Structural Determinants for Geometry and Information Decoding of tRNA by T Box Leader RNA

被引:43
|
作者
Grigg, Jason C. [1 ]
Ke, Ailong [1 ]
机构
[1] Cornell Univ, Dept Mol Biol & Genet, Ithaca, NY 14850 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
TRANSCRIPTION ANTITERMINATION; MESSENGER-RNA; CRYSTAL-STRUCTURE; RIBOSOME; SEQUENCE; MOTIF; LOOP; CONSERVATION; FEATURES; SYSTEMS;
D O I
10.1016/j.str.2013.09.001
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
T box riboswitches are cis-acting RNA elements that bind to tRNA and sense its aminoacylation state to influence gene expression. Here, we present the 3.2 angstrom resolution X-ray crystal structures of the T box Stem I-tRNA complex and tRNA, in isolation. T box Stem I forms an arched conformation with extensive intermolecular contacts to two key points of tRNA, the anticodon and D/T-loops. Free and complexed tRNA exist in significantly different conformations, with the contacts stabilizing flexible D/T-loops and a rearrangement of the D-loop. Using a designed T box RNA/tRNA system, we demonstrate that the T box riboswitch monitors the length and orientation of two essential contacts. Length or orientation mismatches engineered into the T box riboswitch and tRNA disrupt the complex, whereas simultaneous insertion of full helical turns realigns the interfaces and restores interaction between artificially elongated T box riboswitch and tRNA molecules.
引用
收藏
页码:2025 / 2032
页数:8
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