Loss of full length CtBP1 expression enhances the invasive potential of human melanoma
© Winklmeier et al; licensee BioMed Central Ltd. 2009
Received: 01 August 2008
Accepted: 12 February 2009
Published: 12 February 2009
The C-terminal binding protein 1 (CtBP1) is a known co-repressor of gene transcription. We recently revealed that CtBP1 expression is lost in melanoma cells and melanoma inhibitory activity (MIA) expression is subsequently increased. The present study was performed to evaluate a more general role of CtBP1 in human melanoma and identify further CtBP1-regulated target genes.
Sequence analysis and expression profile of CtBP1 in melanoma cell lines were done by PCR. Boyden Chamber assays and co-immunoprecipitation were performed to investigate the functional role of CtBP1. Gene expression analysis and micro array data were used to define target genes.
Interestingly, we detected an alternative splice product of CtBP1 with unknown function whose expression is induced at reduction of full length CtBP1. Overexpression of full length CtBP1 in melanoma cells had no effect on cell proliferation but did influence cell migration and invasiveness. To understand the effect of CtBP1 we identified putative LEF/TCF target genes found to be strongly expressed in melanoma using DNA microarray analysis. We focused on fourteen genes not previously associated with melanoma. Detailed analysis revealed that most of these were known to be involved in tumor metastasis. Eleven genes had expression profiles associated with melanoma cell invasiveness.
In summary, this study revealed that reduction of CtBP1 expression is correlated with migratory, invasive potential of melanoma cells.
CtBP1 was first identified as a cytoplasmatic protein which binds the COOH-terminal region of the adenoviral protein E1A to attenuate its ability to activate transcription. CtBP1 recognizes PXDLS and RRT motifs in DNA-binding proteins and functions as a transcriptional co-repressor in Drosophila, Xenopus, and mammals. CtBP1 contains a central NAD(H)-binding domain and exhibits a weak dehydrogenase activity. This domain is also important for dimerization of CtBP1 contributing to the recruitment of transcriptional regulators. Recent studies revealed that the repressor function of CtBP1 is mediated by binding to enzymes catalyzing histone modification as class 1 HDACs (for review see ). A number of studies have provided evidence that CtBP1 binds to and regulates HMG-box proteins as TCF4  implicating them in context-dependent transcriptional repression. Transcription factors of the LEF/TCF family contain a homologous HMG-box, recognizes a conserved consensus sequence and regulates expression of genes also involved in melanoma development . In previous work we could show that CtBP1 functions as a strong repressor of melanoma inhibitory activity (MIA) expression by negatively regulating MIA promoter activity in malignant melanoma, and that this repressor function requires the TCF binding element in the MIA promoter . Expression of MIA is an early event in melanoma development and correlates with tumor progression in vivo. MIA promotes invasion and metastasis of melanoma cells regulating cell-matrix attachment (for review see ).
CtBPs has a wide impact in tumorigenesis interacting with transcriptional repressors influencing oncogenic and pro-survival pathways (for review see ). It was previously shown that CtBP interacts with Snail contributing to tumor progression [7, 8]. Further analyses revealed CtBP1 to be strongly expressed in primary melanocytes whereas in melanoma cells in vitro and in vivo full length CtBP1 expression is lost or strongly downregulated suggesting an important role of CtBP1 in melanoma progression . To define the role of CtBP1 in melanoma more clearly we performed a screening for CtBP1 target genes.
The melanoma cell lines Mel Im hi, Mel Im si, Mel Im, Mel Ju, Mel Juso, Mel Ho, Mel Ei, Mel Wei, Sk Mel 3, Sk Mel 28 and HTZ 19d were described previously [9, 10]. Cells were maintained in DMEM supplemented with penicillin (400 U/ml), streptomycin (50 μg/ml), L-glutamine (300 μg/ml) and 10% fetal calf serum (FCS; Sigma, Deisenhofen, Germany) and split at a 1:5 ratio every three days. Normal human epidermal melanocytes (NHEM) derived from normal skin were cultivated in melanocyte medium MGM-3 (Promocell, Heidelberg, Germany) under a humidified atmosphere of 5% CO2 at 37°C. Cell proliferation was determined using the XTT assay (Roche, Mannheim, Germany).
A panel of Mel Im cell clones with CtBP1 expression was established by stable transfection using a pCMX-PL1-CtBP1 expression plasmid . Plasmids were cotransfected with pcDNA3 (Invitrogen), containing the selectable marker for neomycin resistance. Mock controls received pcDNA3 alone. Transfections were performed using lipofectamin plus (Invitrogen). One day after transfection, cells were placed in selection medium containing 50 μg/ml G418 (Sigma). After 25 days of selection, individual G418-resistant colonies were subcloned.
RNA isolation and reverse transcription
Total cellular RNA was isolated from cultured cells (4 × 106). cDNAs were generated by reverse transcriptase reaction performed in 20 μl reaction volume containing 2 μg of total cellular RNA, 4 μl of 5× first strand buffer (Invitrogen, Groningen, The Netherlands), 2 μl of 0.1 M DTT, 1 μl of dN6-primer (10 mM), 1 μl of dNTPs (10 mM) and DEPC-water. The reaction mixture was incubated for 10 min at 70°C, 200 units of Superscript II reverse transcriptase (Invitrogen) were added and RNAs were reverse transcribed for 1 hour at 37°C. Reverse transcriptase was inactivated at 70°C for 10 minutes and the RNA was degraded by digestion with 1 μl RNase A (10 mg/ml) at 37°C for 30 minutes. The quality of cDNA was controlled and normalized by RT-PCR amplification of the house keeping gene β-actin.
Analysis of gene expression
Primers used for quantitative RT-PCR
For further analysis of gene expression, we used the micro array data of Smith et al. (GDS1989 ) and Hoek et al. . Via Pigment Cell & Melanoma Research Homepage http://www.pigment.org/genearray_home.asp, these data are available for public.
Sequence analysis of the splice donor and splice acceptor site of CtBP exon 4 was performed on a DNA fragment amplified by conventional PCR using the primers CtBP1 Exon4 for: 5'-TTC AAA CCC GCT CCA GTC-3' and CtBP1 Exon4 rev: 5'-TCA GTC CTG TCC TGG GT TG-3'.
Western Blot analysis
3 × 106 cells were lysed in 200 μl RIPA-buffer (Roche) and incubated for 15 minutes at 4°C. Insoluble fragments were removed by centrifugation at 13000 rpm for 10 minutes and the supernatant lysate was immediately shock frozen and stored at -80°C. 40 μg RIPA-cell lysate of each sample of melanoma cell lines were loaded and separated on 8.75% SDS-PAGE gels and subsequently blotted onto a PVDF membrane (1 hour, 150 mA). After blocking for 1 hour with 3% BSA/PBS the membrane was incubated for 16 hours with the primary antibody (anti-CtBP1 antibody, Transduction Lab, 1:2500) or beta-actin (Sigma, 1:2500). Then the membrane was washed three times in PBS, incubated for 1 hour with 1:4000 of an alkaline phosphate-coupled secondary antibody (Chemicon) and then washed again. Finally immunoreactions were visualized by NBT/BCIP (Sigma) staining.
For co-immunoprecipitation cell lysates dissolved in binding buffer (20 mM NaPO4, 150 mM NaCl, pH 7.5) were incubated with 2 μg of the anti-TCF4  or anti-Snail antibody (Cell Signaling, USA) with shaking at 4°C overnight. Then 20 μl protein G Sepharose 4 Fast Flow (Amersham, Biosciences) was added for 1 h, pelleted, washed three times with binding buffer, resuspended in 20 μl of Laemmli's buffer, heated at 95°C for 5 min, separated on 10% SDS-polyacrylamide gels and subsequently blotted onto a PVDF membrane (1 hour, 150 mA). After blocking for 1 hour with 3% BSA/PBS the membrane was incubated for 16 hours with the primary antibody (anti-CtBP1 antibody (1:2500)). Then the membrane was washed three times in PBS, incubated for 1 hour with 1:2000 of an alkaline phosphate-coupled secondary antibody (Chemicon) and then washed again. Finally, immunoreactions were visualized by NBT/BCIP (Sigma) staining.
Migration and invasion assay
Migration and invasion assays were performed using Boyden Chambers containing polycarbonate filters with 8 μm pore size (Costar, Bodenheim, Germany), essentially as described previously . Filters were coated with gelatine or Matrigel (diluted 1:3 in H2O; Becton Dickinson, Heidelberg, Germany), respectively. The lower compartment was filled with fibroblast-conditioned medium, used as a chemo-attractant. Mel Im cells and CtBP1 cell clones were harvested by trypsinization for 2 min, resuspended in DMEM without FCS at a density of 3 × 104 cells/ml (migration) and 2 × 105 cells/ml (invasion) and placed in the upper compartment of the chamber. After incubation at 37°C for 4 hours, the filters were collected and the cells adhering to the lower surface fixed, stained and counted. Each assay was repeated at least three times.
Results are expressed as mean ± SD (range) or percent. Comparison between groups was made using the Student's unpaired t-test. A p value < 0.05 was considered statistically significant. All calculations were performed using the GraphPad Prism software (GraphPad software Inc, San Diego, USA).
CtBP1 target genes
Details on genes regulated by CtBP1 associated to melanoma development Genes with TCF/LEF binding sites in their promoter were analyzed.
GDS1989 [xfold ind., Nevus set as 1] 
CtBP1 clones versus mock
Hoek et al.
x fold ind.
adaptor-related protein complex 1. sigma 1 subunit
ATPase. Na+/K+ transporting. beta 1 polypeptide
claudin 11 (oligodendrocyte transmembrane protein)
collagen type I alpha 2
ectodermal-neural cortex (with BTB-like domain)
ectonucleotide pyrophosphatase/phosphodiesterase 2 (autotaxin)
FAT tumor suppressor homolog 1 (Drosophila)
fascin homolog 1. actin-bundling protein (Strongylocentrotus purpuratus)
fusion (involved in t(12;16) in malignant liposarcoma)
myeloid/lymphoid or mixed-lineage leukemia 5 (trithorax homolog. Drosophila)
solute carrier family 26 (sulfate transporter). member 2
transmembrane emp24 protein transport domain containing 4
To get more information about the relevance of the genes found to be regulated by CtBP1 for malignant melanoma we used DNA microarray data obtained from proliferative and invasive phenotype cultures . This showed that expression of 11 CtBP1-regulated genes (73%) were significantly associated with the invasive phenotype recently characterized by Hoek et al.  and none with the proliferative cluster supporting our functional data that CtBP1-regulated genes control cellular migration (table 2).
CtBP1 is a known co-repressor involved in gene regulation with several other transcription factors. Recently, we described the loss of CtBP1 expression in melanoma . In this study, we aimed to evaluate the importance of this loss and subsequent changes to regulated genes in more detail.
Interestingly, Western blot and RT-PCR studies revealed the existence of a CtBP1 splice variant (CtBP1splice) in melanoma cells. This variant lacks exon 4 (in frame) leading to a CtBP1 variant missing aa 114–182, and does not bind TCF4 or Snail suggesting that CtBP1 co-repressor activity may not be fulfilled by this variant. However, expression of the variant seems to be important in tumors as CtBP1splice was also detected in breast, colon and hepatocellular carcinoma cells which lack full length CtBP1 expression (data not shown). Several other splice forms of CtBP1 have been previously detailed , however the splice variant we describe is novel. The lack of the PAK phosphorylation site could lead to changes in the control of nuclear-to-cytosolic translocation and co-repressor function . In addition, NAD binding to CtBP1 and CtBP1 dimerization may be affected. As NAD(H)-dependent dimerization is required for transcriptional repression, repressor functions could also be influenced. Additionally, changes in the two protein binding sites could impact the binding of transcription factors to CtBP1splice [16, 17]. CtBP1splice expression after reduction of full length CtBP1 could be important in tumor cells due to general functions recently been described for CtBP as CtBP1 was shown to be involved in Golgi morphogenesis by association to centrosomes  and in vesicular trafficking. Interestingly, some publications also hint at a role for CtBP as a tumor promoter . Jin et al. describe upregulation of MDR1 by CtBP1 leading to drug resistance . This effect could not be shown to be modulated by histone modification which led the authors to suggest regulation via CtBP1 by an unknown mechanism. In addition, CtBP1 was shown to activate expression of Wnt genes in a TCF-independent manner . It can only be speculated that these tumor promoting effects can be achieved by CtBP1splice. Further studies are necessary to understand the function and role of CtBP1splice in carcinogenesis.
CtBP1 has been speculated to be involved in normal cell growth control. It was shown previously that the binding of CtBP to adenoviral E1A correlates with inhibition of E1A and H-ras cotransformation, tumorigenesis, and metastasis . Furthermore, a repressor function of CtBP on E2F-medited transcription via RB was detected . In our study, proliferation was unchanged after reexpression of CtBP1 whereas migration and invasion assays pointed to a role of CtBP1 in cell migration as reexpression of CtBP1 induced a reduction of the migratory potential. This finding was further supported by detailed analysis of CtBP1-regulated genes. By comparison of genes carrying a LEF/TCF site with cDNA array data (GDS1989)  on melanoma fourteen genes showing a correlation with melanoma development and progression were determined. Regulation of these genes by CtBP1 was confirmed performing quantitative RT-PCR. Interestingly, expression of most CtBP1-regulated genes discussed here is associated with the invasive state recently described by Hoek and co-workers . This supports the finding that loss of CtBP1 enhances the migratory behavior of cells.
Only two of the CtBP1-regulated genes were previously described as playing a role in melanoma. ENPP2 (Autotaxin) was originally isolated from melanoma cells and shown to augment the invasive potential of melanoma cells by inducing uPA expression [23, 24]. Versican was also previously described to be expressed in melanoma and to be an inducer of metastasis . The remaining genes have not previously been described to play a role in melanoma, however, deregulation and implication in other kinds of cancer has been noted. ATP1B1, an Na2K-ATPase, was found to be involved in progression and metastasis of prostate cancer . Collagen type I alpha2 and FUS were found to be deregulated in gastric cancer and speculated to play a role in invasion and metastasis . Changes in Claudin 11 were shown during progression of epithelial tumors leading to acquisition of migratory potential . Upregulation of ENC1, an actin-binding protein, contributes to colorectal carcinogenesis . Regulation of ENC1 gene expression by LEF/TCF was already shown. FAT, a cadherin-family molecule, and FCSN1, a protein involved in the assembly of actin filament bundles, were described to play a role in general cell migratory processes [30, 31]. Enhanced FSCN1 expression was associated with increased invasiveness in urinary cancer. TMED4 was significantly induced in invasive adenocarcinoma . In summary, the data available on the functional role of CtBP1-regulated genes hint to an implication in migratory and invasive processes.
It therefore appears that loss of the CtBP1 co-repressor function may be a critical event in the pathogenesis of melanoma. In future, it would be highly interesting to extend the analysis and perform in vivo analysis to look at effects of full length CtBP1 upon tumor growth in a nude mouse model.
In melanoma cells loss of full length CtBP1 expression, a known co-repressor involved in gene regulation with several other transcription factors, is accompanied by induction of a CtBP1 splice variant. This variant lacks exon 4 (in frame) leading to a CtBP1 variant which is unable to bind TCF4 or Snail suggesting that CtBP1 co-repressor activity may not be fulfilled by this variant. Interestingly, in some reports also hint at a role for CtBP as a tumor promoter. The data generated in this study on the functional role of CtBP1-regulated genes suggest an implication in migratory and invasive processes. It, therefore, appears that loss of the CtBP1 co-repressor function may be a critical event in the pathogenesis of melanoma, however, important tumor promoting effects of CtBP can be achieved by CtBP1splice.
We are indebted to Dr. J. Johnson (University of Munich, Germany) for providing melanoma cell lines and to Sibylla Lodermeier and Susanne Wallner for excellent technical assistance. This work was supported by grants from the Deutsche Krebshilfe to A. B. (Melanoma Network).
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