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Crosstalk between DNA methylation and histone acetylation triggers GDNF high transcription in glioblastoma cells
Clinical Epigenetics volume 12, Article number: 47 (2020)
Glial cell line-derived neurotrophic factor (GDNF) is highly expressed in glioblastoma (GBM) and blocking its expression can inhibit the initiation and development of GBM. GDNF is a dual promoter gene, and the promoter II with two enhancers and two silencers plays a major role in transcription initiation. We had previously reported that histone hyperacetylation and DNA hypermethylation in GDNF promoter II region result in high transcription of GDNF in GBM cells, but the mechanism remains unclear. In this study, we investigated whether these modifications synergistically regulate high GDNF transcription in GBM.
Cyclic AMP response element binding protein (CREB) expression and phosphorylation at S133 were significantly increased in human GBM tissues and GBM cell lines (U251 and U343). In U251 GBM cells, high expressed CREB significantly enhanced GDNF transcription and promoter II activity. CREB regulated GDNF transcription via the cyclic AMP response elements (CREs) in enhancer II and silencer II of GDNF promoter II. However, the two CREs played opposite regulatory roles. Interestingly, hypermethylation of CRE in silencer II occurred in GBM tissues and cells which led to decreased and increased phosphorylated CREB (pCREB) binding to silencer II and enhancer II, respectively. Moreover, pCREB recruited CREB binding protein (CBP) with histone acetylase activity to the CRE of GDNF enhancer II, thereby increasing histone H3 acetylation and RNA polymerase II recruitment there and at the transcription start site (TSS), and promoted GDNF high transcription in U251 cells. The results indicated that high GDNF transcription was attributable to DNA hypermethylation in CRE of GDNF silencer II increasing pCREB binding to CRE in enhancer II, which enhanced CBP recruitment, histone H3 acetylation, and RNA polymerase II recruitment there and at the TSS.
Our results demonstrate that pCREB-induced crosstalk between DNA methylation and histone acetylation at the GDNF promoter II enhanced GDNF high transcription, providing a new perspective for GBM treatment.
Glial cell line-derived neurotrophic factor (GDNF) is a member of the transforming growth factor (TGF-β) superfamily. The GDNF gene was initially cloned from the rat B49 glial cell line . In human cells, GDNF is a single-copy gene with two promoters. Promoter I is located upstream of exon IV. Promoter II is located upstream of exon I and contains two enhancers, two silencers, and various transcription factor binding sites; it plays a major role in transcription initiation [2, 3]. Numerous studies have shown that as an important neurotrophic factor for promoting embryonic midbrain dopaminergic neuron survival and differentiation, GDNF also has nutritional and protective effects on peripheral sympathetic, parasympathetic, sensory, and motor neurons [4,5,6], participating in the regulation of renal cell differentiation and spermatogenesis [7,8,9]. GDNF has been well-known as a specific physiological neurotrophic factor and a differentiation-promoting factor for many years. However, Wiesenhofer et al. changed the understanding of GDNF when they reported abnormally increased GDNF expression in primary gliomas and multiple GBM cell lines, which was positively correlated with pathological grade . Subsequent studies have demonstrated that abnormally increased GDNF is a powerful factor in promoting GBM cell proliferation and migration [11, 12]. Knockdown of GDNF or its binding receptor, GFRα1, effectively inhibits GBM progression [13, 14]. High GDNF concentrations protect astrocytes against DNA damage-induced apoptosis . In addition, GDNF is also abnormally expressed in other malignant tumors such as pancreatic, breast, and prostate cancers, which promotes invasive tumor cell growth . Abnormally high expression of GDNF is closely related to the initiation and development of malignant tumors. However, little is known about the regulatory mechanism(s). Our previous study suggested that high GDNF expression in GBM cells is mainly caused by its high transcription rather than gene mutations . Moreover, abnormal DNA methylation and histone acetylation in GDNF promoter II exist in GBM tissue and cells, both of which are involved in regulating high GDNF transcription [18, 19]. However, it is not clear whether there is crosstalk between the two modifications and if so, what the mechanism is.
Uchida et al. recently reported that GDNF expression was synergistically regulated by DNA methylation and various histone modifications in different brain regions of mice . Zhao et al. pointed out that the nuclear transcription factor, peroxisome proliferator-activated receptor γ was involved in the transcriptional regulation of CCAAT/enhancer binding protein α (C/EBPα) in bone marrow stromal cells as a cofactor for DNA methylation and histone acetylation in the C/EBPα promoter . In addition, our previous studies indicated that abnormal epigenetic modifications in GBM cells affect the binding of multiple transcription factors to GDNF promoter II [17, 22]. Thus, we speculate that DNA methylation and histone acetylation may synergistically regulate high GDNF transcription through the abnormal binding of transcription factors. The cyclic AMP response element binding protein (CREB) is a methylation-sensitive nuclear transcription factor involved in tumor cell immortalization and transformation. It binds to the cyclic AMP response element (CRE) in the promoter as a homodimer or heterodimer and activates gene expression by binding to the KID-interacting domain (KIX) in the CREB binding protein (CBP) via its own kinase-inducible domain (KID) [23, 24]. Due to its intrinsic histone acetylase activity, CBP can efficiently acetylate histones H3 and H4 [25,26,27], directly stimulate the recruitment of RNA polymerase II, and loosen chromatin (especially the first nucleosome) at the transcription start site (TSS) by histone acetylation, thereby promoting eukaryotic gene expression . Our previous studies revealed that hyperacetylation of histone H3 in GDNF promoter II in C6 GBM cells was significantly reduced by a CBP inhibitor, curcumin [19, 22, 29], suggesting that hyperacetylation may be caused by CBP. CREs are present in silencer II and enhancer II of GDNF promoter II, and abnormal methylation of promoter II affects the binding of CREB to promoter II in GBM tissue . A recent study reported abnormally high expression and constitutive activation of CREB in glioma tissues, and latter increased with pathological grade . Moreover, drug-induced phosphorylation of CREB promotes GDNF expression in C6 cells . We hypothesized that CREB may be a coupling factor for DNA methylation and histone acetylation in GDNF promoter II. The abnormal DNA methylation in GDNF promoter II, especially hypermethylation in silencer II, results in selective CREB binding to CRE in enhancer II and increases the acetylation of histone H3 and RNA Pol II recruitment in GDNF promoter II by recruiting CBP, thus increasing GDNF transcription.
To test the above hypothesis, expression of CREB and the effect of CREB on GDNF expression were measured by real-time polymerase chain reaction (PCR), RNA interference (RNAi), and a dual-luciferase reporter system; regulation of GDNF transcription by the CRE in the two cis-acting elements of the GDNF promoter II and the methylation status and CREB binding of the two CREs were assessed by site-directed mutagenesis, CRISPR/Cas9, bisulfite sequencing PCR (BSP), and chromatin immunoprecipitation (ChIP)-PCR; effects of S133 phosphorylated CREB (pCREB) on GDNF transcription and recruitment of CBP were determined by point mutation, co-immunoprecipitation (co-IP), and re-ChIP-PCR; effects of CBP on histone H3 acetylation and RNA polymerase II recruitment in the CRE in enhancer II and the TSS of GDNF were examined by RNAi and ChIP-PCR. Our results reveal the molecular mechanisms of synergistic upregulation of GDNF by DNA methylation and histone acetylation in GBM cells, providing a new target for GBM treatment.
CREB expression in GBM tissues and cell lines is significantly increased and significantly promotes GDNF transcription in GBM cells
Bioinformatics analysis and Baecker et al.  showed a potential binding site, CRE, for the transcription factor, CREB, in both enhancer II and silencer II of GDNF promoter II, and the binding sites located at − 984/− 977 nt and − 311/− 304 nt, respectively (Fig. 1a). To clarify the relationship between CREB and GDNF transcription, CREB expression was interrogated in the Cancer Genome Atlas (TCGA) database, which revealed significantly higher CREB mRNA expression in GBM tissue than in normal brain (NB) tissue (P < 0.01) (Fig. 1b). To verify this result, CREB mRNA and protein expression in NB and low- and high-grade glioma (GBM) tissues were determined by real-time PCR and western blot, respectively. The results showed that CREB mRNA and protein expression were very significantly higher (P < 0.01) in GBM tissue, whereas the increase was not significant (P > 0.05) in low-grade glioma tissue compared with NB tissue (Fig. 1c, d). Furthermore, significantly higher CREB mRNA and protein expression were also observed in the human astroglioma cell lines, U251 and U343, compared to normal human astrocytes (NHA, ScienCell) (P < 0.05, Fig. 1e, f).
To investigate the relationship between highly expressed CREB and GDNF transcription, RNAi knockdown (KD) and protein overexpression (OE) of CREB were performed in U251 GBM cells. CREB mRNA expression was very significantly decreased after lentivirus CREB-KDs infection. The lowest expression was observed in the CREB-KD1 group, which was 61% lower than that of the NC group (P < 0.01) (Fig. 1g). A very significant decrease in CREB protein expression was also observed in this group (P < 0.01) (Fig. 1h). Therefore, CREB-KD1 was used for subsequent knockdown experiments. CREB mRNA and protein expression were very significantly increased after infection with CREB-OE lentivirus (P < 0.01) (Fig. S1A, B). On this basis, we found that GDNF mRNA and protein expression in U251 cells were very significantly decreased by CREB knockdown (P < 0.01) (Fig. 1i-j) and very significantly increased by CREB overexpression (P < 0.01) (Fig. S1C, D), suggesting CREB is involved in regulating GDNF transcription in GBM cells.
To clarify whether CREB regulates GDNF transcription by affecting promoter II activity, the effect of CREB knockdown and protein overexpression on GDNF promoter II activity in U251 cells was analyzed using a dual-luciferase reporter system. GDNF promoter II activity was significantly decreased by CREB knockdown and increased by CREB overexpression (both P < 0.01) (Fig. 1k). To determine whether CREB regulation of GDNF promoter II activity is dependent on its binding to promoter II, wild-type CREB and DNA-binding domain-mutated CREB (KCREB) were overexpressed in U251 cells (Fig. S2). The effect of overexpression of the two types of CREB proteins on GDNF transcription was assessed by real-time PCR. Overexpression of wild-type CREB significantly increased GDNF transcription (P < 0.05); whereas KCREB overexpression did not have a significant effect (P > 0.05) (Fig. 1l). Moreover, overexperession of wild-type CREB significantly increased the binding of CREB to CRE in enhancer II of the GDNF promoter II (P < 0.01) (Fig. 1m), suggesting CREB binding to GDNF promoter II is necessary for regulating GDNF transcription.
CRE in the two different cis-acting elements of GDNF promoter II plays an opposite role in the regulation of GDNF transcription in GBM cells
To determine whether CREB is involved in GDNF transcription through different CREs in GDNF promoter II, we assessed the effect of CRE deletion and mutation in different cis-acting elements on GDNF promoter II activity. The results showed that the activity of GDNF promoter II decreased slightly, but not significantly, following deletion or mutation of both CREs (P > 0.05). In contrast, promoter II activity was significantly increased by the deletion or mutation of CRE in silencer II (P < 0.01) and significantly decreased by that in enhancer II (P < 0.01), indicating that both mutation and deletion can block CREB binding to a specific CRE (Fig. 2a). To further clarify which binding site plays a major role in CREB regulation, we examined the effect of CREB overexpression on the activity of GDNF promoter II with different CRE mutations. Compared with wild-type GDNF promoter II plus EGFP group, promoter activity was significantly increased for the wild-type GDNF promoter II and that containing a CRE mutation in silencer II only and decreased for that containing CRE mutation in enhancer II only by CREB overexpression (P < 0.01), but it did not change significantly for that containing mutations of both CREs (P > 0.05). Compared with the EGFP-NC group with each type of promoter II, CREB overexpression only significantly increased promoter activity for the wild-type GDNF promoter II and that containing CRE mutation in silencer II only (P < 0.01). Compared with wild-type GDNF promoter II overexpressing CREB, promoter activity with CREB overexpression was significantly decreased for GDNF promoter II containing CRE mutation in enhancer II only (P < 0.01) and increased for that containing CRE mutation in silencer II only (P < 0.01). These findings indicate that the binding of CREB to CREs in the two cis-acting elements play opposing role in the regulation of GDNF transcription, and CRE in enhancer II may play a stronger role (Fig. 2b).
To corroborate the above results, we designed and packaged sgRNA lentiviruses, sgRNA-CRE-E and sgRNA-CRE-S, targeting the CRE in GDNF enhancer II and silencer II, respectively (Fig. 2c, Table S4). These were used to infect a U251 cell line stably expressing Cas9 protein (Cas9-U251 cells). The cleavage induced by sgRNA-CRE-E and sgRNA-CRE-S and GDNF transcription was then assessed by CruiserTM assay and real-time PCR. sgRNA-CRE-E and sgRNA-CRE-S were able to direct Cas9 to cleave the CRE in enhancer II and silencer II in Cas9-U251 cells (Fig. 2d). GDNF transcription was significantly decreased and increased by infection with sgRNA-CRE-E (P < 0.05) and sgRNA-CRE-S (P < 0.01), respectively (Fig. 2e).
The binding of CREB to CRE in GDNF enhancer II is significantly increased in GBM cells
To determine whether CREB binds to the CRE in different cis-acting elements of GDNF promoter II in GBM cells, the binding of CREB to the CRE in enhancer II and silencer II in U251 cells was detected by electrophoretic mobility shift assay (EMSA). CREB specifically bound to CRE in GDNF enhancer II and silencer II in vitro, and hypermethylation of silencer II reduced CREB binding (Fig. 3a, b). To further investigate intracellular binding of CREB to the CRE in different cis-acting elements of GDNF promoter II, the binding of CREB to the CRE in enhancer II and silencer II in U251 and NHA cells was detected by ChIP-seq. The results showed that some pileup signals of CREB existed in different cis-acting elements of GDNF promoter, but there was no significant binding peak in U251 and NHA cells after peak calling by MACS2 (Fig. 3c). Then, ChIP-PCR was used to recheck the intracellular binding of CREB to the CRE in different cis-acting elements of GDNF promoter II in U251, U343, and NHA cells. The results showed that CREB bound to CRE in different cis-acting elements of GDNF promoter II to varying degrees; the binding of CREB to CRE in enhancer II was significantly increased (P < 0.05) (Fig. 3d) and that in silencer II was significantly decreased (P < 0.01) (Fig. 3e) in U251 and U343 cells compared with NHA cells; relative binding to enhancer II was significantly increased in U251 and U343 cells (P < 0.01, Fig. 3f).
Hypermethylated CRE occurs in silencer II of GDNF promoter II and promotes CREB-mediated high GDNF transcription in GBM cells
The conserved binding sequence of CREB is 5'-TGACGTCA-3', which contains a CpG dinucleotide that is a DNA methylation-sensitive motif (Fig. 4a). Therefore, CREB binding is sensitive to DNA methylation. We previously reported that the DNA methylation of GDNF enhancer II was unchanged in GBM tissue and cells, whereas hypermethylation occurred in silencer II [17, 18]. To further examine CRE methylation in different cis-acting elements of GDNF promoter II in GBM tissue and cells, DNA methylation of CRE in silencer II and enhancer II of GDNF promoter II was quantitatively assessed in GBM and NB tissues, as well as in U251, U343, and NHA cells. CRE methylation in silencer II of GDNF promoter II was significantly higher in GBM tissue than in NB tissue (P < 0.01), whereas no significant change was observed in enhancer II (P > 0.05, Fig. 4b, c). Similarly, CRE methylation in silencer II of GDNF promoter II was significantly higher in U251 and U343 cells compared to NHA cells (P < 0.01), whereas no significant change was observed in enhancer II (P > 0.05, Fig. 4d, e).
To elucidate the effect of silencer II hypermethylation on CREB-mediated regulation of GDNF transcription, the effect of CREB overexpression on the activity of GDNF promoter II in different methylation patterns was assessed by sequence-specific methylation followed by plasmid recircularization. Circular plasmids containing GDNF promoter II with different methylation patterns were successfully generated (Fig. 4f and Fig. S3). Hypermethylation of silencer II significantly increased GDNF promoter II activity (P < 0.05). CREB overexpression significantly increased the activity of the unmethylated promoter II and hypermethylated silencer II (P < 0.01). Moreover, promoter II with hypermethylated silencer II had significantly higher activity than unmethylated promoter II (Fig. 4g). This suggests that silencer II hypermethylation is involved in CREB-mediated, high GDNF transcription.
pCREB recruits the histone acetylase CBP to CRE in GDNF enhancer II to increase GDNF transcription in GBM cells
S133 phosphorylation is a key modification for CREB regulation of gene transcription . A previous study found that S133 phosphorylation was abnormally increased in GBM tissue and cells , which is consistent with our findings (Fig. 5a). To determine whether CREB regulation of high GDNF transcription is dependent on S133 phosphorylation, the effect of overexpression of wild-type and S133 mutant (CR133) CREBs (Fig. 5b) on GDNF transcription in U251 cells was tested by real-time PCR. GDNF transcription was significantly increased by overexpression of wild-type CREB (P < 0.05) and significantly decreased by CR133 overexpression (P < 0.05, Fig. 5c), indicating that CREB regulation of GDNF transcription is dependent on S133 phosphorylation.
pCREB (S133) is capable of recruiting CBP with histone acetylase activity to promote gene transcription . To determine whether pCREB promotes GDNF transcription by recruiting CBP, the binding of pCREB to CBP in U251 cells was assessed by immunofluorescence and co-IP. Both pCREB and CBP were present in cells and partially overlapped in the nucleus and perinuclear region (Fig. 5d), and pCREB was also able to bind to CBP (Fig. 5e). To clarify whether pCREB can recruit CBP to CRE binding sites in GDNF promoter II, the binding of pCREB to CREs in GDNF promoter II and its recruitment of CBP in U251 and NHA cells were examined by re-ChIP-PCR. pCREB mainly bound to CRE in enhancer II and recruited CBP to this site in both cell lines (Fig. 5f). pCREB binding to CRE and CBP recruitment in GDNF enhancer II was significantly increased in U251 cells compared with NHA cells (P < 0.01); whereas the binding of pCREB to CRE in silencer II was significantly decreased (P < 0.01), and CBP recruitment was decreased but not significantly (Fig. 5g, h).
To confirm that CBP is recruited to GDNF enhancer II by CREB, CBP binding to GDNF enhancer II in U251 cells infected with NC or CREB-KD1 virus was detected by ChIP-PCR. CREB knockdown significantly reduced CBP binding to enhancer II (P < 0.01, Fig. 5i). To confirm that pCREB regulation of GDNF transcription is dependent on CBP recruitment, U251 cells were treated with 0, 10, 25, 50, or 100 μM 2-Naphthol-AS-E phosphate (KG-501, Sigma-Aldrich) for 12, 24, or 36 h to inhibit pCREB binding to CBP. GDNF transcription was then measured by real-time PCR. The results showed that GDNF transcription was significantly and dose-dependently decreased by KG-501 treatment compared to the solvent control group (dimethyl sulfoxide) (P < 0.01, Fig. 5j).
Highly recruited CBP significantly increases histone H3 acetylation and RNA polymerase II recruitment in the CRE of enhancer II and the TSS of GDNF in GBM cells
CBP possesses intrinsic histone acetylase activity [25,26,27] that allows it to directly stimulate RNA polymerase II recruitment and loosen chromatin (especially the first nucleosome) by histone acetylation, thereby promoting gene expression . To determine whether CBP recruited to CRE in GDNF enhancer II has the same functions, we used ChIP-PCR to measure CBP binding, histone H3 acetylation, and RNA polymerase II recruitment in the CRE of GDNF enhancer II and at the TSS in GBM and NB tissue and in U251 and NHA cells. All three measured parameters at both sites of GDNF promoter II were significantly higher in GBM tissue than in NB tissue (P < 0.05, Fig. 6a-c). The same results were obtained in U251 cells versus NHA cells (P < 0.01, Fig. 6d-f).
A TCGA database search revealed significantly increased CBP expression in GBM tissue (P < 0.01) (Fig. 6g), which is consistent with our results (Fig. 6h). To clarify the relationship between high CBP expression and histone H3 hyperacetylation and high RNA polymerase II recruitment in GDNF promoter II and GDNF transcription, CBP knockdown was performed in U251 cells by infection with CBP shRNA lentiviral particles (Fig. 6i, j). ChIP-PCR revealed that CBP knockdown significantly reduced histone H3 acetylation (Fig. 6k) and RNA polymerase II recruitment (Fig. 6l) in the CRE of GDNF enhancer II and at the TSS in U251 cells (both P < 0.05). Real-time PCR revealed that CBP knockdown significantly decreased GDNF transcription in U251 cells (P < 0.01) (Fig. 6m).
To investigate the mechanism of crosstalk between DNA methylation and histone acetylation in regulating high GDNF transcription in GBM cells, we examined expression of the proto-oncogene CREB in different grades of glioma tissues and GBM cell lines. CREB expression was abnormally increased in GBM tissue and cell lines, which is consistent with previously reported results [30, 34]. Drug-induced CREB phosphorylation increases GDNF transcription in C6 GBM cells , suggesting that high CREB expression may be involved in regulating high GDNF transcription in GBM cells. Our results confirmed this hypothesis and revealed that GDNF expression and transcription were significantly decreased or increased by knockdown or enhancement of CREB expression, respectively. Moreover, overexpression of mutant KCREB did not significantly alter GDNF transcription, and overexperession of wild-type CREB significantly increased the binding of CREB to CRE in enhancer II of the GDNF promoter II, indicating that CREB regulation of GDNF transcription is dependent on its binding to promoter II.
CREB binds to DNA sequences via the CRE motif . Bioinformatics analysis revealed CREs in both enhancer II and silencer II of GDNF promoter II . To clarify whether CREB is involved in regulating GDNF transcription through different CREs, the effect of CRE deletion in different cis-acting elements on GDNF transcription was assessed using a dual-luciferase reporter system and CRISPR/Cas9. GDNF transcription was significantly increased and decreased by CRE deletion in silencer II and enhancer II, respectively. The CRE in enhancer II may play a larger role in regulating GDNF transcription. CREB binding to different CREs in GDNF promoter II was assessed by EMSA and ChIP-PCR, which revealed that CREB bound to CREs in both enhancer II and silencer II. The binding in enhancer II was significantly higher in U251 and U343 cells than in NHA cells, which was associated with CRE hypermethylation in silencer II. Moreover, hypermethylation of silencer II significantly enhanced the effect of CREB overexpression in promoting GDNF transcription. High methylation of silencer II decreases CREB binding to CRE in silencer II and increases that in enhancer II, thereby promoting GDNF transcription. However, why does increased binding of CREB to CRE in enhancer II increase GDNF transcription? Is it related to histone H3 hyperacetylation in GDNF promoter II? These questions need to be addressed in future studies.
CREB is activated by Ser133 phosphorylation through oncogenic signaling pathways . Our study found significantly increased phosphorylation of CREB at Ser133 in GBM tissue and cells, which is consistent with the results of Valeria et al. . Moreover, overexpression of S133 mutant CREB significantly reduced GDNF transcription. Takebayashi and Hisaoka groups showed that drug-induced phosphorylation of CREB at Ser133 increased GDNF production through extracellular signal-regulated kinase (ERK) signal pathway in rat C6 glioma cells [38,39,40]. In addition, Patel et al. recently reported that activated CREB by sodium benzoate significantly upregulated GDNF transcription in mouse astrocytes in vivo . These results indicate that overactivated CREB is involved in regulating GDNF transcription in GBM cells. Valeria et al. found that CREB phosphorylation was only significantly increased in astrocytoma; no significant changes were seen in oligodendroglioma . TCGA database analysis also revealed significantly increased GDNF expression in astrocytoma but no significant change in oligodendroglioma (data not shown). It suggests that pCREB may only be involved in regulating high GDNF transcription in astroglioma cells. Phosphorylated CREB is able to enter the nucleus and recruit coactivators by forming homodimers or heterodimers . It has been suggested that phosphorylated CREB can bind to the KIX of its transcriptional coactivator, CBP, via its own KID and recruit CBP to the CRE motif of the target gene promoter, thereby activating target gene expression . We therefore hypothesize that pCREB may promote high GDNF transcription by recruiting CBP to the CRE in GDNF enhancer II. To test this hypothesis, the binding of pCREB and CBP in the nuclei of GBM cells was confirmed by immunofluorescence and co-IP. A significant increase in pCREB-mediated CBP recruitment in the CRE of GDNF enhancer II was detected by re-ChIP-PCR. Furthermore, RNAi knockdown of CREB significantly reduced the binding of CBP to CRE in GDNF enhancer II, indicating that high recruitment of CBP in the CRE of enhancer II is achieved by pCREB. Finally, U251 cells were treated with different concentrations of KG-501, a small-molecule inhibitor that inhibits pCREB-CBP complex formation by directly targeting the KIX domain of CBP, thereby inhibiting CREB-mediated gene transcriptional activation [43, 44]. Treatment with KG-501 significantly and dose-dependently decreased GDNF transcription. Collectively, the results suggest that pCREB promotes GDNF transcription in GBM cells by increasing CBP recruitment in the CRE of enhancer II.
CBP recruited by pCREB has histone acetylase activity and can efficiently acetylate histones (H3 and H4) in mammalian cells [45, 46]. We found significantly higher CBP expression in GBM tissue and cells, which is consistent with TCGA database results. Our previous studies demonstrated hyperacetylation of histone H3 in GDNF promoter II in C6 cells, which could be significantly reduced by a CBP inhibitor, curcumin [19, 22, 29]. Hence, we hypothesize that CBP may be responsible for histone H3 hyperacetylation in GDNF promoter II. To test this hypothesis, ChIP-PCR was performed to measure CBP binding and histone H3 acetylation in the CRE of GDNF enhancer II in GBM and NB tissues and in U251 and NHA cells. The results showed that both parameters were significantly increased in GBM tissue and cells. Histone H3 acetylation in the CRE of GDNF enhancer II was significantly decreased in U251 cells by CBP knockdown, indicating that CBP is involved in the hyperacetylation of histone H3 in GDNF enhancer II. Numerous studies have shown that histone H3 hyperacetylation can open the promoter chromatin, thereby facilitating the binding of regulatory factors . In addition, CBP can bind to the DNA region involving H3K36 acetylation by the bromodomain . CBP phosphorylated at Y1126 can bind to acetylated histones, H3K27, H3K14, H3K9, and H3K4 . Thus, it can be seen that CBP increases histone H3 acetylation in the CRE of GDNF enhancer II, and then promotes the binding of CBP and enhancer II through the two mechanisms indicated above, thereby forming a positive feedback pathway to maintain hyperacetylation of histone H3 in the CRE of enhancer II in GBM cells. Moreover, CBP has been shown to promote the recruitment and release of promoter-proximal RNA polymerase II by increasing histone acetylation in the first nucleosome, thereby promoting the expression of eukaryotic genes . Our previous study has shown that histone H3 hyperacetylation in GDNF promoter II in C6 cells promotes the increase in RNA polymerase II recruitment at the TSS . However, the mechanism of action is not clear. Thus, we hypothesize that CBP recruited to the CRE of GDNF enhancer II may act on the TSS via a loop structure, thereby increasing histone H3 acetylation and RNA polymerase II recruitment at this site. This hypothesis is confirmed by the findings that CBP binding, histone H3 acetylation, and RNA polymerase II recruitment at the TSS of GDNF were significantly increased in GBM tissue and cells, and that histone H3 acetylation and RNA polymerase II recruitment at this site were significantly decreased by CBP knockdown.
In summary, this study provides the first evidence that the proto-oncogene CREB promotes GDNF transcription in GBM cells as a coupling factor for DNA methylation and histone acetylation. The molecular mechanisms are as follows: (1) CREB is highly expressed in GBM cells and is activated by S133 phosphorylation; (2) hypermethylation of GDNF silencer II, especially in its CRE, inhibits pCREB binding to silencer II, which results in an increase in its selective binding to CRE in enhancer II as a homodimer; (3) CBP has histone acetylase activity, is highly expressed in GBM cells, binds to pCREB, and is recruited to the CRE of GDNF enhancer II; (4) CBP recruited by pCREB significantly increases histone H3 acetylation in the CRE of GDNF enhancer II, which facilitates CBP binding; and CBP also acts on the TSS of GDNF via a DNA loop structure to increase histone H3 acetylation and RNA polymerase II recruitment at this site, thereby increasing GDNF transcription (Fig. 7). Our future study will focus on investigating how pCREB activates silencer II to downregulate GDNF transcription in GBM cells or normal astrocytes.
Normal brain (NB) tissue samples were obtained from 6 patients with acute brain trauma who underwent intracranial decompression, and 12 human glioma tissue samples (World Health Organization [WHO] grades I-IV) were acquired from the affiliated hospitals of Xuzhou University. Biopsied glioma tissues derived from patients who had not yet undergone cancer therapy were randomly sampled. Specimens with pathological grades I-II and IV were assigned to the low- and high-grade glioma (glioblastoma, GBM) groups, respectively.
Human U251 and U343 GBM cell lines were obtained from ATCC between years 2015 and 2018 and cultured as described previously . The cell lines were authenticated by short tandem repeat profiling by ATCC or Shanghai Genechem Co., Ltd. and passaged continuously for fewer than 6 months after receipt in our laboratory for relevant studies reported here. Normal Human Astrocytes (NHA, ScienCell, Carlsbad, CA, USA) were cultured in Astrocyte Medium (AM, ScienCell) as described previously .
Oncomine database analysis
The Oncomine cancer microarray database (http://www.oncomine.org) was used to identify changes in gene expression in GBM . “Brain Glioblastoma vs. Normal” was established as a filter to assess the mRNA levels of specific genes, and the human genome U133A brain microarray with 557 samples and 12,624 measured genes (TCGA Brain, no associated paper, 2013) was identified in the TCGA database. Specific genes were used as a filter to examine differences in mRNA expression between GBM and normal brain tissue.
RNA extraction and real-time PCR
RNA extraction and real-time PCR were performed as previously described . Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) mRNA expression was used as the internal reference, and the relative mRNA expression levels of the target genes were calculated by relative quantification (2−ΔΔCT). The primer sequences for the target genes and internal reference gene are shown in Supplementary Table S1.
Radioimmunoprecipitation assay lysis buffer was used to isolate the total protein. Samples from each group were subjected to western blotting as described previously . Detailed information of the primary antibodies used in western blotting analysis is listed in Supplementary Table S2. GAPDH was used as the internal reference.
Recombinant lentivirus construction and infection
Full-length human wild-type CREB ORF (NM_134442.3) and mutant CREB ORF (CREB-133 and K-CREB) fragments were amplified from the CREB dominant-negative vector set (pCMV-CREB, pCMV-CREB133, and pCMV-KCREB; Clontech, Mountain View, CA, USA) by PCR technology. CREB133 contains a serine-to-alanine mutation corresponding to amino acid 133 that blocks protein phosphorylation. KCREB contains mutations in its DNA-binding domain, preventing it from binding to CRE. Three types of CREB ORF were subcloned into lentiviral vector pLenti6.3-MCS-IRES-EGFP/V5 DEST. Three pairs of miRNA oligos targeting the human CREB mRNA (Supplementary Table S3) were synthesized and cloned into the lentiviral vector of pLenti6.3-EmGFP-MCS/V5 DEST. Two sgRNAs targeting different regions in human GDNF promoter II (AF053749) were synthesized and cloned into the lentiviral vector of pLenti6.3-MCS-IRES-EGFP/V5 DEST (Supplementary Table S4). Sequence alignment was performed to ensure correctness of the constructs. Recombinant lentiviruses were produced by 293 T cells, termed as CREB-OE, CREB133-OE, K-CREB-OE, CREB-KD1, CREB-KD2, CREB-KD3, sgRNA-CRE-E, and sgRNA-CRE-S. We used pLenti6.3-MCS-IRES-EGFP/V5 DEST or pLenti6.3-EmGFP-NC-miR as a negative control (NC). CBP (sc-29244-V) and control (sc-108080) shRNA lentiviral particles were purchased from Santa Cruz Biotechnology (Dallas, TX, USA). U251 cells without or with stably transfected Cas9 were plated at a density of 2 × 104 cells/well in a 24-well plate (Corning, Corning, NY, USA). After 24 h, cells were infected by 1 μL concentrated lentivirus in the presence of polybrene (8 μg/mL).
CruiserTM assay was performed to check the lentivirus-sgRNA’s cleavage by using a knockout and mutation detection kit (GENESci, Shanghai, China) according to the manufacturer’s instructions. Briefly, genomic DNA was extracted from U251 cells with stably transfected Cas9 after 72 h of infection with sgRNA lentiviruses using a QIAamp DNA Mini and Blood Mini Handbook kit (Qiagen, Hilden, Germany). The products were amplified by two pairs of PCR primers (Supplementary Table S5). The amplification consisted of initial denaturation at 95 °C for 90 s; 35 cycles of denaturation at 95 °C for 30 s, annealing at 55 °C for 30 s, and extension at 72 °C for 20 s; 72 °C for 5 min; 98 °C for 3 min. The system was then allowed to cool to below 40 °C to obtain the mismatched hybrid DNA products for cleavage by CruiserTM detecase, a member of the CEL family of mismatch-specific nucleases. Positive clones were identified on 2% agarose gel electrophoresis. The size of the amplified fragment for the positive control was 456 bp, and the digested fragments were 303 and 151 bp.
Construction and mutagenesis of the GDNF promoter-reporter construct
According to the human GDNF promoter II sequence obtained from GenBank (accession no. AF053749), the following sequences were obtained by chemical synthesis with a KpnI restriction site introduced into the 5'-end and a HindIII restriction site into the 3'-end: wild-type GDNF promoter II (− 1300/+ 149) sequence, CRE-WT; mutant or deletion sequences: mtCRE-E or △CRE-E, with CRE mutant or deletion in enhancer II; mtCRE-S or △CRE-S, with CRE mutant or deletion in silencer II; mtCRE-ES or △CRE-ES, with CRE mutant or deletion in both enhancer II and silencer II, respectively. The sequences were digested with KpnI and HindIII and ligated into the pGL3-basic vector (Promega, Madison, WI, USA). The mutant sequences of the constructs are listed in Supplementary Table S6. All constructed vectors were verified by DNA sequencing.
GDNF promoter activity assay
GDNF promoter activity assays were performed as previously described . Relative luciferase activity = luciferase activity of the experimental group/luciferase activity of the control group. Relative luciferase activity of the control group was defined as 1.
Electrophoretic mobility shift assay
Electrophoretic mobility shift assay was performed with the non-radioactive EMSA kit (Viagene Biotech, Tampa, FL, USA) according to the user manual. The double-stranded DNA probes (wild-type CREB-E: 5'-AAGCCACTGGAGGGCACGTCACGGAGT G-3', − 997 to − 970 nt; wild-type CREB-S: 5'-CGCGCCGGTTGACGTGGTGTCTCGTTCG-3', − 321 to − 293 nt, underline denotes CREs; methyl-CREB-S: 5'-CGCGCCGGTTG ACGTGGTGTCTCGTTCG-3', − 321 to − 293 nt, all the cytosines in the CpG of the probe were methylated) containing the consecutive putative CREB-binding site was synthesized with and without a biotin label. We mixed 10 μg of cell nuclear extracts and a 100-fold molar excess of unlabeled competing probes (including the mutated CREB-E probe: 5'-AAGCCACTGGAGGGCTACACACGGAGTG-3' and the mutated CREB-S probe: 5'-CGCGCCGGTTGTACAGGTGTCTCGTTCG-3', mutated bases are underlined) and incubated at room temperature for 20 min followed by the addition of 15 μL of labeled probes (0.1 μmol) for 20 min. For the supershift assay, samples were incubated with 1 μL of an anti-CREB monoclonal antibody (#9197, cell signaling) for an additional 20 min at room temperature. Protein/DNA complexes were then separated by non-denaturing polyacrylamide gel electrophoresis on 6% gels and transferred to nitrocellulose membranes (Millipore). Protein/DNA complexes were analyzed using streptavidin–horseradish peroxidase and developed with an enhanced chemiluminescence system (Amersham Pharmacia Biotech, Little Chalfont, UK).
ChIP-seq, ChIP-PCR, and re-ChIP-PCR
ChIP-PCR assays were performed as previously described . For re-ChIP assays, the cells were cross-linked with 0.5 M di (N-succinimidyl) glutarate and 37% formaldehyde (Sigma-Aldrich, St. Louis, MO, USA). The chromatin collected after the first ChIP was treated with re-CHIP elution buffer and subjected to the second ChIP. For ChIP-seq assays, the immunoprecipitated DNA from the CREB antibody was quantified by high-throughput sequencing, and the data were analyzed using MACS2. Peak calling was calculated by MACS2 with parameter -B -SPMR -nomodel -extsize 200 -q 0.05. Q-values are calculated from P values using Benjamini-Hochberg procedure. Pileup signals (bedgraph files) were converted to big-wig files using bedGraphToBigWig and visualized in the Integrative Genomics Viewer software. The results for ChIP-PCR and re-ChIP-PCR were calculated as %Input: %Input = 2(CtInput−CtChIP) × Input dilution factor × 100. Antibody information and primer sequences are shown in Supplementary Table S2 and Table S7, respectively.
BSP was performed as previously described [17, 18]. Two pairs of BSP primers (see Table S8 for sequences) were designed and synthesized for the sequence around CRE in different cis-acting elements of promoter II. Each sample was analyzed for methylation using software on the website http://quma.cdb.riken.jp/.
Specific sequence methylation followed by plasmid recircularization
This assay was performed according to the method previously reported by our group . Briefly, the plasmid pGL3-GDNF-promoter II-mt containing the mutant GDNF promoter II was extracted. In this plasmid, a methylation-insensitive single restriction site (5'-MluI-silencer II-XhoI-3') was introduced into both ends of silencer II in GDNF promoter II (− 1300/+ 149) by point mutation, which did not affect promoter activity . Next, 10 μg of pGL3-GDNF-promoter II-mt plasmid was digested with the restriction enzymes MluI and XhoI. The vector backbone and corresponding silencer II fragment were recovered by agarose gel electrophoresis. Part of the recovered silencer II fragment (3 μg) was methylated using CpG methyltransferase (M.SssI; New England Biolabs, Ipswich, MA, USA) according to the manufacturer’s instructions, and then ligated back into the corresponding luciferase vector backbone with T4 ligase (methylated fragment: vector backbone = 3:1). The remaining unmethylated silencer II fragment was also ligated back into the luciferase vector backbone as a control. Ligated components were separated by gel electrophoresis. Circular plasmid DNA with a high migration rate was recovered. After BSP confirmed > 90% DNA methylation of silencer II in GDNF promoter II treated with M.SssI, the circular plasmid DNA was transfected into U251 cells. Promoter activity was measured using a dual-luciferase reporter system.
The U251 cells were grown on coverslips in a 24-well plate, fixed with 4% paraformaldehyde (w/v) for 40 min, washed for 5 min with PBS three times and permeabilized with 0.5% (w/v) Triton X-100 in PBS for 15 min. The cells were then blocked for 30 min in PBS containing 10% bovine serum albumin followed by overnight incubation with the primary antibodies against pCREB and CBP diluted in PBS containing 10% FBS. After series of washings with PBS, cells were incubated for 2 h with secondary antibodies (Life, US) conjugated with fluorescein isothiocyanate or tetra methyl rhodamine isothiocyanate in dark moist environment. After several additional washing steps, the coverslips were mounted with Hydromount containing DAPI to stain the nuclei (KeyGEN BioTECH, China). The localization of pCREB and CBP protein was examined using fluorescence confocal microscope (Leica Microsystems).
Co-immunoprecipitation and immunoblotting
Equal amounts of nuclear protein extracts prepared from U251 cells were incubated with the pCREB antibody, CBP antibody, or normal IgG (sc-2027X, SCBT) overnight at 4 °C. Then, the agarose-conjugated protein-A/G beads (SCBT) were added into the immunocomplex and the mixture was incubated at 4 °C for another 12 h. After extensive washing with ice-cold WB/IP lysis buffer with protease inhibitors, the beads were mixed with SDS loading buffer and boiled. The proteins in the supernatant were separated by SDS-PAGE and transferred to NC membranes. Blots were incubated with blocking reagent (TBST solution containing 5% non-fat milk), primary and secondary antibodies diluted in TBST, and then developed with enhanced chemiluminescence (ECL) + plusTM Western blotting system kit (Amersham). X-ray film was exposed to the membrane and then developed.
All data were processed with SPSS 25.0 (IBM Corp. Armonk, NY, USA). Data are expressed as mean ± standard deviation (SD). Independent sample t tests were used to identify significant differences in mean values between two groups. One-way analysis of variance (ANOVA) and Tukey’s post hoc test were used to compare the mean values of multiple groups. P < 0.05 was considered statistically significant for all tests.
Availability of data and materials
All data is available from the corresponding author on reasonable request.
Bisulfite sequencing PCR
CCAAT/enhancer binding protein α
CREB binding protein
S133 mutant CREBs
Cyclic AMP response element
Cyclic AMP response element binding protein
Electrophoretic mobility shift assay
Glial cell line-derived neurotrophic factor
DNA-binding domain-mutated CREB
Normal human astrocyte
Polymerase chain reaction
The Cancer Genome Atlas
Transforming growth factor-β
Transcription start site
World Health Organization
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We thank Zhonglin Li (the affiliated hospitals of Xuzhou University, China) for providing clinical human glioma samples.
This project was supported by the National Natural Science Foundation of China (nos. 81602464, 81772688, and 81372698), Natural Science Foundation of Jiangsu (BK20130212), China and Jiangsu Postdoctoral Science Foundation funded project (2013 M540466 and 1301068C), Six Talent Peaks in Jiangsu Province Jiangsu (SWYY-088), Qing Lan Project in Jiangsu Province (2017 to B.L. Zhang), and a Project Funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD).
Ethics approval and consent to participate
This study was approved by the Ethics Committee of the affiliated hospitals of Xuzhou University, and written informed consent was obtained from all subjects.
Consent for publication
The authors declare that they have no competing interests.
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Zhang, B., Gu, X., Han, X. et al. Crosstalk between DNA methylation and histone acetylation triggers GDNF high transcription in glioblastoma cells. Clin Epigenet 12, 47 (2020). https://doi.org/10.1186/s13148-020-00835-3
- DNA methylation
- Histone acetylation