Abstract
Zc3h12a is a lipopolysaccharide-inducible gene and has a CCCH-type zinc-finger domain. Zc3h12a knockout mice develop spontaneous autoimmune diseases accompanied by splenomegaly and by lymphadenopathy. Subsequent studies show that Zc3h12a is a nuclease involved in destabilization of interleukin (IL)-6 and IL-12 mRNAvia the stem loop structure within the 30 UTR of these genes. Thus, we renamed it regulatory RNase-1 (Regnase-1) based on its function. IkB kinases phosphorylate and degrade Regnase-1 protein in macrophages in response to IL-1R/Toll-like receptor (TLR) stimulation. T-cell-specific deletion of Regnase-1 produces pathogenic T cells with hyperactivated phenotypes as well as autoimmune diseases. Regnase- 1 protein is cleaved by Malt1 and inactivated in response to T-cell receptor stimulation. Thus, Regnase-1 is a key molecule in the regulation of immune responses. © 2013 Cold Spring Harbor Laboratory Press.
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CITATION STYLE
Akira, S. (2013). Regnase-1, a ribonuclease involved in the regulation of immune responses. Cold Spring Harbor Symposia on Quantitative Biology, 78(1), 51–60. https://doi.org/10.1101/sqb.2013.78.019877
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