Fas is a cell surface death receptor that signals apoptosis. Several proteins have been identified that bind to the cytoplasmic death domain of Fas. Fas-associated death domain (FADD), which couples Fas to procaspase-8, and Daxx, which couples Fas to the Jun NH2-terminal kinase pathway, bind independently to the Fas death domain. We have identified a 130-kD kinase designated Fas-interacting serine/threonine kinase/homeodomain-interacting protein kinase (FIST/HIPK3) as a novel Fas-interacting protein. Binding to Fas is mediated by a conserved sequence in the COOH terminus of the protein. FIST/HIPK3 is widely expressed in mammalian tissues and is localized both in the nucleus and in the cytoplasm. In transfected cell lines, FIST/HIPK3 causes FADD phosphorylation, thereby promoting FIST/HIPK3–FADD–Fas interaction. Although Fas ligand–induced activation of Jun NH2-terminal kinase is impaired by overexpressed active FIST/HIPK3, cell death is not affected. These results suggest that Fas-associated FIST/HIPK3 modulates one of the two major signaling pathways of Fas.
Fas (APO-1/CD95) is a member of the TNFR family and induces apoptosis when cross-linked with Fas ligand (FasL) 1. The Fas–FasL system has an important role in the immune system, where it is involved in the effector function of cytolytic T cells and in the downregulation of immune responses 2. Clustering of Fas upon binding of the membrane-bound form of FasL recruits the bipartite molecule Fas-associated death domain (FADD), composed of an NH2-terminal death effector domain (DED) and a COOH-terminal DD (death domain). FADD binds to Fas via homophilic DD–DD interactions and recruits the upstream DED-containing caspase-8 to the receptor via DED–DED interactions. Neighboring caspase-8 molecules within this newly formed death-inducing signaling complex then proteolytically activate each other and initiate apoptosis by subsequent cleavage of downstream effector caspases (caspase-3, -6, and -7).
An alternative pathway of Fas signaling involves the Fas-binding protein Daxx 3, although these data have been recently challenged 4. It was proposed that upon Fas activation, Daxx interacts with and activates a mitogen-activated protein kinase kinase kinase termed ASK1 (apoptosis signal-regulating kinase 1), leading to the activation of the Jun NH2-terminal kinase (JNK) and p38 mitogen-activated protein kinase pathways 5,6. JNK has been implicated in activating apoptosis in vitro and in vivo 7,8,9, but its functional role in death receptor signaling, as assayed by expressing dominant negative proteins, has been controversial 10,11. JNK activation has also been reported to occur downstream of caspases via the cleavage and activation of MEKK1, a JNK kinase kinase 12.
Aside from FADD and Daxx, the intracellular domain of Fas was reported to interact with several other proteins, including FAF-1, FAP-1, SUMO-1/Sentrin, and UBC9. FAF-1 augments apoptosis when overexpressed in mammalian cells 13, in contrast to the phosphatase FAP-1, which has been proposed to act as an inhibitor of cell death 14. The ubiquitin-like protein SUMO 15 and its ligase UBC9 16,17 are involved in the modification of a number of proteins, thereby targeting them to the nuclear membrane and certain intranuclear structures 18.
Here we report the identification of a novel Fas-interacting protein that we have named Fas-interacting serine/threonine (Ser/Thr) kinase (FIST)3. FIST3, which is identical to homeodomain-interacting protein kinase (HIPK)3, is a Ser/Thr kinase that is capable of inducing FADD phosphorylation. Moreover, FIST/HIPK3 modulates FasL-induced JNK activation.
Materials And Methods
Antibodies used for immunoprecipitation, JNK activation assay, immunofluorescence and Western blot include: anti-Flag M2 (Sigma-Aldrich), anti-FADD (Signal Transduction Labs.), anti-Fas C-20 (Santa Cruz Biotechnology, Inc.), anti-PML (promyelocytic leukemia protein) C7 (a gift of H. de Thé, Hopital St. Louis, Paris, France), anti–phospho-JNK (New England Biolabs), peroxidase- or Cy5-conjugated secondary antibodies (Jackson ImmunoResearch Laboratories), peroxidase-conjugated anti-IgG1 secondary antibody (Southern Biotechnology Associates, Inc.), and Alexa-conjugated secondary antibodies (Molecular Probes). Rabbit polyclonal antibodies were raised against amino acids (aa) 775–878 (clone 25 isolated from the two-hybrid screen) of murine (m)FIST/HIPK3 and aa 766–920 of the rat homologue (a gift of J. Palvimo, Institute of Biomedicine, Helsinki, Finland).
A mouse embryo cDNA library cloned into the NotI site of the vector pVP16 19, which codes for fusion proteins of the viral transcription activation domain VP16, was provided by S. Hollenberg (Vollum Institute, Portland, Oregon). The two-hybrid screen and the generation of cytoplasmic mutants of Fas were previously described 16.
Cloning of FIST/HIPK3 cDNA.
A cDNA clone for mFIST/HIPK3 was isolated from a mouse testis cDNA library (Stratagene) using a 32P-labeled DNA fragment (random-primed DNA labeling kit; Boehringer Mannheim) encoding aa 775–878. Double-stranded sequencing revealed an open reading frame of 3,576 nucleotides encoding a protein of 1,192 aa with a putative Ser/Thr kinase domain. EST clones encoding the human homologue of murine FIST/HIPK3 were identified in the dbEST database at the National Center for Biotechnology Information (EST clones H37893 and R57262) by performing a database search using mFIST/HIPK3 (http://ncbi.nlm.nih.gov). The accession numbers (available from EMBL/GenBank/DDBJ) for the human and murine FIST/HIPK3 cDNA sequences reported in this paper are AF305238 and AF305239, respectively.
Northern Blot Analysis.
Northern blot analysis was performed using human and mouse multiple tissue and human cancer cell Northern blots (CLONTECH Laboratories, Inc.) with a 32P-labeled antisense RNA probe encoding aa 531–658 of hFIST/HIPK3 or a cDNA probe encoding aa 333–591 of mFIST/HIPK3 according to the manufacturer's instructions.
mFIST/HIPK3 isolated from the mouse testis cDNA library or fragments containing the kinase domain (aa 142–608) or the COOH-terminal domain of mFIST/HIPK3 (aa 592–1192) were subcloned into a derivative of the pCR3 expression vector (Invitrogen), in frame with an NH2-terminal Flag tag. Mutations of the kinase domain of mFIST/HIPK3 (Lys226 → Ser, K226S or Asp322 → Asn, D322N) were achieved by site directed mutagenesis with two sequential rounds of PCR, using oligonucleotides containing the target mutation. PCR products were cloned into pCR-blunt (Invitrogen) and subcloned into the pCR3-derived expression vector, in frame with an NH2-terminal Flag. Human Fas cDNA was cloned into pCR3 with or without an NH2-terminal Flag tag. Vesicular stomatitis virus (VSV)-tagged mutant FADD lacking aa 202–208 or 191–208, respectively, were generated as described above. The following expression plasmids were obtained from the indicated sources: Flag-JNK (C. Widmann, Institute of Cell Biology and Morphology, Lausanne, Switzerland) and PML (H. de Thé, Hopital St. Louis, Paris, France).
293T cells were seeded in 6-cm plates and transfected for 8–15 h with the calcium phosphate precipitation method 20. Cells were harvested 24–36 h after the onset of transfection and lysed in lysis buffer containing 0.1% NP-40, 50 mM Tris-HCl, pH 7.4, 150 mM NaCl, and protease inhibitors (Complete™; Boehringer Mannheim), followed by three freeze–thaw cycles. After preclearing for at least 1 h on Sepharose 6B (Amersham Pharmacia Biotech), Flag-tagged proteins were immunoprecipitated for at least 2 h with anti-Flag agarose. Immunoprecipitates were washed three times in lysis buffer without protease inhibitors before analysis by SDS-PAGE and Western blotting.
Sample fractionation with nonionic NP-40 detergent was performed as described 21. In brief, the NP-40–soluble fraction was separated from the insoluble fraction by centrifugation. The pellet was washed twice in PBS and after sonication, both the washed pellet and the initial supernatant were solubilized in SDS sample buffer containing 100 mM dithiothreitol. For the induction of apoptosis, Jurkat cells were treated with 100 ng/ml SuperFasL (Alexis) for 5 h in the presence and the absence of z-VAD-fmk (50 μM).
In Vitro Kinase Assay and Phosphoamino Acid Analysis.
Expression plasmids for wild-type or mutant Flag-tagged mFIST/HIPK3 (full length or kinase domain) were transfected in 293T cells in 10-cm plates. After cell lysis in buffer containing 1% Brij-96, 20 mM Tris-HCl, pH 7.5, 150 mM NaCl, 1 mM EGTA, 1 mM MgCl2, 50 mM NaF,1 mM NaVO4, 10 μg/ml leupeptin, 10 μg/ml aprotinin, 250 μg/ml pefablock, and 10 mM Na4P2O7, immunoprecipitated Flag-tagged proteins were subjected to in vitro kinase assay in 0.05% Brij-96, 1 mM Tris-HCl, pH 7.5, 7.5 mM NaCl, 25 mM Hepes, pH 7.3, 10 μM MgCl2 in the presence of 10 μCi γ-[32P]ATP as previously described 22. The presence of Flag-tagged proteins was confirmed by Western blotting.
For phosphoamino acid analysis, phosphorylated proteins were separated by SDS-PAGE. Dried bands containing phosphorylated FIST/HIPK3 were excised and proteins were extracted from the gel by incubation in 50 mM NH4HCO3, 0.1% SDS, 1% β-mercaptoethanol for 10 min at 100°C and 2 h at room temperature. Proteins were precipitated in presence of 20 μg of RNase A, 15% TCA for 90 min at 4°C and washed once in 10% TCA and once in ethanol/ether (1:1) before drying. Proteins were lysed in 6 M HCl for 70 min at 110°C and 10 min on ice, dried, and resuspended in acetic acid/formic acid/H2O (156:44:1,800), pH 1.9, containing cold phospho-serine, phospho-threonine, and phospho-tyrosine (250 μg/ml each). Samples were analysed by two-dimensional electrophoresis on cellulose TLC plates (Merck) at 1,600 V in acetic acid/formic acid/H2O (156:44:1,800), pH 1.9, for the first dimension and at 2,000 V in 5% acetic acid, 0.5% pyridine for the second dimension. Standards were revealed with 0.2% ninhydrine in acetone.
JNK Activation Assays.
For JNK activation assays, transfected 293T cells were treated for 4 h with SuperFasL (Alexis) and lysed as described before. Cell lysates were analysed by Western blotting for protein expression and the presence of activated (phosphorylated) JNK.
Confocal Immunofluorescence Microscopy.
293T cells seeded on glass coverslips in 6-cm plates were transfected. 2 d after transfection, cells were washed with PBS, fixed with 4% paraformaldehyde in PBS, and permeabilized in 0.1% saponin in PBS. After washing, cells were blocked in PBS containing 0.1% saponin and 2% skim milk, incubated with appropriate primary and secondary antibodies in blocking buffer, and mounted in fluorsave reagent (Calbiochem). Confocal microscopy was performed on a ZEISS Axiovert 100 microscope (ZEISS Laser Scanning Microscope 410) with a 63× oil objective. To detect Cy5 fluorochrome, a helium laser was filtered at 633 nm. An argon laser at 488 nm was used to detect Alexa fluorochrome. Under standard imaging conditions, no signal from one fluorochrome could be detected on the other filter set. Standardized conditions for the pinhole size, for gain and offset (brightness and contrast), were used for image capture, and each image was the average of 16 scans.
Results And Discussion
To identify novel proteins interacting with Fas, we used the yeast two-hybrid system to screen for proteins that bind to the cytosolic domain of murine Fas (Ser183 → Glu306). A library of murine embryo cDNA fused to the transcription activation domain VP16 23 was screened for possible interaction with the Fas bait. 15 positive clones were obtained from 5 × 106 clones screened. Sequencing of the inserts revealed that four inserts corresponded to the murine SUMO-E2 ligase UBC9 as previously reported 16,17,24. Another group of 6 clones contained identical (4 clones) or highly homologous sequences (2 clones) (Fig. 1 A). In the two-hybrid system, the protein fragments (we named the protein FIST for Fas-interacting Ser/Thr kinase) encoded by the insert of the various clones all strongly interacted with the complete cytoplasmic domain of Fas but not with TNFR1, lamin A, LDL receptor, or poly Ig receptor (not shown). An EMBL/GenBank/DDBJ search revealed that the sequences of clones 4, 16, 18, and 25 were contained in a murine gene recently identified as HIPK3, whereas clones 10 and 12 corresponded to murine HIPK1 25. We cloned the full-length murine and human homologue of FIST/HIPK3, whose aa sequences were found to be more than 90% identical (Fig. 1 B). FIST/HIPK3 contains an NH2-terminal kinase domain, followed by the domain that interacts with homeoproteins and a PEST sequence. For HIPK2, it was demonstrated that it binds to the SUMO-E2 ligase UBC9 through the PEST domain and that the protein is consequently modified on a lysine close to the COOH terminus by the ubiquitin-like SUMO-1 21. The Fas-interacting domain of FIST/HIPK3 (aa 775–868), which was deduced from the original yeast two-hybrid clones, partly overlaps with the UBC9 binding domain and is highly conserved. Interestingly, this sequence (and the kinase sequence but not the remainder) is highly conserved in a sequence found in the Caenorhabditis elegans genome (F20B6). The kinase domain of FIST/HIPK3 shows extensive sequence homology with the Ser/Thr kinase YAK1 from Saccharomyces cerevisiae 26 and the minibrain gene that is implicated in learning defects associated with Down's syndrome 27.
We tested whether the predicted Ser/Thr kinase domain of murine FIST/HIPK3 was functionally active. The kinase-containing region of FIST/HIPK3 (FIST/HIPK3kin; aa 142–608), tagged at the NH2 terminus with a Flag epitope, was expressed in 293T cells, immunoprecipitated with an anti-Flag antibody, and subjected to an in vitro kinase assay. SDS-PAGE analysis revealed a 32P-labeled 50-kD band, indicating that FIST/HIPK3 is a protein kinase that becomes autophosphorylated, in agreement with a recent report on the rat homologue of FIST/HIPK3 28. Similar results were obtained with full-length FIST/HIPK3 (data not shown). The kinase activity was impaired when either of the conserved residues, Lys226 or Asp322, two invariant residues essential for the enzymatic activity of protein kinases 29, were mutated to Ser and Asn, respectively (Fig. 1 C). Two-dimensional gel electrophoresis revealed that phosphorylation occurred on Thr and Ser residues (Fig. 1 C).
FIST/HIPK3 mRNA is widely expressed. Northern blot analysis revealed that FIST/HIPK3 is constitutively expressed as a transcript of ∼7.5 kb in most human and murine tissues (Fig. 2A and Fig. C) and in a panel of human cell lines (Fig. 2 B). In murine (and human, detectable after longer exposure) testis, an additional transcript of 4.4 kb was detected. The human FIST/HIPK3 gene is localized on chromosome 7 30.
Subcellular localization of FIST/HIPK3 was assessed in 293T cells transiently transfected with either FIST/HIPK3 or kinase-defective FIST/HIPK3 (Fig. 3 A). In agreement with previous reports on the subcellular localization of HIPK2, a large part of FIST/HIPK3 was localized to nuclear bodies, also referred to as PML bodies or nuclear domain (ND)10, where it colocalized with PML 21. However, FIST/HIPK3 also showed diffuse cytoplasmic staining. The kinase-defective mutant of FIST/HIPK3 displayed an identical subcellular localization. This localization pattern was confirmed using cell fractionation studies of Jurkat T cells where a substantial amount of the kinase was recovered in the detergent-soluble, nonnuclear fraction (Fig. 3 B).
To map FIST/HIPK3 and Fas interaction more precisely, several truncated versions of the Fas cytosolic domain (Fig. 4 A) were constructed. In yeast, clone 25/FIST/HIPK3 (Fig. 1) interacted strongly with the entire cytosolic domain of Fas (Arg166–Glu306) and with the fragments that lacked either 17 aa adjacent to the membrane-interacting segment (Ser183–Glu306) or the COOH-terminal 18 aa (Arg166–Asp288) (Fig. 4 A). Weak interaction was observed with Fas containing the lprcg mutation in the DD that prevents FADD recruitment and thus renders Fas inactive 31. No binding at all was observed with the fragment of Fas corresponding to the DD (Ile207–Asp288) alone or with the COOH-terminal 18 aa (Leu289–Glu306). Thus, efficient binding of FIST/HIPK3 to the cytosolic domain of Fas requires both a functional DD and part of the membrane proximal segment.
To determine whether FIST/HIPK3 also interacts with Fas in mammalian cells, both proteins were expressed in 293T cells. Transfection with Flag-tagged FIST/HIPK3 constructs and subsequent immunoprecipitation revealed that full-length FIST/HIPK3 and its kinase-inactive version interacted with Fas. Moreover, the Flag–FIST/HIPK3 COOH-terminal domain (FIST/HIPK3-C; aa 592–1,192), which includes the segment that interacts with Fas in yeast (Fig. 1), was able to pull down Fas (Fig. 4 B). In contrast, no interaction was detectable with the region containing the kinase domain only. Interestingly, no FIST/HIPK3 was detected when Fas was immunoprecipitated, suggesting that overexpression of Fas which triggers signaling leads to a weakening of the Fas–FIST/HIPK3 interaction.
We next investigated whether FADD would compete with the binding of FIST/HIPK3 to Fas, as both FADD and FIST/HIPK3 interact with overlapping segments of Fas. FADD, Fas, and FIST/HIPK3 were therefore expressed in 293T cells and while analyzing the data, we made an interesting observation (Fig. 4 C). In SDS-PAGE, endogenous or overexpressed FADD always migrates as two molecular species, which correspond respectively to the phosphorylated and unphosphorylated protein 32. Phosphorylation occurs on Ser194 close to the COOH terminus of human FADD 33,34. The role of FADD phosphorylation is not known, and the kinase responsible for this modification has not been identified. Whenever full-length FIST/HIPK3 or the kinase domain of FIST/HIPK3 were coexpressed, the phosphorylated FADD species was predominantly detected, suggesting that FADD was a substrate of FIST/HIPK3. In contrast, no induction of FADD phosphorylation was seen with kinase-dead FIST/HIPK3. Phosphorylation occurred at or close to the natural phosphorylation site (Ser194), as a mutant FADD lacking aa residues 191–208 (Fig. 4 D) was not phosphorylated. In an in vitro kinase assay, where immunoprecipitated FIST/HIPK3 was added to purified glutathione S-transferase–FADD, incorporation of 32P into FADD was very weak (data not shown). Thus, phosphorylation of FADD by FIST/HIPK3 may be indirect via a FIST/HIPK3-activated kinase. The fact that full-length FIST/HIPK3 was less active than the FIST/HIPK3 kinase domain alone can be explained by different expression levels (full-length FIST/HIPK3 is usually expressed poorly as compared with the kinase domain alone; Fig. 4C and Fig. E).
These experiments raised the possibility that FADD is directly interacting with FIST/HIPK3, and indeed, when FADD and Flag–FIST/HIPK3 constructs were overexpressed in 293T cells, FADD was detected in anti-Flag immunoprecipitates (Fig. 4 E). Similar to the FIST/HIPK3–Fas interaction, the COOH-terminal segment but not the kinase domain appeared to mediate the FIST/HIPK3–FADD interaction. FIST/HIPK3 associated only weakly with FADD in the absence of Fas, suggesting that Fas was required for the stabilization of the FIST/HIPK3–FADD complex (Fig. 4 E).
FIST/HIPK3–Fas–FADD interaction was also observed in cells in which Fas and FADD were not overexpressed (Fig. 4 F). The formation of the trimolecular complex composed of transfected Flag-tagged FIST/HIPK3 and endogenous FADD and Fas was only detected with FIST/HIPK3, which contained the COOH-terminal part. No FIST/HIPK3 was found to coimmunoprecipitate with Fas when the complex was precipitated with antibodies to Fas or via Flag-tagged soluble FasL, in agreement with the data obtained with cells that overexpress these proteins (data not shown). Using anti-FIST/HIPK3 antibodies to immunoprecipitate endogenous FIST/HIPK3, no complex formation was observed, suggesting that the epitopes recognized by the antibodies in Western blots are masked in the FIST–FADD–Fas complex. To ascertain that the observed Fas–FADD–Flag–FIST/HIPK3 interaction was of physiological significance, we adjusted the levels of exogenous Flag–FIST/HIPK3 so that they were only slightly higher than that of endogenous FIST/HIPK3 (Fig. 4 F).
It is well known that phosphorylated and unphosphorylated FADD interact equally well with Fas (Fig. 4 G; reference 32). In contrast, under conditions where FADD was not completely phosphorylated by FIST/HIPK3, the phosphorylated form was predominant in FIST/HIPK3 immunoprecipitates, suggesting that phosphorylation of FADD induced by FIST/HIPK3 leads to an increased association of the kinase with FADD (Fig. 4 G).
From the above results, it appears that FIST/HIPK3 is a protein capable of interacting with a surface receptor but at the same time also functions as a nuclear protein. This is reminiscent of Daxx 3, and we therefore investigated whether the two proteins interact. Daxx and FIST/HIPK3 were coexpressed in 293T cells, and strong binding between full-length FIST/HIPK3 and the NH2-terminal portion (aa 1–433) was indeed detected (Fig. 4 H). By contrast, the COOH-terminal, Fas-interacting segment of Daxx (aa 628–740) 3 failed to bind FIST/HIPK3 (data not shown). Interestingly, binding of FIST/HIPK3 to Daxx was dependent on the kinase activity of FIST/HIPK3, as the kinase-dead version of FIST/HIPK3 exhibited a greatly diminished binding activity (Fig. 4 H). The significance of this observation is presently unclear.
Transient transfection assays were used to examine the consequences of FIST/HIPK3 overexpression and FADD phosphorylation on Fas-induced cell death. We found that death signals were transmitted normally in the presence of FIST/HIPK3. A second signaling pathway triggered by Fas leads to the activation of JNK, whose activation can ultimately lead to caspase-8–independent apoptosis 3. This second activity has been attributed to Daxx, which interacts with the cytoplasmic domain of Fas and whose overexpression results in an ASK1-dependent JNK activation 5. We activated JNK by adding FasL to 293T cells and found that under these conditions, JNK activation was maximal 4 h after stimulation and was mostly independent of caspase activation, as the general caspase inhibitor z-VAD had little effect (Fig. 5 A). When FIST/HIPK3 was overexpressed, JNK activation was severely impaired, but only when the catalytic site was intact, suggesting that phosphorylation of an unknown target protein negatively regulates signals that lead to FasL-induced JNK activation (Fig. 5 B). When overexpressed, CARDIAK/RIP2 and viral E10 are both potent inducers of JNK activation 22,35. The presence of FIST/HIPK3, however, did not modulate JNK activation under these conditions (Fig. 5 C), indicating that FIST/HIPK3 does not modulate all pathways leading to JNK activation.
In summary, we have identified FIST/HIPK3 as a kinase that interacts with Fas and FADD. FIST/HIPK3 appears to belong to a growing family of proteins that shuttle between the cytoplasm and nuclear PML bodies in a SUMO-dependent manner 18. For HIPK2 it has been shown that SUMO modification occurs on a lysine close to the COOH terminus 21 that is conserved in all three HIPKs. It is therefore likely that such posttranscriptional modification also occurs in the FIST/HIPK3 protein, considering also the physical presence of the molecules required for SUMO modification (the cytoplasmic domain of Fas has been previously shown to interact with both the SUMO ligase UBC9 and its substrate SUMO). One of several plausible models would predict that Fas-associated FIST/HIPK3 becomes SUMO modified by UBC9 upon Fas activation and subsequently translocates to PML bodies. Although the role of PML bodies remains elusive despite links to oncogenesis and viral replication, it is noteworthy that inhibition of PML body formation caused by the deletion of the PML protein suppresses Fas-induced apoptosis 36. Considering that FIST/HIPKs are also potent repressors of transcription 25, it is tempting to speculate that FIST/HIPK3 may participate in a Fas-dependent nuclear response. This function is similar to the role suggested for Daxx, which interestingly is also modified by SUMO and proposed to shuttle from Fas to the nucleus 3,37,38. Moreover, Daxx interacts with FIST/HIPK3, at least upon overexpression, and it is therefore likely that the two proteins modulate each other's activities in a yet undefined manner.
Additional work is also required to determine the exact functional significance of the Fas–FADD–FIST/HIPK3 interaction. FADD becomes phosphorylated in the presence of FIST/HIPK3, and this phosphorylation is important for FADD–FIST/HIPK3 interaction to occur. In agreement with other studies, FADD phosphorylation does not appear to regulate apoptosis, as FasL-induced apoptosis is not affected by FIST/HIPK3 overexpression. Recently, several uncharacterized Fas-associated Ser/Thr kinase activities were described that phosphorylate Fas and FADD 39. One of these kinases exhibits a molecular mass of ∼120 kD and could therefore correspond to FIST/HIPK3. We found that FasL-mediated JNK activation is impaired by active FIST/HIPK3, but whether this is due to FADD phosphorylation remains to be established in future studies.
We thank Slavica Masina and Margot Thome for critical reading of this manuscript and for insightful discussions. We thank the group of M. Peter, ISREC, Epalinges for help in the kinase assays.
This work was supported by grants of the Swiss National Science Foundation (to J. Tschopp).
Abbreviations used in this paper: aa, amino acid(s); DED, death effector domain; FADD, Fas-associated death domain; FasL, Fas ligand; FIST, Fas-interacting serine/threonine kinase; HIPK, homeodomain-interacting protein kinase; JNK, Jun NH2-terminal kinase.