| First Author | Liang Z | Year | 2023 |
| Journal | EMBO Rep | Volume | 24 |
| Issue | 5 | Pages | e55835 |
| PubMed ID | 36975179 | Mgi Jnum | J:338600 |
| Mgi Id | MGI:7512696 | Doi | 10.15252/embr.202255835 |
| Citation | Liang Z, et al. (2023) The phenotype of the most common human ADAR1p150 Zalpha mutation P193A in mice is partially penetrant. EMBO Rep 24(5):e55835 |
| abstractText | ADAR1 -mediated A-to-I RNA editing is a self-/non-self-discrimination mechanism for cellular double-stranded RNAs. ADAR mutations are one cause of Aicardi-Goutieres Syndrome, an inherited paediatric encephalopathy, classed as a "Type I interferonopathy." The most common ADAR1 mutation is a proline 193 alanine (p.P193A) mutation, mapping to the ADAR1p150 isoform-specific Zalpha domain. Here, we report the development of an independent murine P195A knock-in mouse, homologous to human P193A. The Adar1(P195A/P195A) mice are largely normal and the mutation is well tolerated. When the P195A mutation is compounded with an Adar1 null allele (Adar1(P195A/-) ), approximately half the animals are runted with a shortened lifespan while the remaining Adar1(P195A/-) animals are normal, contrasting with previous reports. The phenotype of the Adar1(P195A/-) animals is both associated with the parental genotype and partly non-genetic/environmental. Complementation with an editing-deficient ADAR1 (Adar1(P195A/E861A) ), or the loss of MDA5, rescues phenotypes in the Adar1(P195A/-) mice. |
