Title: STAT5-induced Id-1 transcription involves recruitment of HDAC1 and deacetylation of C/EBPbeta
Abstract: Article17 February 2003free access STAT5-induced Id-1 transcription involves recruitment of HDAC1 and deacetylation of C/EBPβ Min Xu Min Xu Oklahoma Medical Research Foundation, 825 NE 13th Street, Oklahoma City, OK, 73104 USA Department of Cell Biology, New York University School of Medicine, New York, NY, 10016 USA Search for more papers by this author Lei Nie Lei Nie Oklahoma Medical Research Foundation, 825 NE 13th Street, Oklahoma City, OK, 73104 USA Search for more papers by this author Seung-Hwan Kim Seung-Hwan Kim Oklahoma Medical Research Foundation, 825 NE 13th Street, Oklahoma City, OK, 73104 USA Search for more papers by this author Xiao-Hong Sun Corresponding Author Xiao-Hong Sun Oklahoma Medical Research Foundation, 825 NE 13th Street, Oklahoma City, OK, 73104 USA Search for more papers by this author Min Xu Min Xu Oklahoma Medical Research Foundation, 825 NE 13th Street, Oklahoma City, OK, 73104 USA Department of Cell Biology, New York University School of Medicine, New York, NY, 10016 USA Search for more papers by this author Lei Nie Lei Nie Oklahoma Medical Research Foundation, 825 NE 13th Street, Oklahoma City, OK, 73104 USA Search for more papers by this author Seung-Hwan Kim Seung-Hwan Kim Oklahoma Medical Research Foundation, 825 NE 13th Street, Oklahoma City, OK, 73104 USA Search for more papers by this author Xiao-Hong Sun Corresponding Author Xiao-Hong Sun Oklahoma Medical Research Foundation, 825 NE 13th Street, Oklahoma City, OK, 73104 USA Search for more papers by this author Author Information Min Xu1,2, Lei Nie1, Seung-Hwan Kim1 and Xiao-Hong Sun 1 1Oklahoma Medical Research Foundation, 825 NE 13th Street, Oklahoma City, OK, 73104 USA 2Department of Cell Biology, New York University School of Medicine, New York, NY, 10016 USA *Corresponding author. E-mail: [email protected] The EMBO Journal (2003)22:893-904https://doi.org/10.1093/emboj/cdg094 PDFDownload PDF of article text and main figures. ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinked InMendeleyWechatReddit Figures & Info Transcriptional activation is associated commonly with recruitment of histone acetylases, while repression involves histone deacetylases (HDACs). Here, we provide evidence to suggest that STAT5 activates gene expression by recruiting HDAC. The interleukin-3 (IL-3)-dependent expression of the Id-1 gene, encoding a helix–loop–helix (HLH) transcriptional inhibitor, is activated by both C/EBPβ and STAT5 transcription factors bound to its pro-B-cell enhancer (PBE), but is inhibited by HDAC inhibitors in Ba/F3 cells. STAT5 interacts with HDAC1 in the PBE region, resulting in deacetylation of histones, as well as C/EBPβ, whose acetylation diminishes its DNA-binding activity. Consistently, expression of an acetylation-resistant mutant of C/EBPβ results in IL-3-independent expression of the Id-1 gene. Thus, we propose a novel mechanism by which STAT5 mediates the deacetylation of C/EBPβ, allowing transcriptional activation. Introduction The Id-1 gene encodes a dominant-negative inhibitor of basic helix–loop–helix (bHLH) transcription factors such as E2A, HEB and E2-2 (Norton et al., 1998; Massari and Murre, 2000). Ablation of the function of these bHLH proteins arrests B- and T-cell development at early progenitor stages (Engel and Murre, 2001). Although the bHLH proteins are expressed constitutively, Id-1 expression is regulated during lymphocyte development, which in turn controls bHLH function and lymphocyte differentiation (Sun, 1994; Heemskerk et al., 1997; Kim et al., 1999). Id-1 is highly expressed in hematopoietic stem cells and down-regulated during B-cell differentiation in the bone marrow (Jaleco et al., 1999; Igarashi et al., 2002), a process probably controlled by growth factors and cytokines critical for lymphocyte development. Therefore, knowledge of how the Id1 gene is regulated and what the signal transduction pathways are leading to its regulation will facilitate an understanding of lymphocyte development. Regulation of specific gene expression is achieved largely by controlling production of transcription factors responsible for the expression of target genes, alteration of the activities of transcription factors through post-translational modifications and localized remodeling of chromatin structures. Recently, histone acetylation has attracted tremendous attention. Acetylation of histone proteins, particularly H3 and H4, is thought to lead to relaxed chromatin structure and, therefore, an enhanced rate of transcription. Acetylation reactions are catalyzed by various families of coactivators with histone acetyl transferase activities, represented by PCAF, TAF250 and p300/CBP (H.Chen et al., 2001; Marmorstein and Roth, 2001). On the other hand, deacetylation of histone proteins by histone deacetylases (HDACs) is believed to cause chromosomal condensation and gene repression (Struhl, 1998; Tyler and Kadonaga, 1999). In addition to modification of histone proteins, acetyl ation has been shown to impact on the activities of transcription factors (Kouzarides, 2000). Acetylation of components in the basal transcriptional machinery, such as TFIIEβ and TFIIF, may impact directly on transcription of genes controlled by PCAF, p300 and TAF250 (Imhof et al., 1997). Acetylation of p53, EKLF, GATA1 and MyoD increases in DNA binding or transactivating abilities (Gu and Roeder, 1997; Boyes et al., 1998; Zhang and Bieker, 1998; Hung et al., 1999; Sartorelli et al., 1999; Yamagata et al., 2000). The acetylated p65 subunit of NF-κB has lower affinity for IκB (L.Chen et al., 2001). Despite these different underlying mechanisms, a common outcome of acetylation is to favor transcription controlled by acetylated factors. However, it is also possible that acetylation might negatively influence the activities of transcription factors. For instance, acetylation has been shown to disrupt interaction between coactivators and ACTR or TCF (Waltzer and Bienz, 1998; Chen et al., 1999). Recently, it has been found that β-catenin is acetylated at a single lysine residue frequently mutated in thyroid anaplastic cancer. An unacetylatable form of β-catenin activates c-myc gene expression more efficiently than the wild-type protein (Wolf et al., 2002). In this report, we provide evidence that expression of the Id-1 gene depends on HDAC activities through a molecular mechanism involving the deacetylation of C/EBPβ, a transcription factor essential for Id-1 expression. Previous studies of Id-1 gene regulation led to identification of a pro-B-cell-specific enhancer (PBE), located 3 kb downstream of the gene (Saisanit and Sun, 1995; Saisanit and Sun, 1997). Within this 460 bp PBE enhancer, a C/EBPβ-binding site was found to be important to the enhancer activity, which can be abolished by an inhibitor of C/EBPβ, CHOP (Saisanit and Sun, 1997). We have now demonstrated that HDAC activities are required for STAT5-mediated Id-1 gene expression in the presence of interleukin-3 (IL-3). Consistent with this observation, an acetylation-resistant mutant of C/EBPβ enables Id-1 expression in the absence of IL-3. It thus appears that HDAC activities recruited by STAT5 proteins may be necessary for the deacetylation of C/EBPβ and its transcriptional activation of the Id-1 gene. Results Three C/EBPβ-binding sites in PBE are required for Id-1 expression We have shown previously that a C/EBPβ-binding site is important for the enhancer activity of PBE (Saisanit and Sun, 1995, 1997). Further examination of the PBE sequence revealed two additional C/EBPβ-binding sites with considerably divergent sequences (Figure 1A). These sites, named β1–β3, are clustered within an 80 bp region. Electrophoretic mobility shift assays (EMSAs) with each site as a probe revealed that nuclear extracts from Ba/F3 cells formed three complexes, C1–C3, which were supershifted with antibodies against C/EBPβ (Figure 1B). The C1 complex co-migrates with a non-specific complex, which can be separated from the C1 complex upon prolonged electrophoresis (data not shown). Figure 1.The C/EBPβ-binding site is required for Id-1 expression. (A) Three C/EBPβ-binding sites are diagrammed as filled boxes, and their sequences shown on top. Mutations are indicated with lower case letters. The position of PBE (gray box) relative to Id-1 exons (hatched boxes) is illustrated. (B) EMSA with each of the three C/EBPβ-binding sites as probes. A 70 bp probe containing the β1, β2 or β3 site was incubated with Ba/F3 nuclear extracts with or without antibodies against C/EBPβ. The binding reactions were analyzed on a 6% poly acrylamide gel in Tris–glycine buffer. C/EBPβ-containing complexes are labeled as C1–C3. Supershifted complexes are marked with an open arrow. Additional bands are non-specific complexes found in all cell types. (C) Mutational analysis in transient transfection assays using Ba/F3 cells. Constructs containing the 460 bp PBE placed upstream of a luciferase reporter gene driven by a c-fos minimal promoter are diagrammed. Filled and open boxes represent wild-type and mutant C/EBPβ sites, respectively. Luciferase activities were normalized against the β-galactosidase activity. The data are presented as activities relative to that of the PBE-luc construct and are averages of at least three independent experiments with standard deviations. (D) Mutational analysis in stable Ba/F3 cell lines. The ΔId-1 gene is diagrammed as in (A). Three independent cell lines stably transfected with the indicated constructs were analyzed using RPAs, and transcripts were detected with the probes as labeled. Download figure Download PowerPoint The functional significance of the C/EBPβ-binding sites for PBE activity was tested by mutational analyses using a luciferase reporter gene. Transient transfection of the reporter gene driven by wild-type PBE into Ba/F3 cells usually resulted in >100-fold increases in luciferase activity compared with the construct without the enhancer. Mutations of 2 bp in each of the C/EBPβ sites caused ∼70% reduction in the enhancer activity, suggesting that all three sites are necessary for the enhancer activity. Mutations in all three binding sites almost completely abolished the enhancer activity (Figure 1C). To examine further the importance of these three sites in directing Id-1 expression, stable Ba/F3 cell lines were generated by using an Id-1-minigene, ΔId-1 (Saisanit and Sun, 1995). The ΔId-1 gene, controlled by its 6 kb of 5′- and 7 kb of 3′-flanking sequences, contains a 200 bp deletion in its exon 1 so that its transcript can be distinguished from the endogenous Id-1 transcript. Ribonuclease protection assays (RPAs) revealed that the ΔId-1 gene controlled by wild-type PBE (15K/wt) was expressed at high levels in multiple cell lines, but ΔId-1 expression was dramatically inhibited by mutations in the three C/EBPβ-binding sites (Figure 1D). Therefore, data obtained from both transient and stable transfection assays strongly suggest that the three C/EBPβ-binding sites are essential for Id-1 expression in Ba/F3 cells. Combinations of C/EBPβ dimeric proteins are bound to its binding sites in PBE The C/EBPβ gene encodes three polypeptides through differential usage of AUG codons within the same transcript (Descombes and Schibler, 1991). The 31 and 29 kDa polypeptides contain an N-terminal transcriptional activation domain (Williams et al., 1995), generally referred to as LAP (liver-enriched transcriptional activator protein). The 16 kDa form of C/EBPβ lacks the activation domain, and is called LIP (liver-enriched transcriptional inhibitory protein). These leucine zipper-containing proteins bind to DNA as dimers. To determine the identities of the C1–C3 complexes found in Ba/F3 cells, we compared the mobility of these complexes with those formed with LAP and/or LIP proteins expressed in NIH-3T3 cells (Figure 2A). Although NIH-3T3 cells produced LAP and LIP proteins, which exist as LAP–LAP and LAP–LIP dimers, expression of LAP or LIP led to increased levels of LAP–LAP or LIP–LIP dimers. The LAP construct also makes a small amount of LIP because of internal translation initiation, which formed LAP–LIP dimers. LIP-expressing cells had an increased amount of LAP–LIP dimers due to interaction with endogenous LAP. Expression of both LAP and LIP generated LAP and LIP homo- and heterodimers. The C1–C3 complexes in Ba/F3 cells co-migrated with complexes of LAP–LIP, LIP–LIP and LAP–LAP dimers, respectively, suggesting that these complexes are likely to be combinations of different products of the C/EBPβ gene. Intriguingly, western blot analysis showed that Ba/F3 cells produced a larger amount of LAP than LIP (Figure 2A), but the amount of DNA-binding complexes formed with LAP–LAP dimers (the C3 complex) was much less than those with LAP–LIP and LIP–LIP dimers. In contrast, similar amounts of LAP and LIP proteins co-expressed in NIH-3T3 fibroblasts readily formed the LAP–LAP complex (Figure 2A). These results thus suggested that the LAP protein might be modified post-translationally specifically in Ba/F3 cells such that its DNA-binding activity was inhibited. Figure 2.Identities of the C1–C3 complexes. (A) EMSA was performed with nuclear extracts from NIH-3T3 cells transfected with the indicated constructs. 'C' stands for extracts transfected with an empty vector, pcDNA3. The positions of the indicated homo- and heterodimers of LAP and LIP are labeled on the left, while C1–C3 complexes in Ba/F3 cells are marked on the right. Supershifted complexes with antibodies against C/EBPβ are indicated by an open arrow. Nuclear extracts used in lanes 4 and 5 were analyzed using a western blot with antibodies against the C-terminus of C/EBPβ. The doublets represent the 29 and 31 kDa LAP. (B) ChIP assays with antibodies against C/EBPβ and a negative control, Skp2. A fragment containing all three C/EBP-binding sites was amplified. (C) Transient co-transfection assay of Ba/F3 cells with the indicated constructs; normalized luciferase activities are shown relative to that of PBE-luc. Download figure Download PowerPoint To demonstrate that C/EBPβ binds to PBE in vivo, we performed chromatin immunoprecipitation (ChIP) using cross-linked protein–DNA complexes prepared from Ba/F3 cells cultured with or without IL-3. The immunoprecipitates obtained with antibodies against the C-terminus of C/EBPβ and a non-specific control protein were used as templates to amplify a 170 bp DNA fragment containing all three C/EBP sites (Figure 2B). Indeed, anti-C/EBPβ but not control antibodies brought down the PBE fragment in Ba/F3 cells cultured with and without IL-3. Because the antibodies recognize both LAP and LIP, this assay could not distinguish the different dimers of C/EBPβ bound to the enhancer region. However, the above results suggest that C/EBPβ does bind to the three sites found in PBE. We then tested if C/EBPβ could activate PBE-mediated transcription. The PBE-luc reporter construct was co-transfected into Ba/F3 cells with plasmids expressing LAP, LIP or LGL, which is a forced dimer between LAP and LIP connected through a glycine hinge. LAP increased the reporter activity by 8-fold, but LIP and LGL had no effect on reporter expression (Figure 2C), suggesting that LAP–LAP dimers, but not LIP–LIP or LAP–LIP dimers, are able to activate transcription through PBE. Furthermore, expression of a potent inhibitor of C/EBPβ, CHOP (Ron and Habener, 1992), resulted in a 10-fold reduction of the reporter activity (Figure 2C), indicating that C/EBPβ proteins, specifically LAP–LAP dimers, are probably responsible for the basal activity of PBE-luc in Ba/F3 cells. IL-3-dependent Id-1 expression correlates with STAT5 activation Ba/F3 is an IL-3-dependent cell line (Kinashi et al., 1988), and thus serves as a good model system to study the signaling pathways that influence Id-1 gene expression. Stimulation through the IL-3 receptor leads to activation of STAT5 (Reddy et al., 2000). It has been shown previously that a dominant-negative STAT5 mutant can inhibit Id-1 expression in Ba/F3 cells (Mui et al., 1996). Consistently, we found that upon IL-3 deprivation, levels of Id-1 mRNA decreased immediately, along with levels of phospho-STAT5 proteins, suggesting an involvement of STAT5 in Id-1 gene regulation (Figure 3A). Furthermore, Id-1 expression upon IL-3 re-stimulation occurred in the presence of cycloheximide and hence the absence of new protein synthesis (Figure 3B), perhaps through activation of pre-existing STAT5 transcription factors. Figure 3.STAT5 mediates IL-3-dependent Id1 expression. (A) Northern and western blots (NB and WB) for the levels of Id-1 mRNA and phospho-STAT5 protein in Ba/F3 cells cultured without IL-3 for the indicated times. The levels of GAPDH mRNA and C/EBPβ protein were used as internal controls. Twenty percent of WEHI-3 conditioned medium was used as a source of IL-3 in all experiments. (B) Northern blots for Id-1 and GAPDH mRNA levels in Ba/F3 cells: lane 1, continuously cultured in IL-3; lane 2, deprived of IL-3 for 5 h; lane 3, as lane 2 plus treatment with CHX at 50 μg/ml for the last 80 min; lane 4, re-stimulated with IL-3 for 60 min after a 4 h starvation; and lane 5, as lane 4 plus treatment with CHX at 50 μg/ml for the last 80 min. Download figure Download PowerPoint STAT5 is bound to PBE Although both C/EBPβ and STAT5 are involved in the regulation of Id-1 expression, mutations that destroy the three C/EBPβ-binding sites almost completely abolish Id-1 expression (Figure 1C and D). This thus raises the question of how STAT5 contributes to the regulation of Id-1 expression. We hypothesized that STAT5 could potentiate the transcriptional activity of C/EBPβ. If so, STAT5 would probably bind to sequences near the C/EBPβ sites. To locate STAT5-binding sites, we searched a 1.4 kb sequence surrounding PBE, and found three putative sites (S1–S3) within PBE (Figure 4A). EMSA was performed using the S1 site as a probe, which is identical to the STAT5 consensus binding sequence, TTCNNNGAA (Wakao et al., 1994). A specific binding complex was supershifted by antibodies against STAT5, and competed off by oligonucleotides containing a known STAT5 site or the S1 site (Figure 4A). The S2 site, whose sequence resembles the consensus sequence poorly, did not compete for binding. The S3 site only competed at a high concentration. Therefore, the S1 site appeared to have the highest affinity for STAT5, as judged by EMSA. However, it is not clear whether the S2 and S3 sites, being close to each other, can be bound by STAT5 in vivo. Figure 4.STAT5 binds to PBE. (A) Identification of STAT5-binding sites. Three potential sites shown in triangles, named S1–S3, were found within PBE (thin line). The three C/EBPβ-binding sites are marked as in Figure 1. EMSA was performed using end-labeled 30 bp oligonucleotides containing the S1 site. STAT5 binding and supershifted complexes are indicated by filled and open arrows. Unlabeled 30 bp oligonucleotides containing the S1, S2 or S3 site, plus a known STAT5 site, were used as competitors at the indicated molar excess to the probe. (B) ChIP assays with anti-STAT5a antibodies. Fragments containing the S1 site (S1), S2 plus S3 sites (S23) and C/EBP sites (C/EBP), as diagrammed in (A), were amplified using DNA templates before (input) or after immunoprecipitation (IP) with anti-STAT5 and control antibodies. (C) Effect of deletion of STAT sites on PBE activity. Left: Ba/F3 cells were transfected with the indicated constructs along with the CMV-LacZ construct. Luciferase activities are normalized with that of β-galactosidase and are shown as averages of activities relative to that of PBE-luc obtained from at least three independent experiments. Right: C/EBP-dependent activity is the ratio of relative activities between enhancers with wild-type and mutant C/EBP sites (open and closed ovals). Download figure Download PowerPoint To determine whether STAT5 binds to the PBE region in vivo, ChIP assays were performed with antibodies against STAT5 (Figure 4B). The amount of DNA brought down in the precipitates was determined by PCR using primers specific to regions containing the S1 or the S2 and S3 sites (S23). A larger amount of S1- and S23-containing DNA was recovered from the anti-STAT5 precipitates of cells cultured with IL-3 than those without IL-3, or those from the precipitates with control antibodies. As a negative control, an intervening region between the S1 and S23 sites, containing the C/EBP sites (Figure 4A), was not precipitated specifically by anti-STAT5 antibodies, suggesting that the S1- and S23-containing fragments were brought down as separate fragments due to their independent binding to STAT5. Taken together, these results indicate that STAT5 indeed binds to the DNA sequences in PBE in Ba/F3 cells. Interestingly, EMSA did not reveal high affinities of the S2 and S3 sites for STAT5; these sites together could bind to STAT5 in vivo, perhaps through cooperation. If STAT5 can potentiate the transcriptional activity of C/EBPβ, deletion of these STAT sites would have a negative impact on C/EBP-mediated transcription. Indeed, we found that deletion of all three STAT sites in the ΔPBE construct led to a 55% reduction of overall PBE activity even though all three C/EBP sites are intact (Figure 4C). Furthermore, C/EBP-dependent activities can be determined by comparing the activity of PBE or ΔPBE with that of its cognate construct lacking C/EBP sites. Such activities for PBE and ΔPBE were therefore estimated to be 6.25- and 1.5-fold, which meant that deletion of the STAT sites caused a 76% reduction of the C/EBP-dependent activity in ΔPBE (Figure 4C). This would suggest that the STAT5 sites contribute to the enhancer activity of PBE, most probably by influencing the function of C/EBPβ. The increased activity of ΔPBE-luc-β123 compared with PBE-luc-β123 is probably due to removal of unknown inhibitory sequences in PBE. Histone deacetylase activities are involved in activation of Id-1 transcription To explore the possibility that Id-1 expression is regulated by changes in chromatin structure, we examined histone acetylation in the Id-1 locus using ChIP assays with antibodies against both acetylated histones H3 and H4 (Figure 5A). Regions near the STAT sites (regions B and C) were analyzed along with a region in the promoter (region A) (Figure 5A). Surprisingly, levels of acetylated histones H3 and H4 bound within PBE were significantly and reproducibly lower in cells cultured with IL-3 than those without IL-3. In contrast, the amounts of acetylated histone H3 and H4 in the promoter region (region A) did not decrease under the same condition, suggesting that histone deacetylation occurred specifically in the PBE region (Figure 5A). Furthermore, the reductions in acetylated histone H3 and H4 bound to PBE were not due to decreased histone occupancy because similar or slightly larger amounts of histone H3 and H2B proteins were found in the presence of IL-3 (Figure 5A). Figure 5.Deacetylase activities are necessary for PBE-mediated transcription of the Id-1 gene. (A) ChIP assays of the Id-1 locus depicted as in Figure 1. PCR fragments corresponding to various regions in the locus are shown as short black bars and labeled A–C. Each fragment was amplified from immunoprecipitates of Ba/F3 cells cultured in medium plus or minus IL-3. Fragment B was also amplified using DNA preparations prior to IP as input controls. Data shown are representative of three independent experiments with the indicated antibodies. (B) Northern blot analyses of Id-1 and GAPDH levels in 4 h IL-3-deprived Ba/F3 cells, which were re-stimulated with (lanes 5–7) or without (lanes 2–4) IL-3 for 1 h. TSA (lane 3, 4, 6 and 7) was added 1 h before and during re-stimulation at the indicated concentrations. Lane 1 contains RNA from Ba/F3 cells continuously cultured with IL-3. The percentage Id-1 re-stimulation (lanes 5–7) was calculated by comparing Id-1 levels normalized with levels of GAPDH and shown in the bar graph. (C) Northern blots to measure the levels of Id-2 and GAPDH mRNA. Treatments in lanes 1–6 were identical to those in lanes 2–7 of (B). (D) Transient transfection assays for expression of the indicated reporter genes under the following conditions: (1) continuous culture in IL-3; (2) IL-3 deprivation for 16 h; (3) IL-3 deprivation for 10 h followed by 6 h re-stimulation; (4) the same as (3) plus TSA treatment 1 h before and during IL-3 re-stimulation. SEAP activities accumulated in media during the last 6 h of the treatment were normalized against β-galactosidase activities. Data are presented as activities relative to SEAP activities under condition 1. Download figure Download PowerPoint To test whether histone deacetylation is of any functional significance, IL-3-dependent expression of Id-1 was measured in cells treated with a deacetylase inhibitor, trichostatin A (TSA). Pre-treatment of IL-3-deprived cells with TSA for 1 h inhibited Id-1 expression by 60% upon IL-3 re-stimulation (Figure 5B). As a negative control, expression of an IL-3-independent gene, Id-2, was not inhibited by TSA, suggesting that inhibition of Id-1 expression is not due to any potential deleterious effects on Ba/F3 cells (Figure 5C). Therefore, IL-3-stimulated Id-1 expression appears, at least in part, to depend on a deacetylase activity, most probably operating at the PBE region. We next tested if histone deacetylation is important for PBE activity by using a secreted alkaline phosphatase (SEAP) reporter gene in transient transfection assays. The SEAP reporter allows us to assay for transcriptional activities within defined time periods after different treatments (Figure 5D). Removal of IL-3 for 16 h diminished SEAP expression by at least 70%, indicating that PBE could mediate IL-3-stimulated expression of SEAP. More importantly, treatment with TSA inhibited PBE-SEAP expression upon IL-3 re-stimulation, suggesting that deacetylase activities played an important role in PBE-activated gene expression even in the context of a heterologous promoter and a reporter gene. As a control, IL-3 removal and TSA treatment had little effect on expression of the CMV-SEAP construct. Because the IL-3 response and deacetylase dependence of PBE can be recapitulated when taken out of its natural context, it is unlikely that histone deacetylation or nucleosomal positioning of the enhancer is crucial for Id-1 expression in vivo. Histone deacetylation observed in the PBE region might be a by-product of HDACs recruited to the vicinity. Instead, deacetylase activities could be important for activities of other transcription factors involved in Id-1 expression. STAT5 recruits histone deacetylase 1 Since IL-3-dependent Id-1 expression required protein deacetylation, we tested whether STAT5 could recruit deacetylases by performing co-IP assays. Immuno precipitates obtained with antibodies against STAT5a were western blotted with antibodies against HDAC1. Anti-STAT5a antibodies brought down not only STAT5a but also HDAC1 from total extracts of Ba/F3 cells cultured with IL-3, but not those without IL-3 (Figure 6A). Control mouse IgG precipitated neither STAT5a nor HDAC1. Co-precipitation of STAT5a and HDAC1 was also observed in 293T cells transfected with both STAT5a and HDAC1 expression constructs, but not either alone (Figure 6B). Consistently, we have shown using a ChIP assay that an increased amount of HDAC1 was present near the S1 STAT5 site in the PBE (region B), but not in the promoter (region A), in cells cultured with IL-3 compared with those without IL-3 (Figure 6C). These results thus suggest that STAT5, by recruiting HDAC1 to PBE, is responsible for the deacetylase activity associated with PBE. Figure 6.Interaction between STAT5 and HDAC1. (A) Total cell extracts derived from Ba/F3 cells cultured with or without (+ or −) IL-3 were precipitated with the indicated antibodies. Immunoprecipitates and inputs were analyzed using western blots with antibodies against HDAC1 or STAT5a. (B) 293T cells were transfected with the indicated constructs, and nuclear extracts were analyzed after IP with antibodies against HDAC1 and western blotting with anti-STAT5 antibodies. Inputs were analyzed using western blots with the indicated antibodies. (C) ChIP assay was performed using antibodies against HDAC1 and Ba/F3 cells cultured with or without IL-3. PCR products for regions A and B were as described in Figure 5A. Download figure Download PowerPoint Acetylation of C/EBPβ inhibits its DNA-binding activity What are the intended targets, if not histones, of HDAC1 recruited by STAT5? Since C/EBPβ is crucial for Id-1 expression, it becomes a logical candidate. From studies on acetylation of p53 and GATA1 (Gu and Roeder, 1997; Boyes et al., 1998), an acetylation motif of K/RXKK has been derived, where the acetyl group is usually added to the two adjacent lysine residues (Figure 7A). A similar motif, KAKK, was found in a region N-terminal to the DNA-binding domain of C/EBPβ, which is evolutionarily conserved (Figure 7A). To determine whether C/EBPβ can be acetylated, partially purified recombinant LAP proteins were used in an in vitro acetylation reaction with [14C]acetyl-CoA. Immunoprecipitates containing CBP overexpressed in 293T cells or partially purified GST–PCAF fusion proteins were used as the sources of acetylases. Indeed, LAP was acetylated in vitro by both CBP and PCAF (Figure 7B). Furthermore, mutations of the acetylation site (Lys215 and Lys216 to arginine) greatly reduced the acetylation in LAP (Figure 7A and B). These results thus suggest that C/EBPβ can be a