In search of critical dsRNA targets of ADAR1

被引:10
|
作者
Levanon, Erez Y. [1 ]
Cohen-Fultheim, Roni [1 ]
Eisenberg, Eli [2 ]
机构
[1] Bar Ilan Univ, Mina & Everard Goodman Fac Life Sci, IL-5290002 Ramat Gan, Israel
[2] Tel Aviv Univ, Raymond & Beverly Sackler Sch Phys & Astron, IL-6997801 Tel Aviv, Israel
基金
以色列科学基金会;
关键词
DOUBLE-STRANDED-RNA; ADENOSINE-DEAMINASE; IDENTIFICATION; ENZYME; GENE; ALU; MUTATIONS; RESPONSES; SEQUENCE; SITES;
D O I
10.1016/j.tig.2023.12.002
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Recent studies have underscored the pivotal role of adenosine-to-inosine RNA editing, catalyzed by ADAR1, in suppressing innate immune interferon responses triggered by cellular double -stranded RNA (dsRNA). However, the specific ADAR1 editing targets crucial for this regulatory function remain elusive. We review analyses of transcriptome-wide ADAR1 editing patterns and their evolutionary dynamics, which offer valuable insights into this unresolved query. The growing appreciation of the significance of immunogenic dsRNAs and their editing in inflammatory and autoimmune diseases and cancer calls for a more comprehensive understanding of dsRNA immunogenicity, which may promote our understanding of these diseases and open doors to therapeutic avenues.
引用
收藏
页码:250 / 259
页数:10
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