Depletion of T-cell intracellular antigen proteins promotes cell proliferation
© Reyes et al.; licensee BioMed Central Ltd. 2009
Received: 15 July 2009
Accepted: 26 August 2009
Published: 26 August 2009
T-cell intracellular antigen-1 (TIA-1) and TIA-1 related/like protein (TIAR/TIAL1), two DNA/RNA binding proteins broadly expressed in eukaryotic cells, participate in the regulation of gene expression through RNA metabolism. Despite the biological relevance of these regulators, there are no genome-wide studies assessing global transcriptomic and phenotypic impacts after changes in the expression and/or function of these proteins.
Using high-throughput gene expression profiling, we found that the TIA-1/TIAR-depleted cell phenotype is linked to a transcriptome involved in the control of inflammation, cell-cell signaling, immune-suppression, angiogenesis, metabolism and cell proliferation. Induced genes included pro-inflammatory cytokines, inflammatory chemokines, growth-stimulating factors and pro-angiogenic inducers. Repressed genes involved the RAS oncogene family member RAB40B, regulators of cytoskeleton organization and biogenesis and a mitochondrial modulator. Consistent with these observations, depletion of TIA proteins in HeLa cells results in increased cell proliferation, altered cell-cycle and anchorage-independent growth. Mechanistically, the changes associated with the steady-state target mRNA levels regulated by TIA proteins are consistent with overlapping effects on gene basal transcription rate and mRNA turnover.
Collectively, our findings suggest a role for TIA proteins as cellular sensors that modulate gene expression control at the transcriptional and post-transcriptional levels, coupling cell proliferation responses and metabolic homeostasis to cell survival and growth.
One of the most important challenges resulting from our knowledge of the human genome - and, in general, of all genomes - is to understand how the collection of RNAs and proteins that define us as an organism are generated. Nowadays, we accept that the origin of our transcriptomic and proteomic diversity is due not just to the number of genes present in our genome but also to the dynamic and differential regulation of their expression. The characterization of transcriptional and post-transcriptional events leading to the generation of multiple RNAs, proteins and functions from a single or distinct RNA precursors reveals the existence of multiple layers and networks involved in regulating the diverse biological functions controlled by the transcriptome .
T-cell intracellular antigen (TIA)-1 and TIA-1 related/like factor (TIAR/TIAL1) are two proteins that play important roles in many aspects of RNA biology, from RNA transcription to splicing, stability and translation. Indeed, TIA proteins have been shown to interact with RNA polymerase II , DNA [3, 4] and RNA  and to participate in the control of alternative pre-mRNA splicing [6–8]. TIA proteins bind to uridine-rich sequences, which are mostly located in the introns, and seem to facilitate the recruitment of U1 small nuclear ribonucleoprotein, thus promoting the recognition and processing of atypical 5' splice sites [9, 10]. The cytoplasmic pool of these proteins has been linked to the control of translation and/or stability of some mRNAs through binding to adenine- and uridine-rich sequences located in 3' untranslated regions [11–14]. Additionally, these proteins are involved in cell responses to metabolic and genotoxic stresses as well as the formation of stress granules [15, 16]. It has also been reported that these proteins play a relevant role in the control of cell death [17–19] and viral replication . In fact, mice that lack either TIA-1 or TIAR show high rates of embryonic lethality, indicating a relevant role for these proteins during embryonic development [12, 21]. Furthermore, recent studies have identified a set of mRNAs that interact and are regulated by these proteins [22–24].
Altogether, these findings strongly support a key role for TIA-1 and TIAR proteins in the control of different aspects of RNA metabolism and function. However, little is known about how these regulators control the transcriptome and about the specific and/or overlapping functions associated with TIA proteins at this level. Here, we use a loss-of-function approach combined with global mRNA expression pattern and phenotypic profiling analyses to identify targets and pathways regulated by TIA proteins. Our data suggest that these proteins are involved in the transcriptional and post-transcriptional regulation of specific transcripts associated with the control of key cellular functions, such as inflammation, cell proliferation and anchorage-independent growth responses.
Gene expression profiling of TIA-1 and TIAR-depleted HeLa cells
In an attempt to address the functional relevance of the observed changes in high-density DNA microarrays, Gene Ontology (GO) analyses were performed for the up- and down-regulated genes. GO analysis was able to identify the main categories that had significant representation (P < 0.01) of differentially expressed genes controlled by TIA proteins (Figure 2c, d; Additional data file 3). GO categories related to inflammation and immune responses, cell proliferation, cell-cell signaling, chemotaxis, cell motility, angiogenesis and anagen were among the enriched categories in up-regulated genes (Figure 2c). On the other hand, GO categories associated with apoptosis induction, humoral immune response, cell differentiation and chromatin modifications were particularly prevalent in down-regulated genes (Figure 2d).
In the same vein, Kyoto Encyclopedia of Genes and Genomes (KEGG) database analysis integrating individual components into unified pathways was used to identify the enrichment of specific pathway components in functionally regulated gene groups (Figure 2e, f; Additional data file 3). The results indicate that six KEGG pathways were significantly enriched (P < 0.05) in up-regulated genes, including cytokine-cytokine receptor interaction, apoptosis inhibition, epithelial cell signaling in Helicobacter pylori infection, hematopoietic cell lineage, Toll-like receptor signaling pathway and gamma-hexachlorocyclohexane degradation (Figure 2e; Additional data file 3), and five KEGG pathways were significantly enriched (P < 0.05) in down-regulated genes, involving several metabolic pathways such as tryptophan metabolism, amino acid degradation, propionate metabolism, limonene and pinene degradation and vitamin B6 metabolism (Figure 2f; Additional data file 3).
Taken together, these results suggest the activation of inflammation and proliferation-promoting pathways followed by alterations in apoptotic and immune responses as well as in cell signaling and metabolism that can mediate or modulate their own pathway or the cross-talk between pathways that account for the functional reprogramming of TIA-1/TIAR-depleted HeLa cells.
Distinct and overlapping functions of TIA-1 and TIAR in the control of the transcriptome
To determine whether TIA-1 and TIAR have selective and specific effects on the control of the gene expression pathways described above, we next performed gene expression profiling analyses in HeLa cells in which either TIA-1 or TIAR was inactivated (Additional data files 4 and Additional data files 5). Inactivation of TIA-1 revealed 124 differentially expressed genes (P < 0.05), of which 36 and 88 were up- and down-regulated, respectively (Additional data file 4). On the other hand, knockdown of TIAR resulted in the differential expression (P < 0.05) of 94 genes, of which 23 and 71 were up- and down-regulated, respectively (Additional data file 5).
Next, GO biological process categories and KEGG pathway analyses were performed as before. A summary of GO annotations by biological process categories is provided in Additional data file 6a-d. GO categories (P < 0.01) associated with both TIA-1 (Additional data files 6a and Additional data files 7) and TIAR (Additional data files 6b and Additional data files 8) knockdown are related to inflammation and cell proliferation processes, including up-regulated genes in the following categories: cell-cell signaling, inflammatory response, chemotaxis, negative and positive regulation of cell proliferation, immune response, G-protein coupled receptor protein signaling pathway, cell adhesion, angiogenesis, cell motility, transduction and cell surface receptor mediated signaling. These results agree with the observations previously found in HeLa cells under TIA-1 and TIAR double silencing (Figure 2c), indicating that TIA-1 and TIAR are redundant in the control of these pathways. However, GO categories (P < 0.01) of down-regulated genes associated with the depletion of either TIA-1 (Additional data files 6c and Additional data files 7) or TIAR (Additional data files 6d and Additional data files 8) showed striking differences in the gene clusters. Indeed, whereas GO categories of down-regulated genes in TIA-1 knockdown cells are linked to genes involved in apoptosis induction, negative regulation of cytokine biosynthesis and metabolic responses (Additional data files 6c and Additional data files 7, GO categories of down-regulated genes in TIAR knockdown cells were limited to genes implicated in RNA processing (Additional data files 6d and Additional data files 8).
Results from KEGG pathway analysis (P < 0.05) are provided in Additional data file 6e-h. KEGG data for up-regulated genes in TIA-1 (Additional data files 6e and Additional data files 7) and TIAR (Additional data files 6f and Additional data files 8) knockdown cells are associated with genes related to cytokine-cytokine receptor interaction, apoptosis inhibition, and immune, chemotaxis, inflammatory, proliferative and metabolic responses, in agreement with the results described above (Additional data file 6a, b). On the other hand, KEGG data for down-regulated genes in TIA-1 knockdown cells are linked to vascular epidermal growth factor signaling pathway and citrate and reductive carboxylase cycles (Additional data files 6g and Additional data files 7), and KEGG data for TIAR knockdown cells are associated with several pathways related to the metabolism of amino acids, vitamins, fatty acids, glycerophospholipids and energy availability (Additional data files 6h and Additional data files 8), suggesting that both TIA-1 and TIAR can regulate specific aspects of cell metabolism.
Collectively, these results indicate that TIA-1 and TIAR regulate specific and overlapping aspects of the transcriptome, suggesting that their functional effects can be redundant, additive and/or independent, in agreement with previous findings [8, 12, 21, 27].
A molecular hallmark involving cytokines, chemokines and growth-stimulating factors is associated with the depletion of TIA proteins
Validation of microarray-predicted changes in gene expression patterns
Depletion of TIA proteins alters both mRNA stability and basal gene transcription
Given that the results on mRNA turnover do not conclusively explain the steady-state target mRNA levels in TIA-1/TIAR-depleted HeLa cells, we decided to estimate the contribution of the TIA-1/TIAR-induced silencing on transcription activation of two target genes. For this purpose, control and TIA-1/TIAR-depleted HeLa cells were cotransfected transiently with PTGS2 and IL-6 promoter-driven firefly luciferase constructs [30, 31] and a β-galactosidase-expressing plasmid used as a transfection control. Sixteen hours after transfection, cells were stimulated with dimethyl sulfoxide (DMSO) or phorbol 12-myristate 13-acetate (PMA), as described in the Materials and methods section, and 6 hours after stimulation both luciferase and β-galactosidase activities were measured in whole-cell extracts. As shown in Figure 5c, d, the depletion of TIA proteins was able to promote a significant and reproducible induction (2- to 2.5-fold) of both luciferase constructs under the control of PTGS2 (Figure 5c) and IL-6 (Figure 5d) human promoter sequences, suggesting that reduced expression of TIA proteins deregulates the basal transcriptional activity of both promoters. Taken together, these results could suggest that the gene expression patterns detected in TIA-1/TIAR-depleted HeLa cells might be the result of an overlapping regulation, implying the involvement of several molecular events at the post-transcriptional and transcriptional levels.
Silencing of TIA proteins results in increased cell proliferation and anchorage-independent growth
Gene expression profiling has revolutionized our ability to understand the concerted and global response of the human transcriptome at the molecular level. Collectively, our data suggest that either expression or suppression of TIA-1 and/or TIAR proteins triggers pathway-specific and biologically coherent regulatory programs linked to an acute inflammation and cell proliferation-promoting transcriptome. They also reveal that TIA proteins can provide a novel regulatory layer of mechanisms for cross-talk between different pathways that coordinate cellular phenotypes such as metabolic homeostasis, cell survival and growth. Most importantly, we would like to indicate that our findings agree with and can explain at the molecular level previous observations based on mice models where suppression of TIA-1 expression promotes chronic inflammatory responses as well .
Why should inflammation and cell proliferation signaling result in a coherent transcriptional and post-transcriptional program of gene regulation targeting similar classes of genes? Promotion of cell proliferation and growth can be achieved through either abnormally activated or deregulated signaling pathways involved in cell cycle regulation or, quite often, abnormal growth signals outside the transformed cell, which are usually not considered. In this regard, TIA-1/TIAR target genes regulating proliferation include those encoding growth- and survival-stimulating factors, such as the epidermal growth factor receptor (EGFR)/pan-HER ligand epiregulin (EREG), the epidermal growth factor-like growth factor amphiregulin (AREG), and a member of the transforming growth factor-beta (TGF-beta) superfamily known as growth differentiation factor-15 (GDF15) (Figure 7). Moreover, the cellular processes and pathways promoting these growth-stimulating factors can be reinforced by IL-6 and IL-8, the chemokines CXCL1 and 2 and cyclooxygenase-2, which contribute to cell growth through self-sufficiency in growth signals, evasion of apoptosis, insensitivity to growth inhibitors as well as inflammatory and angiogenic potential responses [33–36].
These findings provide novel insights into the critical role of individual regulators such as TIA proteins to control, indirectly rather than directly, protein output from hundreds of target genes in a given cellular context. These regulators may impact physiological processes by regulating the concentrations of a few key cellular proteins that may be components of a single or functionally interrelated pathways. This is an interesting observation because it suggests that the molecular links that lead to gene expression control are intimately interconnected, pointing to a widespread role for TIA proteins in the negative regulation of transcriptional rates of the human genome. Thus, these proteins may function as adaptors or coupling factors to facilitate cross-talk between different layers that define the complex interactions involved in the regulation of the human transcriptome.
A close inspection of differentially expressed genes between control versus TIA-1/TIAR-depleted HeLa cells reveals the up-regulation of cell-cycle activators such as CDC23 and the down-regulation of cell-cycle suppressors such as CHES1, MPHOSPH9, CCNB1 (encoding cyclin B1), ANAPC7, NASP and CDC7, which could also account for the enhanced proliferation. Additionally, genes for cell-cycle controlling transcription factors - for example, TFDP1, TFDP2 and E2F8 - as well as other cell-cycle progression related factors - UHRF1, BARD1, RABGAP1, PSRC1, PCGF6 and SEPT6 - are also down-regulated in HeLa cells with TIA-1/TIAR-induced silencing (Additional data files 9 and Additional data files 10). To our knowledge, this is the first study to analyze, in parallel, global transcriptomic and phenotypic impacts after changes in the expression and/or function of TIA proteins.
What could be the molecular mechanism that mediates the changes in steady-state mRNA levels triggered by TIA proteins? We propose that, in addition to mediating some of the signaling effects of the cytokines, chemokines and growth-stimulating factors, the putative molecular mechanism may implicate the activation of basal transcriptional machinery through up-regulation of the gene TAF5L as well genes for nuclear transcription factors - for example, the CREM and MAFF families - together with the down-regulation of genes for transcription repressors, such as PCGF2, NR2F2, SUDS3 and PCGF6 (Additional data files 9 and Additional data files 10). Constitutive activation/repression of basal transcriptional machinery and/or selective transcription factors is an emerging hallmark of various transformed cell types [33–35]. In addition, they have specifically been implicated in the development of proliferative phenotypes through autocrine and paracrine mechanisms. Our TIA-1/TIAR silencing signature is associated with the up-regulation of critical NF-κB and CREM effectors, including CXCL1, CXCL2, PTGS2, IL-6 or IL-8, which have been implicated in cell proliferation and growth [33–35]. In summary, TIA-1/TIAR-depleted HeLa cells are characterized by a molecular signature indicative of global and constitutive activation of NF-κB and CREM downstream effector genes associated with cell proliferation. Presumably, the up-regulation of genes required for proliferation, survival and inhibition of apoptosis might be essential for anchorage-independent growth. These conjectures, however, will have to be proven by additional studies in order to determine the precise role of these genes in the phenotypes observed in this study.
Nevertheless, the coordinate expression of inflammation and/or growth-stimulating genes requires both transcriptional and post-transcriptional regulation . Indeed, this gene coordination is also able to exert a positive effect on inflammation and cell proliferation or a positive feedback control on these pathways by regulating the expression of some of its components in TIA-1/TIAR-dependent regulatory events. These multifunctional proteins have been implicated in several steps of RNA dynamics and metabolism, including transcription, RNA splicing, RNA stability and translation, but little is known about the putative mechanisms and selectivity of transcriptional repression exerted by these proteins. It is important to note that these regulators have been localized on the carboxy-terminal domain of RNA polymerase II ; therefore, they could interact with basal transcription machinery and influence its activity. In addition, both proteins contain three RNA-binding motifs and are structurally close to heterogeneous ribonucleoproteins . Consistently, both TIA proteins directly bind to RNA as well as to single- and double-stranded DNA [3–5]. It is tempting to speculate that TIA proteins could also interact with specific promoter sequences and/or with gene-specific/general transcription factors [3, 4]. In this regard, it is more than reasonable to suggest that these proteins can carry out functions during transcription. Further, an increasing body of evidence indicates that transcription and RNA splicing processes are coupled .
Collectively, we postulate that, during transcription, TIA-1 and/or TIAR proteins can be recruited from the carboxy-terminal domain of RNA polymerase II to interact with genomic DNA sequences and/or basal transcription machinery and subsequently slow down RNA polymerase II and, therefore, the rate of transcription. Moreover, these proteins can perform triple functions during chromatin structure organization, transcription and splicing because they can potentially shuttle between DNA and RNA substrates and it has been demonstrated that factors affecting the rate of RNA polymerase II-mediated transcriptional elongation/initiation could influence alternative splicing patterns .
On the other hand, the prevalent role of these proteins as gene expression post-transcriptional modulators in the regulation of processes of alternative pre-mRNA splicing as well as their role in the stability and translation of specific cellular mRNAs is well-documented [8, 12–14, 22–24]. TIA proteins regulate the alternative pre-mRNA splicing of approximately 15% of alternative cassette human exons through binding to U-rich intronic elements, facilitating atypical 5' splice site recognition by U1 small nuclear ribonucleoproteins [6–10]. These proteins have also been well characterized as regulators of the stability and translation of cellular mRNAs in the cytosol. The proteins have been implicated in stress-induced translational arrest, colocalizing after stress with poly(A)+ RNA in the cytoplasmic foci known as stress granules . TIA-1 and TIAR are both able to bind to the 3'-untranslated regions of the stability/translation regulatory U- and AU-rich elements [5, 11–14, 16]. This aspect of TIA-1/TIAR function has recently been the focus of a broad and systematic analysis to identify mRNAs associated with both RNA-binding proteins [22–24]. However, it is interesting to note that no overlap is observed between gene targets reported to be repressed by TIA-1 at the translation level  and genes regulated by TIA1/TIAR at the alternative splicing level . This suggests that TIA proteins regulate distinct subsets of genes at the splicing and translation levels. Indeed, TIA-1 and/or TIAR proteins might independently switch on/off molecular plasticity in gene regulation machineries such as transcription, alternative splicing, stability and/or translation to coordinate the establishment of the diversity of specific transcriptomes and proteomes that are required in complex cellular responses such as cell proliferation and growth. Thus, the roles of these regulators and further newly identified targets in these physiological processes deserve further investigation.
The data presented in this manuscript illustrate specific changes in transcriptomic dynamics associated with cell-cell signaling, immuno-suppression, inflammation, angiogenesis, metabolism and cell proliferation-related mRNAs upon silencing of TIA-1 and/or TIAR proteins in HeLa cells. A gene cluster including cytokines, chemokines and growth-stimulating factors was identified as a molecular hallmark/signature associated with the depletion of TIA proteins. From a mechanistic viewpoint, TIA proteins could modulate transcriptional and post-transcriptional events associated with the control of target gene promoter basal activity and specific mRNA turnover. Additionally, the results also show that the knockdown of TIA-1 and/or TIAR proteins in HeLa cells triggers cell proliferation and anchorage-independent growth. In silico simulation of a biochemical interaction network incorporating up- and down-regulated target genes is consistent with a set of functions coherent with the different roles of several in vivo pathways to activate the acquisition of cell proliferation and anchorage-independent growth phenotypes detected after TIA-1/TIAR silencing. Collectively, our results argue that silencing of TIA proteins can trigger pathway-specific changes and affect genes with coherent functions that are important for cell proliferation and growth responses.
Materials and methods
Cell culture and RNA interference analysis
Transfections, luciferase and β-galatosidase assays
The human PTGS2 promoter [GenBank:AF276953.2] construct containing the full-length promoter sequence fused to a firefly luciferase reporter gene, named p2-1900 (-1,796, +104), was generated as described previously . The human IL-6 gene promoter [GenBank:AF372214.2] construct containing a 651-bp fragment of the human promoter sequence was fused to a firefly luciferase reporter gene, named pIL-6-luc651, as described previously . Both constructs were kindly provided by Dr Y Revilla. The β-galactosidase plasmid pcDNA3.1/myc-His/lacZ (Invitrogen, Carlsbad, CA, USA) was kindly provided by Dr J Berlanga. Control and TIA-1/TIAR-depleted HeLa cells, as described above, were co-transfected transiently with 50 and 500 ng of specific reporter lacZ and firefly luciferase plasmids, respectively, in six-well plates. The cells were incubated at 37°C for 16 h and then post-transfected cells were stimulated with DMSO or 20 ng/ml of PMA in DMSO. Six hours after stimulation, cells were lysed with 200 μl of cell culture lysis reagent (Promega, Madison, WI, USA) and microcentrifuged at 14,000 rpm for 5 minutes at 4°C, and 20 and 40 μl of each supernatant was used to determine firefly luciferase activity in a Monolight 2010 luminometer (Analytical Luminescence Laboratory, San Diego, CA, USA). β-Galactosidase activity was measured as described previously . Luciferase activity was expressed as relative light units (RLU) per milligram of protein determined by the bicinchoninic acid method (Pierce, Rockford, IL, USA) and normalized to β-galactosidase-specific activity expressed as nmoles of hydrolyzed o-nitrophenyl-β-D-galactopyranoside (Sigma, St. Louis, MO, USA) per minute and milligram of protein at 37°C. Co-transfection experiments were performed in triplicate and the data are presented as the means of the ratio RLU/β-galactosidase, expressed as fold induction relative to the corresponding control values (means ± standard error of the mean).
Proliferation and cell-cycle analyses
For cell growth analysis, post-transfected HeLa cells (2 × 104) were seeded and collected for counting from triplicate at the indicated time points for 6 days. Cell proliferation was also quantified by measuring the conversion of methyl thiazolyl tetrazolium into DMSO-soluble formazan by living cells, with absorbance measured at 560 nm using a spectrophotometer. Cell-cycle analysis was carried out by flow cytometry after propidium iodide staining.
Anchorage-independent growth assays
Soft agar colony formation was assayed by plating in duplicate 1 × 103 cells in 0.35% agarose in 10% fetal calf serum containing media on a 0.8% agarose base in six-well plates. After 14 days, the resulting colonies were stained with 0.01% crystal violet solution, counted and photographed under a light microscope at 100× magnification.
Preparation of cell extracts and western blot analysis
Whole-cell extracts were performed and processed as described previously . Immunoblots were carried out using the following antibodies: anti-U2AF65 (MC3; provided by J Valcárcel); anti-PTGS2 (provided by MA Íñiguez), anti-TIA-1, anti-TIAR and anti-HuR (Santa Cruz Biotechnology, Santa Cruz, CA, USA), anti-Mcl-1 (Biomol, Farmingdale, NY, USA) and anti-α-tubulin (Sigma, St. Louis, MO, USA).
RNA purification, semiquantitative and quantitative RT-PCR analyses and in vivoRNA decay determination
Cytoplasmic RNA isolations and semiquantitative RT-PCR analysis were carried out as described previously [10, 25–27]. The expression of selected genes was assessed independently by quantitative RT-PCR as described in . A list of primer pairs is given in Additional data file 11. RNA turnover experiments were performed by adding actinomycin D (5 μg/ml) to the growth medium.
RNA quality checks, amplification, labeling, hybridization with Human Genome U133 Plus 2.0 Array Chips (approximately 55,000 transcripts; Affymetrix Inc., Santa Clara, CA, USA) and initial data extraction were performed at the Genomic Array Core Facility in Scientific Park, Madrid at the Universidad Complutense de Madrid . Comparison of multiple cDNA array images (three independent experiments per biological condition tested) was carried out by using an average of all of the gene signals on the array (global normalization) to normalize the signal between arrays (Additional data file 1). Heat map and sample clustering plots as well as GO and KEGG database analyses were performed using software programs provided by Integromics™ . Networks of biochemical relationships between gene clusters identified as up-regulated and down-regulated by microarray analysis were created using the Pathway Studio software (version 6.0) and the 'ResNet Mammalian' database developed by Ariadne Genomics, Inc. (Rockville, MD, USA) . Microarray data have been deposited in the EMBL-EBI ARRAY EXPRESS database  and are accessible through the ArrayExpress accession number [ArrayExpress:E-MTAB-93].
Represented values are shown as means ± standard error of the mean. Differences were tested for significance by means of the Student's t-test. TIA-1/TIAR siRNA effects on HeLa cells were compared with respect to the control siRNA transfection. A probability level P < 0.05 was considered significant.
Additional data files
The following additional data are available with the online version of this paper: variability of data as function of the mean (MvA), RNA digestion, raw and normalized data box plots (Additional data file 1); summary of differentially expressed genes in TIA-1 and TIAR-depleted HeLa cells (Additional data file 2); summary of GO and KEGG database analyses of microarray-predicted genes from TIA-1 and TIAR-depleted HeLa cells (Additional data file 3); summary of differentially expressed genes in TIA-1-depleted HeLa cells (Additional data file 4); summary of differentially expressed genes in TIAR-depleted HeLa cells (Additional data file 5); global mRNA expression patterns in TIA-1 or TIAR-depleted HeLa cells (Additional data file 6); summary of GO and KEGG database analyses of microarray-predicted genes from TIA-1-depleted HeLa cells (Additional data file 7); summary of GO and KEGG database analyses of microarray-predicted genes from TIAR-depleted HeLa cells (Additional data file 8); global network of genes modulated after TIA-1 and TIAR silencing (Additional data file 9); list of genes up- and down-regulated after TIA-1/TIAR silencing that function as transcription and/or cell-cycle modulators (Additional data file 10); list of primer pair sequences used to validate microarray-predicted genes by real-time PCR analysis (Additional data file 11).
pan-HER ligand epiregulin
growth differentiation factor
Kyoto Encyclopedia of Genes and Genomes
relative light units
small interfering RNA
T-cell intracellular antigen-1
TIA-1 like/related protein.
We wish to thank JM Sierra and JM Zapata for assistance, help and encouragement. We are grateful for the generosity of J Valcárcel, MA Íñiguez, Y Revilla, O Eickelberg and J Berlanga, who have helped us with different reagents as mentioned in Materials and methods. This work was supported by grants from Fondo de Investigaciones Sanitarias (PI051605) and Ministerio de Ciencia e Innovación (BFU2008-00354). R Reyes is a recipient of a postgraduate fellowship from the Ministerio de Ciencia e Innovación. The CBMSO receives an institutional grant from Fundación Ramón Areces.
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