TY - JOUR
T1 - Effect of codon adaptation on codon-level and gene-level translation efficiency in vivo
AU - Nakahigashi, Kenji
AU - Takai, Yuki
AU - Shiwa, Yuh
AU - Wada, Mei
AU - Honma, Masayuki
AU - Yoshikawa, Hirofumi
AU - Tomita, Masaru
AU - Kanai, Akio
AU - Mori, Hirotada
N1 - Funding Information:
We thank Nozomi Abe for technical assistance; Yoshihiro Toya, Motomu Matsui, and Atsuko Shinhara for help in informatics; and Giselda Bucca and Colin Smith for discussions and critical reading of the manuscript. We thank the authorities at Tsuruoka City and Yamagata Prefecture for supporting this study at Keio University Institute for Advanced Biosciences. This work was supported by Japan Society for the Promotion of Science Grants-in-Aid for Scientific Research (B) numbers 20310117 and 24310148. This work was also supported by a co-operative research grant of the Genome Research for Bioresource, NODAI Genome Research Center, Tokyo University of Agriculture.
Publisher Copyright:
© Nakahigashi et al.; licensee BioMed Central.
PY - 2014/12/16
Y1 - 2014/12/16
N2 - Background: There is a significant difference between synonymous codon usage in many organisms, and it is known that codons used more frequently generally showed efficient decoding rate. At the gene level, however, there are conflicting reports on the existence of a correlation between codon adaptation and translation efficiency, even in the same organism. Results: To resolve this issue, we cultured Escherichia coli under conditions designed to maintain constant levels of mRNA and protein and subjected the cells to ribosome profiling (RP) and mRNA-seq analyses. We showed that the RP results correlated more closely with protein levels generated under similar culture conditions than with the mRNA abundance from the mRNA-seq. Our result indicated that RP/mRNA ratio could be used as a measure of translation efficiency at gene level. On the other hand, the RP data showed that codon-specific ribosome density at the decoding site negatively correlated with codon usage, consistent with the hypothesis that preferred codons display lower ribosome densities due to their faster decoding rate. However, highly codon-adapted genes showed higher ribosome densities at the gene level, indicating that the efficiency of translation initiation, rather than higher elongation efficiency of preferred codons, exerted a greater effect on ribosome density and thus translation efficiency. Conclusions: These findings indicate that evolutionary pressure on highly expressed genes influenced both codon bias and translation initiation efficiency and therefore explains contradictory findings that codon usage bias correlates with translation efficiency of native genes, but not with the artificially created gene pool, which was not subjected to evolution pressure.
AB - Background: There is a significant difference between synonymous codon usage in many organisms, and it is known that codons used more frequently generally showed efficient decoding rate. At the gene level, however, there are conflicting reports on the existence of a correlation between codon adaptation and translation efficiency, even in the same organism. Results: To resolve this issue, we cultured Escherichia coli under conditions designed to maintain constant levels of mRNA and protein and subjected the cells to ribosome profiling (RP) and mRNA-seq analyses. We showed that the RP results correlated more closely with protein levels generated under similar culture conditions than with the mRNA abundance from the mRNA-seq. Our result indicated that RP/mRNA ratio could be used as a measure of translation efficiency at gene level. On the other hand, the RP data showed that codon-specific ribosome density at the decoding site negatively correlated with codon usage, consistent with the hypothesis that preferred codons display lower ribosome densities due to their faster decoding rate. However, highly codon-adapted genes showed higher ribosome densities at the gene level, indicating that the efficiency of translation initiation, rather than higher elongation efficiency of preferred codons, exerted a greater effect on ribosome density and thus translation efficiency. Conclusions: These findings indicate that evolutionary pressure on highly expressed genes influenced both codon bias and translation initiation efficiency and therefore explains contradictory findings that codon usage bias correlates with translation efficiency of native genes, but not with the artificially created gene pool, which was not subjected to evolution pressure.
KW - Chloramphenicol
KW - Codon preference
KW - Codon usage
KW - Ribosome profiling
KW - Translation efficiency
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U2 - 10.1186/1471-2164-15-1115
DO - 10.1186/1471-2164-15-1115
M3 - Article
C2 - 25512115
AN - SCOPUS:84925659421
SN - 1471-2164
VL - 15
JO - BMC Genomics
JF - BMC Genomics
IS - 1
M1 - 1115
ER -