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The Effects of the Context-Dependent Codon Usage Bias on the Structure of the nsp1αof Porcine Reproductive and Respiratory Syndrome Virus
Author(s) -
Yaozhong Ding,
Yanan You,
Dong-jie Sun,
Hao-tai Chen,
Yong-lu Wang,
Hui-yun Chang,
Li Pan,
Yu-zhen Fang,
Zhong-wang Zhang,
Peng Zhou,
Jian-liang Lv,
Xin-sheng Liu,
Jun-jun Shao,
Fu-rong Zhao,
Tong Lin,
L. Stipkovits,
Z. Pejsak,
Yong-guang Zhang,
Jie Zhang
Publication year - 2014
Publication title -
biomed research international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.772
H-Index - 126
eISSN - 2314-6141
pISSN - 2314-6133
DOI - 10.1155/2014/765320
Subject(s) - codon usage bias , transfer rna , biology , context (archaeology) , synonymous substitution , protease , folding (dsp implementation) , genetics , porcine reproductive and respiratory syndrome virus , gene , rna , biochemistry , paleontology , genome , electrical engineering , enzyme , engineering
The information about the crystal structure of porcine reproductive and respiratory syndrome virus (PRRSV) leader protease nsp1 α is available to analyze the roles of tRNA abundance of pigs and codon usage of the nsp1 α gene in the formation of this protease. The effects of tRNA abundance of the pigs and the synonymous codon usage and the context-dependent codon bias (CDCB) of the nsp1 α on shaping the specific folding units ( α -helix, β -strand, and the coil) in the nsp1 α were analyzed based on the structural information about this protease from protein data bank (PDB: 3IFU) and the nsp1 α of the 191 PRRSV strains. By mapping the overall tRNA abundance along the nsp1 α , we found that there is no link between the fluctuation of the overall tRNA abundance and the specific folding units in the nsp1 α , and the low translation speed of ribosome caused by the tRNA abundance exists in the nsp1 α . The strong correlation between some synonymous codon usage and the specific folding units in the nsp1 α was found, and the phenomenon of CDCB exists in the specific folding units of the nsp1 α . These findings provide an insight into the roles of the synonymous codon usage and CDCB in the formation of PRRSV nsp1 α structure.

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