Causal signals between codon bias, mRNA structure, and the efficiency of translation and elongation

被引:171
|
作者
Pop, Cristina [1 ]
Rouskin, Silvi [2 ]
Ingolia, Nicholas T. [3 ]
Han, Lu [4 ]
Phizicky, Eric M. [4 ]
Weissman, Jonathan S. [2 ]
Koller, Daphne [1 ]
机构
[1] Stanford Univ, Dept Comp Sci, Stanford, CA 94305 USA
[2] Univ Calif San Francisco, Dept Cellular & Mol Pharmacol, Calif Inst Quantitat Biol, Ctr RNA Syst Biol,Howard Hughes Med Inst, San Francisco, CA 94143 USA
[3] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[4] Univ Rochester, Med Ctr, Sch Med & Dent, Rochester, NY 14642 USA
关键词
codon usage bias; elongation; mRNA structure; translation efficiency; GENOME-WIDE ANALYSIS; SECONDARY-STRUCTURE; IN-VIVO; ESCHERICHIA-COLI; GENE-EXPRESSION; INDIVIDUAL CODONS; PROTEIN-SYNTHESIS; INITIATOR CODONS; SINGLE RIBOSOMES; SELECTION;
D O I
10.15252/msb.20145524
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
Ribosome profiling data report on the distribution of translating ribosomes, at steady-state, with codon-level resolution. We present a robust method to extract codon translation rates and protein synthesis rates from these data, and identify causal features associated with elongation and translation efficiency in physiological conditions in yeast. We show that neither elongation rate nor translational efficiency is improved by experimental manipulation of the abundance or body sequence of the rare AGG tRNA. Deletion of three of the four copies of the heavily used ACA tRNA shows a modest efficiency decrease that could be explained by other rate-reducing signals at gene start. This suggests that correlation between codon bias and efficiency arises as selection for codons to utilize translation machinery efficiently in highly translated genes. We also show a correlation between efficiency and RNA structure calculated both computationally and from recent structure probing data, as well as the Kozak initiation motif, which may comprise a mechanism to regulate initiation.
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页数:15
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