Activation of resting T lymphocytes initiates differentiation into mature effector cells over 3–7 days. The chemokine CCL5 (RANTES) and its major transcriptional regulator, Krüppel-like factor 13 (KLF13), are expressed late (3–5 days) after activation in T lymphocytes. Using yeast two-hybrid screening of a human thymus cDNA library, PRP4, a serine/threonine protein kinase, was identified as a KLF13-binding protein. Specific interaction of KLF13 and PRP4 was confirmed by reciprocal coimmunoprecipitation. PRP4 is expressed in PHA-stimulated human T lymphocytes from days 1 and 7 with a peak at day 3. Using an in vitro kinase assay, it was found that PRP4 phosphorylates KLF13. Furthermore, although phosphorylation of KLF13 by PRP4 results in lower binding affinity to the A/B site of the CCL5 promoter, coexpression of PRP4 and KLF13 increases nuclear localization of KLF13 and CCL5 transcription. Finally, knock-down of PRP4 by small interfering RNA markedly decreases CCL5 expression in T lymphocytes. Thus, PRP4-mediated phosphorylation of KLF13 plays a role in the regulation of CCL5 expression in T lymphocytes.
A fundamental question in inflammatory disease is how immune cells move from the bloodstream to sites of disease. This process is central to the development of a variety of acute and chronic immune-mediated diseases. Critical components in this process are chemokines that direct the movement and infiltration of specific subsets of inflammatory cells to the site of inflammation (1). This family of small proteins also plays an important role in the control of leukocyte recruitment, activation, and effector function, as well as hemopoiesis, the modulation of angiogenesis, and aspects of adaptive immunity (2, 3, 4, 5, 6). CCL5, a member of the C-C chemokine family, is a potent chemoattractant of T lymphocytes, monocytes, eosinophils, basophils, and NK cells (7, 8, 9, 10, 11). CCL5 also activates T lymphocytes, causes degranulation of basophils, and mediates a respiratory burst in eosinophils (12, 13, 14). Collectively, these functions implicate CCL5 as an important mediator of both acute and chronic inflammation. The chemokine receptor CCR5, which binds CCL5 and the related chemokines MIP-1α and MIP-1β, serves as a coreceptor for HIV to enter target cells (15, 16, 17, 18, 19). Thus, CCL5 has become an important therapeutic target for immune-mediated diseases. The development of anti-inflammatory agents capable of blocking CCL5 expression may inhibit the generation of cellular infiltrate in autoimmunity and transplant rejection. In contrast, inducing CCL5 expression may be therapeutic for cancer and AIDS.
CCL5 is ubiquitously expressed in a variety of tissues under different conditions (20, 21, 22, 23). In fibroblasts, epithelial cells, and monocytes/macrophages, the expression of CCL5 is elevated within hours of stimulation and is regulated by NF-κB (24, 25). In contrast, in T lymphocytes, the induction of CCL5 occurs 3–5 days after activation (26) and is regulated by a complex of proteins recruited by Krüppel-like factor 13 (KLF13)3 (27, 28). These late kinetics of expression help to amplify the immune response in both time and space, and are consistent with the late expression of other genes involved in T cell effector function including perforin, granulysin, and granzymes A and B. KLF13 binds to the CTCCC element of the human CCL5 promoter present in the A/B site (27). Silencing of KLF13 expression in human T lymphocytes with small interfering RNA (siRNA) decreases the expression of CCL5 mRNA and protein (28). Although KLF13 mRNA levels are similar in resting and activated T lymphocytes, KLF13 protein is only expressed in actively proliferating and differentiating T lymphocytes (translational regulation), coincident with CCL5 gene expression (29). Interestingly, KLF13 is highly phosphorylated in activated T lymphocytes (27), suggesting that, like many transcription factors, its activity is regulated by kinases. To identify binding partners and potential regulators of KLF13 function, yeast two-hybrid screening was performed in the present study. PRP4 kinase, a member of the MAPK family, was found to bind KLF13 and to regulate CCL5 expression in human T lymphocytes.
Materials and Methods
RFLAT-1 (C-19) Ab for supershifting KLF13 was purchased from Santa Cruz Biotechnology. Alexa Fluor 488-conjugated anti-GFP and Alexa Fluor 555 goat anti-mouse IgG2b(γ2b) were purchased from Molecular Probes. Anti-hemagglutinin (HA) mouse mAb (clone 12CA5) was purchased from Roche Diagnostic Systems. Anti-V5 mouse mAb was purchased from Sigma-Aldrich. Anti-α-actinin was obtained from Upstate Biotechnology. Rabbit polyclonal antisera to KLF13 was produced as described previously (27). Rabbit polyclonal antisera to PRP4 was produced by immunizing rabbits with synthetic peptides LKKLNDADPDDKFHC (residues 736–750) and CQRLPEDQRKKVHQLK (residues 962–977) conjugated to keyhole limpet hemocyanin (Washington Biotechnology).
pGL3-RP-luc was constructed by inserting −195 to +54 bp of the CCL5 promoter into the pGL3-basic vector (Promega). pSOS-KLF13 construct was obtained by subcloning the PCR-amplified full-length KLF13 into NcoI/SacI sites of the bait vector pSOS (Stratagene). pME-HA-PRP4, which contains full-length PRP4, was a gift from Dr. M. Hagiwara (Tokyo Medical and Dental University, Tokyo, Japan). pcDNA3.1-KLF13 and pcDNA3.1/CT-GFP-KLF13 constructs were obtained by subcloning a PCR product encoding full-length human KLF13 cDNA into the mammalian expression vector pcDNA3.1−+
Yeast two-hybrid analysis
The CytoTrap two-hybrid system (Stratagene) was used to identify proteins that bind to KLF13 using pSOS-KLF13 as the bait construct. This construct was cotransfected into a mutant yeast strain cdc25Hα with a CytoTrap XR Human Thymus cDNA Library cloned in pMyr vector following the manufacturer’s protocol. Plasmids were extracted from putative positive colonies and transformed into Escherichia coli to be further analyzed by DNA sequencing. Only peptide sequences that were in frame in pMyr were considered for further validation.
Cell culture, transfection, and luciferase assays
Human peripheral blood T lymphocytes were isolated from leukopacs (Stanford Blood Bank) by negative selection (RosetteSep) according to the manufacturer’s protocol (StemCell Technologies). T lymphocytes and COS7 cells were cultured at 37°C with 5% CO2l-glutamine, and 100 U/ml penicillin-streptomycin, respectively. T lymphocytes were stimulated with 5 μg/ml PHA for up to 7 days. Transient transfection of COS7 cells was performed using FuGENE 6 transfection reagent (Roche Diagnostics Systems) according to the manufacturer’s recommendation. For luciferase reporter assays, COS7 cells (2.5 × 105) were transfected with pGL3-RP-luc (0.6 μg) plus pcDNA3.1-KLF13 (0.3 μg) and/or pME-HA-PRP4 (0.3 μg). Corresponding empty vectors were used to keep the total amount of DNA constant. A pRL-TK plasmid (20 ng; Promega) encoding a Renilla luciferase gene was included as an internal control. The cells were harvested and lysed 36-h posttransfection, and luciferase activity was determined using a Dual Luciferase Assay Kit (Promega). Firefly luciferase activities were normalized to Renilla activities to account for differences in transfection efficiency.
Immunoprecipitation and kinase assay
Transfected COS7 cells were lysed in buffer A containing 20 mM HEPES (pH 7.9), 1.5 mM MgCl2, 420 mM NaCl, 0.2 mM EDTA, 25% glycerol, 1 mM DTT, and protease inhibitors. Lysates were clarified at 15,000 × g for 20 min at 4°C. Immunoprecipitations from cell lysates were conducted using corresponding Ab along with protein A/G agarose beads. After incubating for 16 h at 4°C, immune complexes were collected by centrifugation and then washed two times with lysis buffer and two times with PBS. For kinase assays, the immunoprecipitants were washed one more time with kinase buffer (25 mM Tris-HCl (pH 7.6), 10 mM MgCl2, 1 mM EGTA, and 1 mM DTT). In the kinase reaction, His-tagged full-length or aa 264–288-truncated KLF13 was used as substrate. Purification of recombinant KLF13 protein through a Ni+ column was described previously (27). The immunocomplexes were incubated at 30°C in kinase buffer supplemented with 1 mM ATP, 1 μCi [γ-32P]ATP, and 1 μg of recombinant KLF13 in a volume of 30 μl for 15 min. The reaction was terminated by the addition of SDS-PAGE loading buffer and the samples were subjected to SDS-PAGE. Phosphorylated KLF13 was visualized by autoradiography. For EMSA, phosphorylated recombinant KLF13 was made using cold ATP instead of [γ-32P]ATP in the kinase reaction.
Total RNA was extracted from human T lymphocytes using the RNeasy Mini Kit according to the manufacturer’s instructions (Qiagen). Twenty micrograms of total RNA was used for Northern blotting as previously described (30). The membrane was hybridized with 32P-labeled PRP4 cDNA, stripped, and then reprobed with 32P-labeled 28S rRNA antisense oligonucleotide to confirm equal loading and transfer. Relative quantification was performed using densitometry.
T lymphocytes were lysed in buffer A as described above. T cell lysates or immunoprecipitants from transfected COS7 cells were subjected to SDS-PAGE and the membrane was hybridized with Abs against KLF13 or PRP4. ECL Western blotting detection reagents were used for detection (Amersham Biosciences). Loading and transfer efficiency were confirmed by blotting with a mouse Ab against α-actinin.
A double-stranded oligonucleotide corresponding to the A/B site of the CCL5 promoter was used as a probe for EMSA as previously described (27). The labeled probe (20,000 cpm) was incubated with 1 μg of recombinant KLF13 from the kinase reaction, 1.5 μg of poly(dI:dC), 10 mM Tris-HCl (pH 7.5), 80 mM NaCl, 1 mM EDTA, 1 mM DTT, and 5% glycerol for 20 min at room temperature. EMSA was also performed using immunoprecipitants from COS7 cells transfected with either empty vector (vector) or pME-HA-PRP4 (PRP4) in the absence of KLF13 as additional negative controls. For supershift assays, 2 μg of Ab was added to the binding mixture. DNA-protein complexes were analyzed on a 5% nondenaturing polyacrylamide gel in 0.5 × Tris-borate-EDTA buffer.
Cellular localization experiments
To visualize the intracellular localization of KLF13 and PRP4, COS7 cells (2 × 104) grown on tissue culture glass slides were transfected with pcDNA3.1-GFP-KLF13 (0.2 μg) and pME-HA-PRP4 (0.2 μg), either alone or in combination using FuGene 6 transfection reagent. Corresponding empty vector was used as a control. After 24 h, the transfected cells were fixed and permeabilized. KLF13 and PRP4 were detected by immunofluorescence as described by Kojima et al. (31
siRNA and real-time quantitative PCR (RT-qPCR)
Knock-down of PRP4 mRNA was achieved using double-stranded siRNA oligonucleotides obtained from Qiagen. Nonsilencing siRNA (5′-UUCUCCGAACGUGUCACGUdTdT-3′), which has no homology to any known mammalian gene, was used as a negative control. A total of 1.5 μg of siRNA was nucleofected into 5 × 106−ΔΔCt, where ΔΔCt = (ΔCt(silencing)) − (ΔCt(non-silencing)) and ΔCt = (Ct(sample) − Ct(Gus)). Values represent the fold change of target gene expression from PRP4 siRNA-transfected vs nonsilencing siRNA-transfected primary T lymphocytes.
CCL5 protein levels were measured in the culture supernatant using the Endogen Human RANTES ELISA Kit (Pierce) according to the manufacturer’s instruction.
PRP4 binds KLF13 in human thymocytes
The CytoTrap yeast two-hybrid system was used to screen a human thymus library for proteins that bind to KLF13. Approximately 2 × 106 transformants were screened with a pSOS-KLF13 construct, and 19 putative positive clones were identified. Comparison of cDNA sequences of the clones with the GenBank database revealed that one of them is the human homolog of the yeast serine-threonine kinase PRP4. To further confirm the physical interaction between KLF13 and PRP4, reciprocal coimmunoprecipitation experiments were performed. COS7 cells were cotransfected with pME-HA-PRP4 construct and pcDNA3.1-KLF13. Replacement of one expression plasmid with its corresponding empty vector was used to show specificity of coimmunoprecipitation. Only HA-PRP4-transfected COS7 lysates immunoprecipitated with an anti-HA Ab against tagged PRP4 pulled down KLF13 (Fig. 1⇓A), while the reciprocal experiment using a KLF13 Ab pulled down PRP4 (Fig. 1⇓B). These data confirm that KLF13 binds PRP4.
PRP4, a MAPK, is expressed in T lymphocytes
T lymphocytes were isolated from peripheral blood and activated with the mitogen PHA. PRP4 mRNA and protein were measured in resting T lymphocytes and through 7 days after activation. Low levels of PRP4 mRNA were detected by Northern blot in resting T lymphocytes (Fig. 2⇓A). mRNA levels increased 5-fold 1 day after the activation of T lymphocytes with PHA and, by day 3, had increased ∼20-fold. PRP4 mRNA decreased on day 5 and, by day 7, PRP4 mRNA dropped to the same level seen on day 1. PRP4-specific rabbit antisera were generated to monitor PRP4 protein expression during T lymphocyte activation by Western blot (Fig. 2⇓B). Parallel to the mRNA results, only trace amounts of PRP4 protein were present in resting T lymphocytes. PRP4 protein increased 1 day after activation and continued to increase with a peak of 9-fold induction observed by day 3. Protein levels decreased on days 5 and 7, consistent with mRNA expression. Thus, PRP4 kinase is expressed in human T lymphocytes and displays an activation kinetic peaking in expression at day 3.
PRP4 phosphorylates KLF13, decreasing its binding affinity to the CCL5 promoter A/B site
KLF13 is the major transcription factor regulating CCL5 expression in T lymphocytes (27, 28). KLF13 is expressed late (days 3–5) after T lymphocyte activation, is rapidly phosphorylated, and is present in both the nucleus and the cytosol (27, 32). Because the protein expression patterns of KLF13 and PRP4 are similar, we tested whether PRP4 and NLK, another MAPK family member, could phosphorylate KLF13 (Fig. 3⇓A). The immunoprecipitants derived from PRP4- or NLK-overexpressing COS7 cells were used to phosphorylate recombinant KLF13 in a kinase assay, with immunoprecipitants from corresponding vector-transfected cells used as a negative control. Under these conditions, immunoprecipitated PRP4 phosphorylated both itself and KLF13 (Fig. 3⇓A, lane 4). In contrast, immunoprecipitated NLK phosphorylated itself, but not KLF13 (Fig. 3⇓A, lane 2). We previously found that NLK was recruited to the CCL5 promoter by KLF13 and subsequently phosphorylates serine 10 of histone H3 upon T lymphocyte activation (28). These results suggest that PRP4 and NLK regulate CCL5 expression by phosphorylating different target proteins. Immunoprecipitated PRP4 also phosphorylated KLF13 (1–263) that has 25 aa deleted from the C terminus (Fig. 3⇓A, lane 6). However, phosphorylation was less robust, suggesting that KLF13 may contain multiple PRP4 phosphorylation sites, with one or more sites in the truncated region.
To test whether the phosphorylation of KLF13 by PRP4 affects its interaction with the CCL5 promoter, EMSA was performed using a γ-32P-end-labeled oligonucleotide derived from the A/B region of the CCL5 promoter. Full-length recombinant KLF13 was phosphorylated by immunoprecipitated PRP4 obtained from transfected COS7 cell lysate using unlabeled ATP, with immunoprecipitant from vector-transfected COS7 cell lysate serving as control. An upper doublet and three lower bands were observed. Although the upper doublet most likely corresponds to the full-length KLF13 bound to probe, the lower bands may result from the degradation of the KLF13 substrate during the kinase reaction. All of these DNA-protein complexes were supershifted upon the addition of anti-KLF13 Ab (Fig. 3⇑B), but not with anti-p50 Ab (data not shown), indicating the specificity of binding. In the presence of PRP4, there is a ∼50% decrease in KLF13 bound to the CCL5 promoter A/B site probe (Fig. 3⇑B). Thus, phosphorylation of KLF13 by PRP4 results in lower binding affinity to the CCL5 promoter compared with nonphosphorylated KLF13.
KLF13 and PRP4 synergistically regulate CCL5 expression
Reporter gene assays were performed to examine the effect of PRP4 on CCL5 transcription (Fig. 4⇓). The CCL5 promoter luciferase reporter construct pGL3-RP was transfected into COS7 cells along with KLF13 and/or PRP4 expression constructs. Compared with vector control, expression of KLF13 caused a 2.8-fold induction (p < 0.0001) in CCL5 reporter gene activity, while expression of PRP4 caused a 1.4-fold increase (p = 0.01). However, coexpression of KLF13 and PRP4 resulted in a 5.2-fold increase (p < 0.0001) in CCL5 promoter activity. Of note, we detected endogenous PRP4 in COS7 cells (data not shown), explaining the modest increase in CCL5 promoter activity in the presence of transfected PRP4. These results indicate that PRP4 synergizes with KLF13 to regulate CCL5 expression in vitro.
PRP4 increases the nuclear localization of KLF13
To further investigate the role of PRP4 in regulating CCL5 expression, the effect of PRP4 on intracellular localization of KLF13 was assessed. COS7 cells were transiently transfected with expression vectors corresponding to empty vector, GFP-KLF13, HA-PRP4, or a combination of GFP-KLF13 and HA-PRP4. No signal was detected when cells were transfected with pcDNA3.1, and only a small amount of background signal was observed throughout the cell following transfection of the pME-HA vector (Fig. 5⇓). In the absence of PRP4, overexpressed KLF13 protein was detected in the nuclear compartment of all KLF13-transfected COS7 cells, while 45–50% of these cells also had KLF13 in the cytoplasm (Fig. 5⇓, GFP-KLF13/α-GFPAb). In contrast, when KLF13 was coexpressed with PRP4, KLF13 resided almost exclusively in the nucleus, indicating that PRP4 regulates the nuclear translocation of KLF13 (Fig. 5⇓, GFP-KLF13 + HA-PRP4/α-GFPAb). The arrows in the frames transfected with GFP-KLF13 + HA-PRP4 (Fig. 5⇓) mark a single cell that expresses KLF13, but not PRP4. It is evident that, in the absence of PRP4, overexpressed KLF13 is distributed both in the nuclei and cytoplasm of the cell. In contrast, overexpressed KLF13 resides exclusively in the nuclei of the other cells in the same field that is coexpressing both KLF13 and PRP4, supporting the role of PRP4 in KLF13 nuclear translocation. Overexpressed PRP4 is predominantly expressed in the nucleus of the cell, regardless of the presence or absence of overexpressed KLF13 (Fig. 5⇓, HA-PRP4/αHAAb). Frames of Fig. 5⇓ in each row shows nuclei visualized by Hoechst staining. Composite was generated by merging images from frames 1–3 (Fig. 5⇓) in each row to better visualize colocalization.
Knock-down of PRP4 decreases CCL5 expression in human T lymphocytes
To confirm the role of PRP4 in regulating CCL5 expression in T lymphocytes, two sets of PRP4-specific siRNAs were nucleofected into resting human T lymphocytes. The cells were then stimulated with PHA, and the expression of CCL5 was measured after 30 h using RT-qPCR and ELISA. PRP4 mRNA (Fig. 6⇓A) and protein (Fig. 6⇓B) were suppressed >65% by both sets of siRNA. In contrast, PRP4-specific siRNAs caused only 10–15% suppression of NLK mRNA expression (Fig. 6⇓A), demonstrating the specificity of the siRNAs. Moreover, both sets of PRP4 siRNA repressed CCL5 expression, with ∼55–60% reduction in mRNA transcription and 30–35% reduction in protein expression (Fig. 6⇓). Thus, PRP4 regulates CCL5 expression in T lymphocytes.
KLF13 is the major transcription factor that positively regulates CCL5 expression in activated T lymphocytes (27). We previously reported that KLF13 protein is expressed in the adult spleen and lung, but not in liver, brain, kidney, heart, or reproductive organs, and showed that KLF13 is translationally regulated through its 5′-untranslated region (29). In addition, KLF13 is highly phosphorylated in activated T lymphocytes, suggesting that its activity is regulated by posttranslational modification. In this study, we show that PRP4, a MAPK family member, phosphorylates KLF13 and plays an important role in the regulation of CCL5 expression in human T lymphocytes.
PRP4, originally isolated from the fission yeast Schizosaccharomyces pombe, is involved in pre-mRNA splicing (33, 34). The human homolog of PRP4 is ubiquitously expressed in multiple tissues (31), including spleen and lung, which also express KLF13 (27). In addition, in T lymphocytes, the expression patterns of PRP4 and KLF13 (28) mirror each other with resting cells having very low or undetectable levels of these proteins until 3 days after activation, when both proteins are significantly induced. PRP4 belongs to a family of serine/arginine-rich protein-specific kinases that recognize serine-arginine-rich substrates (34). The catalytic domain of PRP4 shows significant similarity to the JNK/stress-activated protein kinase type of MAPK including the TPY motif, suggesting that PRP4 may play an important role in cell differentiation (35). PRP4 has also been reported to mediate cellular signaling (36). The N terminus of PRP4 interacts with proteins involved in splicing and nuclear hormone-regulated chromatin remodeling (37). Recently, Bennett et al. (38) reported that the C terminus of PRP4 interacts with HIV-2 Gag, although HIV-2 Gag polyprotein is not phosphorylated by PRP4. In our study, a yeast two-hybrid screen demonstrated that PRP4 interacts with KLF13. We confirmed this interaction by reciprocal coimmunoprecipitation experiments, because interactions detectable in multiple binding assays are unlikely to be experimental false positives (39). In addition, we also demonstrated that KLF13 is a substrate of PRP4 in kinase assays using PRP4 immunoprecipitated from transfected COS7 cells. However, PRP4 (499–1007), which retains its kinase domain, showed autophosphorylation, but completely lost its ability to phosphorylate KLF13 (data not shown), indicating that the truncated region of PRP4 is required for the interaction and/or phosphorylation of KLF13. These findings are consistent with the previous results of others, showing that PRP4 is capable of the phosphorylation of both transcription factors and serine/arginine-rich splicing factors (36).
KLF13 contains multiple potential phosphorylation sites. At least 18 putative serine phosphorylation sites and 3 threonine phosphorylation sites are predicted by NetPhos2.0 Server. Whether one or more of these sites is the PRP4 recognition sequence has not yet been determined. Although we have identified several serine phosphorylation sites between aa 264–88 in the C-terminal end of KLF13 (data not shown), deletion of this region does not completely abrogate the phosphorylation by PRP4, suggesting either that these sites are targets of other protein kinases or that multiple PRP4 phosphorylation sites work in concert.
KLF13 binds to the A/B region of the CCL5 promoter in a dose-dependent manner (27). Although phosphorylation of KLF13 by PRP4 results in a decreased affinity of KLF13 for the A/B site as demonstrated by EMSA, reporter gene assays using a CCL5 promoter luciferase reporter indicate that coexpression of KLF13 and PRP4 results in increased CCL5 promoter activity relative to transactivation by KLF13 alone. In contrast, coexpression of KLF13 and PRP4 (499–1007), which retains its kinase domain but is unable to phosphorylate KLF13, did not enhance transcription (data not shown). This indicates that the N-terminal region of PRP4 is not only important for the phosphorylation of KLF13, but also plays a role in regulating CCL5 expression. The apparent dichotomy between decreased KLF13 DNA binding induced by PRP4-mediated phosphorylation and increased CCL5 expression remains unclear, but may be related to the complexity of the CCL5 enhancesome (28). In this regard, Song et al. (40) reported that the transcriptional coactivators p300 CREB-binding protein (CBP) and p300-CBP-associated factor (PCAF) act cooperatively in stimulating KLF13 transcriptional activity. Nevertheless, p300/CBP and PCAF acetylate specific lysine residues in the zinc finger DNA-binding domain of KLF13 which disrupt KLF13 DNA binding. In comparison, we found that the mutation of two amino acids in the same zinc finger DNA-binding domain of KLF13 causes a dramatic increase in CCL5 reporter gene activity, although the mutated KLF13 bound to the CCL5 A/B site with much lower affinity (data not shown). Moreover, we recently confirmed that KLF13 recruits p300/CBP and PCAF to the CCL5 promoter in activated T lymphocytes (28). Studies are currently underway to determine whether PRP4 mediates changes in the acetylation states of KLF13 in concert with other acetyltransferase proteins, such as p300/CBP and PCAF and, therefore, reduces its DNA-binding affinity. We hypothesize that the phosphorylation of KLF13 by PRP4 may facilitate the assembly or disassembly of the multiprotein complex at the CCL5 promoter, enabling PRP4 to further modify transcriptional coactivators or repressors by phosphorylation, as many ERK/MAPK and cyclic-dependent kinases have been shown to associate with and phosphorylate transcription factors or transcriptional coactivators (41).
Control of CCL5 expression in T lymphocytes is complex. CCL5 transcription is controlled by an enhancesome composed of different factors at various times after T lymphocyte activation (28). KLF13, a sequence-specific DNA transcription factor, coordinates the induction of CCL5 expression in T lymphocytes by ordered recruitment of proteins to the CCL5 promoter, including Brahma-related gene 1 (Brg-1) (28). Brg-1 is an ATPase subunit of the SWI-SNF chromatin-remodeling complexes (42). It is recruited to chromatin by direct interactions with DNA-binding proteins (43). Interestingly, Dellaire et al. (37) demonstrated that Brg-1 interacts with the hypophosphorylated form of PRP4 in a transcription-dependent manner and appears to be a PRP4 substrate in vitro. Nuclear receptor corepressor, a component of the nuclear hormone corepressor complex, also interacts in vivo with human PRP4. In summary, PRP4 binds to and phosphorylates KLF13, enhancing CCL5 expression. Therefore, PRP4 is an important component of the enhancesome assembling over time at the CCL5 promoter in activated T lymphocytes.
The authors have no financial conflict of interest.
The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.
↵1 This work was supported by a grant (to A.M.K.) from the National Institutes of Health (NIH R37 DK35008-23). A.M.K. is the Shelagh Galligan Professor of Pediatrics.
↵2 Address correspondence and reprint requests to Dr. Alan M. Krensky, Division of Immunology and Transplantation Biology, Stanford University, 300 Pasteur Drive, Stanford, CA 94305. E-mail address:
↵3 Abbreviations used in this paper: KLF13, Krüppel-like factor 13; HA, hemagglutinin; siRNA, small interfering RNA; RT-qPCR, real-time quantitative PCR; NLK, Nemo-like kinase; GUS, β-glucuronidase; Brg-1, Brahma-related gene 1; Ct, threshold cycle; CBP, CREB binding protein; PCAF, p300/CBP-associated factor.
- Received December 22, 2006.
- Accepted April 2, 2007.
- Copyright © 2007 by The American Association of Immunologists