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Codon Usage Influences the Local Rate of Translation Elongation to Regulate Co-translational Protein Folding
被引:405
作者:

Yu, Chien-Hung
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Univ Texas SW Med Ctr Dallas, Dept Physiol, Dallas, TX 75390 USA Univ Texas SW Med Ctr Dallas, Dept Physiol, Dallas, TX 75390 USA

Dang, Yunkun
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Univ Texas SW Med Ctr Dallas, Dept Physiol, Dallas, TX 75390 USA Univ Texas SW Med Ctr Dallas, Dept Physiol, Dallas, TX 75390 USA

Zhou, Zhipeng
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Univ Texas SW Med Ctr Dallas, Dept Physiol, Dallas, TX 75390 USA Univ Texas SW Med Ctr Dallas, Dept Physiol, Dallas, TX 75390 USA

Wu, Cheng
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机构:
Texas A&M Univ, Dept Biol, College Stn, TX 77843 USA Univ Texas SW Med Ctr Dallas, Dept Physiol, Dallas, TX 75390 USA

Zhao, Fangzhou
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Univ Texas SW Med Ctr Dallas, Dept Physiol, Dallas, TX 75390 USA Univ Texas SW Med Ctr Dallas, Dept Physiol, Dallas, TX 75390 USA

Sachs, Matthew S.
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h-index: 0
机构:
Texas A&M Univ, Dept Biol, College Stn, TX 77843 USA Univ Texas SW Med Ctr Dallas, Dept Physiol, Dallas, TX 75390 USA

Liu, Yi
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h-index: 0
机构:
Univ Texas SW Med Ctr Dallas, Dept Physiol, Dallas, TX 75390 USA Univ Texas SW Med Ctr Dallas, Dept Physiol, Dallas, TX 75390 USA
机构:
[1] Univ Texas SW Med Ctr Dallas, Dept Physiol, Dallas, TX 75390 USA
[2] Texas A&M Univ, Dept Biol, College Stn, TX 77843 USA
基金:
美国国家卫生研究院;
关键词:
IN-VITRO TRANSLATION;
FIREFLY LUCIFERASE;
ESCHERICHIA-COLI;
CONSERVED MECHANISM;
NEUROSPORA-CRASSA;
GENE-EXPRESSION;
RIBOSOME;
EFFICIENCY;
BIAS;
SELECTION;
D O I:
10.1016/j.molcel.2015.07.018
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:
Codon usage bias is a universal feature of eukaryotic and prokaryotic genomes and has been proposed to regulate translation efficiency, accuracy, and protein folding based on the assumption that codon usage affects translation dynamics. The roles of codon usage in translation, however, are not clear and have been challenged by recent ribosome profiling studies. Here we used a Neurospora cell-free translation system to directly monitor the velocity of mRNA translation. We demonstrated that the preferred codons enhance the rate of translation elongation, whereas non-optimal codons slow elongation. Codon usage also controls ribosome traffic on mRNA. These conclusions were supported by ribosome profiling results in vitro and in vivo with template mRNAs designed to increase the signal-to-noise ratio. Finally, we demonstrate that codon usage regulates protein function by affecting co-translational protein folding. These results resolve a long-standing fundamental question and suggest the existence of a codon usage code for protein folding.
引用
收藏
页码:744 / 754
页数:11
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