Roles for Synonymous Codon Usage in Protein Biogenesis

被引:207
作者
Chaney, Julie L. [1 ]
Clark, Patricia L. [1 ,2 ]
机构
[1] Univ Notre Dame, Dept Chem & Biochem, Notre Dame, IN 46556 USA
[2] Univ Notre Dame, Dept Chem & Biomol Engn, Notre Dame, IN 46556 USA
来源
ANNUAL REVIEW OF BIOPHYSICS, VOL 44 | 2015年 / 44卷
关键词
translation; ribosome; cotranslational folding; protein aggregation; protein degradation; NASCENT POLYPEPTIDE-CHAINS; HORIZONTAL GENE-TRANSFER; TRANSFER-RNA ABUNDANCE; ESCHERICHIA-COLI; MESSENGER-RNA; IN-VIVO; CODING-SEQUENCE; ANGSTROM RESOLUTION; SECONDARY STRUCTURE; ELONGATION RATES;
D O I
10.1146/annurev-biophys-060414-034333
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Owing to the degeneracy of the genetic code, a protein sequence can be encoded by many different synonymous mRNA coding sequences. Synonymous codon usage was once thought to be functionally neutral, but evidence now indicates it is shaped by evolutionary selection and affects other aspects of protein biogenesis beyond specifying the amino acid sequence of the protein. Synonymous rare codons, once thought to have only negative impacts on the speed and accuracy of translation, are now known to play an important role in diverse functions, including regulation of cotranslational folding, covalent modifications, secretion, and expression level. Mutations altering synonymous codon usage are linked to human diseases. However, much remains unknown about the molecular mechanisms connecting synonymous codon usage to efficient protein biogenesis and proper cell physiology. Here we review recent literature on the functional effects of codon usage, including bioinformatics approaches aimed at identifying general roles for synonymous codon usage.
引用
收藏
页码:143 / 166
页数:24
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