Active role of elongation factor G in maintaining the mRNA reading frame during translation

被引:35
|
作者
Peng, Bee-Zen [1 ]
Bock, Lars V. [2 ]
Belardinelli, Riccardo [1 ]
Peske, Frank [1 ]
Grubmueller, Helmut [2 ]
Rodnina, Marina V. [1 ]
机构
[1] Max Planck Inst Biophys Chem, Dept Phys Biochem, D-37077 Gottingen, Germany
[2] Max Planck Inst Biophys Chem, Dept Theoret & Computat Biophys, D-37077 Gottingen, Germany
关键词
GTP HYDROLYSIS; RIBOSOME; TRANSLOCATION; SUBUNIT; MOVEMENT; KINETICS; GENE; SITE;
D O I
10.1126/sciadv.aax8030
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 translation, the ribosome moves along the mRNA one codon at a time with the help of elongation factor G (EF-G). Spontaneous changes in the translational reading frame are extremely rare, yet how the precise triplet-wise step is maintained is not clear. Here, we show that the ribosome is prone to spontaneous frameshifting on mRNA slippery sequences, whereas EF-G restricts frameshifting. EF-G helps to maintain the mRNA reading frame by guiding the A-site transfer RNA during translocation due to specific interactions with the tip of EF-G domain 4. Furthermore, EF-G accelerates ribosome rearrangements that restore the ribosome's control over the codon-anticodon interaction at the end of the movement. Our data explain how the mRNA reading frame is maintained during translation.
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页数:8
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