Adar null mutant mouse embryos die with aberrant double-stranded RNA (dsRNA)-driven interferon induction, and Adar Mavs double mutants, in which interferon induction is prevented, die soon after birth. Protein kinase R (Pkr) is aberrantly activated in Adar Mavs mouse pup intestines before death, intestinal crypt cells die, and intestinal villi are lost. Adar Mavs Eifak2 (Pkr) triple mutant mice rescue all defects and have long-term survival. Adenosine deaminase acting on RNA 1 (ADAR1) and PKR co-immunoprecipitate from cells, suggesting PKR inhibition by direct interaction. AlphaFold studies on an inhibitory PKR dsRNA binding domain (dsRBD)-kinase domain interaction before dsRNA binding and on an inhibitory ADAR1 dsRBD3-PKR kinase domain interaction on dsRNA provide a testable model of the inhibition. Wild-type or editing-inactive human ADAR1 expressed in A549 cells inhibits activation of endogenous PKR. ADAR1 dsRNA binding is required for, but is not sufficient for, PKR inhibition. Mutating the ADAR1 dsRBD3-PKR contact prevents co-immunoprecipitation, ADAR1 inhibition of PKR activity, and co-localization of ADAR1 and PKR in cells.

Central European Institute for Technology at Masaryk University Building E35 Kamenice 735 5 625 00 Brno Czechia

Central European Institute for Technology at Masaryk University Building E35 Kamenice 735 5 625 00 Brno Czechia; National Centre for Biomolecular Research Faculty of Science Masaryk University Kamenice 5 625 00 Brno Czechia

Institute of Molecular Genetics of the Czech Academy of Sciences Prumyslova 595 252 50 Vestec Czechia

Laboratory of Embryology and Genetics of Human Malformation Imagine Institute INSERM UMR 1163 Université de Paris Cité 75015 Paris France

Laboratory of Epigenetic Regulation Institute of Molecular Genetics of the Czech Academy of Sciences Vídeňská 1083 142 20 Prague Czechia

Citace poskytuje Crossref.org

Distinct interactomes of ADAR1 nuclear and cytoplasmic protein isoforms and their responses to interferon induction