Targeted RNA editing: novel tools to study post-transcriptional regulation

被引:16
作者
Xu, Weijin [1 ,3 ]
Biswas, Jeetayu [2 ,4 ]
Singer, Robert H. [2 ]
Rosbash, Michael [1 ]
机构
[1] Brandeis Univ, Howard Hughes Med Inst, Dept Biol, Waltham, MA 02451 USA
[2] Albert Einstein Coll Med, Dept Anat & Struct Biol, Bronx, NY 10461 USA
[3] CD Capital, Shanghai 200041, Peoples R China
[4] Weill Cornell Med, New York Presbyterian Hosp, Dept Med, New York, NY 10021 USA
关键词
MESSENGER-RNA; ADENOSINE-DEAMINASE; BINDING PROTEINS; GENETIC-CODE; HITS-CLIP; MECHANISTIC INSIGHTS; CATALYTIC SUBUNIT; NONCODING RNAS; IDENTIFICATION; REVEALS;
D O I
10.1016/j.molcel.2021.10.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
RNA binding proteins (RBPs) regulate nearly all post-transcriptional processes within cells. To fully under-stand RBP function, it is essential to identify their in vivo targets. Standard techniques for profiling RBP targets, such as crosslinking immunoprecipitation (CLIP) and its variants, are limited or suboptimal in some situations, e.g. when compatible antibodies are not available and when dealing with small cell popula-tions such as neuronal subtypes and primary stem cells. This review summarizes and compares several ge-netic approaches recently designed to identify RBP targets in such circumstances. TRIBE (targets of RNA binding proteins identified by editing), RNA tagging, and STAMP (surveying targets by APOBEC-mediated profiling) are new genetic tools useful for the study of post-transcriptional regulation and RBP identification. We describe the underlying RNA base editing technology, recent applications, and therapeutic implications.
引用
收藏
页码:389 / 403
页数:15
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