Androgen responsive intronic non-coding RNAs
© Louro et al; licensee BioMed Central Ltd. 2007
Received: 01 September 2006
Accepted: 30 January 2007
Published: 30 January 2007
Transcription of large numbers of non-coding RNAs originating from intronic regions of human genes has been recently reported, but mechanisms governing their biosynthesis and biological functions are largely unknown. In this work, we evaluated the existence of a common mechanism of transcription regulation shared by protein-coding mRNAs and intronic RNAs by measuring the effect of androgen on the transcriptional profile of a prostate cancer cell line.
Using a custom-built cDNA microarray enriched in intronic transcribed sequences, we found 39 intronic non-coding RNAs for which levels were significantly regulated by androgen exposure. Orientation-specific reverse transcription-PCR indicated that 10 of the 13 were transcribed in the antisense direction. These transcripts are long (0.5–5 kb), unspliced and apparently do not code for proteins. Interestingly, we found that the relative levels of androgen-regulated intronic transcripts could be correlated with the levels of the corresponding protein-coding gene (asGAS6 and asDNAJC3) or with the alternative usage of exons (asKDELR2 and asITGA6) in the corresponding protein-coding transcripts. Binding of the androgen receptor to a putative regulatory region upstream from asMYO5A, an androgen-regulated antisense intronic transcript, was confirmed by chromatin immunoprecipitation.
Altogether, these results indicate that at least a fraction of naturally transcribed intronic non-coding RNAs may be regulated by common physiological signals such as hormones, and further corroborate the notion that the intronic complement of the transcriptome play functional roles in the human gene-expression program.
Non-coding RNAs (ncRNAs), particularly those transcribed from genomic regions spanning introns of spliced genes, have been proposed as a fundamental advance in the genetic operating system of higher organisms by influencing the genomic program of differentiation and development in individuals and species [1, 2]. Many functions, such as transcriptional or translational regulation, RNA splicing, gene silencing, imprinting and dosage compensation, have been assigned to mammalian ncRNAs . Most functionally characterized ncRNAs belong to classes of small RNAs such as microRNAs  and small nucleolar RNAs (snoRNAs) . While several novel long ncRNAs have been described in mammalian organisms [6, 7] few have been characterized in more detail, the ~15 kb Xist RNA involved in inactivation of chromosome X being an exception .
Recent studies based on computational analysis and experimental validation have revealed that both introns and intergenic regions constitute major sources of ncRNAs [3, 9, 10]. Extensive analyses of the human expressed sequence tags (EST) database have focused particularly on spliced mRNAs, and ESTs that overlap at least one exon have identified an abundant number of sense-antisense transcript pairs in humans [7, 11, 12], mice  and plants , pointing to a well-conserved mechanism of post-transcriptional regulation of gene expression in eukaryotes.
Recently, microRNAs have been shown to be consistently altered in normal and tumor cells, allowing the identification of tissue-specific expression signatures . Using a custom-built cDNA microarray enriched in ESTs corresponding to fragments of intronic transcripts, we previously detected transcription of a set of totally intronic ncRNAs, which are long (0.6–1.1 Kb), unspliced, and oriented in the antisense direction relative to the corresponding protein-coding transcript . Moreover, expression levels of 23 intronic ncRNAs were shown to correlate with the degree of tumor differentiation in prostate cancer . The potential role of long ncRNAs in human cancer is also exemplified by MALAT-1, a 7-kb RNA that was reported to be associated with metastatic non-small cell lung cancer . Other reports have shown that totally or partially intronic long antisense transcripts may have regulatory functions, such as modulating the methylation status of promoters  or the alternative splicing pattern of the corresponding protein-coding gene . However, little attention has been given to the mechanism used by the cell to control the expression of these long intronic RNAs.
Androgens have been implicated in central events governing the regulation of distinct and diverse physiological processes in normal and neoplastic prostate cells. These hormones are known to promote cell division and proliferation of epithelial cells, to modulate programmed cell death and cell quiescence [20, 21] and to regulate cellular metabolism . More recently, several studies have characterized the temporal transcriptional program reflecting the cellular response to androgens, which led to the identification of novel androgen-regulated protein-coding genes [23–25].
In the present study, to identify androgen-responsive non-coding intronic RNAs, we used a custom-built spotted cDNA microarray enriched in intronic transcribed sequences and a prostate cancer cell line (LNCaP) cultured in the presence of a synthetic androgen. Using orientation-specific reverse transcription followed by PCR (RT-PCR) we determined the sense or antisense direction of a subset of intronic transcripts. We found that the levels of these intronic RNAs in androgen-treated and control cells correlate with the levels of message or to the alternative usage of exons in the corresponding protein-coding transcript. Additional approaches such as rapid amplification of the cDNA ends (RACE) and chromatin immunoprecipitation assays (ChIP) demonstrated that these intronic messages represent long and unspliced RNA transcripts that may be directly regulated by the androgen receptor (AR) in vivo. These findings indicate that transcription of long intronic ncRNAs may be controlled by mechanisms common to protein-coding transcripts, such as those involving hormonal control of gene-promoter activation. In addition, our results indicate that a fraction of this class of long unspliced intronic RNAs may have a role in post-transcriptional regulation of gene expression by modulating transcript stability and alternative splicing.
Results and discussion
Identification of intronic RNAs regulated by androgen
Androgen-regulated intronic RNAs could be grouped into three clusters based on their different temporal patterns of expression after androgen exposure (Figure 1B). Cluster I contained RNAs whose levels were 2–3-fold downregulated within 24 h after androgen exposure and were restored at 48 h. Clusters II and III included intronic RNAs that were upregulated by androgen within 24 h and later restored. Cluster II grouped RNAs that were 2-t3-fold increased, and cluster III grouped RNAs that were upregulated 3–6-fold. All of these intronic RNAs are unspliced messages, and apparently have no coding potential as determined by ESTScan analysis  (a complete list of androgen-regulated intronic RNAs is provided in Additional file 4).
Most mammalian snoRNAs  and a large fraction of microRNAs  are derived from intronic sequences of protein-coding and noncoding genes. To investigate the possibility that some of the androgen-regulated intronic transcripts might be primary transcripts that, after processing, could generate known small RNAs of those classes, we compared the sequence of the 39 androgen-regulated intronic RNAs with those of 346 snoRNAs  and 383 microRNAs ; no similarity was found.
We then investigated the enrichment of specific gene ontology (GO) categories for androgen-regulated exonic and intronic transcripts using BiNGO, a gene ontology comparison tool . We postulated that intronic transcripts represent a new class of RNAs that might act as cis-regulatory factors . Thus, for each androgen-regulated intronic transcript we used the GO annotation assigned to the corresponding protein-coding mRNA mapping to the same genomic locus. We found no significant enrichment of specific GO categories (p < 0.05) among the selected sets of exonic or intronic androgen-regulated transcripts when a correction for multiple testing was applied. However, we noted that 13 of the set of 39 androgen-regulated intronic transcripts belonged to the signal-transduction GO category (GO no. 0007165). Indeed, some of these loci have already been implicated in cellular events related to prostate cell growth and differentiation. For example, the protein encoded by GAS6 mRNA is a ligand of the Axl receptor tyrosine kinase, and the Gas6/Axl complex has been shown to exhibit mitogenic activity in human prostatic cancer cell lines by modulating the PI3K/AKT and MEK signal-transduction pathways . Similarly, the transcription factor encoded by ERG, a member of the ETS family of central genes involved in integrating signals that regulate cell growth and differentiation, stress responses and tumorigenesis, has been previously identified as the most frequently overexpressed proto-oncogene in malignant prostate epithelial cells .
Characterization of androgen-regulated intronic RNAs
Orientation-specific RT-PCR was performed (see Methods for details) on a selected set of androgen-regulated intronic RNAs (Figure 1C). Sense or antisense orientation of the intronic RNA relative to the corresponding protein-coding gene could be unambiguously assigned in most cases (13 of 17). For most of these (10 of 13) an intronic antisense RNA could be detected (Figure 1D). For six of these antisense RNAs (DNAJC3, SAP18, KDELR2, FLJ10154, MYO5A and ATF2) we detected an overlapping intronic sense message transcribed in the opposite strand. Four RNAs (GAS6, RAB25, ITGA6 and ADD3) were only detected in the antisense orientation, and three intronic messages (ACTN4, STARD13 and ERG) were only detected in the sense orientation (Figure 1D). The intronic sense transcripts of ACTN4, STARD13 and ERG did not show coding potential as determined by ESTScan. Without further experimentation, we could not determine if these intronic sense transcripts are novel non-coding exons present in alternative splicing forms, or if they represent ncRNAs originated from independent intronic transcriptional units located in the sense strand. However, the latter explanation concurs with sense intronic transcriptional units that have been observed elsewhere [9, 36].
A strand-specific northern blot confirmed the expression of a long (~5 kb) GAS6 antisense transcript in various human tissues (Figure 2F). The observation that androgen-regulated intronic RNAs could be detected in tissues that are not particularly responsive to this hormone (Figure 2, panel F) suggests that regulation of the steady-state levels of these transcripts may also proceed through an androgen-independent pathway.
Effect of androgen in the levels of intronic RNAs and corresponding protein-coding transcripts
Of the androgen-regulated transcripts identified in our analysis, only KDELR2 and ADD3 showed detectable changes in expression levels of both intronic and exonic transcripts. The intronic ADD3 transcript increased 4.9-fold (log2 ratio = 2.3) in androgen-treated cells, whereas the corresponding protein-coding transcript decreased 3.3-fold (log2 ratio = -1.7) in the same experiment. Intronic KDELR2 transcript levels increased 2-fold (log2 ratio = 1), and the corresponding exonic transcript increased 2.3-fold (log2 ratio = 1.2) in cells exposed to androgen relative to control cells (see Additional files 3 and 4). These results indicate that for a given intronic-exonic pair transcribed in the same locus, the intronic message may be directly or inversely modulated with respect to the exonic message after androgen treatment.
To accumulate further evidence of functional involvement of antisense intronic non-coding transcripts on the splicing mechanism [19, 33], we investigated the existence of correlation between their relative levels and the levels of the corresponding protein-coding mRNAs, using primers designed to probe regulated exons, that is, exons that are absent in at least one documented transcript isoform. At the KDELR2 locus, we found that exons 2 and 3 were upregulated (2-fold) after androgen treatment (Figure 3C, exonic panel). Notably, exon 2 was absent in one KDELR2 transcript isoform [GenBank: BP269541]. Therefore, it is conceivable that the observed increase in the level of intronic antisense RNA for KDELR2 after androgen treatment may induce increased retention of exon 2. We could not detect any notable androgen-driven change in the levels of transcripts containing exons 1 and 3 or exons 1 and 4 (Figure 3C, exonic panel). Notwithstanding, we observed that exon 1 for KDELR2 was downregulated 2.4-fold after androgen treatment when a pair of primers designed to probe only this exon was used (Figure 3C, exonic panel). This result can only be accounted for by the accumulation after androgen treatment of an as yet uncharacterized alternative KDELR2 transcript with a shorter 3' end.
At the ITGA6 locus we found that the levels of a protein-coding transcript isoform containing a longer terminal exon (exon 22D) were downregulated 4.2-fold after androgen treatment (Figure 3D, exonic panel), and thus inversely correlated with the 4.2-fold increase observed in the antisense intronic RNA under the same conditions (Figure 3D, intronic panel). However, it was not possible to determine whether this result was actually due to downregulation of the ITGA6 mRNA isoform containing exon 22D, as we also detected downregulation of another intronic transcript naturally transcribed in the ITGA6 locus [GenBank: BX537483] that spans the 3' terminal exon of the gene (Figure 3D).
Non-coding RNAs have been shown to affect splicing of protein-coding genes [19, 39]. HBII-52, a snoRNA was found to regulate alternative splicing of the serotonin receptor gene 5-HT2CRA in trans, by binding to a silencing element in exon Vb of 5-HT2CRA . Lack of HBII-52 expression causes defective 5-HT2CRA pre-mRNA processing and probably accounts for the behavioral problems observed in patients with congenital Prader-Willi syndrome . A previous study on the FAS locus has identified a partially intronic antisense RNA that is naturally transcribed from the first intron of the gene, which was named Saf . In vitro overexpression of Saf induced skipping of several 3' exons of Fas mRNA, resulting in a Fas protein that was no longer able to anchor to the cell membrane or to induce Fas-mediated apoptosis . Our results identify novel intronic antisense RNAs that might be involved in regulatory mechanisms of alternative splicing of protein-coding genes, in analogy to those observed for HBII-52 and Fas/Saf.
Increased binding of the androgen receptor to an androgen response element motif upstream of asMYO5A
Androgen-mediated transcriptional regulation involves direct hormone interaction with the AR protein and the translocation of this complex to the nucleus, promoting specific interactions with DNA (i.e. androgen response element; ARE) motifs located near or within the target sequences . To support a mechanism of direct transcriptional control of androgen-regulated intronic RNAs, we used a bioinformatics approach  to look for putative ARE motifs located upstream of the identified androgen-regulated intronic RNAs. At least one putative ARE motif was identified for 24 androgen-regulated intronic transcripts (a complete list of identified putative ARE motifs is presented in Additional file 5).
The presence of a weak band for asMYO5A ARE in control cell lysates immunoprecipitated with anti-AR (Figure 4B, asMYO5A ARE), indicating that binding of AR to asMYO5A ARE may occur to some extent in untreated cells. This may be explained by the presence of trace amounts of androgen remaining in charcoal-stripped fetal calf serum added to the cell-culture medium. An alternative explanation for the background signal of asMYO5A ARE measured in control cells may be the existence of small amounts of AR constitutively bound to the chromatin, as described for another transcription factor, cyclic AMP-responsive element-binding protein (CREB) .
The increased binding of AR to the asMYO5A ARE motif is in agreement with the androgen-induced increased expression of the antisense intronic MYO5A RNA (asMYO5A) detected by microarray (Figure 1), and confirmed by orientation-specific reverse transcription followed by real-time PCR (Figure 4A). MYO5A encodes an actin-based processive motor involved in intracellular trafficking and exocytosis . Tissue-specific Myo5a isoforms are originated from alternative exon usage of the primary transcript, which in turn is thought to modulate the protein specificity for different cargoes within the cell . It is conceivable that the increase in asMYO5A levels in prostate cells in response to androgen affects the relative levels of the alternatively spliced forms of MYO5A, thus modulating protein activity or specificity. Together, these results suggest that functional binding of androgen-AR activated complexes to regulatory ARE regions is required to modulate the levels of intronic antisense RNAs after androgen treatment of prostate cells.
Although there is still no conclusive evidence about the molecular mechanisms involved in response to androgen, we postulate that intronic transcripts exert their regulatory functions by acting in cis through Watson-Crick base-pairing to complementary sense pre-mRNA . The results presented here corroborate the notion that at least a fraction of these intronic transcripts may directly affect the levels and/or splicing of the protein-coding transcript originating in the opposite strand, and concur with previous reports in the literature [44, 45].
It is not yet clear if the intronic transcripts identified in this work exert their potential regulatory functions as long (0.5–5 kb) RNAs, or alternatively, as shorter RNAs resulting from processing of the primary transcript. Processing of these androgen-regulated ncRNAs into shorter RNAs of defined sizes would also raise the possibility that some may modulate transcriptional or post-transcriptional events in messages from different loci, in a manner similar to microRNAs . The identification of possible short RNAs modulated by androgen will require further work, such as 15% denaturing polyacrylamide gel electrophoresis or northern blots of prostate cells exposed to androgen in time-course experiments to document the accumulation of the long intronic RNAs, the time course of their conversion to short RNAs, and the accumulation of possible short RNA intermediates.
Previous reports have shown that a large number of transcription-factor binding sites (TFBSs) for well-characterized transcription factors such as Sp1, c-Myc, p53 and Creb lie upstream to transcriptionally active intronic regions [41, 46], some of which generate transcripts that are oriented antisense relative to the known gene . Notably, Cawley et al  found that comparable fractions of protein-coding genes and ncRNAs having an experimentally determined upstream TFBS region were regulated after exposure to retinoic acid. The results presented here provide further evidence that ncRNAs transcribed from intronic segments of the human genome may be regulated by physiological signals that commonly act on protein coding-transcripts such as hormones. Similar results were observed in mice when the effect of lipopolysaccharide stimulation on the levels of several long ncRNAs was measured . Together, these results strongly suggest that at least in mammalian cells intronic ncRNAs are transcribed in a regulated fashion and therefore must exert physiological roles, which corroborates the existence of a yet underappreciated complex RNA-based regulatory system involving non-coding messages in higher organisms [2, 3, 48].
Cell culture and RNA isolation
The experimental design was based on recent published work . In summary, prostate carcinoma cell lines LNCaP, DU145 and PC3 were obtained from the American Type Culture Collection and maintained using the suggested medium supplemented with 10% (v/v) fetal calf serum (FCS), 3 mM L-glutamine, 100 μg/ml streptomycin and 100 U/ml penicillin. LNCaP cells were grown in RPMI 1640, and DU145 and PC3 cells were cultured in DMEM. For the androgen-response experiments, LNCaP cells were cultured for 24 hours in androgen-deprived medium (RPMI 1640) with 5% (w/v) charcoal-stripped fetal calf serum (FCS; Invitrogen, Carlsbad, CA, USA). After 24 hours, cells were placed in fresh RPMI 1640 medium, with 10% (w/v) charcoal-treated FCS, and either 1 nM of the synthetic androgen R1881 (Perkin Elmer, Wellesley, MA, USA) or equivalent volume of vehicle (ethanol) was added. Cells were harvested after 0, 6, 9, 12, 18, 24, and 48 hours for RNA isolation. Two independent cultures of androgen-treated cells and of control cells (independent biological replicates), were used for RNA isolation.
In parallel, cells were harvested after 4 hours of hormone treatment for isolation of DNA that was subsequently used in ChIP assays, as described below. Total RNA was purified from experimental and control cells by caesium chloride cushion  after cell lysis (4 M guanidine isothiocyanate; 0.1 M β-mercaptoethanol; 25 mM sodium citrate pH 7.0). Total RNA (100 μg sample) was treated with RNase-free DNase (RNeasy kit; Qiagen, Hilden, Germany) for 15 min in the medium recommended by the manufacturer to minimize genomic DNA contaminants, and kept at -80°C until use.
The microarray platform used in this study was constructed using PCR-amplified cDNA fragments derived from ORESTES clones , and spotted onto Type 7 STAR glass slides (GE Healthcare, Piscataway, NJ, USA) as previously described . This consists of a 9216-element microarray (3355 unique cDNA probes spotted in duplicate, plus positive and negative controls) enriched in probes representing intronic (822 probes) and intergenic (241 probes) ncRNAs. For each time point, 15 μg of DNAse-treated total RNA from androgen-treated or untreated control LNCaP cells were used to generate fluorescent targets by incorporation of Cy5-dUTP in reverse transcription reactions using the CyScribe First strand cDNA labeling kit (GE Healthcare) and the protocol recommended by the manufacturer. Fluorescent targets labeled with Cy3-dUTP were generated in parallel from a reference RNA pool consisting of equimolar quantities of DNAse-treated total RNA from LNCaP, DU145 and PC3 cells.
For each independent biological replicate hybridization, fluorescently labeled targets from each experimental time point and the reference pool were combined and hybridized on an automated slide processor (GE Healthcare) using protocols recommended by the manufacturer. For each time point, two independent biological replicate hybridizations were performed. Each hybridization used one RNA, isolated from a different biological replicate of androgen-treated or untreated control cells. Processed slides were scanned in a microarray scanner (GenePix 4000 B; Molecular Devices, Sunnyvale, CA, USA). More detailed information about microarray experiments and analysis is provided as supplementary material (see Additional file 6) following MIAME guidelines .
Data acquisition and statistical analysis
Background-subtracted artifact-removed median intensities of both Cy3 and Cy5 emissions were extracted for each spot from raw images using image analysis software (ArrayVision version 8.0; GE Healthcare). Only spots with signal intensity above the average plus 3 SD from a set of negative controls (plant and bacterial DNA) were used in subsequent analyses. As each microarray contains two replicates of each spotted cDNA, a total of four replicate measurements was obtained for each spot at each time point. We evaluated the average coefficient of variation between replicates of expression ratios between treated and control cells calculated in two different ways. For each time point, expression ratios between treated and control cells were reconstructed either from (i) ratios relative to the reference pool or (ii) Cy5 intensities obtained from androgen-treated and control cells using a one-color approach . A smaller average coefficient of variation between replicates was obtained with the latter approach, and therefore we opted to use only the Cy5-labeled sample measurements to calculate the treatment:control sample ratios. We used the mean intensity signal (40% trimmed) of each dataset for normalization between experiments. Raw and normalized microarray intensities were deposited in the Gene Expression Omnibus (GEO) database  (accession number GSE5345).
Transcripts with statistically significant changes in expression in response to androgen stimulation were identified using the statistical analysis of microarrays (SAM) method . Only transcripts showing significant expression changes in at least three consecutive time points were selected for further analysis, using as parameters the two-class response (paired data), 1000 permutations, K-nearest neighbors imputer, fold change ≥ 1.5 and FDR < 5%. Expression profiles of SAM-selected transcripts were grouped using hierarchical clustering (UPGMA with Euclidean distance) and visualized using software (Spotfire Decision Site; Spotfire, Somerville, MA, USA).
Orientation-specific RT-PCR and orientation-specific real-time quantitative RT-PCR
Orientation-specific RT-PCR was performed as previously described . Briefly, 4 μg of DNase-treated total RNA from androgen-treated or control LNCaP cells were used to generate strand-specific cDNA. RNA samples were selected from experimental time points that showed higher fold change relative to control cells as identified in microarray hybridizations. The same RNA samples were used in microarray hybridizations and real-time PCR reactions. To determine the levels of sense and antisense intronic transcripts in androgen-treated and control cells, we performed one orientation-specific reverse transcription reaction for each strand using a single RNA sample, and gene specific (forward or reverse) primers. RNA samples plus 0.9 μM of specific primer for either antisense or sense strand of each intronic segment were heated to 75°C for 10 minutes to minimize artifacts derived from the formation of secondary structure. Reverse transcription was performed at 50°C for 60 min in a 50-μl volume, using 200 U of reverse transcriptase (SuperscriptII; Invitrogen). Controls for the absence of self-priming were obtained by performing reverse transcription in the absence of primers, and controls for the absence of genomic DNA contamination were obtained by incubation with primers in the absence of reverse transcriptase enzyme. A reaction containing a primer complementary to the coding region of TUBA6 (reverse primer: AGTGCCAGTGCGAACTTCATC) was carried out in parallel. Reverse transcriptase was denatured for 30 min at 95°C. One pair of internal primers for PCR amplification of either the tubulin gene or the desired target intronic segment under study was added. For each intronic transcript, cDNAs with sense or antisense orientation relative to the corresponding gene were analyzed by three replicate measurements in quantitative real-time PCR reactions. For exonic transcripts, cDNA was obtained by reverse transcription of RNA samples using oligo-dT primers, and the levels of each message was also determined by three replicate measurements in real-time PCR reactions with gene specific primers. All real-time PCR reactions were carried out in a volume of 20 μl for 40 cycles, according to the manufacturer's instructions for the reagent (Sybr-Green PCR core reagent; Applied Biosystems, Foster City, CA, USA) using an automated sequence analyser (GenAmp 5700; Applied Biosystems). For quantitative results, the levels of each transcript detected by real-time quantitative PCR was normalized to the level of tubulin, and represented as fold change using the ΔCt method . Quantitative results for a transcript in androgen-treated cells were expressed as relative fold change with respect to the value of the target transcript in the control (ethanol vehicle), which was set at unity.
Rapid amplification of cDNA ends-PCR and northern blot
For RACE-PCR we used a commercial cDNA library prepared from poly(A)+ RNA isolated from a human prostatic adenocarcinoma cell line (Human XG marathon-ready cDNA, catalog no. 7498-1; BD Biosciences, Palo Alto, CA, USA). Two rounds of PCR reactions were performed for each intronic transcript using two pairs of gene-specific primers in nested PCR reactions. To obtain a long (~5 kb) transcript corresponding to asGAS6, a gene-specific PCR was performed using a forward primer complementary to the partial asGAS6 cDNA sequence deposited in the microarray and a reverse primer complementary to the antisense transcript deposited in [GenBank: AK123478]. The PCR product was sequenced to confirm the identity. To confirm the size and orientation of the full-length asGAS6 obtained by PCR, a northern blot was performed using a commercial membrane containing 2 μg poly(A)+ RNA from 10 human tissues (First Choice Human Blot 4; Ambion, Austin, TX, USA), using a probe complementary to the antisense strand of GAS6 intronic transcript spotted onto the microarray. Sense α-[32P]-CTP-labeled RNA probes were obtained by in vitro transcription using T7 RNA polymerase (Riboprobe; Promega, Madison, WI, USA). Hybridization and wash procedures were carried out as described in the human blot manufacturer's protocol (Ambion). The probed blot was processed in a phosphorimager (Storm; GE Healthcare).
Putative identification of androgen-responsive elements and chromatin immunoprecipitation assay
Using a bioinformatics approach, we searched for regions with similarity to the palindromic ARE consensus AGAACAnnnTGTTCT , obtained from the TRANSFAC database of eukaryotic cis-acting regulatory DNA elements . The search was conducted within a 3-kb region of genomic sequence, upstream of the putative transcriptional start sites of the 39 androgen-regulated intronic transcripts identified in the microarray analysis. When available, RACE-extended fragments were used. ChIP assays were performed as described in the literature [56–58], and specific PCR primers were designed to detect binding of the androgen receptor to the putative ARE promoter sequence of asMYO5A, identified by in silico analysis. A chromatin immunoprecipitation assay kit (catalog no. 17–295, Millipore, Billerica, MA, USA) was used, with the protocols recommended by the manufacturer. Briefly, LNCaP cells treated with androgen or vehicle as described above were fixed with 1% formaldehyde for 10 min at room temperature and lysed with sodium dodecyl sulfate lysis buffer. Cell lysates were sonicated to shear the DNA between 200 and 1000 bp using a sonic dismembrator (Model 500; Fischer Scientific, Waltham, MA, USA). Aliquots of the lysate (100 μL). containing approximately 2 × 106 cells were diluted in 900 μL dilution buffer, and 10 μL from each aliquot (1% of total lysate) were separated and used subsequently as loading controls for input DNA. Parallel chromatin immunoprecipitation reactions were performed with either 3 μg polyclonal antibody anti-AR (H-280; Santa Cruz Technologies, Santa Cruz, CA, USA) or 1 μg normal mouse IgG (negative control). Immunoprecipitated chromatin fractions and respective loading control fractions were treated for cross-link reversal, treated with RNase A and proteinase K, and DNA fragments were purified using Spin Columns. An aliquote (2 μl) from each eluted DNA was used as template in PCR reactions with the following primers flanking the putative asMYO5A ARE: forward, TTTGCTGGATAAGGATTCCCA; reverse, AGTTCCTTAAACTTTAGCTTAGAAAAAGGA. Similar reactions were performed with control primers designed to the known AREIII motif of the PSA (prostate-specific antigen) enhancer (positive control) (forward primer: GCTCAGCCTTTGTCTCTGATGA, reverse: TGCAAGATGATATCTCTCTCAGATCC) and to the TUBA6 non-related upstream genomic sequence (negative control) (forward primer: GACTACAGGTGTGCGCCATCAT, reverse: TGCCGTGTTCCAGGCAGTAG). For each DNA target, semi-quantitative PCR was performed by running parallel reactions with increasing numbers of PCR cycles (25, 30 or 40 cycles). Cycle runs of 25 and 30 PCR cycles resulted in non-saturated amplification of each DNA target in immunoprecipitated and input DNA fractions from androgen-treated or control cells (data not shown). Equal volumes from each PCR reaction were loaded and separated in a 3% agarose gel. The intensity of PCR-amplified bands was determined by gel densitometry (Image Master; GE Healthcare).
We have deposited in GenBank the following sequence data under the indicated accession numbers (in parentheses): antisense intronic ITGA6 [GenBank: DQ866759], antisense intronic DNAJC3 [GenBank: DQ866760], antisense intronic MYO5A [GenBank: DQ866761], intronic STARD13 [GenBank: DQ866762], antisense intronic GAS6 [GenBank: DQ866763], antisense intronic RAB25 [GenBank: DQ866751], antisense intronic ADD3 [GenBank: DQ866752], intronic ACTN4 [GenBank: DQ866753], intronic SAP18 [GenBank: DQ866754], intronic ERG [GenBank: DQ866755], intronic KDELR2 [GenBank: DQ866756], intronic FLJ10154 [GenBank: DQ866757], and intronic ATF2 [GenBank: DQ866758].
Authors thank Junio Cota Silva and Vinícius Coutinho for technical help with RACE experiments. This work was mainly funded by grant 02/13283-6 from Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) to SVA and AMDS, by grant 03-465 RG/BIO/LA from TWAS to EMR, by grant 01/10707-7 to MCS from FAPESP and by fellowships to RL and HIN from FAPESP. Fellowships from Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) supported PPA and FF. MCS, AMDS and SVA were partially supported by CNPq.
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