Unusual base pairing during the decoding of a stop codon by the ribosome

被引:127
作者
Fernandez, Israel S. [1 ]
Chyan Leong Ng [1 ]
Kelley, Ann C. [1 ]
Wu, Guowei [2 ]
Yu, Yi-Tao [2 ]
Ramakrishnan, V. [1 ]
机构
[1] MRC Lab Mol Biol, Cambridge CB2 0QH, England
[2] Univ Rochester, Med Ctr, Dept Biochem & Biophys, Rochester, NY 14642 USA
基金
美国国家卫生研究院; 英国医学研究理事会; 英国惠康基金;
关键词
TRANSFER-RNA; MECHANISM; PSEUDOURIDINE; REFINEMENT; TU;
D O I
10.1038/nature12302
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
During normal translation, the binding of a release factor to one of the three stop codons (UGA, UAA or UAG) results in the termination of protein synthesis. However, modification of the initial uridine to a pseudouridine (Psi) allows efficient recognition and readthrough of these stop codons by a transfer RNA(tRNA), although it requires the formation of two normally forbidden purine-purine base pairs(1). Here we determined the crystal structure at 3.1 angstrom resolution of the 30S ribosomal subunit in complex with the anticodon stem loop of tRNA(Ser) bound to the Psi AG stop codon in the A site. The Psi A base pair at the first position is accompanied by the formation of purine-purine base pairs at the second and third positions of the codon, which show an unusual Watson-Crick/Hoogsteen geometry. The structure shows a previously unsuspected ability of the ribosomal decoding centre to accommodate non-canonical base pairs.
引用
收藏
页码:107 / U136
页数:5
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