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Review
. 2007 Jun-Jul;89(6-7):789-98.
doi: 10.1016/j.biochi.2007.02.006. Epub 2007 Feb 20.

Diverse functions of RNase L and implications in pathology

Affiliations
Review

Diverse functions of RNase L and implications in pathology

Catherine Bisbal et al. Biochimie. 2007 Jun-Jul.

Abstract

The endoribonuclease L (RNase L) is the effector of the 2-5A system, a major enzymatic pathway involved in the molecular mechanism of interferons (IFNs). RNase L is a very unusual nuclease with a complex mechanism of regulation. It is a latent enzyme, expressed in nearly every mammalian cell type. Its activation requires its binding to a small oligonucleotide, 2-5A. 2-5A is a series of unique 5'-triphosphorylated oligoadenylates with 2'-5' phosphodiester bonds. By regulating viral and cellular RNA expression, RNase L plays an important role in the antiviral and antiproliferative activities of IFN and contributes to innate immunity and cell metabolism. The 2-5A/RNase L pathway is implicated in mediating apoptosis in response to viral infections and to several types of external stimuli. Several recent studies have suggested that RNase L could have a role in cancer biology and evidence of a tumor suppressor function of RNase L has emerged from studies on the genetics of hereditary prostate cancer.

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Figures

Figure 1
Figure 1
A) The 2–5A/RNase L pathway B) Structure of the 2–5A4: 2′–5′ oligoadenylates tetramer.
Figure 2
Figure 2
Structure of the RNase L.

References

    1. Zhou A, Hassel BA, Silverman RH. Expression cloning of 2–5A-dependent RNAase: a uniquely regulated mediator of interferon action. Cell. 1993;72:753–765. - PubMed
    1. Meurs E, Chong K, Galabru J, Thomas NS, Kerr IM, Williams BR, Hovanessian AG. Molecular cloning and characterization of the human double-stranded RNA- activated protein kinase induced by interferon. Cell. 1990;62:379–390. - PubMed
    1. Kerr IM, Brown RE, Ball LA. Increased sensitivity of cell-free protein synthesis to double-stranded RNA after interferon treatment. Nature. 1974;250:57–59. - PubMed
    1. Brown GE, Lebleu B, Kawakita M, Shaila S, Sen GC, Lengyel P. Increased endonuclease activity in an extract from mouse Ehrlich ascites tumor cells which had been treated with a partially purified interferon preparation: dependence of double-stranded RNA. Biochem Biophys Res Commun. 1976;69:114–122. - PubMed
    1. Sen GC, Lebleu B, Brown GE, Kawakita M, Slattery E, Lengyel P. Interferon, double-stranded RNA and mRNA degradation. Nature. 1976;264:370–373. - PubMed

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