Measles virus, a paramyxovirus of the Morbillivirus genus, is responsible for an acute childhood illness that infects over 40 million people and leads to the deaths of more than 1 million people annually (C. J. Murray and A. D. Lopez, Lancet 349:1269-1276, 1997). Measles virus infection is characterized by virus-induced immune suppression that creates susceptibility to opportunistic infections. Here we demonstrate that measles virus can inhibit cytokine responses by direct interference with host STAT protein-dependent signaling systems. Expression of the measles V protein prevents alpha, beta, and gamma interferon-induced transcriptional responses. Furthermore, it can interfere with signaling by interleukin-6 and the non-receptor tyrosine kinase, v-Src. Affinity purification demonstrates that the measles V protein associates with cellular STAT1, STAT2, STAT3, and IRF9, as well as several unidentified partners. Mechanistic studies indicate that while the measles V protein does not interfere with STAT1 or STAT2 tyrosine phosphorylation, it causes a defect in IFN-induced STAT nuclear accumulation. The defective STAT nuclear redistribution is also observed in measles virusinfected cells, where some of the STAT protein is detected in cytoplasmic bodies that contain viral nucleocapsid protein and nucleic acids. Interference with STAT-inducible transcription may provide a novel intracellular mechanism for measles virus-induced cytokine inhibition that links innate immune evasion to adaptive immune suppression.Cytokine signal transduction is essential for normal immune function and controls the quality of responses to a wide variety of microbial infections. Innate and adaptive host responses to virus infections are regulated by autocrine and paracrine cytokine signaling systems. For most cytokines, receptor binding triggers an intracellular signaling cascade involving one or more signal transducer and activator of transcription (STAT) proteins. Diverse cytokine and growth factor signaling pathways produce active STAT transcription factors that specify mRNA induction profiles (26). For example, the alpha and beta interferon (IFN-␣/␤) family is of primary importance for both innate and adaptive antiviral immunity (reviewed in references 1, 49, and 53). In the innate antiviral system, IFN-␣/␤ initiates a receptor-mediated signaling system that produces an activated STAT1-STAT2-IRF9 heterotrimeric transcription complex known as ISGF3 (27). The ISGF3 complex translocates to the nucleus, where it can bind to target gene promoter elements and induce the transcription of host antiviral genes. Similarly, IFN-␥, a cytokine that mediates both innate and adaptive immune responses critical for defense against microbial infections and cancer (21), activates a homodimeric STAT1 transcription factor, GAF (9). Interleukin 6 (IL-6), a cytokine required for acute-phase responses, liver regeneration, B-cell maturation, and macrophage differentiation, activates STAT3 homodimers, a response in common with growth factor pathways (69) and onco...

Signal transducer and activator of transcription (STAT) proteins are normally long-lived, but infection with certain Paramyxoviruses results in efficient loss of IFN-responsive STAT1 or STAT2. Expression of a virus-encoded protein called "V" is sufficient to mediate the destruction of STAT proteins. STAT degradation is blocked by proteasome inhibitors, strongly implicating the ubiquitin (Ub)-proteasome targeting system. We demonstrate that cellular expression of V proteins from simian virus 5 (SV5) and type II human parainfluenza virus (HPIV2) induces polyubiquitylation of STAT1 and STAT2 targets. In vitro, the V proteins catalyze Ub transfer in an ATP-dependent process that requires both Ub-activating (E1) and Ub-conjugating (E2) activities. Furthermore, SV5 and HPIV2 V-interacting protein partners were isolated by affinity purification from human cells and reveal a complex of associated cellular proteins. This complex includes both STAT1 and STAT2, and the damaged DNA binding protein, DDB1. In addition, a protein related to a family of cellular Ub ligase complex subunits, cullin 4A (Cul4A), associated with the V proteins. The roles of both DDB1 and Cul4A in STAT1 degradation by SV5 infection were analyzed using small interfering RNAs. These findings demonstrate the assembly of a V-dependent degradation complex that includes STAT1, STAT2, DDB1, and Cul4A. In agreement with prior nomenclature on SCF-type cellular E3 enzymes, we refer to this complex as VDC.

Mumps virus is a common infectious agent of humans, causing parotitis, meningitis, encephalitis, and orchitis. Like other paramyxoviruses in the genus Rubulavirus, mumps virus catalyzes the proteasomal degradation of cellular STAT1 protein, a means for escaping antiviral responses initiated by alpha/beta and gamma interferons. We demonstrate that mumps virus also eliminates cellular STAT3, a protein that mediates transcriptional responses to cytokines, growth factors, nonreceptor tyrosine kinases, and a variety of oncogenic stimuli. STAT1 and STAT3 are independently targeted by a single mumps virus protein, called V, that assembles STAT-directed ubiquitylation complexes from cellular components, including STAT1, STAT2, STAT3, DDB1, and Cullin4A. Consequently, mumps virus V protein prevents responses to interleukin-6 and v-Src signals and can induce apoptosis in STAT3-dependent multiple myeloma cells and transformed murine fibroblasts. These findings demonstrate a unique cytokine and oncogene evasion property of mumps virus that provides a molecular basis for its observed oncolytic properties.Gene expression and biological responses to cytokines and polypeptide growth factors are often mediated by signal transducer and activator of transcription (STAT) proteins (12). The activities of various STAT proteins control cell growth and differentiation, organogenesis, embryonic development, and host responses to cancer and infection. Inappropriate activation of STAT signaling is frequently observed in human diseases, including inflammation, asthma, autoimmunity, and cancer, suggesting that inhibitors of STAT factors might be of wide-ranging therapeutic value (reviewed in reference 55 and references therein).Of the seven mammalian STAT proteins, STAT1, STAT2, and STAT3 exhibit the broadest expression profiles and respond to activating stimuli in most cell types (70, 71). A transcription factor complex, ISGF3, containing activated STAT1 and STAT2 is essential for induction of alpha/beta interferon (IFN-␣/␤) target genes that establish an innate cellular antiviral state (54). Similarly, the transcriptional response to IFN-␥ is mediated by a STAT1 homodimer that is required for IFN-␥-dependent innate and adaptive immune responses (31). The third widely expressed STAT protein, STAT3, is activated by many cytokine systems, including interleukin 6 (IL-6), leukemia inhibitory factor, ciliary neurotrophic factor, oncostatin M, and leptin (reviewed in reference 28). STAT3 is also activated by growth factor receptors with intrinsic protein tyrosine kinase activity (e.g., platelet-derived and epidermal growth factor receptors [53,61]) as well as cellular and viral cytoplasmic tyrosine kinases (e.g., c-Src and v-Src [6,68]).Targeted disruption of STAT3 in mice results in early embryonic lethality (57). Tissue-specific disruption has revealed diverse STAT3 functions in mammary gland, liver, keratinocytes, thymus, blood, and neurons that are involved in growth and differentiation, inflammation, liver regeneration, acutephase responses...

The primary antiviral cytokines produced by higher eukaryotes are the alpha/beta interferons (IFN-␣ and IFN-␤; referred to herein as IFN) that function directly on target cells by creating an antiviral state that blocks virus replication (24). The molecular basis for most antiviral effects induced by IFN requires IFN-induced mRNA and protein synthesis (46). IFN activates a transcriptional complex, ISGF3, composed of three proteins. Two subunits are members of the signal transducer and activator of transcription (STAT) family, STAT1 and STAT2, that heterodimerize and complex with a third protein, IRF9, a member of the interferon regulatory factor (IRF) family that provides DNA recognition.The general mechanism leading to activation of ISGF3 has been well characterized (reviewed in references 20 and 46). IFN binding induces aggregation of a multichain receptor, causing the receptor-associated tyrosine kinases Jak1 and Tyk2 to phosphorylate the receptor cytoplasmic domain. The receptor phosphotyrosine provides a docking site for the src homology 2 (SH2) domain of the latent cytoplasmic STAT2 and/or STAT2-IRF9 complexes (28). STAT2 then becomes phosphorylated on tyrosine 690, providing a docking site for the latent STAT1. Following STAT1 phosphorylation on tyrosine 701, the two STATs heterodimerize via intermolecular SH2 domain-phosphotyrosine interaction (44) and, together with IRF9, form an active ISGF3 heterotrimer that can bind to IFN-stimulated gene (ISG) promoter IFN-stimulated response elements (ISRE). STAT proteins are long-lived, and their inactivation has been shown to involve dephosphorylation by a nuclear protein tyrosine phosphatase and recycling of the inactivated STATs (3,17,18,33,36).It is not surprising to find that many, if not all, viruses have evolved strategies to impede host IFN responses (15). Evolution of enhanced IFN resistance can lead to highly infectious viruses and/or persistent infections (4,11,13,14,27,47). Recently, the IFN antagonist strategies used by some negativestranded RNA viruses have been determined to act directly on the ISGF3 STAT protein subunits. The paramyxovirus simian virus 5 (SV5) was found to evade IFN responses by specifically targeting the STAT1 protein for proteolytic degradation. This destruction of STAT1 was found to be mediated by expression of a single virus-encoded protein called V (11,12,54). Human parainfluenza virus 2 (HPIV2) blocks IFN signaling by preferentially inducing degradation of STAT2 and not STAT1 (40,55). In common with SV5, the expression of the HPIV2 V protein from a cDNA clone is sufficient to abolish IFN-responsive transcription as a result of STAT2 destabilization (40). These two paramyxovirus V proteins have ϳ50% amino acid sequence identity in their ϳ220-amino-acid length, yet they specifically recognize and catalyze the destruction of only one of the two IFN-responsive STAT proteins.The mechanistic basis for the selective STAT protein degradation mediated by paramyxovirus V proteins is not entirely understood, but the available evidence i...

Transcription regulators STAT1 and STAT2 are key components of the interferon signaling system leading to innate antiviral immunity. The related STAT3 protein is a regulator of interleukin-6-type cytokine signals and can contribute to both cell growth and death important for cancer gene regulation and tumor survival. These three STAT proteins are targeted for proteasome-mediated degradation by RNA viruses in the Rubulavirus genus of the Paramyxoviridae. A single viral protein, the V protein, assembles STAT-specific ubiquitin ligase complexes from cellular components. Simian virus 5 (SV5) targets STAT1, human parainfluenza virus 2 targets STAT2, and mumps virus targets both STAT1 and STAT3. Analysis of the V-dependent degradation complex (VDC) composition and assembly revealed several features contributing to targeting specificity. SV5 and mumps V proteins require STAT2 to recruit the STAT1 target, yet mumps V protein binds STAT3 independent of STAT1 and STAT2. All Rubulavirus V proteins tested require cellular DDB1 to target STATs for degradation but differ in the use of Roc1, which is essential for mumps V STAT3 targeting. Protein interaction analysis reveals that paramyxovirus V proteins can homo-and heterooligomerize and that the conserved cysteine-rich zinc-binding C-terminal domain is necessary and sufficient for oligomerization. Purified SV5 V protein spontaneously assembles into spherical macromolecular particles, and similar particles constitute SV5 and mumps VDC preparations.