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Weak 5′-mRNA Secondary Structures in Short Eukaryotic Genes

机译:短真核基因中的弱5-mRNA二级结构。

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摘要

Experimental studies of translation have found that short genes tend to exhibit greater densities of ribosomes than long genes in eukaryotic species. It remains an open question whether the elevated ribosome density on short genes is due to faster initiation or slower elongation dynamics. Here, we address this question computationally using 5′-mRNA folding energy as a proxy for translation initiation rates and codon bias as a proxy for elongation rates. We report a significant trend toward reduced 5′-secondary structure in shorter coding sequences, suggesting that short genes initiate faster during translation. We also find a trend toward higher 5′-codon bias in short genes, suggesting that short genes elongate faster than long genes. Both of these trends hold across a diverse set of eukaryotic taxa. Thus, the elevated ribosome density on short eukaryotic genes is likely caused by differential rates of initiation, rather than differential rates of elongation.
机译:翻译的实验研究发现,在真核生物中,短基因比长基因倾向于表现出更大的核糖体密度。短基因上核糖体密度的升高是由于起始速度加快还是延伸动力学较慢仍是一个悬而未决的问题。在这里,我们使用5'-mRNA折叠能作为翻译起始速率的代表,而密码子偏向作为延伸速率的代表,以计算方式解决这个问题。我们报告了在较短的编码序列中减少5'-二级结构的显着趋势,表明短基因在翻译过程中启动更快。我们还发现短基因有更高的5'-密码子偏倚趋势,这表明短基因比长基因的延伸快。这两种趋势都存在于各种真核生物分类中。因此,短真核生物基因上核糖体密度的升高很可能是由不同的起始速率而不是不同的延伸速率引起的。

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