|Ribonuclease L (2',5'-oligoisoadenylate synthetase-dependent)|
PDB rendering based on 1wdy.
|Symbols||; PRCA1; RNS4|
|External IDs||ChEMBL: GeneCards:|
|RNA expression pattern|
Ribonuclease L or RNase L (for latent), known sometimes as ribonuclease 4 or 2'-5' oligoadenylate synthetase-dependent ribonuclease — is an interferon (IFN)-induced ribonuclease which, upon activation, destroys all RNA within the cell (both cellular and viral). RNase L is an enzyme that in humans is encoded by the RNASEL gene.
This gene encodes a component of the interferon-regulated 2'-5'oligoadenylate (2'-5'A) system that functions in the antiviral and antiproliferative roles of interferons. RNase L is activated by dimerization, which occurs upon 2'-5'A binding, and results in cleavage of all RNA in the cell. This can lead to activation of MDA5, an RNA helicase involved in the production of interferons.
Synthesis and activation
RNase L is present in very minute quantities during the normal cell cycle. When interferon binds to cell receptors, it activates transcription of around 300 genes to bring about the antiviral state. Among the enzymes produced is RNase L, which is initially in an inactive form. A set of transcribed genes codes for 2’-5’ Oligoadenylate Synthetase (OAS). The transcribed RNA is then spliced and modified in the nucleus before reaching the cytoplasm and being translated into an inactive form of OAS. The location of OAS in the cell and the length of the 2’-5’ oligoadenylate depends on the post-transcriptional and post-translational modifications of OAS.
OAS is only activated under a viral infection, when a tight binding of the inactive form of the protein with a viral dsRNA, consisting of the retrovirus’ ssRNA and its complementary strand, takes place. Once active, OAS converts ATP to pyrophosphate and 2’-5’-linked oligoadenylates (2-5A), which are 5’ end phosphorylated. 2-5 A molecules then bind to RNase L, promoting its activation by dimerization. In its activated form RNase L cleaves all RNA molecules in the cell leading to autophagy and apoptosis. Some of the resulting RNA fragments can also further induce the production of INF-β as noted in the Significance section.
This dimerization and activation of RNase L can be recognized using Fluorescence Resonance Energy Transfer (FRET), as oligoribonucleotides containing a quencher and a fluorophore on opposite sites are added to a solution with inactive RNase L. The FRET signal is then recorded as the quencher and the fluorophore are very close to each other. Upon the addition of 2-5A molecules, RNase L becomes active, cleaving the oligoribonucleotides and interfering in the FRET signal.
RNase L is part of the body's innate immune defense, namely the antiviral state of the cell. When a cell is in the antiviral state, it is highly resistant to viral attacks and is also ready to undergo apoptosis upon successful viral infection. Degradation of all RNA within the cell (which usually occurs with cessation of translation activity caused by protein kinase R) is the cell's last stand against a virus before it attempts apoptosis.
Interferon beta (INF-β), a type I interferon responsible for antiviral activity, is produced by RNAse L and melanoma differentiation-associated protein 5 (MDA5) in the infected cell. The relationship between RNAse L and MDA5 in the production of INFs has been confirmed with siRNA tests silencing the expression of either molecule and noting a marked decline in INF production. MDA5, an RNA helicase, is known to be activated by long dsRNA transcribed from the viral genome. In a cell with RNAse L, MDA5 activity may be further enhanced. When active, RNAse L cleaves and identifies viral RNA and feeds it into MDA5 activation sites, enhancing the production of INF-β. The RNA fragments produced by RNAse L have double stranded regions, as well as specific markers, that allow them to be identified by the RNAse L and MDA5. Some studies have suggested that high levels of RNAse L may actually inhibit INF-β production, but a clear linkage still exists between RNAse L activity and INF-β production.
Furthermore, it has been shown that RNase L is involved in many diseases. In 2002, the “hereditary prostate cancer 1” locus (HPC1) was mapped to the RNASEL gene, indicating that mutations in this gene cause a predisposition to prostate cancer. Impairments of the OAS/RNase L pathway in chronic fatigue syndrome (CFS) have been investigated.
- Squire J, Zhou A, Hassel BA, Nie H, Silverman RH (Jun 1994). "Localization of the interferon-induced, 2-5A-dependent RNase gene (RNS4) to human chromosome 1q25". Genomics 19 (1): 174–5. doi:10.1006/geno.1994.1033. PMID 7514564.
- N. Sarkar, Saumendra; Pandley, Mitali; C. Sen, Ganes (2005). Interferon Methods and Protocols. Totowa, New Jersey, USA: Human Press Inc. pp. 81–102. ISBN 978-1-58829-418-0.
- Liang, Shu-Ling; Quirk, David; Zhou, Aimin (September 2006). "RNase L: Its Biological Roles and Regulation". Life 58 (9): 508–514. doi:10.1080/15216540600838232.
- Banerjee, Shuvojit; Chakrabarti, Arindam; Kant Jha, Babal; R. Weiss, Susan; H. Silverman, Robert (25 February 2014). "Cell-Type-Specific Effects of RNase L on Viral Induction of Beta Interferon" (PDF). mBio 5 (2): 1–6. doi:10.1128/mBio.00856-14. Retrieved 14 October 2014.
- S. Thakur, Chandar; Xu, Zan; Wang, Zhengfu; Novince, Zachary; H. Silverman, Robert (2005). Interferon Methods and Protocols. Totowa, New Jersey, USA: Human Press Inc. pp. 103–114. ISBN 978-1-58829-418-0.
- Luthra, Priya; Sun, Dengyun; H. Silverman, Robert; He, Biao (18 January 2011). "Activation of IFN-β expression by a viral mRNA through RNase L and MDA5". Proceedings of the National Academy of Sciences of the United States o America 108 (5): 2118–2123. doi:10.1073/pnas.1012409108.
- Pichlmair, Andreas; Schulz, Oliver; Tan, Choon-Ping; Rehwinkel, Jan; Kato, Hiroki; Takeuchi, Osamu; Akira, Shizuo; Way, Michael; Schiavo, Giampietro; Reis e Sousa, Caetano (October 2009). "Activation of MDA5 Requires Higher-Order RNA Structures Genereated during Virus Infection". Journal of Virology 83 (20): 10761–10769. doi:10.1128/JVI.00770-09.
- "Entrez Gene: RNASEL ribonuclease L (2',5'-oligoisoadenylate synthetase-dependent)".
- Carpten J, Nupponen N, Isaacs S et al. (February 2002). "Germline mutations in the ribonuclease L gene in families showing linkage with HPC1". Nature Genetics 30 (2): 181–4. doi:10.1038/ng823. PMID 11799394.
- Nijs J, De Meirleir K (Nov–Dec 2005). "Impairments of the 2-5A synthetase/RNase L pathway in chronic fatigue syndrome". In Vivo 19 (6): 1013–21. PMID 16277015.
- Suhadolnik RJ et al. (1997). "Biochemical evidence for a novel low molecular weight 2-5A-dependent RNase L in chronic fatigue syndrome". J Interferon Cytokine Res 17 (7): 377–85. doi:10.1089/jir.1997.17.377. PMID 9243369.
- Urisman A, Molinaro RJ, Fischer N, Plummer SJ, Casey G, Klein EA, Malathi K, Magi-Galluzzi C, Tubbs RR, Ganem D, Silverman RH, DeRisi JL (March 2006). "Identification of a novel Gammaretrovirus in prostate tumors of patients homozygous for R462Q RNASEL variant". PLoS Pathog. 2 (3): e25. doi:10.1371/journal.ppat.0020025. PMC 1434790. PMID 16609730.
- Chakrabarti A, Jha BK, Silverman RH (January 2011). "New insights into the role of RNase L in innate immunity". J. Interferon Cytokine Res. 31 (1): 49–57. doi:10.1089/jir.2010.0120. PMC 3021357. PMID 21190483.
- Castelli J, Wood KA, Youle RJ (1999). "The 2-5A system in viral infection and apoptosis.". Biomed. Pharmacother. 52 (9): 386–90. doi:10.1016/S0753-3322(99)80006-7. PMID 9856285.
- Leaman DW, Cramer H (1999). "Controlling gene expression with 2-5A antisense.". Methods 18 (3): 252–65. doi:10.1006/meth.1999.0782. PMID 10454983.
- Silverman RH (2003). "Implications for RNase L in prostate cancer biology.". Biochemistry 42 (7): 1805–12. doi:10.1021/bi027147i. PMID 12590567.
- Kieffer N, Schmitz M, Scheiden R et al. (2006). "Involvement of the RNAse L gene in prostate cancer.". Bulletin de la Société des sciences médicales du Grand-Duché de Luxembourg (1): 21–8. PMID 16869093.
- Bisbal C, Silverman RH (2007). "Diverse functions of RNase L and implications in pathology.". Biochimie 89 (6-7): 789–98. doi:10.1016/j.biochi.2007.02.006. PMC 2706398. PMID 17400356.
- Carter BS, Beaty TH, Steinberg GD et al. (1992). "Mendelian inheritance of familial prostate cancer.". Proc. Natl. Acad. Sci. U.S.A. 89 (8): 3367–71. doi:10.1073/pnas.89.8.3367. PMC 48868. PMID 1565627.
- Dong B, Xu L, Zhou A et al. (1994). "Intrinsic molecular activities of the interferon-induced 2-5A-dependent RNase.". J. Biol. Chem. 269 (19): 14153–8. PMID 7514601.
- Bisbal C, Martinand C, Silhol M et al. (1995). "Cloning and characterization of a RNAse L inhibitor. A new component of the interferon-regulated 2-5A pathway.". J. Biol. Chem. 270 (22): 13308–17. doi:10.1074/jbc.270.22.13308. PMID 7539425.
- Zhou A, Hassel BA, Silverman RH (1993). "Expression cloning of 2-5A-dependent RNAase: a uniquely regulated mediator of interferon action.". Cell 72 (5): 753–65. doi:10.1016/0092-8674(93)90403-D. PMID 7680958.
- Hassel BA, Zhou A, Sotomayor C et al. (1993). "A dominant negative mutant of 2-5A-dependent RNase suppresses antiproliferative and antiviral effects of interferon.". EMBO J. 12 (8): 3297–304. PMC 413597. PMID 7688298.
- Smith JR, Freije D, Carpten JD et al. (1996). "Major susceptibility locus for prostate cancer on chromosome 1 suggested by a genome-wide search.". Science 274 (5291): 1371–4. doi:10.1126/science.274.5291.1371. PMID 8910276.
- Egesten A, Dyer KD, Batten D et al. (1997). "Ribonucleases and host defense: identification, localization and gene expression in adherent monocytes in vitro.". Biochim. Biophys. Acta 1358 (3): 255–60. doi:10.1016/S0167-4889(97)00081-5. PMID 9366257.
- Eeles RA, Durocher F, Edwards S et al. (1998). "Linkage analysis of chromosome 1q markers in 136 prostate cancer families. The Cancer Research Campaign/British Prostate Group U.K. Familial Prostate Cancer Study Collaborators.". American Journal of Human Genetics 62 (3): 653–8. doi:10.1086/301745. PMC 1376940. PMID 9497242.
- Dong B, Silverman RH (1999). "Alternative function of a protein kinase homology domain in 2', 5'-oligoadenylate dependent RNase L.". Nucleic Acids Res. 27 (2): 439–45. doi:10.1093/nar/27.2.439. PMC 148198. PMID 9862963.
- Carpten JD, Makalowska I, Robbins CM et al. (2000). "A 6-Mb high-resolution physical and transcription map encompassing the hereditary prostate cancer 1 (HPC1) region.". Genomics 64 (1): 1–14. doi:10.1006/geno.1999.6051. PMID 10708513.
- Zhou A, Nie H, Silverman RH (2001). "Analysis and origins of the human and mouse RNase L genes: mediators of interferon action.". Mamm. Genome 11 (11): 989–92. doi:10.1007/s003350010194. PMID 11063255.
- Dong B, Niwa M, Walter P, Silverman RH (2001). "Basis for regulated RNA cleavage by functional analysis of RNase L and Ire1p.". RNA 7 (3): 361–73. doi:10.1017/S1355838201002230. PMC 1370093. PMID 11333017.