- Research article
- Open Access
Systems genetics analyses predict a transcription role for P2P-R: Molecular confirmation that P2P-R is a transcriptional co-repressor
© Peidis et al; licensee BioMed Central Ltd. 2010
Received: 7 May 2009
Accepted: 25 February 2010
Published: 25 February 2010
The 250 kDa P2P-R protein (also known as PACT and Rbbp6) was cloned over a decade ago and was found to bind both the p53 and Rb1 tumor suppressor proteins. In addition, P2P-R has been associated with multiple biological functions, such as mitosis, mRNA processing, translation and ubiquitination. In the current studies, the online GeneNetwork system was employed to further probe P2P-R biological functions. Molecular studies were then performed to confirm the GeneNetwork evaluations.
GeneNetwork and associated gene ontology links were used to investigate the coexpression of P2P-R with distinct functional sets of genes in an adipocyte genetic reference panel of HXB/BXH recombinant strains of rats and an eye genetic reference panel of BXD recombinant inbred strains of mice. The results establish that biological networks of 75 and 135 transcription-associated gene products that include P2P-R are co-expressed in a genetically-defined manner in rat adipocytes and in the mouse eye, respectively. Of this large set of transcription-associated genes, >10% are associated with hormone-mediated transcription. Since it has been previously reported that P2P-R can bind the SRC-1 transcription co-regulatory factor (steroid receptor co-activator 1, [Ncoa1]), the possible effects of P2P-R on estrogen-induced transcription were evaluated. Estrogen-induced transcription was repressed 50-70% by the transient transfection of P2P-R plasmid constructs into four different cell types. In addition, knockdown of P2P-R expression using an antisense oligonucleotide increased estrogen-mediated transcription. Co-immunoprecipitation assays confirmed that P2P-R interacts with SRC-1 and also demonstrated that P2P-R interacts with estrogen receptor α.
The findings presented in this study provide strong support for the value of systems genetics, especially GeneNetwork, in discovering new functions of genes that can be confirmed by molecular analysis. More specifically, these data provide evidence that the expression of P2P-R co-varies in a genetically-defined manner with large transcription networks and that P2P-R can function as a co-repressor of estrogen-dependent transcription.
Systems genetics is an evolving new speciality that can be used to define biological networks and to predict molecular interactions. It is based on the analysis of transcripts whose expression co-vary within genetic populations, such as the BXD strains of mice and the HXB strains of rats or other genetic reference panels. GeneNetwork http://www.genenetwork.org is an example of a bioinformatics tool that can be used to explore systems genetics data.
The importance of defining biological networks and predicting molecular interactions has been emphasized by several reports [1, 2]. Such studies emphasize that when knowledge about DNA variation within populations is interfaced with data on gene expression, protein interactions and DNA-protein binding, biological networks can be constructed that are predictive of the physiological molecular interactions and of disease susceptibility.
In 2005, we published the first report documenting the ability of the systems genetics tool GeneNetwork to predict interactions between molecules that could be then confirmed by molecular analysis . The P2P-R gene, coding for a hnRNP-related protein  that binds both the p53  and Rb1  tumor suppressor proteins was used as a test molecule. P2P-R was entered into GeneNetwork to search for a co-variant that was most highly co-expressed in three tissues of the BXD mouse genetic reference panel, ie,, cerebellum, hematopoietic stem cells and whole brain specimens. The outcome of that study was the identification of Pum2 as the gene product that showed a strong positive expression covariance with P2P-R. Pum2 is a member of the highly conserved Puf family of RNA binding proteins that often function as gene-specific translation regulators, through their association with specific elements located in the 3' untranslated region (UTR) of their target mRNAs [6, 7]. The 3' UTR of the P2P-R mRNA was found to contain one perfect consensus and two near-perfect consensus Pum2 binding sequences, while pull-down assays combined with reverse transcription and RT-PCR confirmed that Pum2 does indeed bind P2P-R mRNA to modulate its expression .
From the time when P2P-R was cloned it has been implicated in multiple cellular processes such as mitosis [8, 9], mRNA processing  and translation . In addition, recent studies have suggested that P2P-R has a role in ubiquitination and degradation of p53 and YB-1 proteins [11, 12], while it has been shown to be highly up-regulated in oesophageal cancer, being a promising target for immunotherapy against the disease . To further investigate the functional potential of P2P-R, we used the GeneNetwork database to evaluate if genetically-defined mechanisms modulate the co-expression of any distinct sets of gene products with P2P-R. An adipocyte genetic reference panel of HXB/BXH recombinant strains of rats and an eye genetic reference panel of BXD recombinant inbred strains of mice have been employed for these studies. These two genetic reference panels were chosen because P2P-R was cloned and characterized using primarily proadipocytes  and because the GeneNetwork eye database represents the most genetically diverse BXD reference panel available for analysis.
The outcome of these systems genetics studies implies that P2P-R is an important member of large genetically-defined transcription networks in adipose and eye tissues. That prediction was then confirmed by data showing that P2P-R can function as a co-repressor of estrogen-induced transcription. Immunoprecipitation experiments strengthen such functional studies by confirming that P2P-R interacts with SRC-1 and by demonstrating that P2P-R also interacts with estrogen receptor α (ERα). These data suggest that P2P-R may be a component of large macromolecular complexes that impact steroid-dependent transcription.
P2P-R is part of a genetically-defined transcription network in fat cells
Since most studies concerning the cloning and characterization of P2P-R were performed using the 3T3T proadipocyte system , we initiated the current studies focusing on the rat fat cell GeneNetwork microarray database to evaluate if genetically-defined mechanisms modulate the co-expression of any distinct sets of transcripts with P2P-R. The results show that in rat fat cells , P2P-R is co-expressed with a large set of transcription-associated gene products.
The above data were then normalized using the Robust Multiarray Method (RMA, http://odin.mdacc.tmc.edu/~zhangli/PerfectMatch/) . In such studies it is worthwhile to evaluate databases using at least two normalization approaches. Therefore, the Mas5 normalization tool was also used. Both normalization methods confirmed that a large network of transcription-association gene transcripts is indeed co-expressed with P2P-R in rat fat cells (data not shown). In support of the above data based on analysis of the fat cell GeneNetwork database derived from HXB/BHX recombinant inbred rats, limited analysis were also performed on the GeneNetwork mouse adipose tissue database wherein it was found that 13.5% of the transcripts whose expression co-varies with P2P-R with a correlation coefficient of ≥ 0.5 has transcription-associated functions (data not shown). This percentage is comparable to the one observed in studies on the fat cell database of recombinant inbred HXB/BHX rats.
P2P-R is part of a genetically-defined transcription network in the eye
Even more detailed analysis of the 135 members of the eye transcription network, reveals the following network characteristics:
1) ~80% of the 135 transcription network gene products have nucleotide binding characteristics.
2) >40% of the 135 transcription network gene products bind zinc.
3) ~30% of the 135 transcription network gene products bind both nucleotides and zinc, and
4) ~10% of the 135 members of the P2P-R transcription network gene products are associated with hormone-mediated transcription. These include the following transcription factors or co-factors: Nr3c1 [+0.8472], Ep300 [+0.8056], Pparbp [+0.7709], Glcci1 [+0.7690], Esrrg [+0.7574], Srebf2 [-0.7568], Ncoa6 [+0.7423], Ncor1 [+0.7115], Ncoa1 (Src-1) [+0.6987] and Ncoa2 [+0.6787] and Nr2f6 [-0.6653] (the parenthetic numbers indicate positive or negative expression correlation coefficients with P2P-R expression).
The findings from studies on fat cell-adipose and eye tissues therefore strongly suggest that P2P-R has the potential to function as a member of a genetically-defined transcription complex. Two important questions arise from these findings. Does a P2P-R-associated transcription network exist in all tissues? Can the role of P2P-R in transcription be confirmed by molecular studies? To address the first question, studies were performed on several other tissues in the GeneNetwork database to search for additional P2P-R transcription networks. There was no evidence of a P2P-R-associated transcription network in liver or whole brain databases, however, in a cerebellum database a smaller P2P-R-associated transcription set could be identified (data not shown). These data suggest that the role of P2P-R in transcription may be tissue specific. The studies in the following sections address the second question and show that P2P-R can indeed function as a transcriptional co-repressor.
Repression of estrogen-induced transcription by P2P-R
Several members of the transcription network co-expressed with P2P-R participate in steroid-regulated transcription (Nr3c1, Glcci1, Esrrg, Srebf2, Ncoa6, Ncor1, Ncoa1, Ncoa2). In this regard, of special note is the April 1, 2005 report in the Nuclear Receptor Signaling Atlas online database http://www.nursa.org that P2P-R interacts with Ncoa1 (SRC-1), a well-known steroid receptor co-regulator (for review see ref. . This datum was placed in the NURSA database by Jung SY, Luo H, Malovannaya A, Kim T, Zhang J, Qin J and O'Malley BW under the designation of proteomic analysis of steady-state nuclear hormone receptor coactivator complexes.
To identify which domain of the P2P-R protein is responsible for the observed repression of E2-induced transcription, MCF-7 cells were transiently co-transfected with an ERα-reporter construct with an empty vector or with plasmid constructs that encode specific P2P-R domains as illustrated in Figure 5B. The five P2P-R plasmid constructs that were employed include: the near full length P2P-R (aa 25-1560); the N-terminal half of P2P-R (aa 1-760); the C-terminal half of P2P-R (aa 761-156); a C-terminal sub-domain of P2P-R (aa 1156-1560) and the C-terminal most domain of P2P-R (aa 1314-1560) [8, 18]. As shown in Figure 5C, all four P2P-R constructs that encode the C-terminal regions of P2P-R, repressed estrogen-dependent transcription to more or less the same extent as full-length P2P-R, whereas the N-terminal half of P2P-R showed minimal repressor activity. It appears therefore that a region within the 246 amino acids of the C-terminal most segment of P2P-R is the primary effector that functions to inhibit estrogen-dependent transcription.
The P2P-R protein interacts with ERα and SRC-1
The data reported in this paper establish that the function of gene products can be confidently predicted by determining their association with specific genetically-defined biological networks, using systems genetics approaches and tools, such as GeneNetwork. GeneNetwork has been previously used to predict a molecular interaction between P2P-R and Pum2, the gene transcript which is most consistently co-expressed with P2PR in three tissues of the BXD mouse genetic reference panel. That prediction was confirmed by molecular studies showing that Pum2 binds to a specific sequence in the 5'UTR of P2PR mRNA to modulate P2PR expression .
The current studies expand the use of GeneNetwork databases in an attempt to identify biological networks in which P2P-R is a member, leading to the prediction of new function(s). Data derived using these systems genetics approaches suggest that P2P-R is an important member of large genetically-defined transcription networks in adipose and eye tissues, thereby having the potential to impact the expression of many hundreds of genes. That prediction was then confirmed by molecular studies showing that P2P-R can indeed function as a transcriptional co-repressor.
The results specifically demonstrate that P2P-R acts as a co-repressor of estrogen-dependent transcription in four different cell systems including MCF-7, Ishakawa, HeLa and 293T cells. The co-repressor activity of P2P-R was further confirmed by evidence that knocking down P2P-R protein expression, using an antisense oligonucleotide, facilitates estrogen-induced transcription. Immunoprecipitation experiments support those functional studies by showing that the P2P-R protein is a component of the estrogen-transcription complex that includes ERα and SRC-1. Preliminary data also suggest that P2P-R interacts with the Mad2 mitotic protein (Scott RE, unpublished observation), which is of interest in this context, since it has previously been reported that Mad2 associates with estrogen receptor beta .
An important question concerns how P2P-R might affect estrogen-induced transcription. Since P2P-R is a hnRNP-like protein that associates with the nuclear matrix , [Peidis P, Giannakouros T and Scott RE, unpublished observations], we propose that estrogen-dependent transcription might also be linked to the nuclear matrix in association with P2P-R. In this respect it has been reported that estrogen-dependent transcription is mediated by immobilizing the transcription regulatory complex to DNAse resistant nuclear matrix-like entities, in a manner that allows for continued turnover of some of the its components . Furthermore, the scaffold attachment factor B1 (SAFB1) , which can bind to the S/MAR (S caffold/M atrix A ttachment R egions) elements of the nuclear matrix, was shown to interact with the C-terminal domain of RNA polymerase II, and with ERα and to suppress ERα-mediated transcription [22–25]. Interestingly, we have previously shown by pull-down assays that the RS domain of P2P-R binds to SAFB1 . We therefore speculate that P2P-R's transcription co-repressor function might stem from its ability to complex with SAFB1 and form dynamic structural and functional entities that influence the organization of chromatin or control the stringency by which various components of the estrogen receptor complex associate with the nuclear matrix, thereby regulating their rate of turnover, and consequently influencing the transcription rate.
It should be also noted that the C-terminal most domain of P2P-R (aa 1314-1560) that is responsible for the observed inhibition of estrogen-dependent transcription is an unusual lysine rich region, reminiscent of the basic N-termini of several histones [4, 5]. Core histones are known to undergo acetylation that loosens the DNA-histone contacts, thereby making the DNA more accessible to transcription factors and promoting transcription initiation. The positively charged lysine rich region in P2P-R has been reported to undergo in vitro acetylation . It is therefore possible that this region is similarly modified in vivo, in a way that mimics histone acetylation, thus acting as a competitive inhibitor of histone acetylation and consequently of chromatin remodeling.
The above suggested mechanisms by which P2P-R might influence transcription will need to be the focus of many more detailed studies. However, based on the data presented in this paper, it is now clear that P2P-R does have an important role in transcription, specifically in estrogen-dependent transcription and that this discovery was predicted using GeneNetwork.
This study strongly supports the conclusion that GeneNetwork is an excellent tool that can be used to confidently predict new functions for genes. Using GeneNetwork, it was established that large genetically-defined transcription networks that include P2P-R exist in fat cells and eye tissues. Based on a previous report that P2P-R can interact with SRC-1, a well known steroid receptor co-regulator, and given that a significant percentage of the transcription genes within these networks are associated with hormone-mediated transcription, the effects of P2P-R on estrogen-dependent transcription were evaluated. The data presented corroborate the outcome of the systems genetics analyses and clearly show that P2P-R can function as a co-repressor of estrogen-dependent transcription. Immunoprecipitation experiments strengthen those functional studies by confirming that P2P-R interacts with SRC-1 and by demonstrating that P2P-R also interacts with ERα. P2P-R may therefore be a component of large macromolecular complexes that impact steroid-dependent transcription.
Use of the GeneNetwork database to identify genetically-modulated co-expression of P2P-R transcripts with transcription gene products
GeneNetwork is a web resource that contains many large gene expression data sets for populations of rats and mice. Using this system it is possible to extract sets of transcripts that co-vary tightly with a target transcript across genetically diverse populations. Patterns of co-variation can be studied in multiple experimental crosses and in multiple tissues [27, 28]. We have used the following subset of the GeneNetwork expression data in the present study:
1. Peritoneal fat cells derived from young males of 32 HXB/BHX recombinant inbred rat strains were the sources of the GeneNetwork database . Microarrays were performed using Affymetrix 230A GeneChip with the RMA2z+8 normalization system. The P2P-R (Rbbp6) probset used was [1376947_at].
2. Eye tissue of pooled female and male specimens derived from 68 recombinant inbred BXD mouse strains plus 35 strains of a mouse diversity panel plus 6 knockout mouse stains were selected to provide maximum diversity to this genetic reference panel . Affymetrix M430 2.0 GeneChips were employed and all data were normalized using the RMA system. The P2P-R (Rbbp6) probeset [1426487_a_at] was primarily used.
Additional details on each of these datasets is available online at http://www.genenetwork.org. In many studies lists of expression covariates were exported to the gene ontology program, WebGestalt, to identify functional gene subsets whose co-expression was enriched . Such enriched sets of genes with common functions are designated genetically-defined networks. When these networks are illustrated in graphic form in various figures of this paper, the color of the lines connecting the genes indicates the degree to which their expression co-varies among the strains evaluated (red = very high positive correlation, orange = moderate positive correlation, blue = very high negative correlation, green = moderate negative correlation).
Human HeLa, MCF-7, Ishikawa and 293T cells and mouse 3T3T cells were used in this study. All cells were cultured in Dulbecco's modified Eagle's medium supplemented with 10% (v/v) fetal bovine serum (FBS) and antibiotics, unless otherwise described, such as, in assays to measure estrogen-dependent effects where phenol red and charcoal stripped (CS), estrogen-depleted media was employed.
Steroid-induced Transcription Assays
MCF-7 and Ishikawa cells, that contain endogenous ERα, were cultured in steroid and phenol red free medium for 48 h. The cells were then plated in 12-well plates at 5 × 105 cells/well in the same medium, allowed to attach overnight and then transfected with 300 ng/well of a luciferase reporter construct (pGl2-ERE2X-TK), containing two copies of the vitellogenin estrogen response element (ERE) linked to the luciferase gene plus 15 ng/well of pRL vector (Promega) expresing renilla luciferase, with or without co-transfection with FLAG-tagged P2P-R constructs that were prepared as previously described [8, 18]. HeLa and 293T cells, that lack endogenous ERα, were also co-transfected with plasmid constructs encoding ERα (50 ng pSG5-ERα/well). Transfections were performed using Effectene (Qiagen, Valencia, CA) as per manufacturer's instructions. Five hours after transfection, cultures were refed fresh media with vehicle (DMSO) or with 100 pM 17-beta estradiol and the cells were therein incubated for 18 h at 37°C prior to processing for analysis of the extent of ERE-dependent transcription. Luciferase activity was measured using 30 μl of cell extract and 100 μl of Luciferase Assay Substrate (Promega, Madison, WI) in a Berthold AutoLumat Plus luminometer. The transcription assays were performed in triplicate, as described in the Dual-Luciferase Reporter Assay System Manual (Promega) using Renilla Luciferase as internal control. Data are expressed as Relative Luciferase Activity (RLA) of E2-dependent transcription. RLA represents the firefly luciferase RLU (Relative Light Units) divided by those of the renilla luciferase RLU in the presence of E2 minus the firefly luciferase RLU divided by the renilla luciferase RLU in the presence of DMSO. Additional information concerning this method has been previously reported .
Effect of P2P-R knockdown on estrogen-induced transcription
Native 3T3T cells and 3T3T cells that had been stably transfected with a P2P-R anti-sense oligonucleotide resulting in a 50-70% knockdown in P2P-R protein levels , were transfected with ERE-luciferase plasmid (300 ng/well) and pSG5-ERα (50 ng/well), using Effectene (Qiagen, Valencia, CA) as per manufacturer instructions. Transfected cells were incubated for 18-24 h in phenol-red free DMEM with 5% CS-FBS in the presence of DMSO or 100 pM 17 β-estradiol. Cells were harvested and luciferase activity was measured.
Immunoprecipitation and Western blotting
Human HeLa and MCF-7 cells were used to perform co-immunopreciptiation experiments concerning P2P-R, SRC-1 and ERα. These assays employed the following antibodies: anti- P2P-R [#M56 - Santa Cruz Biotechnology, Inc., Santa Cruz, CA], anti-SRC-1 [#05-522 - Upstate Biotechnology, Lake Placid, NY] and anti-ERα [ERα (H-184), #SC-7207, Santa Cruz Biotechnology]. Immunoprecipitations were performed as previously described . Each immunoprecipitation employed approximately one milligram of total cell extract. Native and immunopreciptated proteins were analyzed by Western blotting as previously described [8, 18], using the above described antibodies against P2P-R and SRC-1. For Western blotting analysis of ERα, the anti-ERα antibody (D-12) was used [#SC-8005, Santa Cruz Biotechnology].
TG was supported by grants from the Greek Ministry of Education (HPAKΛEITOΣ grant 21768), while MEB was supported by NIH grant DK059389. PP was a recipient of a fellowship from the Greek National Fellowship Foundation. RES is supported by Varigenix, Inc. in his role as company president. RWW and GeneNetwork are supported by NCI grant U01CA105417. The authors acknowledge Dr. Sizhi Gao for preparation and validation of the P2P-R (1-760) plasmid construct and Drs. David Lonard and Bert O'Malley for performing selected confirmatory experiments.
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