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Regulation of Interleukin 4-Mediated Signaling by Naturally Occurring Dominant Negative and Attenuated Forms of Human Stat6
Bharvin K. R. Patel, Jacalyn H. Pierce and William J. LaRochelle
Proceedings of the National Academy of Sciences of the United States of America
Vol. 95, No. 1 (Jan. 6, 1998), pp. 172-177
Published by: National Academy of Sciences
Stable URL: http://www.jstor.org/stable/44435
Page Count: 6
You can always find the topics here!Topics: Protein isoforms, Surface antigens, Complementary DNA, Phosphorylation, Mice, Molecules, Transcriptional activation, Messenger RNA, T lymphocytes, 3T3 cells
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Interleukin (IL)-4-mediated nuclear signaling by Stat6 has been implicated in lymphoid cell proliferation and the transcriptional activation of genes encoding major histocompatability complex (MHC) class II molecules and Fc receptors. To investigate IL-4-mediated transcriptional events, we cloned two naturally occurring human Stat6 isoforms, Stat6b and Stat6c, that encoded an NH2-terminal truncation or an SH2 domain deletion, respectively. Stat6 variant mRNAs were differentially expressed in many human tissues. To elucidate the biologic role of each isoform, we examined the consequences of overexpression in IL-4-responsive FDC-P2 cells. Stat6 and Stat6b (to a lesser extent) enhanced DNA synthesis, up-regulated endogenous MHC class II and Fcγ receptors, and became tyrosine phosphorylated in response to IL-4 stimulation. In contrast, Stat6c, which lacks functionally critical SH2 domain residues, unexpectedly inhibited IL-4-mediated mitogenesis and cell surface antigen expression and was not tyrosine phosphorylated. Although Stat6c only modestly diminished endogenous Stat6 tyrosine phosphorylation, it abolished endogenous Stat6 Fcγ RI and Iε DNA binding activity and Fcγ RI-luciferase reporter transcriptional activation. Our results indicate that the molecular mechanism of inhibition by Stat6c was due to suppression of endogenous Stat6 dimer formation. Thus, Stat6b and Stat6c are naturally occurring attenuated and dominant negative Stat6 variants, respectively, that affect IL-4-mediated biologic responses through differential transcriptional regulation.
Proceedings of the National Academy of Sciences of the United States of America © 1998 National Academy of Sciences