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Identification of new p53 target microRNAs by bioinformatics and functional analysis
© Bisio et al.; licensee BioMed Central Ltd. 2013
Received: 28 April 2013
Accepted: 5 November 2013
Published: 21 November 2013
The tumor suppressor p53 is a sequence-specific transcription factor that regulates an extensive network of coding genes, long non-coding RNAs and microRNAs, that establish intricate gene regulatory circuits influencing many cellular responses beyond the prototypical control of cell cycle, apoptosis and DNA repair.
Using bioinformatic approaches, we identified an additional group of candidate microRNAs (miRs) under direct p53 transcriptional control. To validate p53 family-mediated responsiveness of the newly predicted target miRs we first evaluated the potential for wild type p53, p63β and p73β to transactivate from p53 response elements (REs) mapped in the miR promoters, using an established yeast-based assay.
The REs found in miR-10b, -23b, -106a, -151a, -191, -198, -202, -221, -320, -1204, -1206 promoters were responsive to p53 and 8 of them were also responsive to p63β or p73β. The potential for germline p53 mutations to drive transactivation at selected miR-associated REs was also examined. Chromatin Immuno-Precipitation (ChIP) assays conducted in doxorubicin-treated MCF7 cells and HCT116 p53+/+ revealed moderate induction of p53 occupancy at the miR-202, -1204, -1206, -10b RE-containing sites, while weak occupancy was observed for the miR-23b-associated RE only in MCF7 cells. RT-qPCR analyses cells showed modest doxorubicin- and/or Nutlin-dependent induction of the levels of mature miR-10b, -23b, -151a in HCT116 p53+/+ and MCF7 cells. The long noncoding RNA PVT1 comprising miR-1204 and −1206 was weakly induced only in HCT116 p53+/+ cells, but the mature miRs were not detected. miR-202 expression was not influenced by p53-activating stimuli in our cell systems.
Our study reveals additional miRs, particularly miR-10b and miR-151a, that could be directly regulated by the p53-family of transcription factors and contribute to the tuning of p53-induced responses.
The master regulator p53 is a prominent tumor suppressor gene, functioning in the cell as a tetrameric (dimer of dimers) sequence-specific transcription factor, able to bind to two copies of a decameric sequence with the RRRCWWGYYY consensus (where R stands for a purine, W for A/T and Y for a pyrimidine) representing the so called p53-response element (p53-RE) . p53 is known to be inducible in response to a large number of cellular stress signals that, besides genotoxic stress, include carbon and oxygen deficiencies, perturbations of the translation apparatus, excessive proliferation signals, alteration in microtubule dynamics [2, 3]. There are >100 established p53 targets genes that link p53 to cell cycle arrest, apoptosis, DNA repair and inhibition of angiogenesis [3–6]. More recently, p53 was demonstrated to modulate the expression of genes able to modify glucose as well as lipid metabolism, induction of autophagy, immune responses and cell motility [7–11].
A direct role of p53 on the activation of microRNA (miRs) expression as well as a role on selective maturation of microRNA precursors has been recently established [12, 13]. miRs are small non coding RNAs typically of 21–25 nucleotides in length that regulate gene expression by inhibiting translation or repressing stability of target messenger RNAs including those coding for oncogenes and tumor suppressor proteins . Dysregulation in miR expression has been reported in various cancers and can contribute to tumorigenesis . The first evidence of a p53-dependent regulation of miR genes was provided by He et al., who identified a family of miRs, namely miR-34a-c, whose expression reflected the p53 status . The authors demonstrated that genes encoding miR-34 family cluster were direct transcriptional targets of p53 and that their induced expression levels upon genotoxic or oncogenic stress was dependent on p53 expression, both in vitro and in vivo. Moreover, He et al. identified the DNA sequences responsible for the p53 responsiveness of those miRs. A year later another group of miRs, (miR-192, -194 and −215) was identified as targets of p53 and their ability to increase the level of CDKN1A (p21CIP1) and to function as drivers of cell cycle arrest was established . Examples of feedback loops or regulatory circuits comprising p53, a target miR and target mRNAs were discovered. For example, p53-directed repression of c-Myc has also been linked to p53-dependent induction of miR-145 . miR-107 was demonstrated to be activated by p53 and to cooperate in its cancer suppressive function through the inhibition of HIF-1β and, consequently, tumor angiogenesis . The p53 targeted miR-34a was shown to modulate SIRT1 . More recently, Jin et al. surprisingly found that p53 directly induced the transcription of miR-149*, which in turn can target the glycogen synthase kinase-3α mRNA, resulting in elevated expression of Mcl-1 and resistance to apoptosis in melanoma cells, thus providing a rational explanation for the poor ability of p53 to suppress melanoma progression .
Furthermore, it has been demonstrated that p53 itself can be indirectly activated by the miR-29 family members (miR-29a, -29b and -29c), which inhibit the expression of p85 alpha (the regulatory subunit of the phosphatidylinositol-3 kinase, PI3K) and CDC42 (Cell division cycle 42, a Rho family GTPase), thereby decreasing their inhibitory effect on p53 . Alternatively, miRs can also negatively regulate p53 expression as observed for miR-1285, miR-504, miR-33, miR-380, miR-30d, miR-25 and miR-125b [23–28].
The mechanisms regulating in vivo p53 transactivation specificity still need to be fully understood, but require in most cases the interaction of p53 with its response element sequences (REs) at target promoters . Recent evidences, including our studies using functional as well as DNA binding assays in yeast or mammalian cells or with cell extracts, demonstrated that maximal transactivation potential requires adjacent dimer binding sites [29–34]. A spacer between dimer sites even of 1 or 2 nucleotides conferred a negative impact, particularly for the p53-related protein p73 [31, 35, 36]. We also established that p53 can stimulate transcription, albeit at a reduced levels, from noncanonical response elements (half-sites and ¾ sites) , that do not provide for a p53 tetramer binding site. The same sequence-specific requirements that were shown to maximize the transactivation potential from full-site REs, appeared to be valid for the half-site REs . This information is relevant to optimize pattern-based motif searches aiming at identifying functional p53 response elements within genomes [37–39].
In this study we used a regression-based predictor for p53 transactivation , to identify additional p53-target miRs through the presence of functional p53-REs in their promoter regions or in promoter regions of long noncoding RNA that are precursors of those miRs. We then used a yeast-based functional assay to determine the relative transactivation capacity of p53 family proteins towards the identified REs and Chromatin Immuno-Precipitation (ChIP) assays in human cells to investigate genotoxic-stress dependent p53 occupancy at the chromosomal sites containing those REs. Changes in the expression levels for mature miRs or precursors were measured by real-time qPCR using cell lines and treatments probing the direct involvement of p53. We propose miR-10b, -23b and -151a to be included in the list of direct p53 target miRs contributing to the fine-tuning of p53-induced responses.
Yeast reporter strains and media
List of predicted p53-REs mapped nearby miR genes
p53-RE Genomic location
p53-RE distance miRNA
Distance from sense transcript TSS
p53- RE organization
N = 0 - 13
Chr 1 - 9242203
- 30,476 bp
+ 123 bp
Chr 2 - 177013750
- 1,281 bp
+ 12,065 bp
Chr 9 - 97818687
- 28,803 bp
+ 135 bp
Chr X - 133309906
- 5,678 bp
Chr 5 - 148786372
- 23,837 bp
+ 68 bp
Chr 8 - 141734774
- 2,349 bp
- 75,874 bp
Chr 3 - 49063594
- 5,543 bp
+ 5,103 bp
Chr 3 - 120112741
+ 1,774 bp
- 57,359 bp
Chr 10 - 135058647
+ 2,368 bp
- 2,748 bp
Chr X - 45599946
+ 5,639 bp
Chr 9 - 116880600
- 91,114 bp
- 49,395 bp
Chr 8 - 22095461
+ 7,014 bp
Chr 16 - 67331546
- 95,322 bp
+ 98,475 bp
Chr 7 - 150896632
- 38,875 bp
- 32,953 bp
Chr 8 - 128808017
- 191 bp
+ 1,238 bp
Chr 8 - 129002467
- 18,677 bp
+ 1,037 bp
Yeast cells were grown in 1% yeast extract, 2% peptone, 2% dextrose with the addition of 200 mg/L adenine (YPDA medium). Selective minimal plates lacking tryptophan or leucine but containing adenine (200 mg/L) and dextrose as carbon sources were used (transformation in yeast and luciferase-based assay).
Yeast expression vectors
For the expression of p53 family protein in yeast we used available CEN/ARS expression vectors (pTSG- or pLSG-based) harbouring alternatively the cDNA wild-type of p53, p63 or p73 under the control of the GAL1,10 inducible promoter . Among the various isoforms of p53 family members, we selected the full-length wild type p53 and the TA-p63β and TA-p73β isoforms as they showed the maximal transactivation potential in our experimental settings. The expression levels were modulated by the concentration of galactose in the culture medium (0.008%, 0.128% or 1%). The whole panel of 104 p53 germline missense mutants from the IARC R11 database (http://p53.iarc.fr) cloned in the pLS-Ad vector (providing for a constitutive expression of p53 mutants)  were used to test transactivation capability towards the miR-34a p53 RE. The pRS-314 or pRS-315 empty vectors were included as controls; these vectors contain respectively the TRP1 (as pTSG-) or LEU2 (as pLSG-) yeast selectable markers.
Luciferase assays in yeast
The p53 family responsiveness of miRNA-associated REs was examined by transforming the panel of yLFM-RE strains with the p53 expression vectors. Transformants were obtained using the LiAc method and selected on minimal plates lacking tryptophan or leucine but containing adenine (200 mg/L) and dextrose as carbon source to allow respectively the growth of white colonies of normal shape and to keep the expression of p53 family members inhibited. After 3 days of growth at 30°C, transformants were streaked onto the same plates and allowed to grow for an additional day. For each reporter strain, the basal luciferase activity was measured from pRS314- or pRS315-transformants and used to calculate the fold of induction due to the expression of each p53 family member. For the luciferase assay we exploited the recently developed miniaturized yeast assay . Transformant colonies were grown in 100 μl of the selective medium with 2% raffinose as carbon source (raffinose result in basal level of expression from the GAL1,10 promoter), supplemented with different concentrations of galactose (0.008% and 0.128% for p53; 0.008% and 1% for the other members of the family, to obtain a low, moderate or high expression of the proteins) in a transparent 96-well plate and incubated under 150 rpm shaking for 16–24 hours at 30°C. OD600 was measured directly in the multi-well plate to normalize for cell density using a multilabel plate reader (Infinite M200-Pro, Tecan, Milan, Italy). 10 μl of cells suspensions were transferred to a white 384-well plate (Brand, Milan Italy) and mixed with an equal volume of PLB buffer 2X (Passive Lysis Buffer, Promega, Milan, Italy). After 15 minutes of shaking at room temperature, 10 μl of Firefly luciferase substrate (Bright Glo Luciferase Reporter Assay, Promega) were added. Luciferase activity was measured at the plate reader, using a luminescence program with 1” integration time.
Cell lines and treatments
The human breast adenocarcinoma-derived MCF7 cell line was obtained from the InterLab Cell Line Collection bank, ICLC (Genoa, Italy). The colon adenocarcinoma HCT116 (p53+/+) cell line and its p53−/− derivative were obtained from B. Vogelstein’s group (The Johns Hopkins Kimmel Cancer Center, Baltimore, Maryland, USA). Cells were normally maintained in DMEM or RPMI supplemented with 10% FCS and antibiotics (100 units/ml penicillin plus 100 mg/ml streptomycin).
Cells were treated for 24 hours with 1.5 μM doxorubicin (DXR) or 10 μM Nutlin-3A for p53 stabilization/activation. Stock solutions of Nutlin-3A were dissolved in 100% DMSO (stock solution 10 mM); DXR was dissolved in H2O (stock 10 mM). DXR was bought from Sigma-Aldrich® (Milan, Italy) whereas Nutlin-3A from Alexis® Biochemicals (Enzo Life Sciences, Exeter, UK). All the treatments were performed when cells reached 70-80% of confluence.
RNA extraction and RT-qPCR
RNA extraction from human cell lines was done with Trizol reagent (InVitrogen, Life Technologies, Milan, Italy) following the manufacturer’s protocol. Cells were treated with 1.5 μM DXR or 10 μM Nutlin-3A for 24 hours prior to Trizol extraction. Quantification of mature microRNA expression was carried out using TaqMan MicroRNA Assay kits according to the manufacturer’s protocol (Applied Biosystems, Life Technologies), as described in Barbareschi et al. . Specifically, ready-made TaqMan MicroRNA Assays (containing microRNA-specific forward and reverse PCR primers and microRNA-specific Taqman MGB probe) were used for the investigation of miR-34a (ABI P/N 000426), miR-10b (ABI P/N 000388), miR-23b (ABI P/N 000400), miR-151a (ABI P/N 002254), and miR-202 (ABI P/N 002363). We also quantified the U6 small nuclear RNA (RNU6B) (ABI P/N 4373381) as an endogenous control to normalize the levels of target microRNA. Complementary DNA was generated using the Taqman MicroRNA Reverse Transcription (RT) Kit (ABI P/N 4366596) according to the manufacturer’s instructions. Reverse transcriptase reactions contained 10 ng of total RNA as the template, 3 μl of gene specific stem-loop RT primer, 1.5 μl of 10X RT buffer, 0.15 μl of 100 mM dNTPs, 1 μl of MultiScribe reverse transcriptase, and nuclease-free water. The 15 μl reactions were incubated on a GeneAmp PCR System (Bio-Rad, Hercules, CA) for 30 minutes at 16°C, 30 minutes at 42°C, 5 minutes at 85°C, and then kept at 4°C. Quantitative RT-PCR was carried out using the Rotorgene 6000 (Corbett Life Science, Ancona, Italy) in 20 μl PCR reactions containing 1.33 μl of RT product, 10 μl of FastStart TaqManProbe Master (Roche, Milan, Italy, P/N04673417001), 7.67 μl of nuclease–free water, and 1 μl of MicroRNA Assay (Applied Biosystems, Life Technologies) buffer. Reactions were incubated at 95°C for 10 minutes, followed by 40 cycles of incubation at 95°C for 15 seconds and at 60°C for 1 minute. The quantification of protein coding mRNAs was performed using a Sybr green RT-qPCR approach. Total RNAs extracted with Trizol were converted using the RevertAid™ First Strand cDNA Synthesis Kit containing the M-MuLV Reverse Transcriptase following the manufacture’s recommendation (Thermo Scientific Inc., M-Medical, Milan, Italy). qPCR were carried out using the KAPA Sybr Green PCR mix (Kapa Biosystems, Resnova, Rome, Italy) with 12.5 ng of cDNA on the CFX384 real-time PCR detection system (BioRad, Milan, Italy). Primers were picked using the Primer-BLAST online tool (http://www.ncbi.nlm.nih.gov/tools/primer-blast/); sequences are available upon request. The Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) and β2-microgobulin (B2M) were used as reference genes for normalization.
In all the qPCR assays, the threshold cycle data (Ct) and baselines were determined using auto settings. The Ct value was defined as the fractional cycle number at which the fluorescence passed a fixed threshold. Fold changes were calculated using the comparative Ct method (ΔΔCt).
Western blot analysis
To evaluate p53, p63 or p73 protein levels in yeast we cultured transformant colonies for 24 hours using selective medium containing 0.128% (p53) or 1% (p63β and p73β) galactose to induce the expression. Yeast cells were harvested, washed in ddH2O and lysed mechanically with glass beads as previously described . 15 μg (p53) and 75 μg (p63β and p73β) were loaded on a 7.5% Acrylamide gel and separated by SDS-PAGE. DO-1, 4A4 (Santa Cruz Biotechnology, Milan, Italy) and ER-15 (Calbiochem, Merck, Millipore, Milan, Italy) antibodies were used for p53, p63 and p73 immunodetection, respectively. PhosphoGlycerate Kinase 1 (PGK1, detected by Ab clone number 22C5D8, InVitrogen, Life Technologies) was used as loading control.
To demonstrate p53 stabilization and activation upon treatment with doxorubicin or Nutlin-3A, MCF7, HCT p53+/+ and HCT p53−/− cells were harvested 16–18 hours after the treatments and lysed using RIPA (Radio Immuno Precipitation Assay) buffer (150 mM sodium chloride; 1.0% NP-40; 0.5% sodium deoxycholate; 0.1% SDS, sodium dodecyl sulphate; 50 mM Tris, pH 8.0) supplemented with Protease Inhibitors cocktail (Roche, Milan, Italy) . 50 μg of the soluble extracts were loaded on a 12% Acrylamide gel and separated by SDS-PAGE. p53 and p21 endogenous protein levels were detected with incubation with monoclonal antibodies (DO-1 and C-19 clones against p53 and p21 respectively, Santa Cruz Biotechnology). Glyceraldehyde 3-phosphate dehydrogenase protein (GAPDH, Ab clone 6C5, Santa Cruz Biotechnology) served as loading control. All antibodies were diluted in 1% non-fat skim milk dissolved in PBS-0.1% Tween20.
Chromatin immunoprecipitation (ChIP) analysis
HCT116 p53+/+ and HCT116 p53−/− or MCF7 cells were grown on 150-mm dishes and treated with 1.5 μM doxorubicin for 24 hours. Proteins were cross-linked with DNA by addition of 1% formaldehyde. After 10 minutes incubation at room temperature the reaction was stopped by addition of glycine at a final concentration of 0.125 M followed by additional incubation for 5 minutes. Cells were washed twice with 10 ml cold PBS, harvested in 1 ml PBS plus protease inhibitors (PI) (Complete EDTA-free, Roche), and lysed using an SDS lysis buffer (1% SDS, 50 mM Tris–HCl pH 8, 20 mM EDTA, 0.1 mg/mL Sonicated Salmon sperm DNA, 1X PI). In order to eliminate soluble p53 protein, lysates were incubated with gently shaking for 10 min and insoluble material was collected by centrifugation at 800 g at 4°C for 5 min. Pellets were resuspended in 0.5 ml of sonication buffer containing 0.25% SDS, 200 mM NaCl, 100 mg/ml of sonicated salmon sperm DNA and protease inhibitors and were sonicated to shear DNA to lengths between 150 and 500 base pairs (bp) using a Misonix S-4000 sonicator with a plate horn (Misonix, Newtown, Connecticut, USA). After 10-fold dilution in ChIP dilution buffer (16.7 mM Tris, 0.01% SDS, 1.1% Triton X-100, 1.2 mM EDTA, 167 mM NaCl), IPs were carried out overnight at 4°C with 2 μg of anti-p53 (DO-1, Santa Cruz Biotechnology) or 2 μg of normal IgG as a negative control. Fifty microliters of Dynabeads protein G magnetic beads (Invitrogen, Life Technologies) were added to each sample for 2–3 h, and the beads were then washed as indicated in the Upstate Biotechnology ChIP protocol. DNA was eluted firstly with 100 μL of TE with 1% SDS for 10 min at 65°C and a second time with 150 μL of TE with 0.67% SDS for an additional 10 min at 65°C. The cross-links were reversed overnight at 65°C. RNase A was added and incubated at 37°C for 30 min and then Proteinase K for 2 h at 56°C. DNA was then purified by QIAquick PCR purification KIT columns (Qiagen, Milan, Italy). Immunoprecipitated DNA was analyzed for p53 occupancy on selected chromosomal sites surrounding the predicted miR-associated p53 REs by RealTime-qPCR and fold enrichment of p53 binding to the respective DNA sequences was calculated by the comparative Ct method as described previously . RealTime-qPCR was carried out with the KAPA SYBR Green PCR mix (Kapa Biosystems, Resnova) and all primers were checked for equal amplification efficiency. All PCR results were normalized to input controls. Three different DNA loci were used as ChIP negative controls (the CCNB1 exon 9, the Actin and GAPDH promoter). Sequences of all ChIP primers are available upon request.
Results and discussion
Identification of functional p53 response elements in miR genes
Next we tested p63 and p73 responsiveness of the same panel of REs, using the transactivation competent, TA-p63β and TA-p73β isoforms for these proof-of-principle experiments, as they exhibit higher relative transactivation potential compared to N-terminal truncated ΔN- and also compared to TA-p63α and TA-p73α isoforms . As expected the transactivation potential of p63 β and p73β were much lower compared to p53 (Figure 1C and D). Only a subset of p53-responsive REs was active with p63 and p73 and included miR-34a, -202 and −1204 REs. Furthermore, differences in relative transactivation potential were observed in the comparison of the three family members. For example, miR-34a and −1204 were more responsive to p63 than to p73. Furthermore, we observed examples of selective lack of responsiveness: p73 towards miR-10b and −221 REs; p63 towards mir-151a. To verify the protein expression of the three p53 family members in yeast after galactose induction (0.128% and 1% galactose for p53 or p63 and p73, respectively, to match the experimental conditions used for the luciferase assays) we performed a western blot using antibodies specific for each transcription factor (Figure 1E).
Overall these results identify a panel of p53 REs that based on the comparison with well-established REs from coding genes [31, 37] suggest the potential for p53-mediated control of miR gene expression in vivo. Further, results suggested that miRs could be selectively or more specifically (e.g. -10b, -151a; -198) targeted by individual p53 family proteins, possibly contributing to the distinctiveness of the regulated networks and biological outcomes. Finally, the identified p53 miR-REs can be used to refine the functional classification of cancer associated p53 mutant alleles.
p53-occupancy at endogenous miR-associated promoters in human cells
Downstream of and consistent with the yeast-based results, ChIP assays further supported the putative function of the identified p53 REs in modulating p53-mediated responsiveness of miR genes. However, the correlation between occupancy and transactivation is not direct, nor linear . p63 and p73 occupancy was not investigated and awaits further studies to clarify the contribution of p53 family proteins on miR gene expression.
Doxorubicin responsiveness of identified p53 target miRs in p53 wild type human cells
To exclude any impact of the miR maturation processes or low sensitivity of the mature miR assay systems, we also selected primers that can amplify the pre-miR RNA and performed RT-qPCR for miR-1204, miR-1206, miR-202 and miR-34a (Figure 4B). We also analyzed the expression of PVT1, the long non-coding RNA transcript comprising the miR-1204 cluster . Weak, DXR-dependent induction was observed for PVT1, pre-miR-1204 and pre-miR-1206 in HCT116 p53+/+ and MCF7 cells. No changes were observed in HCT116 p53−/− or repression of PVT1 (Figure 4B). To further confirm the direct involvement of p53 in the transcriptional regulation of those miRs we also treated the cells with the MDM2 specific inhibitor Nutlin-3A (Figure 4C). Except for pre-miR-34a, pre-miR-1204, -1206 and even −202 were responsive to Nutlin treatment only in the HCT116 p53+/+ cell line, highlighting cell type and treatment dependencies in the expression regulation. The effect of the treatments on p53 stabilization and activation was examined using western blot (Figure 4D).
miR expression analysis in doxorubicin treated cells differing for p53 status supported p53-mediated responsiveness for miR-10b, -151a and, limited to MCF7 cells, also -23b. The levels of induction were in general comparable to those of miR-34a. Despite the high transactivation potential of the associated p53 REs and the p53 occupancy analysis, the mature miR-202 was not responsive to p53-inducing treatment. This discrepant finding could be related to the relatively large distance between the mapped p53 REs and the pri-miR-202 transcript start site and/or to the inaccessibility of the site due chromatin structure. The p53 RE sequence does not fall within DNAse sensitive sites based on ENCODE data. We were not able to confirm the p53-dependent induction of mature miR-1204 and −1206 in our cell lines, although we detected weak induction of the long noncoding RNA containing the miR-1204 cluster and possibly evidence for an internal transcript comprising pre-miR-1206. A recent study established p53-dependent induction of Plasmacytoma Variant Translocation 1 gene PVT1 and miR-1204  in HCT116 p53 wild type cells treated with doxorubicin. Our results confirm those findings and also suggest p53 recruitment internally to the PVT1 gene locus to possibly further modulate miR-1206 independently or in addition to the activation of the entire miR-1204-1208 cluster. Further studies are needed, including the use of cell lines expressing higher basal levels of PVT1 to examine whether miR-1206, and possibly −1207 and −1208 downstream, can be modulated by p53 family proteins also independently from PVT1 gene transcription. A link between p53 and modulation of miR-23b was also recently described and indirectly related to human papillomavirus (HPV)-mediated responses through inhibition of p53 function . Our results further confirm miR-23b as a p53 target miR in other cancer–derived cell lines. A previous link between p53 and miR-151a, as well as FAK pre-mRNA that contains miR-151a, was proposed based on transient silencing of p53 in the hepatocellular carcinoma-derived HepG2 cells resulting in FAK and miR-151a up-regulation (Figure S4 in ). Our results in different cell models indicate instead the potential for positive modulation of this miR by doxorubicin treatment in p53 wild type cells. Bioinformatics-based predictions, transactivation potential of RE, occupancy and mature miR expression changes in doxorubicin treated cells, consistently indicate, to our knowledge for the first time, miR-10b as a p53 target gene.
An expanded role of p53 in the modulation of microRNA expression
The study of the p53 gene transcriptional networks continues to raise particular interest in the field due to the increasing complexity of regulatory circuits and the functions of the extensive list of target genes spanning a myriad of different biological pathways. The discovery of p53-target miRs has led to the identification of several feedback and feed-forward loops that can lead to fine-tuning of p53-mediated responses. A few p53 target miRs, more prominently miR-34a, have been shown to act as bona-fide tumor suppressor genes [56, 57]. Multiple evidence, comprising gene expression, ChIP-seq and phenotypic studies upon gene silencing or targeting in cell and animal models indicate a complex crosstalk between p53 and the related p63 and p73 proteins at the level of common and exclusive coding gene targets [58–61]. An integrated view of common and p53-family protein specific regulation of miR genes is however largely missing.
This work led to the identification of new p53 target miRs (miR-10b; -151a) and also confirmed or extended recent evidence from the literature (miR-1204, -1206; -23b). Proof-of-principle experiments also suggested miR genes worth of further analysis to ascertain a specific or selective role for p63 or p73 transcription in their expression. The weak p53-responsiveness towards p53 REs associated with miR-106a, -191, -198, -221 and −320 was not pursued in this study and awaits further investigation.
Perhaps surprising is the fact that the miR genes we propose (miR-10b; -151a) or confirm more in detail (miR-23b; -1204; -1206) as direct p53 targets do not fit intuitively with the expected p53-mediated functions. In fact all these miRs have been proposed to exhibit oncogenic activities or at least their over-expression has been correlated to aggressive cancer phenotypes in some tissues [55, 62–66]. For example, the established potential for miR-10b to target both CDKN1A and CDKN2A mRNAs could in principle result in a p53-directed attenuation circuit of cell cycle arrest and senescence . However, KLF4 mRNA has been described as a miR-10b target and KLF4 down-regulation in breast cancer cells has been reported to restore p53 functions leading to apoptosis . Hence, in specific cellular contexts, it is possible that the p53-dependent regulation of miR-10b we discovered could result in a positive feedback loop stimulating p53 activity. Further, CpG islands upstream from the miR10b/10b* locus were found to be hyper-methylated in breast cancers and through ectopic expression an important role for miR-10b* in cell cycle inhibition was established .
It is known that miR functions can be highly context and tissue-dependent and their p53-mediated control in normal cells could potentially affect biological responses also not directly related to cell cycle control or apoptosis. For example, low levels of miR-23b resulting in higher levels of its target urokinase-type plasminogen activator could promote cervical cancer cell migration . Finally, increasing evidence link p53 functions to innate and adaptive immunity and it could be speculated that miR-23b as well as PVT1 and the miR-1204 cluster regulation could be relevant in this context [53, 69]. Interestingly, functional enrichment analyses of predicted targets of both miR-10b and -151a showed enrichment for neuron generation/development and brain-related phenotypes (uncorrected p-value < 0.05; data not shown).
In our study, bioinformatics-based predictions, transactivation potential of putative p53 REs, p53 occupancy at the endogenous RE positions, and mature miR expression changes in cell lines differing for p53 status, were combined to identify miRs that are direct transcriptional targets of wild type p53. We established that miR-10b and miR-151a are new p53 target genes and also confirmed cis-mediated regulation by p53 of miR-1204, -1206 and -23b. Further studies are warranted to establish the biological implications of the newly identified p53 target miRs.
We thank Gilberto Fronza and Paola Monti for sharing the panel of germline Li-Fraumeni derived p53 mutant expression plasmids. This work was partially supported by the AIRC, Italian Association for Cancer Research (Associazione Italiana per la Ricerca sul Cancro, #IG9086 to AI) and by CIBIO start-up funds. YC is supported by a Marie-Curie/Autonomous-Province-of-Trento (PAT) cofund grant (#40101712). VDV is recipient of an Outgoing Marie-Curie/Autonomous-Province-of-Trento (PAT) cofund grant. VDS was supported by a Pezcoller Foundation fellowship.
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