MicroRNA Editing Facilitates Immune Elimination of HCMV Infected Cells.

Nachmani, Daphna; Zimmermann, Albert; Oiknine Djian, Esther; Weisblum, Yiska; Livneh, Yoav; Khanh Le, Vu Thuy; Galun, Eithan; Horejsi, Vaclav; Isakov, Ofer; Shomron, Noam; Wolf, Dana G.; Hengel, Hartmut; Mandelboim, Ofer

The human cytomegalovirus (HCMV) is extremely prevalent in the human population. Infection by HCMV is life threatening in immune compromised individuals and in immune competent individuals it can cause severe birth defects, developmental retardation and is even associated with tumor development. While numerous mechanisms were developed by HCMV to interfere with immune cell activity, much less is known about cellular mechanisms that operate in response to HCMV infection. Here we demonstrate that in response to HCMV infection, the expression of the short form of the RNA editing enzyme ADAR1 (ADAR1-p110) is induced. We identified the specific promoter region responsible for this induction and we show that ADAR1-p110 can edit miR-376a. Accordingly, we demonstrate that the levels of the edited-miR-376a (miR-376a(e)) increase during HCMV infection. Importantly, we show that miR-376a(e) downregulates the immune modulating molecule HLA-E and that this consequently renders HCMV infected cells susceptible to elimination by NK cells.

MICRORNA; HUMAN cytomegalovirus diseases; HUMAN abnormalities; TUMOR growth; RNA editing; KILLER cells

PLoS Pathogens, 2014, Vol 10, Issue 2, p1

1553-7366

Academic Journal

10.1371/journal.ppat.1003963