tRNA m1A modification is essential for gut homeostasis and function of group 3 innate lymphoid cells

Group 3 innate lymphoid cells (ILC3s) play crucial roles in maintaining intestinal homeostasis and defending against bacterial infections. However, the epigenetic mechanisms that regulate ILC3 responses are not well understood. In this study, we show that Trmt61a, the methyltransferase responsible for the m<sup>1</sup>A58 tRNA modification, is predominantly expressed in ILC3s. We found that specific depletion of TRMT61A in ILC3s leads to dysregulated cell cycle and a reduction in cell numbers. Notably, mice with an ILC3-specific TRMT61A deficiency exhibit dysbiosis, but antibiotic treatment can restore colonic ILC3 levels. Furthermore, these mice exhibit increased susceptibility to experimental intestinal inflammation and enteric bacterial infection. Our findings uncover a previously unrecognized role for TRMT61A mediated m<sup>1</sup>A modification in the regulation of intestinal ILC3s, essential for protecting intestinal tissue during inflammation and enhancing innate immunity against enteric pathogens.

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Publication Details

Journal
Cell Discovery
Published
2026-01-03
DOI
https://doi.org/10.1038/s41421-025-00850-9
Primary Topic
IL-33, ST2, and ILC Pathways
Type
article
Field-Weighted Citation Impact
0.00

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article

tRNA m1A modification is essential for gut homeostasis and function of group 3 innate lymphoid cells

Bing Su, H. Li, Huabin Li, Jingyu Li et al.
Cell Discovery
IL-33, ST2, and ILC Pathways
article

tRNA m1A modification is essential for gut homeostasis and function of group 3 innate lymphoid cells

Bing Su, H. Li, Huabin Li, Jingyu Li, Chen Kan, Coco Chu, Longyan Wu, Gaoyang Wang, Xuemin Cai, Z. Tang, Bin Li, Yunzhu Chen
article en

Abstract

Group 3 innate lymphoid cells (ILC3s) play crucial roles in maintaining intestinal homeostasis and defending against bacterial infections. However, the epigenetic mechanisms that regulate ILC3 responses are not well understood. In this study, we show that Trmt61a, the methyltransferase responsible for the m<sup>1</sup>A58 tRNA modification, is predominantly expressed in ILC3s. We found that specific depletion of TRMT61A in ILC3s leads to dysregulated cell cycle and a reduction in cell numbers. Notably, mice with an ILC3-specific TRMT61A deficiency exhibit dysbiosis, but antibiotic treatment can restore colonic ILC3 levels. Furthermore, these mice exhibit increased susceptibility to experimental intestinal inflammation and enteric bacterial infection. Our findings uncover a previously unrecognized role for TRMT61A mediated m<sup>1</sup>A modification in the regulation of intestinal ILC3s, essential for protecting intestinal tissue during inflammation and enhancing innate immunity against enteric pathogens.

Cell DiscoveryVol. 12(1)
Shanxi Medical University (CN), Shanghai Jiao Tong University (CN), Ruijin Hospital (CN), University of Manchester (GB), Sichuan International Studies University (CN), Eye & ENT Hospital of Fudan University (CN), Beijing Tsinghua Chang Gung Hospital (CN), Center for Life Sciences (CN), Chongqing Medical University (CN), Tsinghua University (CN)
Shanghai Municipal Health Commission, National Natural Science Foundation of China, Shanghai Jiao Tong University, School of Medicine, Shanghai Jiao Tong University
Openalex Percentile: Top 98%
IL-33, ST2, and ILC Pathways
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