Emerging role of the RNA-editing enzyme ADAR1 in stem cell fate and function

被引:10
作者
Lu, Di [1 ]
Lu, Jianxi [1 ]
Liu, Qiuli [1 ]
Zhang, Qi [1 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 3, Biotherapy Ctr, Guangzhou 510630, Peoples R China
基金
中国国家自然科学基金;
关键词
Adenosine deaminase acting on RNA-1 (ADAR1); Stem cells; Cell fate; RNA editing; ADENOSINE-DEAMINASE; SELF-RENEWAL; METHYLATION; GENE; N-6-METHYLADENOSINE; DIFFERENTIATION; TRANSCRIPTION; EXPRESSION; LEUKEMIA; CANCER;
D O I
10.1186/s40364-023-00503-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Stem cells are critical for organism development and the maintenance of tissue homeostasis. Recent studies focusing on RNA editing have indicated how this mark controls stem cell fate and function in both normal and malignant states. RNA editing is mainly mediated by adenosine deaminase acting on RNA 1 (ADAR1). The RNA editing enzyme ADAR1 converts adenosine in a double-stranded RNA (dsRNA) substrate into inosine. ADAR1 is a multifunctional protein that regulate physiological processes including embryonic development, cell differentiation, and immune regulation, and even apply to the development of gene editing technologies. In this review, we summarize the structure and function of ADAR1 with a focus on how it can mediate distinct functions in stem cell self-renewal and differentiation. Targeting ADAR1 has emerged as a potential novel therapeutic strategy in both normal and dysregulated stem cell contexts.
引用
收藏
页数:12
相关论文
共 144 条
[61]   Mammalian Staufen1 recruits Upf1 to specific mRNA 3'UTRs so as to elicit mRNA decay [J].
Kim, YK ;
Furic, L ;
DesGroseillers, L ;
Maquat, LE .
CELL, 2005, 120 (02) :195-208
[62]   Dyschromatosis symmetrica hereditaria and reticulate acropigmentation of Kitamura: An update [J].
Kono, Michihiro ;
Akiyama, Masashi .
JOURNAL OF DERMATOLOGICAL SCIENCE, 2019, 93 (02) :75-81
[63]   DOUBLE-STRANDED RNA-DEPENDENT PROTEIN-KINASE ACTIVATES TRANSCRIPTION FACTOR NF-KAPPA-B BY PHOSPHORYLATING I-KAPPA-B [J].
KUMAR, A ;
HAQUE, J ;
LACOSTE, J ;
HISCOTT, J ;
WILLIAMS, BRG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (14) :6288-6292
[64]   Upping the antizyme: AZIN1 directs stem cell fate [J].
Ladel, Luisa ;
Jamieson, Catriona H. M. .
BLOOD, 2021, 138 (20) :1910-1911
[65]   Editing of glutamate receptor B subunit ion channel RNAs by four alternatively spliced DRADA2 double-stranded RNA adenosine deaminases [J].
Lai, F ;
Chen, CX ;
Carter, KC ;
Nishikura, K .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (05) :2413-2424
[66]   ADAR1: "Editor-in-Chief" of Cytoplasmic Innate Immunity [J].
Lamers, Mart M. ;
van den Hoogen, Bernadette G. ;
Haagmans, Bart L. .
FRONTIERS IN IMMUNOLOGY, 2019, 10 :1763
[67]   Alu-dependent RNA editing of GLI1 promotes malignant regeneration in multiple myeloma [J].
Lazzari, Elisa ;
Mondala, Phoebe K. ;
Delos Santos, Nathaniel ;
Miller, Amber C. ;
Pineda, Gabriel ;
Jiang, Qingfei ;
Leu, Heather ;
Ali, Shawn A. ;
Ganesan, Anusha-Preethi ;
Wu, Christina N. ;
Costello, Caitlin ;
Minden, Mark ;
Chiaramonte, Raffaella ;
Stewart, A. Keith ;
Crews, Leslie A. ;
Jamieson, Catriona H. M. .
NATURE COMMUNICATIONS, 2017, 8
[68]   ADAR1 attenuates allogeneic graft rejection by suppressing miR-21 biogenesis in macrophages and promoting M2 polarization [J].
Li, Junjie ;
Xie, Jiangang ;
Liu, Shanshou ;
Li, Xiao ;
Zhang, Dongliang ;
Wang, Xianqi ;
Jiang, Jinquan ;
Hu, Wei ;
Zhang, Yuan ;
Jin, Boquan ;
Zhuang, Ran ;
Yin, Wen .
FASEB JOURNAL, 2018, 32 (09) :5162-5173
[69]   RNA editing underlies genetic risk of common inflammatory diseases [J].
Li, Qin ;
Gloudemans, Michael J. ;
Geisinger, Jonathan M. ;
Fan, Boming ;
Aguet, Francois ;
Sun, Tao ;
Ramaswami, Gokul ;
Li, Yang, I ;
Ma, Jin-Biao ;
Pritchard, Jonathan K. ;
Montgomery, Stephen B. ;
Li, Jin Billy .
NATURE, 2022, 608 (7923) :569-+
[70]   RNA EDITING RNA editing by ADAR1 prevents MDA5 sensing of endogenous dsRNA as nonself [J].
Liddicoat, Brian J. ;
Piskol, Robert ;
Chalk, Alistair M. ;
Ramaswami, Gokul ;
Higuchi, Miyoko ;
Hartner, Jochen C. ;
Li, Jin Billy ;
Seeburg, Peter H. ;
Walkley, Carl R. .
SCIENCE, 2015, 349 (6252) :1115-1120