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Sci. STKE, 20 March 2007
Vol. 2007, Issue 378, p. tw92
[DOI: 10.1126/stke.3782007tw92]


Immunology To Turn On or Turn Off: One Molecule’s Dilemma?

John F. Foley

Science’s STKE, AAAS, Washington, DC 20005, USA

Steroid receptor coactivator-3 (SRC-3) is a member of the SRC family of nuclear receptor coactivators and is known for its function as an enhancer of gene transcription. Although knockout studies show roles for SRC-3 in development, oncogenesis, and tumor suppression, little is known about its contribution to immune responses. In this study, Yu et al. first demonstrated that SRC-3–/– mice were more susceptible to lipopolysaccharide (LPS)-induced endotoxic shock than were wild-type mice. The authors found increased concentrations of the proinflammatory cytokines tumor necrosis factor-{alpha} (TNF-{alpha}), interleukin-6 (IL-6), and IL-1beta in the sera of SRC-3–/– animals. Peritoneal macrophages from SRC-3–/– mice secreted more of these cytokines after treatment with LPS than did macrophages from wild-type mice. These effects were not observed in macrophages from SRC-1–/– or SRC-2–/– mice. Electrophoretic mobility shift assays revealed that LPS-induced activation of the transcription factor NF-{kappa}B was comparable in wild-type and SRC-3–/– cells, ruling out a role for SRC-3 in repressing NF-{kappa}B activation. There were no differences in the abundance or half-lives of proinflammatory cytokine mRNAs when comparing wild-type and SRC-3–/–macrophages, nor were there any differences in the secretion or stability of TNF-{alpha}. Polysomal profile analysis, which estimates the proportion of actively translating cytoplasmic mRNAs, revealed that the increased production of TNF-{alpha} and IL-1beta by SRC-3–/– macrophages was due to enhanced translation. SRC-3, which does not contain RNA-binding motifs, associated with the translational repressors TIA-1 and TIAR, providing a mechanism by which SRC-3 may repress mRNA translation. This study suggests that a coregulator protein can act as a transcriptional coactivator or a translational corepressor, depending on the cellular context.

C. Yu, B. York, S. Wang, Q. Feng, J. Xu, B. W. O’Malley, An essential function of the SRC-3 coactivator in suppression of cytokine mRNA translation and inflammatory response. Mol. Cell 25, 765-778 (2007). [PubMed]

Citation: J. F. Foley, To Turn On or Turn Off: One Molecule’s Dilemma? Sci. STKE 2007, tw92 (2007).

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