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. 2021 Sep 14;54(9):1976-1988.e7.
doi: 10.1016/j.immuni.2021.08.022.

Mutations in the adenosine deaminase ADAR1 that prevent endogenous Z-RNA binding induce Aicardi-Goutières-syndrome-like encephalopathy

Taisuke Nakahama  1 , Yuki Kato  2 , Toshiharu Shibuya  1 , Maal Inoue  1 , Jung In Kim  1 , Tuangtong Vongpipatana  1 , Hiroyuki Todo  1 , Yanfang Xing  1 , Yukio Kawahara  3
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Mutations in the adenosine deaminase ADAR1 that prevent endogenous Z-RNA binding induce Aicardi-Goutières-syndrome-like encephalopathy

Taisuke Nakahama et al. Immunity. .
Free article

Abstract

Mutations in the adenosine-to-inosine RNA-editing enzyme ADAR1 p150, including point mutations in the Z-RNA recognition domain Zα, are associated with Aicardi-Goutières syndrome (AGS). Here, we examined the in vivo relevance of ADAR1 binding of Z-RNA. Mutation of W197 in Zα, which abolished Z-RNA binding, reduced RNA editing. Adar1W197A/W197A mice displayed severe growth retardation after birth, broad expression of interferon-stimulated genes (ISGs), and abnormal development of multiple organs. Notably, malformation of the brain was accompanied by white matter vacuolation and gliosis, reminiscent of AGS-associated encephalopathy. Concurrent deletion of the double-stranded RNA sensor MDA5 ameliorated these abnormalities. ADAR1 (W197A) expression increased in a feedback manner downstream of type I interferons, resulting in increased RNA editing at a subset of, but not all, ADAR1 target sites. This increased expression did not ameliorate inflammation in Adar1W197A/W197A mice. Thus, editing of select endogenous RNAs by ADAR1 is essential for preventing inappropriate MDA5-mediated inflammation, with relevance to the pathogenesis of AGS.

Keywords: ADAR1; AGS; ISG; MDA5; RNA editing; Z-RNA; encephalopathy; hematopoiesis; inosine.

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Conflict of interest statement

Declaration of interests The authors declare no competing interests.

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