- Open Access
Selective repression of retinoic acid target genes by RIP140 during induced tumor cell differentiation of pluripotent human embryonal carcinoma cells
Molecular Cancervolume 6, Article number: 57 (2007)
The use of retinoids as anti-cancer agents has been limited due to resistance and low efficacy. The dynamics of nuclear receptor coregulation are incompletely understood. Cell-and context-specific activities of nuclear receptors may be in part due to distinct coregulator complexes recruited to distinct subsets of target genes. RIP140 (also called NRIP1) is a ligand-dependent corepressor that is inducible with retinoic acid (RA). We had previously shown that RIP140 limits RA induced tumor cell differentiation of embryonal carcinoma; the pluriopotent stem cells of testicular germ cell tumors. This implies that RIP140 represses key genes required for RA-mediated tumor cell differentiation. Identification of these genes would be of considerable interest.
To begin to address this issue, microarray technology was employed to elucidate in a de novo fashion the global role of RIP140 in RA target gene regulation of embryonal carcinoma. Subclasses of genes were affected by RIP140 in distinct manners.
Interestingly, approximately half of the RA-dependent genes were unaffected by RIP140. Hence, RIP140 appears to discriminate between different classes of RA target genes. In general, RIP140-dependent gene expression was consistent with RIP140 functioning to limit RA signaling and tumor cell differentiation. Few if any genes were regulated in a manner to support a role for RIP140 in "active repression". We also demonstrated that RIP140 silencing sensitizes embryonal carcinoma cells to low doses of RA.
Together the data demonstrates that RIP140 has profound effects on RA-mediated gene expression in this cancer stem cell model. The RIP140-dependent RA target genes identified here may be particularly important in mediating RA-induced tumor cell differentiation and the findings suggest that RIP140 may be an attractive target to sensitize tumor cells to retinoid-based differentiation therapy. We discuss these data in the context of proposed models of RIP140-mediated repression.
Retinoids are used in the clinic to prevent and treat select tumors through the process of induced tumor cell differentiation, yet the efficacy of retinoids toward the most common neoplasms has been limited . Therefore, it is important to understand the mechanisms by which tumors are resistant to the ability of retinoids to affect tumor growth and progression. Embryonal carcinoma (EC) is a model of embryonic development as well as tumor cell differentiation . EC is considered to be the malignant counterpart to embryonic stem cells because of a remarkable degree of genetic, morphologic, biochemical and gene expression similarity [3, 4]. EC cells are pluripotent and considered to be the stem cells of male germ cell tumors [3, 4]. In response to all trans retinoic acid (RA), the pluripotent human EC cell line, NT2/D1, differentiates toward a neuronal lineage with associated loss of cell growth and tumorigenicity [5, 6].
Retinoids mediate their effects by binding to and activating retinoid specific nuclear receptors, RARs and RXRs [7, 8]. Corepressors, such as NCoR and SMRT, bind to nuclear receptors in the absence of ligand to assemble large repressor complexes containing chromatin repressing and histone deacetylase activity [9, 10]. Ligand-bound receptors recruit coactivators, such as the p160 family, which recruit histone acetyltransferases and other chromatin remodeling proteins to induce gene transcription .
This classic coregulator paradigm does not fully explain the recent evidence that ligands such as retinoids, estrogen, and vitamin D3, apparently also actively suppress gene expression [12, 13]. These data challenge the current coregulator paradigm by implying that repressor complexes may participate in active repression of ligand-bound receptors. RIP140 is the first member of a unique class of ligand-dependent corepressors [14–18]. RIP140 exhibits intrinsic repression activity when fused to the Gal4-DNA binding domain, and directly recruits histone deacetylases as well as the transcriptional repressor, c-terminal binding protein (CTBP), to nuclear receptors [19, 20]. In addition, RIP140 inhibits the transactivation function of several ligand bound nuclear receptors [14–18]. Since RIP140 preferentially binds and suppresses agonist bound nuclear receptors, it provides a candidate mechanism for active repression of several members of the nuclear receptor superfamily.
Our prior work demonstrated that RIP140 is a direct target of retinoid signaling and that RIP140 can be limiting for both retinoid and estrogen signaling [21–23]. Silencing RIP140 in NT2/D1 cells resulted in RA-dependent increases in expression of model endogenous RA target genes RARβ and LEFTY2, and enhanced and accelerated RA-induced differentiation and growth suppression . This evidence suggests that RA induction of RIP140 constitutes a negative-feedback mechanism to fine-tune retinoid signaling.
Retinoids are pleiotropic agents regulating many gene targets. However, we have shown that RIP140 siRNA accelerates RA-dependent growth suppression and differentiation . The identification of genes normally limited by RIP140 during RA-induced growth and differentiation is of interest since these genes may be particularly important regulators of these processes. The possibility remains that unidentified subclasses of genes may be regulated by RIP140 in distinct manners .
The present study was conducted to characterize, on a genome-wide scale, the role of RIP140 in the regulation of RA signaling in a cancer stem cell model. Together the data demonstrates that RIP140 has profound effects on RA-mediated gene expression. Subclasses of genes were affected by RIP140 in distinct manners while other RA-dependent genes were unaffected suggesting that RIP140 may discriminate between different classes of RA targets. The RIP140-dependent RA target genes identified here may be particularly important in mediating RA-induced tumor cell differentiation.
Validation of RIP140 specific siRNA
We previously established that RIP140 is a target of RA signaling and that RIP140 in turn is a limiting factor for RA activity . Specifically, we showed that knockdown of RIP140 with a RIP140-specific siRNA (RIP140siRNA#1) increased endogenous expression of RA target genes RARβ and LEFTY2, and accelerated immunophenotypic differentiation as measure by A2B5 staining of NT2/D1 cells . A key feature was that knockdown of RIP140 did not affect these endpoints in cells depleted of endogenous retinoids, confirming that RIP140 mainly associates with ligand-bound nuclear receptors. These studies were performed with a constant 1 μM dose of RA and a relatively high, 150 nM dose of siRNA. Prior to global gene expression studies, we wished to further validate the siRNA approach for targeting RIP140.
Experiments were performed under charcoal absorbed sera conditions to deplete the basal levels of retinoids known to be in sera. An additional siRNA, RIP140siRNA#2, also potently enhanced the RA-mediated expression of the RA target gene RARβ at 150 nM and at doses as low as 40 nM (Figure 1A). Importantly, RIP140 siRNA cells also overexpressed RARβ when compared to mock transfected cells (Figure 1A). Low, 40 nM doses of RIP140siRNA#1 and RIP140siRNA#2 resulted in enhanced neuronal differentiation with RA as assessed by expression of the early neuronal ectodermal marker, A2B5 (Figure 1B).
An important control to ensure a given siRNA phenotype is not due to off-target effects is to rescue the siRNA phenotype with overexpression of its target. RIP140siRNA#1, as well as a newly designed siRNA targeting the 3' untranslated region of human RIP140 (siRNA#3) enhanced induction of a RAR-specific reporter construct in a RA-dependent manner (Figure 1C). Further, a RIP140 expression plasmid that does not contain the 3' untranslated region of RIP140 repressed RA signaling in scrambled control cells (Figure 1C). This RIP140 construct potently opposed the effect of RIP140siRNA#3 but not RIP140siRNA#1, which targets the coding region of RIP140. Thus, silencing of RIP140 by siRNA enhanced RA-mediated responses in NT2/D1 cells at low doses of siRNA and this could be rescued by exogenous RIP140. Further, the effects of RIP140 silencing were mainly ligand-dependent since performing these experiments under charcoal absorbed sera conditions resulted in minimal changes in basal RAR activity or in the differentiation of NT2/D1 cells (Figure 1).
We then sought to determine the global effects of RIP140 on RA-dependent and RA-independent gene expression. A dose of siRNA of 90 nM was chosen. Twelve independent hybridizations were performed from mRNA isolated from 12 independent samples (Figure 2A). One scrambled and two independent RISC-free siRNA transfections and transfections with three distinct RIP140 siRNAs were performed in NT2/D1 cells. Each siRNA treatment was further treated with either 10 μM RA or DMSO control for 24 hours. Hence, the design consisted of four groups, the three siRNA controls treated with vehicle, Group 1; the siRNA controls treated with RA, Group 2; siRNA to RIP140 treated with vehicle, Group 3; and siRNA to RIP140 treated with RA, Group 4 (Figure 2A).
The treatments were done in the presence of normal sera, since charcoal absorption of sera removes many small hydrophobic ligands to the nuclear receptor family in addition to retinoids. This measure was taken with the aim to perhaps identify target genes of other nuclear receptors including orphan receptors that could be regulated by RIP140 in the presence of low levels of their cognate ligands. RA treatment of 10 μM for 24 hours was chosen since previous experience with NT2/D1 cells indicated that a reasonably sized set of altered genes would be obtained [5, 24]. In addition, NT2/D1 cells commit to RA-induced differentiation by 48 hours and RIP140 repression accelerates RA-induced differentiation of EC cells [5, 22]. Therefore, the 24-hour time point is well-within the range of the RA commitment "window" and a larger percentage of direct RA-target genes could be expected to be uncovered compared to later time points.
Based on the current understanding of the properties of RIP140 [14–18], a number of potential outcomes were anticipated: 1) RIP140 may limit RA target gene activation by negative-feedback inhibition upon RA addition, 2) RIP140 may participate in "active repression" of gene expression upon RA addition, 3) an unexpected outcome that RIP140 may participate in the activation of a subset of target genes, 4) RIP140 may regulate the transcription of target genes of other nuclear receptors or even non-nuclear receptor transcription factors. The readout from the array design that would support each of these outcomes is depicted in Figure 2B. The extent of RIP140 knockdown and the level of enhancement of RARβ expression in the actual samples used in for array are depicted in Figure 2C.
Silencing of RIP140 quantitatively alters the RA transcriptional response in EC cells
To further ensure that off-target effects were minimized, any gene that differed 1.5-fold or greater between the replicates of the control (Group 1) were removed from the analysis. The expression of the remaining 52,270 probe sets were compared in pairwise fashion between the experimental groups (Figure 3). As expected, comparison of gene expression between the siRNA control cells treated with RA and the control cells treated with vehicle revealed that the great majority of genes are unaltered with RA treatment (Figure 3A). Interestingly, the total number of genes regulated by RA in the RIP140 siRNA cells increased compared to the number of genes regulated by RA in the siRNA control cells (compare the spread in the scatter plots between Figure 3A vs. Figure 3B or 3C). This is apparent regardless of whether RIP140 siRNA RA cells were compared with control siRNA vehicle cells (Figure 3B) or compared to RIP140 siRNA vehicle cells (Figure 3C). The disparity in the overall number of RA-sensitive genes increased as the fold-cut off increased (Figure 3F), suggesting that RIP140 siRNA increases the number of RA altered genes and also amplifies RA-dependent gene alterations. It is important to emphasize that the genes identified here under these experimental conditions may not be direct target genes of liganded RARs. The complete list of genes and expression values for each pairwise comparison is supplied in Supplemental Tables S1 to S5 [see Additional file 1].
A similar trend is also apparent in the scatter plot comparing RIP140 siRNA RA cells with control siRNA RA cells (Group 4 vs. Group 2, Figure 3D). The greatest difference is in RA induced genes, consistent with a role for RIP140 in repressing the activation of ligand engaged RARs. However, a number of repressed genes are also repressed to a greater extend in RIP140 siRNA cells, although this differential expression is lower. Table 1 and supplemental Table S6 [see Additional file 2] list the top genes differentially expressed between siRNA RIP140 RA cells and control siRNA RA cells (Group 4 vs. Group 2). Table 1 ranks the genes by fold-change, while Table S6 [see Additional file 2] ranks the genes by p-value. The known RA-target gene HOXA5 is induced 1.6 fold with RA in siRNA control cells and 20.6-fold with RA in RIP140 siRNA cells for a differential induction of 12.8. RARβ, the primary gene used the establish the negative-feedback model was also identified as being super-induced by RIP140 siRNA (Table 1). Other genes that are highly RIP140-dependent in their RA-alterations include both known (MEIS1, HOXB5, HOXB13) and previously unsuspected (NODAL, TSHZ1) RA target genes. Other noteworthy genes regulated by RA in a RIP140-dependent manner include the nuclear receptor coactivator PCAF and the pluripotency gene FOXD3 which are predicted to be upregulated and downregulated by RA, respectively (Table 1). Including the previously confirmed RARβ gene, we were able to confirm the RIP140-dependent expression pattern of 5 of the top 6 genes from Table 1 (Figure 4).
The majority of RIP140-dependent genes change in a manner consistent with RIP140 limiting RA signaling. Hence, RIP140 siRNA results in enhancement or amplification of the RA signal. Genes induced by RA in control cells are induced to a greater extent by RA in RIP140 siRNA cells and genes repressed by RA in control cells are repressed to a greater extent in RIP140 siRNA cells. This trend holds true whether the effects of RIP140 on RA signaling are ranked by fold-change (Table 1, 47 out of 49 genes) or p-value (Table S6, 37 out of 40 genes). The exceptions are bolded in Tables 1 and Table S6 [see Additional file 2]. In addition only 1 gene in the ranked tables had an expression profile that could be consistent with "active repression" (second pattern in Figure 2B). This gene is boxed in Table S6. The effects of RIP140 had little bias for the extent of RA-induction. For example, a strongly induced gene, PYCR2, is induced by RA in control cells 32.6-fold and in RIP140 siRNA cells by 104.6-fold, while a weakly induce gene INHBB is induce 1.22-fold in control cells and 2.95-fold in RIP140 siRNA cells (Table 1). There are also examples of genes that are not altered with RA in control cells but altered by RA in RIP140 siRNA cells. One interpretation of this result is that the RA alteration of these genes may have been accelerated with RIP140 siRNA and that the 24-hour time point is too early to detect RA-mediated changes in the siRNA control cells.
Silencing of RIP140 does not greatly alter RA-independent gene expression
Although the array experiments were designed to maximize the potential to find RA-independent RIP140 targets, very few genes matching this pattern were found (last pattern in Figure 2B). This is evident by the comparison of Group 3 vs. Group 1 (Figure 3E, and Table 2 and supplemental Table S7 [see Additional file 3]). Reassuringly, one of the genes identified by the array as repressed basally is RIP140 itself. There is a clear bias for repressed genes suggesting that these genes are indirectly regulated by RIP140. The majority of the altered genes in Figure 3E and Table 2 and Table S7 are also altered with RA in siRNA control and RIP140 siRNA cells (Figure 5). Hence, RIP140 siRNA caused basal alterations in some genes that are altered in control siRNA cells treated with RA. One interpretation of this result is that RIP140 siRNA is sensitizing the cells to the basal levels of retinoids in the normal sera media. Two genes that were found to be exclusively expressed in RIP140 siRNA cells independent of RA, and hence fit the pattern of RA-independent RIP140 targets (last pattern in Figure 2B), were doublecortex (DCX, bolded in Table 2) and reticulon 1 (RTN1, just missed fold-cutoff in Table 2). Both of these genes have roles in neuronal development. Interestingly, a third gene that fit this pattern was only induced 1.47 fold in RIP140 siRNA cells but had a highly significant p-value, the repressor protein, c-terminal binding protein 2 (CTBP2) (Table S7). CTBP2 is a known RIP140 co-factor . This suggests that RIP140 may repress transcription of its own cofactor.
RA target genes cluster into distinct groups based on RIP140-dependency
The major influences of RIP140 siRNA were also assessed by hierarchical clustering. There were 1,115 genes with a fold change of 1.8 or greater in any of the four groups with p-value < 0.01 (supplied as Supplemental Table S8 [see Additional file 4]). These were clustered by the Eisen program (Figure 5). Inspection of the cluster confirms that the major pattern of RIP140 siRNA alterations is RA-dependent. In that, very few genes made to threshold cutoffs because of RA-independent alterations in expression (only changed in Group 3 and Group 4 of Figure 5). Further, the pattern associated with active repression (Figure 2B) was not greatly evident (would be green in Group 2 but less green in Group 4 of Figure 5). Genes representative of the major patterns are shown in Figure 5. These include genes that are basally induced or repressed with RIP140 siRNA, and genes that are "super-induced" or "super-repressed" by RIP140 siRNA. Approximately half of the total RA-dependent genes were not influenced by RIP140 in this analysis. Partitioning around mediods (PAM) analysis was also performed on genes with a cut off of 1.5-fold and p-value of < .001, (1065 genes) (Figure 6). There were 542 genes in cluster patterns indicative of little or no change with RIP140 siRNA (Cluster 1 and Cluster 2). There were 312 genes in cluster patterns indicative of super-induction or super-repression with RIP140 siRNA (Cluster 3 and Cluster 4) and 211 genes in clusters indicative of basal induction or basal repression in RIP140 siRNA cells (Cluster 5 and Cluster 6, Figure 6). The list of genes and expression values for each of the six clusters is supplied as Supplementary Tables S9 to S14 [see Additional file 5]. Genes representative of some of the patterns were confirmed in independent samples (Figure 7).
Mode of action of RIP140 in RA signaling
The pattern of gene expression in RIP140 siRNA cells suggests that RIP140 siRNA may influence RA signaling in distinct manners, either to sensitize cells to lowdose RA (basally altered array genes) or to accelerate or amplify RA-dependent gene expression (super-induced or super-repressed array genes). However, the array was performed at a single RA dose and time point. We had shown previously that RIP140 siRNA accelerates and enhances RA-induced differentiation in NT2/D1 cells . RIP140 siRNA was also able to promote differentiation of NT2/D1 cells at low doses of RA (Figure 8A). Time course studies demonstrated that RIP140 siRNA caused a combination of accelerated and amplified alterations in RA target gene expression (Figure 8B). Hence, these data suggests that RIP140 may limit a subset of RA target genes by effecting the rate and extent of target gene expression at a given dose of RA.
Through the use of microarray technology we sought to elucidate, in a de novo fashion, the global role of RIP140 in RA-dependent signaling. The predominant gene expression pattern is consistent with RIP140 limiting RA signaling . Since RIP140 depletion enhances RA-induced differentiation (Figure 1B, 8A) these genes may play an important role in mediating the growth suppression, differentiation and anti-tumorigenic effect of RA in embryonal carcinoma. These data support the notion that the primary effect of the ligand-dependent corepressor RIP140 is to limit the activity of retinoid receptors (Figure 8C). A feature of this model is that RIP140 is itself induced by RA  and that RIP140 inhibits ligand-bound RARs to form a classic negative-feedback loop. One interesting gene predicted to be repressed by RIP140 was the RIP140 cofactor, CTBP2 . This raises the potential of the additional complexity of RIP140 limiting its own activity by regulating CTBP2. Confirming and establishing the importance of RIP140 transcriptional regulation of CTBP2 will require further rigorous studies.
It is tempting to speculate on the importance of RIP140 restriction of RA-target gene expression. One possibility is that RIP140 ensures that cells are exposed to a threshold concentration of RA for a required duration before committing to differentiation. This could be important for developmental timing but an impediment to retinoid therapies in the adult [1, 25]. Alternatively, RIP40 may fine-tune the RA signal to ensure that a critical set of target genes are not overly or toxically expressed.
Our studies suggest that regulation of RAR signaling by RIP140 is more complex than a simple all-or-none effect on global RAR activation. We have identified gene subsets regulated by RA in apparent RIP140-dependent and RIP140-independent manners. It is possible that RIP140 may have a selective ability to affect the actions of different subtypes of retinoid receptors. Alternatively, this differential effect of RIP140 may involve differences in the local chromatin environment of specific genes. First-pass analysis of the predicted promoter regions of RIP140-dependent target genes was unable to identify any cis-acting features that may account for differential sensitivity to RIP140. We believe the RIP140-sensitive RA target genes identified here may have pharmacologic importance during normal retinoid-based cancer therapy or prevention [1, 25]. It would also be interesting to know the number of RIP140 sensitive genes that are direct RA-target genes.
Within the limits of the single RA dose and time-point employed, RIP140-dependent genes can be placed in three categories based on their expression profiles (Figure 5, 6 and 7). Some genes appeared super-induced or super-repressed with RIP140 repression, meaning they were changed with RA to a greater degree in RIP140 siRNA cells compared to control siRNA cells. Some genes were induced with RA in RIP140 siRNA cells but unchanged by RA in control siRNA cells. It may be predicted that this subset of genes is regulated by RA in the control siRNA cells at later time points. Some RA regulated genes in control cells were regulated basally in the siRNA RIP140 cells. We propose that these genes are expressed in RIP140 siRNA cells due to the presence of previously sub-optimal concentrations of retinoids in standard non-charcoal stripped FBS media. Hence, from the data presented here we propose the RIP140 plays a role in finetuning the RA signal by either delaying the timing, decreasing the amplitude or decreasing the effective ligand concentration of RAR activation (Figure 8C).
Recent microarray studies suggest extensive and early ligand-dependent repression of gene expression by nuclear receptors [12, 13]. However, the mechanism for such repression is unclear. Ligand-dependent repressors like RIP140 are candidate mediators of such repression. This is particularly relevant for the steroid nuclear receptors such as the estrogen, progesterone and glucocorticoid receptors. If RIP140 participates in this form of RAR "active repression" one would expect that genes repressed by RA would be de-repressed upon RIP140 silencing. Our data does not support a widespread role for RIP140 in retinoid receptor-mediated active repression. This conclusion is consistent with the finding that RIP140 also inhibits glucocorticoid receptor-mediated repression from a negative GRE . As with other nuclear receptor and coregulator functions, active repression by RIP140 may be cell-, receptor- and context-specific.
While it is known that RIP140 modulates transcription through repressing ligand-dependent nuclear receptors, the possibility exists that RIP140 may function through multiple mechanisms, including nuclear receptor-independent mechanisms. For example, a recent microarray study reported a role for the coactivator, NCoA3/AIB1, in receptor-independent activities, illustrating the diverse functionality of coregulators and highlighting the need for further elucidation of their role in gene transcription . The microarray studies presented here were optimized to investigate gene changes following RA treatment, making it difficult to draw conclusions regarding the effects of RIP140 on other nuclear receptors. Despite the inclusion of normal sera media which may contain limiting quantities of ligand for other nuclear receptors, we were unable to identify many RA-independent targets of RIP140. To address this question, additional RIP140 siRNA array studies should be performed with exogenous ligands for other nuclear receptors.
A limited number of studies have been performed to assess the global effect of RIP140 on gene expression. Expression profiles were performed with murine embryonic fibroblasts in which RIP140 was deleted and reintroduced during adipocytic differentiation . Another study employed 3T3-L1 fibroblasts treated with RIP140 siRNA during adipocytic differentiation . Genes identified to be regulated by RIP140 in these systems were involved in glucose and fatty acid metabolism [28, 29]. An additional study profiled mouse ovaries from RIP140 knockout mice treated with or without human chorionic gonadotropin and pregnant mare serum gonadotropin . There is little overlap in the RIP140-dependent genes identified in these and our study. This is not surprising since RIP140 likely regulates different sets of genes in different tissues based on the ligand/receptor under investigation and the distinct hormone sensitivities of the tissue.
The data demonstrates that RIP140 globally effects RA-mediated gene expression and that RIP140 discriminates between different classes of RA targets in the embryonal carcinoma cancer stem cell model. Maintaining therapeutic doses of RA has proven difficult in the clinic [1, 25]. Understanding the mechanisms that limit RA effectiveness may aid in developing new RA therapeutic strategies. We propose that the combination of RIP140 gene silencing with RA treatment might enhance expression of important RA target genes, thereby enhancing the therapeutic benefit of RA. Future studies should focus on pharmacologic modulation of RIP140 expression or activity as a potential strategy to enhance the chemotherapeutic action of retinoids.
Cell culture, siRNA and transfection protocols
The RA-sensitive human EC cell line, NT2/D1 is a clonal line derived from a xenograft of Tera-2 cells . Cells were cultured in high glucose DMEM (Gibco) with 10% FBS supplemented with glutamine and antibiotics. Repression of RIP140 was achieved using three siRNAs purchased from Dharmacon. RIP140siRNA#1 and RIP140siRNA#2 have been previously described [22, 23]. RIP140siRNA#1 is of sequence 5'-GAAGGAAGCUUUGCUAGCU-3' and corresponds to the human RIP140 cDNA starting 331 bp downstream of the ATG start codon. RIP140siRNA#2 is of sequence 5'-CAAACAGGAUAGCACAUUA-3' and corresponds to human RIP140 cDNA starting 1986 bp downstream of the ATG start codon. RIP140siRNA#3 is of sequence 5'-AACUGUGAGUAGCCUAUGA-3' and corresponds to the 3'-UTR of RIP140 242 bp downstream of the stop codon. Controls were the Scramble II siRNA or RISC-free siRNA from Dharmacon. For microarray experiments, log-phase cells were transfected with 90 nM siRNA using OligofectAMINE (Invitrogen) as described [22, 23]. Briefly, 3.5 × 106 cells per 10 cm plate were transfected with 90 nM siRNA for 16 h. 1 × 106 cells were then replated in normal sera DMEM media per 10 cm dish and 24 hours later treated with either 10 μM RA or DMSO for 24 hours before harvesting for mRNA. For some indicated experiments, NT2/D1 cells were first incubated in charcoal-absorbed sera containing DMEM prior to transfection with siRNA and treatment with indicated dosages of RA.
The reporter, RARE-TK-Luc, and the expression plasmid pSG5-HAhRIP140 have been previously described [21–23]. Cells were plated at 1.5 × 105 cells per well of a six-well plate and transfected with Polyfect (Qiagen) according to the manufacturer's directions. Tranfections were performed in triplicate for each condition with a final concentration of 0.375 μg RARE-TK-Luc, 0.375 μg pRL-TK, 0.75 μg of either pSG5-insertless or pSG5HA-hRIP140, and 50 nM of control or RIP140 siRNA. Cells were exposed to transfection reagent for 16 hours and then washed and cultured in indicated dosages of RA or the vehicle, DMSO. Cells were harvested 48 hours following transfection and Dual Luciferase Reporter analysis was performed (Promega). Luciferase activity was normalized against renilla activity and reported as the average of triplicate transfections with similar results obtained in at least two independent experiments.
Northern and RT-PCR analysis
Total RNA was harvested using TriReagent (Invitrogen). Northern hybridizations for RARβ and RIP140 were performed with 5 μg RNA as previously described . Expression levels of RA-target genes were assessed by semi-quantitative RT-PCR. The cDNA was synthesized using Superscript II RT from 5 μg total RNA. PCR analysis was performed with Taq polymerase (Denville) to varying cycle numbers within the linear range as previously described . The sequence of primers are available upon request.
Indirect fluorescence activated cell sorter (FACS) analysis to evaluate RA-induced neuronal differentiation of NT2/D1 cells was performed using established techniques . Briefly, NT2/D1 cells were harvested by trypsinization and incubated with antibody to the cell surface antigen A2B5 or with isotype-matched monoclonal antibody as controls. The A2B5 antibody recognizes a neuronal epitope on RA-treated NT2/D1 cells and was prepared from hybridoma cultures purchased from ATCC. The cells were indirectly assayed with FITC-conjugated goat-anti-mouse antibody, and fluorescence was measured as described . Mean peak fluorescent values and the percentage of positive cells were measured for the entire population. At least 1 × 104 cells were analyzed per assay.
Total RNA was purified using RNeasy columns (Qiagen). Hybridizations were performed according to Affymetrix guidelines at the Dartmouth College Microarray Shared Resource using an Affymetrix GeneChip Workstation. Biotin-labeled cRNA was generated from 5 μg of total RNA and hybridized to the Human Genome (HG) U133 Plus 2.0 chip which contains over 54,000 probe sets. Unless specifically stated we will refer to each probe set as a "gene". As described in Figure 2A, a total of 12 hybridizations were performed comprising 12-independent biologic samples organized into four groups of three. This data is available at the GEO website under Accession GSE7500 and conforms to MIAME guidelines. Raw data from each hybridization was normalized by RMA, background corrected and filtered for present using GeneSifter software (vizX Labs). As a further filter, any gene that showed a 1.5-fold or greater difference amongst the three samples comprising Group 1 (the siRNA controls) were eliminated from further analysis. The remaining 52,270 probe sets were then analyzed by GeneSifter software. Pairwise comparisons between groups were performed using t-test with p-value and cutoffs as indicated. For hierarchical cluster analysis genes changed 1.8 fold or greater between any of the four groups with p-value < .01 (1115 genes) were clustered via the Cluster program by Michael Eisen using a correlation metric for similarity matrix and average linkage clustering . The clustered data was visualized by Tree-View software. Genes were also divided into clusters using partitioning around medoids (PAM) analysis from the GeneSifter package. Genes changed 1.5-fold or greater with a p-value of < .001 (1065 genes) were used for this analysis using the correlation metric for similarity. The number of clusters (six) was chosen empirically to obtain the best mean silhouette value of 0.560.
nuclear receptor interacting protein 1
retinoic acid receptor
retinoid X receptor
nuclear receptor co-repressor 1
silencing mediator for retinoid and thyroid hormone receptor
c-terminal binding protein.
Freemantle SJ, Spinella MJ, Dmitrovsky E: Retinoids in cancer therapy and chemoprevention: promise meets resistance. Oncogene. 2003, 22: 7305-7315. 10.1038/sj.onc.1206936
Chambers I, Smith A: Self-renewal of teratocarcinoma and embryonic stem cells. Oncogene. 2004, 23: 7150-7160. 10.1038/sj.onc.1207930
Houldsworth J, Korkola JE, Bosl GJ, Chaganti RS: Biology and genetics of adult male germ cell tumors. J Clin Oncol. 2006, 24: 5512-5518. 10.1200/JCO.2006.08.4285
Giuliano CJ, Freemantle SJ, Spinella MJ: Testicular germ cell tumors: Aparadigm for the successful treatment of solid tumor stem cells. Curr Cancer Ther Rev. 2006, 2: 255-270. 10.2174/157339406777934681. 10.2174/157339406777934681 10.2174/157339406777934681
Giuliano CJ, Kerley-Hamilton JS, Bee T, Freemantle SJ, Manickaratnam R, Dmitrovsky E, Spinella MJ: Retinoic acid represses a cassette of candidate pluripotency chromosome 12p genes during induced loss of human embryonal carcinoma tumorigenicity. Biochim Biophys Acta. 2005, 1731: 48-56.
Andrews PW, Damjonov I, Simon D, Banting GS, Carlin C, Dracopoli NC, Fogh J: Pluripotent embryonal carcinoma clones derived from the humanteratocarcinoma cell line Tera-2. Differentiation in vivo and in vitro. Lab Invest. 1984, 50: 147-162.
Chambon P: A decade of molecular biology of retinoic acid receptors. FASEB J. 1996, 10: 940-954.
Mangelsdorf DJ, Umesono K, Evans RM: The Retinoid Receptors. The Retinoids: Biology, Chemistry and Medicine. Edited by: Sporn MB, Roberts AB, Goodman DS. 1994, 319-349. New York: Raven Press,
Horlein AJ, Naar AM, Heinzel T, Torchia J, Gloss B, Kurokawa R, Ryan A, Kamei Y, Soderstrom M, Glass CK, Rosenfeld MG: Ligand-independent repression by the thyroid hormone receptor mediated by a nuclear receptor co-repressor. Nature. 1995, 377: 397-404. 10.1038/377397a0
Chen JD, Evans RM: A transcriptional co-repressor that interacts with nuclear hormone receptor. Nature. 1995, 377: 454-457. 10.1038/377454a0
Hermanson O, Glass CK, Rosenfeld MG: Nuclear receptor coregulators: multiple modes of modification. Trends Endocrinol Metab. 2002, 13: 55-60. 10.1016/S1043-2760(01)00527-6
Lin R, Nagai Y, Sladek R, Bastien Y, Ho J, Petrecca K, Sotiropoulou G, Diamandis EP, Hudson TJ, White JH: Expression profiling in squamous carcinoma cells reveals pleiotropic effects of vitamin D3 analog EB1089 signaling on cell proliferation, differentiation, and immune system regulation. Mol Endocrinol. 2002, 16: 1243-1256. 10.1210/me.16.6.1243
Frasor J, Danes JM, Komm B, Chang KC, Lyttle CR, Katzenellenbogen BS: Profiling of estrogen up- and down-regulated gene expression in human breast cancer cells: insights into gene networks and pathways underlying estrogenic control of proliferation and cell phenotype. Endocrinology. 2003, 144: 4562-4574. 10.1210/en.2003-0567
Augereau P, Badia E, Balaguer P, Carascossa S, Castet A, Jalaguier S, Cavailles VJ: Negative regulation of hormone signaling by RIP140. Steroid Biochem Mol Biol. 2006, 102: 51-59. 10.1016/j.jsbmb.2006.09.005.
White JH, Fernandes I, Mader S, Yang XJ: Corepressor recruitment by agonist-bound nuclear receptors. Vitam Horm. 2004, 68: 123-143.
Christian M, White R, Parker MG: Metabolic regulation by the nuclear receptor corepressor RIP140. Trends Endocrinol Metab. 2006, 17: 243-250. 10.1016/j.tem.2006.06.008
Wei LN: Retinoids and receptor interacting protein 140 (RIP140) in gene regulation. Curr Med Chem. 2004, 11: 1527-1532.
Tazawa H, Osman W, Shoji Y, Treuter E, Gustafsson JA, Zilliacus J: Regulation of subnuclear localization is associated with a mechanism for nuclear receptor corepression by RIP140. Mol Cell Biol. 2003, 23: 4187-4198. 10.1128/MCB.23.12.4187-4198.2003
Wei LN, Hu X, Chandra D, Seto E, Farooqui M: Receptor-interacting protein140 directly recruits histone deacetylases for gene silencing. J Biol Chem. 2000, 275: 40782-40787. 10.1074/jbc.M004821200
Vo N, Fjeld C, Goodman RH: Acetylation of nuclear hormone receptor-interacting protein RIP140 regulates binding of the transcriptional corepressor CtBP. Mol Cell Biol. 2001, 21: 6181-6188. 10.1128/MCB.21.18.6181-6188.2001
Kerley JS, Olsen SL, Freemantle SJ, Spinella MJ: Transcriptional activation of the nuclear receptor corepressor RIP140 by retinoic acid: a potential negative-feedback regulatory mechanism. Biochem Biophys Res Commun. 2001, 285: 969-975. 10.1006/bbrc.2001.5274
White KA, Yore MM, Warburton SL, Vaseva AV, Rieder E, Freemantle SJ, Spinella MJ: Negative feedback at the level of nuclear receptor coregulation. Self-limitation of retinoid signaling by RIP140. J Biol Chem. 2003, 278: 43889-43892. 10.1074/jbc.C300374200
White KA, Yore MM, Deng D, Spinella MJ: Limiting effects of RIP140 in estrogen signaling: potential mediation of anti-estrogenic effects of retinoic acid. J Biol Chem. 2005, 280: 7829-7835. 10.1074/jbc.M412707200
Freemantle SJ, Kerley JS, Olsen SL, Gross RH, Spinella MJ: Developmentally-related candidate retinoic acid target genes regulated early during neuronal differentiation of human embryonal carcinoma. Oncogene. 2002, 21: 2880-2889. 10.1038/sj.onc.1205408
Niles RM: Recent advances in the use of vitamin A (retinoids) in the prevention and treatment of cancer. Nutrition. 2000, 16: 1084-1090. 10.1016/S0899-9007(00)00436-6
Subramaniam N, Treuter E, Okret S: Receptor interacting protein RIP140 inhibits both positive and negative gene regulation by glucocorticoids. J Biol Chem. 1999, 274: 18121-18127. 10.1074/jbc.274.25.18121
Labhart P, Karmakar S, Salicru EM, Egan BS, Alexiadis V, O'Malley BW, Smith CL: Identification of target genes in breast cancer cells directly regulated by the SRC-3/AIB1 coactivator. Proc Natl Acad Sci USA. 2005, 102: 1339-1344. 10.1073/pnas.0409578102
Christian M, Kiskinis E, Debevec D, Leonardsson G, White R, Parker MG: RIP140-targeted repression of gene expression in adipocytes. Mol Cell Biol. 2005, 25: 9383-9391. 10.1128/MCB.25.21.9383-9391.2005
Powelka AM, Seth A, Virbasius JV, Kiskinis E, Nicoloro SM, Guilherme A, Tang X, Straubhaar J, Cherniack AD, Parker MG, Czech MP: Suppression of oxidative metabolism and mitochondrial biogenesis by the transcriptional corepressor RIP140 in mouse adipocytes. J Clin Invest. 2006, 116: 125-136. 10.1172/JCI26040
Tullet JM, Pocock V, Steel JH, White R, Milligan S, Parker MG: Multiple signaling defects in the absence of RIP140 impair both cumulus expansion and follicle rupture. Endocrinol. 2005, 146: 4127-4137. 10.1210/en.2005-0348.
Andrews PW: Teratocarcinomas and human embryology: pluripotent human EC cell lines. APMIS. 1998, 106 (1): 158-168.
Spinella MJ, Freemantle SJ, Sekula D, Chang JH, Christie AJ, Dmitrovsky E: Retinoic acid promotes ubiquitination and proteolysis of cyclin D1 during induced tumor cell differentiation. J Biol Chem. 1999, 274: 22013-22018. 10.1074/jbc.274.31.22013
Eisen MM, Spellmann PT, Brown PO, Botstein D: Cluster analysis and display of genome-wide expression patterns. Proc Natl Acad Sci USA. 1998, 95: 14863-14868. 10.1073/pnas.95.25.14863
This work was supported by the National Institute of Health Grant R01-CA104312 (MJS) and a grant from the Lance Armstrong Foundation (MJS), and a pre-Doctoral Fellowship BC010159 from the Department of Defense (KAW).
The authors declare that they have no competing interests.
KCH carried out sample characterization for the reported arrays, participated in the array experiments and final data analysis, performed Northern and RT-PCR analysis. KAW-B participated in the initial study design, preliminary array experiments and data interpretation, expression confirmations and FACs analysis. DD participated in reporter experiments, RT-PCR, FACS and Northern analysis. CRT directed and supervised microarray studies. JHM participated in extraction and analysis of gene expression data from the microarray. SJF contributed to RNA sample preparation and study design. MJS conceive of the study, directed the study and participated in the extraction and analysis of gene expression data, data interpretation and writing of the manuscript. All authors read and approved the final manuscript.
Kelly C Heim, Kristina A White contributed equally to this work.
Electronic supplementary material
Additional file 4: Supplemental Table 8. The 1,115 genes in Figure 5 with a fold-change of 1.8 or greater in any of the four treatment groups with p-value < 0.01. (XLS 383 KB)
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.