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翻译选择与酵母蛋白质组进化

Translational selection and yeast proteome evolution.

作者信息

Akashi Hiroshi

机构信息

Institute of Molecular Evolutionary Genetics and Department of Biology, 208 Mueller Laboratory, Pennsylvania State University, University Park, PA 16802, USA.

出版信息

Genetics. 2003 Aug;164(4):1291-303. doi: 10.1093/genetics/164.4.1291.

Abstract

The primary structures of peptides may be adapted for efficient synthesis as well as proper function. Here, the Saccharomyces cerevisiae genome sequence, DNA microarray expression data, tRNA gene numbers, and functional categorizations of proteins are employed to determine whether the amino acid composition of peptides reflects natural selection to optimize the speed and accuracy of translation. Strong relationships between synonymous codon usage bias and estimates of transcript abundance suggest that DNA array data serve as adequate predictors of translation rates. Amino acid usage also shows striking relationships with expression levels. Stronger correlations between tRNA concentrations and amino acid abundances among highly expressed proteins than among less abundant proteins support adaptation of both tRNA abundances and amino acid usage to enhance the speed and accuracy of protein synthesis. Natural selection for efficient synthesis appears to also favor shorter proteins as a function of their expression levels. Comparisons restricted to proteins within functional classes are employed to control for differences in amino acid composition and protein size that reflect differences in the functional requirements of proteins expressed at different levels.

摘要

肽的一级结构可能会进行调整,以实现高效合成以及发挥正常功能。在此,利用酿酒酵母基因组序列、DNA微阵列表达数据、tRNA基因数量以及蛋白质的功能分类,来确定肽的氨基酸组成是否反映了自然选择,以优化翻译的速度和准确性。同义密码子使用偏好与转录本丰度估计值之间的强相关性表明,DNA阵列数据可作为翻译速率的充分预测指标。氨基酸使用情况也与表达水平呈现出显著关系。高表达蛋白质中tRNA浓度与氨基酸丰度之间的相关性,比低丰度蛋白质中的更强,这支持了tRNA丰度和氨基酸使用情况的适应性调整,以提高蛋白质合成的速度和准确性。高效合成的自然选择似乎也倾向于根据蛋白质的表达水平选择更短的蛋白质。对功能类别内蛋白质的比较用于控制氨基酸组成和蛋白质大小的差异,这些差异反映了不同水平表达的蛋白质功能需求的差异。

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Translational selection and yeast proteome evolution.翻译选择与酵母蛋白质组进化
Genetics. 2003 Aug;164(4):1291-303. doi: 10.1093/genetics/164.4.1291.
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