Functional analysis of RNA motifs essential for BC200 RNA-mediated translational regulation

被引:4
|
作者
Jang, Seonghui [1 ,2 ]
Shin, Heegwon [1 ]
Lee, Younghoon [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Chem, Daejeon 34141, South Korea
[2] Korea Food Res Inst, Wonju 55365, South Korea
基金
新加坡国家研究基金会;
关键词
A/C-rich domain; Alu domain; BC200; RNA; RNA motifs; Translational regulation; LONG NONCODING RNAS; NEURAL BC1 RNA; POLY(A)-BINDING PROTEIN; NEURONAL BC1; IN-VITRO; EXPRESSION; SEQUENCE; RECOGNITION; LOCATION; SYSTEMS;
D O I
10.5483/BMBRep.2020.53.2.153
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
Brain cytoplasmic 200 RNA (BC200 RNA) is proposed to ad as a local translational modulator by inhibiting translation after being targeted to neuronal dendrites. However, the mechanism by which BC200 RNA inhibits translation is not fully understood. Although a detailed functional analysis of RNA motifs is essential for understanding the BC200 RNA-mediated translation-inhibition mechanism, there is little relevant research on the subject. Here, we performed a systematic domain-dissection analysis of BC200 RNA to identify functional RNA motifs responsible for its translational-inhibition activity. Various RNA variants were assayed for their ability to inhibit translation of luciferase mRNA in vitro. We found that the 111-200-nucleotide region consisting of part of the Alu domain as well as the A/C-rich domain (consisting of both the A-rich and C-rich domains) is most effective for translation inhibition. Surprisingly, we also found that individual A-rich, A/C-rich, and Alu domains can enhance translation but at different levels for each domain, and that these enhancing effects manifest as cap-dependent translation.
引用
收藏
页码:94 / 99
页数:6
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