of MLE-15 nuclear protein extract, the addition of JUN increased the intensity of DNA–protein complexes formed with the −339/−316 oligonucleotide probe. Further analysis, using point mutant oligonucleotides, suggested that multiple transcription factors bound to the −339/−316 probe.
Previous studies demonstrated that C/EBP-β and JUN interacted through their bZIP region in the absence of DNA. Such interactions altered the specificity of DNA binding (54). In our EMSA analyses, C/EBP binding to the Sftpb −339/−316 region, to which JUN by itself cannot bind, was shifted in the presence of purified recombinant JUN protein. These results suggest that the Sftpb −339/−316 region is recognized by C/EBP-α and/or C/EBP-β dimers or C/EBP-α and/or C/EBP-β/JUN heterodimers, and that the formation of heteromeric complexes is key to Sftpb promoter targeting by JUN. The PAR-bZIP DBP also bound to the −339/−316 probe, raising the possibility that other transcription factors or bZIP proteins could bind to the same site.
In conclusion, we analyzed the murine Sftpb promoter encompassing nucleotides −653 to +42. Deletion and site-directed Sftpb promoter reporter mutants and EMSAs indicate that the distal Sftpb promoter region −339 to −316 is a critical regulatory element. Mutagenesis in this region, which contains a C/EBP recognition site, reduced Sftpb promoter activity and sensitivity to JUN-mediated inhibition. Endogenous C/EBP-α and C/EBP-β bind to the Sftpb promoter. The transcription factor JUN can partner with C/EBP-α or c/EBP-β, bind to the identified cis-acting regulatory DNA site, and inhibit Sftpb promoter activity. Thus, the inhibition by JUN of the Sftpb promoter is likely indirect and dependent on heteromeric complex formation.
This study was supported by National Institutes of Health grants ES015675, HL077763, and HL085655 (G.D.L.).
This article has an online supplement, which is accessible from this issue's table of contents at www.atsjournals.org
Originally Published in Press as DOI: 10.1165/rcmb.2010-0260OC on December 10, 2010
Author Disclosure: None of the authors has a financial relationship with a commercial entity that has an interest in the subject of this manuscript.