A loss-of-function human ADAR variant activates innate immune response and promotes bowel inflammation

Inflammatory bowel disease (IBD) arises from genetic-environmental interactions. Adenosine deaminases acting on RNA 1 (ADAR), an RNA-editing enzyme converting adenosine (A) to inosine (I), is essential for tissue homeostasis. Here we report that intestinal ADAR deficiency contributes to IBD pathogenesis in humans with reduced ADAR expression in patient intestinal crypts. Genetic or pharmacological inhibition of ADAR in mice causes spontaneous ileitis and colitis. Organoid studies show that ADAR loss leads to double-strand RNA (dsRNA) and endogenous retroviruses (ERVs) accumulation, disrupting intestinal homeostasis via melanoma differentiation-associated protein 5 (MDA5)-mediated dsRNA sensing and Janus kinase (JAK)-signal transducer and activator of transcription (STAT) signaling. Editome analyses identify Mda5 as an ADAR target, and edited Mda5 exhibits impaired dsRNA sensing. The human ADAR p.N173S mutation is a loss-of-function variant that fails to rescue IBD in intestinal Adar deficient mice, whereas JAK1/2 inhibitor Ruxolitinib attenuates IBD. We conclude that the ADAR-dsRNA/ERVs-MDA5-JAK/STAT axis is a potential therapeutic target for IBD.

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Publication Details

Journal
Nature Communications
Published
2025-09-29
DOI
https://doi.org/10.1038/s41467-025-63554-4
Primary Topic
RNA regulation and disease
Type
article
Field-Weighted Citation Impact
0.00

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article

A loss-of-function human ADAR variant activates innate immune response and promotes bowel inflammation

Da Yang, Pengfei Xu, Xingchen Wang, Wen Li Xie et al.
Nature Communications
RNA regulation and disease
article

A loss-of-function human ADAR variant activates innate immune response and promotes bowel inflammation

Da Yang, Pengfei Xu, Xingchen Wang, Wen Li Xie, Yue Wang, Min Zhang, Jong‐Won Kim, Qingde Wang, Chen Gao, Yue Xi, Songrong Ren, Meishu Xu
article en

Abstract

Inflammatory bowel disease (IBD) arises from genetic-environmental interactions. Adenosine deaminases acting on RNA 1 (ADAR), an RNA-editing enzyme converting adenosine (A) to inosine (I), is essential for tissue homeostasis. Here we report that intestinal ADAR deficiency contributes to IBD pathogenesis in humans with reduced ADAR expression in patient intestinal crypts. Genetic or pharmacological inhibition of ADAR in mice causes spontaneous ileitis and colitis. Organoid studies show that ADAR loss leads to double-strand RNA (dsRNA) and endogenous retroviruses (ERVs) accumulation, disrupting intestinal homeostasis via melanoma differentiation-associated protein 5 (MDA5)-mediated dsRNA sensing and Janus kinase (JAK)-signal transducer and activator of transcription (STAT) signaling. Editome analyses identify Mda5 as an ADAR target, and edited Mda5 exhibits impaired dsRNA sensing. The human ADAR p.N173S mutation is a loss-of-function variant that fails to rescue IBD in intestinal Adar deficient mice, whereas JAK1/2 inhibitor Ruxolitinib attenuates IBD. We conclude that the ADAR-dsRNA/ERVs-MDA5-JAK/STAT axis is a potential therapeutic target for IBD.

Nature CommunicationsVol. 16(1)
University of Pittsburgh (US), Gyeongsang National University (KR), Wuhan University (CN), Hubei Provincial Center for Disease Control and Prevention (CN), Zhongnan Hospital of Wuhan University (CN), PharmacoGenetics (China) (CN)
National Institutes of Health
Openalex Percentile: Top 77%
RNA regulation and disease
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