The seven members of the signal transducer and activator of transcription (STAT) family of transcription factors are activated in response to many different cytokines and growth factors by phosphorylation of specific tyrosine residues. The STAT1 and STAT3 genes are specific targets of activated STATs 1 and 3, respectively, resulting in large increases in the levels of these unphosphorylated STATs (U-STATs) in response to the interferons (STAT1) or ligands that active gp130, such as IL-6 (STAT3). U-STATs drive gene expression by novel mechanisms distinct from those used by phosphorylated STAT (P-STAT) dimers. In this review, we discuss the roles of U-STATs in transcription and regulation of gene expression.
Signal transducers and activators of transcription (STATs) were originally discovered as DNA-binding proteins that mediate interferon (IFN)-dependent gene expression 1, 2, 3. STATs are latent in the cytoplasm until they are activated by extracellular ligands, including cytokines, growth factors, and hormones 4, 5. Binding of these extracellular ligands to their specific receptors leads to the activation of various tyrosine kinases (TKs), including JAKs, receptor TKs, and non-receptor TKs such as SRC and ABL, which can directly phosphorylate STATs in the absence of ligand-induced receptor signaling 6, 7. These TKs phosphorylate a single tyrosine residue of each STAT, followed by homo- or hetero-dimerization of STATs through reciprocal Src homology 2 (SH2)-phosphotyrosine interactions, leading to nuclear translocation of the resulting dimers and activation of target genes. Seven STATs have been identified in mammals: STAT1, STAT2, STAT3, STAT4, STAT5A, STAT5B, and STAT6. Each is differentially activated by specific extracellular ligands, allowing differential intracellular processing of signals transduced across the plasma membrane. The biological role of each STAT has been delineated by investigating the phenotypes of mice lacking their expression 5. Recently, it has been found that STATs 1 and 3 (and probably other STATs) also play important roles in mediating gene expression without tyrosine phosphorylation. The expression of unphosphorylated STATs (U-STATs) 1 and 3 is greatly increased in response to their activation, since the STAT1 gene is strongly activated by phosphorylated STAT (P-STAT) 1 dimers or ISGF3, which are formed in response to type II or type I IFNs, respectively, and, similarly, since the STAT3 gene is strongly activated by P-STAT3 dimers, which are formed in response to IL-6 and other ligands that activate the gp130 common receptor subunit. Ligand-dependent increases in the concentrations of U-STATs drive the expression of genes that are distinct from those activated by P-STATs. The abnormally high levels of U-STAT3 that accompany the abnormal constitutive activation of STAT3 found in many tumors drive the over-expression of several genes that contribute to tumorigenesis.
U-STAT1 mediates constitutive expression of the low molecular mass polypeptide (LMP) 2 gene by collaborating with IRF1 8, and U-STAT3 binds to unphosphorylated NFκB (U-NFκB), in competition with IκB, and the resulting U-STAT3/U-NFκB complex accumulates in the nucleus with help from the nuclear localization signal of STAT3, activating a subset of κB-dependent genes (Figure 1) 9; U-STAT6 cooperates with p300 and binds to a consensus STAT6 binding site located within the COX-2 promoter to enhance COX-2 expression 10. The discovery of these specific mechanisms for how U-STATs mediate gene expression serves as examples for additional mechanisms that have yet to be revealed. Many of the STATs are sticky and interact with many different proteins. STAT1 and IRF1 bind to each other even in the absence of DNA, and this heterodimer binds to a composite element in the LMP2 promoter that recognizes each monomeric component separately. The ternary complex is stable enough to drive the constitutive expression of LMP2, but can be displaced by the more potent STAT1 dimer in IFNγ-treated cells. STATs can form several different homo- and heterodimers and STATs can form heterodimers with other proteins even without tyrosine phosphorylation. Different complexes, which may not be very stable as free forms in solution, can nevertheless form on specific target genes, depending on the stabilization through binding to specific DNA elements in each promoter and probably also through specific interactions with other bound proteins. Thus, we expect many different mechanisms for U-STAT-dependent expression of different genes.
STAT1-dependent gene expression
STAT1, the first member of the multi-gene family to be discovered, is a principal target of both type I and type II IFNs 2, 11, 12, 13. STAT1-null (STAT1−/−) mice have lost responsiveness to both types of IFN and have thus acquired enhanced susceptibility to bacterial and viral pathogens 14. The discovery that the active form of STAT1 is required for IFN-α and IFN-γ to inhibit the growth of cultured cells 15, 16, 17 has led to the assumption that inadequate function of STAT1 might result in cell growth deregulation and disturbed immune function, i.e. disorders that are pertinent to malignancy. The potential involvement of STAT1 in cancer has been supported by several observations reporting inappropriate activation of STAT1 and even loss of its expression in malignant cells derived from different histological types of tumors such as breast cancer, head and neck cancer, melanoma, leukemia, and lymphoma 6, 18, 19, 20, 21. However, convincing evidence on the role of STAT1 in malignant tumors was provided by studies employing STAT1−/− mice. Although some recent data supported that STAT1−/− mice (therefore unresponsive to IFNs) lacking host-cell sensitivity to IFNγ in antitumor immunity form more spontaneous and chemically induced tumors than wild-type mice 22, most literatures observed no increased spontaneous malignancy in STAT1−/− mice. They manifested heightened susceptibility to both chemically induced and transplanted tumors compared to control animals 23, 24. These data support the idea that STAT1 might function as a tumor suppressor 25. Subsequent studies revealed that the involvement of STAT1 in oncogenesis is more complex and that only a part of its tumor growth-suppressing activity is attributable to the loss of IFN-dependent anti-proliferative response when STAT1 is absent. Kaplan et al. 23 demonstrated that the elevated growth of tumor cells in STAT1-deficient, IFN-γ insensitive mice is at least partly due to the absence of well-known effects of IFN-γ on tumor cell immunogenicity and/or host response to tumor antigens. Since IFN-γ represents a critical component of the immune system required for tumor surveillance, it is likely that impaired STAT1 function negatively affects the immunogenic phenotype of developing tumors. Thus, the impaired responsiveness to IFN-γ due to STAT1 dysfunction may provide a selective growth advantage to some malignant cells at an early stage of tumor development, a process known as cancer immuno-editing 26, 27. Several reports showing that some spontaneous human tumors are selectively unresponsive to IFN-γ due to perturbed STAT1 activation suggest that, similarly to animal models, STAT1-dependent tumor surveillance also operates in humans 28, 29, 30, 31, 32. More recently, it was shown that STAT1 can accelerate the development of hematopoietic tumors independently of IFN-dependent signaling. These authors demonstrated that the up-regulation of MHC class I expression represents a general mechanism for escape from tumor surveillance and that a low level of MHC class I expression might be beneficial for leukemia patients 33.
The first indication that STAT1 might function as a transcription factor in the absence of tyrosine phosphorylation came from an analysis of its role in TNF-induced apoptosis 34. STAT1-null U3A cells are resistant to TNF plus cycloheximide, while parental 2fTGH cells or STAT1-deficient U3A cells reconstituted with wild-type STAT1 (U3A-R cells) are sensitive. Furthermore, the expression of caspases 1, 2, and 3 is defective in U3A cells and is induced only in 2fTGH and U3A-R cells but not in U3A cells following TNF treatment. Thus, STAT1 is required for TNF-mediated apoptosis and appears to act in the absence of any phosphorylation of tyrosine 701. Small amounts of constitutively P-STAT1 in 2fTGH and U3A-R cells are not responsible for the observed response since U3A-701 cells, reconstituted with the Y701F mutant of STAT1, which cannot be phosphorylated on tyrosine, are also sensitive to TNF-mediated apoptosis and normal for caspase gene expression 34.
Another indication of a role in transcription for STAT1 without tyrosine phosphorylation came from an analysis of the expression of a gene encoding a component of the 20S proteosome, LMP2 8. The bi-directional promoter that regulates LMP2 expression contains overlapping IFN consensus sequence 2 (ICS2) and gamma-activated sequence (GAS) sites. The IFN-inducible LMP2 gene is also transcribed at a lower level in the absence of IFN 35. In vivo footprinting of the ICS2/GAS element revealed protein-DNA contacts at both sub-sites in unstimulated HeLa cells 36. Thus, both STAT1 and IRF1 appear to be essential for basal transcription of the LMP2 gene. There is barely any LMP2 expression in IRF1-null mice 36. STAT1-deficient U3A cells do not express LMP2, but the gene is transcribed in parental 2fTGH cells and its expression is restored when wild-type STAT1 is put back into U3A cells 8. LMP2 transcription is also restored in U3A-701 cells, in which the mutant Y701F STAT1 cannot be phosphorylated 37.
Using DNA microarrays, a comparison of transcription in U3A cells and U3A-701 cells revealed that the basal expression of many genes is regulated similarly by wild-type U-STAT1 and STAT1 Y701F. The genes include those encoding the MHC class II transactivator (CIITA), hsp70, and Bcl-xL. MHC class I and 2-microglobulin expression was similar in U3A-701 and 2fTGH cells 37. The expression of several caspase genes is also regulated similarly in U3A-701 and 2fTGH cells 34. Constitutive expression of the MHC class I and β2-microglobulin genes is lower in mouse STAT1-null T lymphocytes than in wild-type cells 38. Several other examples of ligand-independent functions of STAT1 have been described more recently. In cardiac myocytes, transcriptional activation of Fas and FasL is dependent on S727 of STAT-1 but independent of Y701. Furthermore, S727 but not Y701 is required for the enhancement of cardiomyocyte cell death by STAT1 following ischemia/reperfusion injury 39. In another instance, 7-ketocholesterol-induced apoptosis requires STAT1 since this phenomenon is not observed in U3A cells, but apoptosis is restored when either Y701F or wild-type STAT1 is put back into U3A cells. However, U3A cells reconstituted with S727A STAT1 are not sensitive to 7-ketocholesterol-induced apoptosis 40.
Thus, serine 727 of STAT1 appears to play an important role in some constitutive functions. Such a role is also indicated by the fact that U3A-S727A cells are resistant to TNF-mediated apoptosis and do not express caspases 1, 2, and 3 34. Serine phosphorylation of STAT1 can be induced independently of tyrosine phosphorylation 41 and STAT1 can be phosphorylated only on serine 727 in response to UV 21, IL-1, or TNF 42. The effect of the S727A mutation of STAT1 on basal transcription of caspase 34, GBP1, TAP1, and IFP53 genes 21 shows that this serine residue, which lies in the transactivation domain, is essential for STAT1 to be an effective transcription factor for certain genes. More examples were found recently. Timofeeva et al. 32 showed that, in Wilms' tumor (WT), one of the most common pediatric solid cancers, STAT1 was found to be constitutively phosphorylated on serine 727 in 19 of 21 primary WT samples and two WT cell lines. The inactivating mutation S727A reduced colony formation of WT cells in soft agar by more than 80% and induced apoptosis under conditions of growth stress. S727-P-STAT1 provided resistance to apoptosis for WT cells by upregulating the expression of heat-shock protein (HSP)27 and the anti-apoptotic protein myeloid cell leukemia (MCL)-1. These findings suggest that serine-P-STAT1 plays a critical role in the pathogenesis of WT and other neoplasms. Although it is tempting to suggest that the phosphorylation of S727 is important for this function, there is at present no direct evidence to rule out the possibility that S727 is important per se, without phosphorylation, for vital protein-protein interactions on certain promoters.
The gene expression patterns induced by U-STAT1 depend strongly on the cell type. Gene expression profiles performed in human fibroblast BJ cells and epithelial HME1 cells in which Y701F-STAT1 was stably expressed at a high level show quite different patterns of gene expression (H Cheon and GR Stark, unpublished data).
STAT3-dependent gene expression
STAT1 has been shown to drive gene expression in the absence of tyrosine phosphorylation 43. In the case of STAT3, an array-based analysis of gene expression revealed that the relative levels of more than a thousand mRNAs changed in response to increased expression of wild type or Y705F-STAT3. In human primary epithelial hTERT-HME1 cells, 1 420 mRNAs changed, positively or negatively, by more than 2-fold in response to a high level of wild-type STAT3 and 1 191 mRNAs changed by the same amount in response to a high level of Y705F-STAT3. Furthermore, 869 mRNAs changed in common by at least 2-fold in both cell populations, and 84 of these changed by more than 4-fold 44. These mRNAs include several that are induced to very high levels (10- to 40-fold). Analysis of mouse cell lines provided complementary data. In addition to the obvious cell-type differences in the two experiments, mouse cells with high level of wild-type or Y705F-STAT3 are compared with STAT3-null cells. In MEFs, more than a thousand mRNAs changed by more than 2-fold in cells with either high level of wild-type STAT3 or high level of Y705F-STAT3. Furthermore, about 400 mRNAs changed in common by more than 2-fold in both cell types 44. Some of these genes are known to be regulated by STAT3 homodimers, including SOCS-3 45, c-Myc and DP1 46, c-Fos and c-Jun 47, 48, 49, and Bcl-x 50.
STAT3 was initially identified as an IL-6-dependent transcription factor important for mediating the inflammatory response, tumorigenesis, and anti-apoptotic effects on cells. Recently, in addition to its ability to form complexes with itself and other STATs, there are several reports that STAT3 and NFκB interact with each other 51. For example, Hagihara et al. 52 demonstrated that STAT3 forms a complex with the p65 subunit of NFκB following stimulation of cells with IL-1 plus IL-6, and that the bound STAT3 interacts with non-consensus sequences near the κB element of the serum amyloid A (SAA) promoter. Moreover, the complex formed by STAT3, p65, and p300 is essential for the synergistic induction by IL-1 and IL-6 of the SAA gene, which does not have a typical STAT3 response element in its promoter. Yu et al. 53 found that U-STAT3, through direct interaction with p65, serves as a dominant-negative inhibitor to suppress the ability of P-NFκB to induce cytokine-dependent activation of the iNOS promoter in mesangial cells. Yoshida et al. 54 showed that STAT3 and p65 physically interact in vivo and that p65 homodimers can cooperate with U-STAT3 when bound to a specific type of κB motif. Reciprocally, this interaction appears to inhibit the function of STAT3 GAS-binding sites. In contrast, the p50 subunit of NFκB can cooperate with P-STAT3 bound to GAS sites 54. Yang et al. 9, 44 demonstrated that an increase in the concentration of endogenous U-STAT3 following long-term treatment with IL-6 allows U-STAT3 to compete effectively with IκB for U-NFκB, to form a novel transcription factor that induces RANTES expression by binding to the proximal κB site of the RANTES promoter. Since the Y705F mutant of STAT3, which cannot be phosphorylated on tyrosine, also activates RANTES expression, this function of U-STAT3 is clearly distinct from the absolute requirement for tyrosine phosphorylation that enables STAT3 dimers to bind to GAS sequences 55, 56, 57.
It should be noted that several researchers have reported that additional phosphorylation of P-STAT3 dimers on Ser727 is needed for maximal activation of transcription, but not for DNA binding 4, 55. However, Ser727 phosphorylation seemed to be not required for activation of RANTES, because STAT3-β, a truncate form of STAT3 which lacks 50 amino acids from the C-terminus, is still capable of driving RANTES expression. It seems possible that the C-terminal domain, with Ser727 phosphorylated, might facilitate the transactivation of promoters other than RANTES in response to binding of the U-STAT3:U-NFκB complex. For example, Ng et al. 58 have shown that STAT3 is phosphorylated on Ser727 but not Tyr705 in response to activation of the TrkA receptor by nerve growth factor, and that serine-P-STAT3 is important in driving signal-dependent gene expression.
Another recent example is that U-STAT6 forms a complex with p300, which is able to directly bind to the cyclooxygenase-2 promoter 10. Surprisingly, the U-STAT6/p300 complex binds to the same GAS element that is presumed to be bound by P-STAT homo- or heterodimers. This result is different from the data obtained by Yang et al. 9, Yoshida et al. 54 and Chatterjee-Kishore et al. 37 for U-STAT3 and U-STAT1.
Nuclear-cytoplasmic transport of U-STATs
Although all STATs share sequence and domain structures, each individual STAT protein that has been studied has evolved a distinct mechanism to regulate its intracellular trafficking. Specifically, the movement of STAT1, STAT2, and STAT3 into the nucleus is governed by different kinds of importin transporters. STAT family members have similar nuclear-localization signals (NLSs) or nuclear-export signals (NESs) domains that govern their passage into and out of the nucleus. STAT1 can be detected in the nuclei of 2fTGH cells in the absence of ligand-dependent stimulation, as can Y701F STAT1 43. A survey of several established cell lines shows that STAT1 is present in the nuclei of all cells in the absence of ligand-dependent stimulation. Treating cells with IFNγ induces an increase in nuclear STAT1 and, although staurosporine inhibits the IFNγ-induced import of STAT1 into nuclei, it does not alter basal levels of nuclear STAT1 59. Unlike the nuclear import of tyrosine-P-STAT1, that of U-STAT1 is sensitive to wheat germ agglutinin and occurs independently of the import receptor p97 59. Soon after the discovery of the importin-α/importin-β-dependent nuclear import pathway, importin-α5 was found to mediate nuclear translocation of tyrosine-P-STAT1 60, 61. Importin-α5 recognizes tyrosine-P-STAT1 either in the form of ISGF3 or as a homodimer 62. In this case, tyrosine phosphorylation of STAT1 induces conformational changes that promote STAT/STAT interactions and facilitate STAT/DNA interactions, which are intimately linked to conditional nuclear import or export signals. However, unlike other STATs, such as STAT1 and STAT2, which accumulate in the nucleus only following their phosphorylation, STAT3 can enter the nucleus independently of its phosphorylation. The mechanisms underlying these differences relate to the involvement of distinct importins used by STATs for their nuclear import. For instance, the phosphorylation of the nuclear localization signal of STAT1 is a prerequisite for its interaction with importin-α5 and subsequent nuclear import 60, 61. In contrast, STAT3 binds constitutively to importin-α3 and α6 63, and the shuttling of STAT3 in and out of the nucleus seems independent of its phosphorylation 63.
DNA binding of STATs without tyrosine phosphorylation
P-STAT1 binds to DNA in the form of homo- or heterodimers. Tyrosine phosphorylation is essential for the ligand-induced formation of STAT1 homodimers or STAT1-2 heterodimers and for their binding to the cis-recognition sequences in the promoters of IFN-regulated genes 13. Without tyrosine phosphorylation, STAT1 does not regulate the transcription of IFN-inducible genes (e.g., IRF1) that have GAS sites in their promoters 37.
The high-resolution structures of DNA-bound STATs 1 and 3 64, 65 and of the N-terminal portion of STAT4 66 indicate that the mutual binding of two STAT monomers is possible without SH2-phosphotyrosine interactions. The structures indicate that each monomer of the DNA-bound STAT dimer contacts only half of the palindromic GAS element. Also, the N-terminal coiled coil domain of the dimer is likely to have very few contacts with DNA and thus is essentially free for additional protein-protein interactions 64, 66. Consistent with this, several recent studies have identified proteins that interact with this domain of STAT3 or other STATs 67, 68, 69, 70, 71. U-STAT1 monomers can bind to DNA on their own by contacting one half of a palindromic GAS. They can also form dimers through mutual interaction of the N-terminal domain of each monomer and bind to GAS sequences in vitro 37. The N-terminal region of STAT1, especially residues 135–200 within the first coiled-coil domain, is required to form dimers of U-STAT1 on the LMP2 GAS in vitro. However, the affinity for U-STAT1 monomers or dimers is much less than that for P-STAT1 homodimers.
Weak STAT binding can be enhanced by increasing the concentration of STAT proteins or by interaction of STAT1 with other proteins, either transcription factors bound to adjacent promoter sites or accessory factors and co-activators. In the case of the LMP2 gene, U-STAT1 binds to IRF1 through the N-terminal domain of STAT1, and the STAT1-IRF1 dimer binds to the overlapping ICS2/GAS site on the LMP2 promoter 37. The adenovirus E1A protein can down-regulate LMP2 transcription by interfering directly with this interaction of U-STAT1 and IRF1 and thus with their binding to the LMP2 promoter 37.
In addition to U-STAT1 37, other U-STATs have been reported to be capable of binding to DNA. It has been shown that U-STAT6 associated with p300 binds directly to the COX-2 GAS element to drive its expression in NSCLC cells 10; U-STAT3 competes with IκB and binds to NFκB and, with the help of importin-α3, brings the U-STAT3/p65/p50 complex to the nucleus, which then binds to a κB site to facilitate RANTES gene expression 9. In addition to its interactions with NFκB, STAT3 has been shown to bind to other transcription factors. For example, it forms a complex with the CRE-binding protein on the JunB promoter 72 and with c-Jun on the α2-macrogloblin APRE 73. Other reports show that STAT3 has an effect on CRE-like sites in the C/EBPβ promoter 74 and on the glucocorticoid response element 75, which lack classical GAS sequences. It should be mentioned that fewer than half of the genes that respond to high-level expression of U-STAT3 respond also to TNF-α. The U-STAT3-responsive genes that do not respond to TNF-α probably do not have functional κB elements, and two such genes do not need p65 in order to respond to U-STAT3. Therefore, it is extremely likely that U-STAT3 interacts productively with one or more transcription factors different from NFκB to drive the expression of this class of genes. Identification of these factors and characterization of their interactions with U-STAT3 are of interest for future studies.
The biology of U-STATs
All seven STAT proteins share a high degree of sequence homology, but they are expressed differently. In resting cells, STATs reside largely in the cytoplasm as inactive homodimers 76. However, upon ligand binding, receptor-associated JAKs become activated, leading to the phosphorylation of specific receptor tyrosine residues, which then direct the SH2-dependent recruitment of specific STATs, which in turn become JAK substrates. As activated STATs are released from the receptor they reorient into an antiparallel dimer, where the SH2 domain of one STAT binds to the phosphotyrosine of the other STAT. Activated STAT dimers translocate to the nucleus and bind to specific elements. STAT homodimers bind to members of the GAS family of enhancers (a palindrome, TTCNNNGAA). Different STATs are activated by phosphorylation of the tyrosine residue in response to different stimuli, for example, STAT1 and 2 by type I and II IFNs, STAT3 by IL-6 and EGF, STATs 4 and 6 by IL-12 and IL-4, and STAT5 by prolactin and IL-3, respectively 77, 78, 79. As noted above, both the STAT1 and STAT3 genes are regulated by their own activation because their promoters contain GAS elements 80, 81, 82. Long-term exposure of cells to IFNs leads to a large (20-fold or more) increase in the concentration of U-STAT1. Similarly, the STAT3 gene has a GAS element that drives its expression in response to the activation of STAT3, for example, in response to IL-6 9, 82. Hu et al. showed that priming with low concentrations of IFN-γ for 2 days leads to increased tyrosine phosphorylation of STAT1 and increases total STAT1 expression in primary human monocytes in response to IFN-α 80. Furthermore, the IL-6 and IFN-γ receptors preferentially activate STAT3 and STAT1, respectively, but also activate the other STATs with lower efficiency. Qing et al. 81 showed that, when STAT1 is absent, IFN-γ activates STAT3 robustly and, conversely, when STAT3 is absent, IL-6 and other gp130-linked cytokines activate STAT1 robustly 83. It is interesting that, in addition to JAK1 and JAK2, SRC-family kinases are required to activate STAT3 in response to IFN-γ 81. Because STAT1 and STAT3 usually have opposite biological effects, their reciprocal activation in response to IFN-γ or IL-6 suggests that their relative abundance, which may vary considerably in different normal cell types, under different conditions, or in tumors, may well have a major impact on how cells behave in response to these two different classes of cytokines 81. The ratio of STAT3 to STAT1 may be as much as hundreds of times different in cells pretreated with IL-6 than in cells pretreated with IFN-γ, with significant consequences for downstream signaling in response to a second cytokine that activates either STAT, for example, IFNβ. Perhaps a more important consequence of up-regulated STAT expression is the ability of U-STATs 1 and 3 to drive gene expression through mechanisms distinct from those used by p-STATs. In recent experiments, van Boxel-Dezaire et al. have observed that, in freshly drawn human blood treated for 30–45 min with IFN-β, STATs 1, 3, and 5 are activated to very different extents in CD4+ and CD8+ T cells, B cells, and monocytes, with little activation of STAT1 in B cells (A van Boxel-Dezaire and GR Stark, unpublished observations). It seems inevitable, therefore, that the IFN-induced patterns of gene expression will be very different in these different cell types, as will the biological consequences of exposure to IFN.
The full biological relevance of the ability of P-STAT3 to increase the intracellular concentration of U-STAT3 remains to be established. In the context of cancer, the constitutive tyrosine phosphorylation of STAT3 in many different tumors is likely to lead to increased expression of U-STAT3, which in turn drives the expression of oncogenes such as MET and MRAS 9, 44. In cell culture systems, long-term treatment with IL-6 increases total U-STAT3, and the levels of RANTES, MET, MRAS, and TIS11D 9, 44 are increased coordinately with U-STAT3. The biological role of U-STAT3-driven gene expression in normal physiology is best addressed by experiments with genetically altered mice. An important attempt to do this was reported by Narimatsu et al. 82, who mutated a GAS element of the endogenous STAT3 promoter. The ability of IL-6 to increase STAT3 expression was abrogated in some tissues but not in others, probably because STAT3-dependent expression of the STAT3 gene can be regulated through additional elements that were not recognized and therefore were not mutated. Incomplete suppression of the response of the STAT3 gene to IL-6 might well account for the mild phenotype of the promoter knock-in mouse observed by Naramatsu et al. Since complete deletion of STAT3 is embryonic lethal 84, it remains to be seen whether mice with complete loss of the STAT3-dependent induction of U-STAT3 expression would have severe defects, as might be expected if the up-regulation of U-STAT3 is important for the full physiological functions of the many cytokines that use the common gp130 receptor subunit to induce the phosphorylation of STAT3.
STATs are ancient transcription factors, present in Dictyostelium 85, Drosophila 86, and zebrafish 87. The seven members of the mammalian STAT family range in size from 750 to 900 amino acids and feature several conserved domains, especially an SH2 domain. It is tempting to speculate that a primordial STAT first functioned as a constitutive transcription factor, with the ability to dimerize through ligand-dependent tyrosine phosphorylation as an additional function that was acquired more recently. Experiments in which the wild-type mouse genes encoding STAT1 or STAT3 are replaced cleanly by the Y-F or S-A mutants should give important new information to distinguish between the ligand-dependent and ligand-independent functions of these STATs in mammals.
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British Journal of Cancer (2016)