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Liangjing Wang

As seen in: Nature, MDPI
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Articles

Targeting NAT10 alleviates colonic senescence and elderly-onset colitis by disrupting N4-acetylation of DYRK1A - Nature Communications

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By Jingyu Chen, Meng Xue, Shuyi Mi, Wenwen Chen, Yuhao Sun, Shenglong Xia, Qiwei Ge, Jiakai Luo, Qiao Yu, Liangjing Wang, Shujie Chen, Anbo Fu
| Nature Verified
Abstract Intestinal aging characterized by imbalance between cell senescence and mucosal self-renewal, increases susceptibility to the elderly-onset ulcerative colitis (UC), while the underlying mechanisms remain elusive. Here, we identify mRNA N4-acetylcytidine (ac4C) modification and its specific writer, N-acetyltransferase 10 (NAT10), as critical regulators of human colonic epithelial cell senescence.
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Publisher Correction: Comprehensive discovery and functional characterization of the noncanonical proteome - Cell Research

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By Chengyu Shi, Shanshan Xie, Qiang Sun, Lingjie Sang, Wei Zhuo, Jian Liu, Qingfeng Yan, Dante Neculai, Qiming Sun, Jianzhong Shao, Wei Liu, Liangjing Wang, Xu Li, Tianhua Zhou
| Nature Verified
Correction to: Cell Research https://doi.org/10.1038/s41422-024-01059-3, published online 10 January 2025 The wrong Supplementary files (Table S12 and Table S13) were originally published with this article due to publisher’s mistake in correction stage; They have now been replaced with the correct files. The original article has been corrected.
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Comprehensive discovery and functional characterization of the noncanonical proteome - Cell Research

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By Chengyu Shi, Shanshan Xie, Qiang Sun, Lingjie Sang, Wei Zhuo, Jian Liu, Qingfeng Yan, Dante Neculai, Qiming Sun, Jianzhong Shao, Wei Liu, Liangjing Wang, Xu Li, Tianhua Zhou
| Nature Verified
Abstract The systematic identification and functional characterization of noncanonical translation products, such as novel peptides, will facilitate the understanding of the human genome and provide new insights into cell biology. Here, we constructed a high-coverage peptide sequencing reference library with 11,668,944 open reading frames and employed an ultrafiltration tandem mass spectrometry assay to identify novel peptides.
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