L
Linda Zhang
Researcher at University of Chicago
Publications - 13
Citations - 569
Linda Zhang is an academic researcher from University of Chicago. The author has contributed to research in topics: Messenger RNA & Medicine. The author has an hindex of 5, co-authored 8 publications receiving 171 citations. Previous affiliations of Linda Zhang include Howard Hughes Medical Institute.
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Journal ArticleDOI
Transcriptome-wide Mapping of Internal N7-Methylguanosine Methylome in Mammalian mRNA.
Li-Sheng Zhang,Chang Liu,Chang Liu,Honghui Ma,Qing Dai,Qing Dai,Hui-Lung Sun,Hui-Lung Sun,Guan-Zheng Luo,Zijie Scott Zhang,Zijie Scott Zhang,Linda Zhang,Linda Zhang,Lulu Hu,Lulu Hu,Xueyang Dong,Chuan He,Chuan He +17 more
TL;DR: This work developed a chemical-assisted sequencing approach that selectively converts internal m7G sites into abasic sites, inducing misincorporation at these sites during reverse transcription and enabled transcriptome-wide mapping of m7g in human tRNA and mRNA, revealing distribution features of the internal m 7G methylome in human cells.
Journal ArticleDOI
Control of Early B Cell Development by the RNA N6-Methyladenosine Methylation
Zhong Zheng,Linda Zhang,Linda Zhang,Xiaolong Cui,Xiaolong Cui,Xianbin Yu,Xianbin Yu,Phillip J. Hsu,Phillip J. Hsu,Ruitu Lyu,Ruitu Lyu,Haiyan Tan,Malay Mandal,Michelle Zhang,Michelle Zhang,Hui-Lung Sun,Hui-Lung Sun,Arantxa Sanchez Castillo,Arantxa Sanchez Castillo,Junmin Peng,Marcus R. Clark,Chuan He,Haochu Huang +22 more
TL;DR: Deletion of Mettl14 impairs interleukin-7 (IL-7)-induced pro-B cell proliferation and the large-pre-B-to-small- pre-B transition and causes dramatic abnormalities in gene expression programs important for B cell development in mice.
Journal ArticleDOI
A New Model of Spontaneous Colitis in Mice Induced by Deletion of an RNA m6A Methyltransferase Component METTL14 in T Cells.
Thomas X. Lu,Zhong Zheng,Linda Zhang,Hui-Lung Sun,Marc Bissonnette,Haochu Huang,Chuan He,Chuan He +7 more
TL;DR: A new mouse model of spontaneous colitis based on perturbation of RNA methylation in T cells is reported, which represents a new tool for elucidating pathogenic pathways, studying the contribution of intestinal microbiome and preclinical testing of therapeutic agents for inflammatory bowel disease.
Journal ArticleDOI
Stabilization of ERK-Phosphorylated METTL3 by USP5 Increases m6A Methylation.
Hui-Lung Sun,Allen C. Zhu,Yawei Gao,Hideki Terajima,Hideki Terajima,Qili Fei,Qili Fei,Shun Liu,Shun Liu,Linda Zhang,Linda Zhang,Zijie Zhang,Zijie Zhang,Bryan T. Harada,Bryan T. Harada,Yu-Ying He,Marc Bissonnette,Mien Chie Hung,Chuan He,Chuan He +19 more
TL;DR: This study reveals an unrecognized function of ERK in regulating m6A methylation, found that ERK phosphorylates METTL3 at S43/S50/S525 and WTAP at S306/S341, followed by deubiquitination by USP5, resulting in stabilization of the m 6A methyltransferase complex.
Journal ArticleDOI
N6-Adenosine Methylation of Socs1 mRNA Is Required to Sustain the Negative Feedback Control of Macrophage Activation.
Jie Du,Wang Liao,Weicheng Liu,Dilip K. Deb,Lei He,Phillip J. Hsu,Tivoli Nguyen,Linda Zhang,Marc Bissonnette,Chuan He,Yan Chun Li +10 more
TL;DR: It is concluded that m6A methylation-mediated SOCS1 induction is required to maintain the negative feedback control of macrophage activation in response to bacterial infection.