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Publication : cDNA cloning and expression analysis of the murine ribonuclease L inhibitor.

First Author  Benoit De Coignac A Year  1998
Journal  Gene Volume  209
Issue  1-2 Pages  149-56
PubMed ID  9524254 Mgi Jnum  J:46859
Mgi Id  MGI:1202153 Doi  10.1016/s0378-1119(98)00040-7
Citation  Benoit De Coignac A, et al. (1998) cDNA cloning and expression analysis of the murine ribonuclease L inhibitor. Gene 209(1-2):149-56
abstractText  The 2-5A/RNase L system is one of the pathways induced by interferon (IFN). It plays a major role in the antiviral and antiproliferative activities of IFNs. Recently, we have shown that the activity of the RNase L could be inhibited by a proteic inhibitor, the RNase L Inhibitor (RLI). Human RLI (Hu-RLI) was cloned and characterized. We describe here the isolation and characterization of the cDNA encoding the murine RLI (Mu-RLI). Hu-RLI and Mu-RLI protein have 98% amino acid identity. Mu-RLI is functionally homologous to Hu-RLI, and all the structural features and amino acid sequence motifs of Hu-RLI are conserved in Mu-RLI. Moreover, reticulocyte lysate translated Mu-RLI protein is also able to inhibit 2-5A binding on 2-5A-dependent RNAse-L. Northern blot analysis revealed that Mu-RLI cDNA hybridizes with one mRNA of 3.5 kb except for the testis where two mRNA of 3.5 and 2.1 kb, respectively, are detected, suggesting a tissue-specific regulation.
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