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Publication : microRNA-induced translational control of antiviral immunity by the cap-binding protein 4EHP.

First Author  Zhang X Year  2021
Journal  Mol Cell Volume  81
Issue  6 Pages  1187-1199.e5
PubMed ID  33581076 Mgi Jnum  J:309694
Mgi Id  MGI:6707958 Doi  10.1016/j.molcel.2021.01.030
Citation  Zhang X, et al. (2021) microRNA-induced translational control of antiviral immunity by the cap-binding protein 4EHP. Mol Cell 81(6):1187-1199.e5
abstractText  Type I interferons (IFNs) are critical cytokines in the host defense against invading pathogens. Sustained production of IFNs, however, is detrimental to the host, as it provokes autoimmune diseases. Thus, the expression of IFNs is tightly controlled. We report that the mRNA 5' cap-binding protein 4EHP plays a key role in regulating type I IFN concomitant with controlling virus replication, both in vitro and in vivo. Mechanistically, 4EHP suppresses IFN-beta production by effecting the miR-34a-induced translational silencing of Ifnb1 mRNA. miR-34a is upregulated by both RNA virus infection and IFN-beta induction, prompting a negative feedback regulatory mechanism that represses IFN-beta expression via 4EHP. These findings demonstrate the direct involvement of 4EHP in virus-induced host response, underscoring a critical translational silencing mechanism mediated by 4EHP and miR-34a to impede sustained IFN production. This study highlights an intrinsic regulatory function for miRNA and the translation machinery in maintaining host homeostasis.
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