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Proofreading neutralizes potential error hotspots in genetic code translation by transfer RNAs

机译:校对通过转移RNA消除了遗传密码翻译中潜在的错误热点

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摘要

The ribosome uses initial and proofreading selection of aminoacyl-tRNAs for accurate protein synthesis. Anomalously high initial misreading in vitro of near-cognate codons by tRNAHis and tRNAGlu suggested potential error hotspots in protein synthesis, but in vivo data suggested their partial neutralization. To clarify the role of proofreading in this error reduction, we varied the Mg2+ ion concentration to calibrate the total accuracy of our cell-free system to that in the living Escherichia coli cell. We found the total accuracy of tRNA selection in our system to vary by five orders of magnitude depending on tRNA identity, type of mismatch, and mismatched codon position. Proofreading and initial selection were positively correlated at high, but uncorrelated at low initial selection, suggesting hyperactivated proofreading as a means to neutralize potentially disastrous initial selection errors.
机译:核糖体使用氨酰基-tRNA的初始和校对选择来进行准确的蛋白质合成。 tRNA His 和tRNA Glu 在体外对近同源密码子的异常误读异常高,表明蛋白质合成中存在潜在的错误热点,但体内数据表明它们被部分中和。为了澄清校对在减少错误中的作用,我们改变了Mg 2 + 离子浓度,以校准无细胞系统与活大肠杆菌细胞的总准确度。我们发现,在我们的系统中,tRNA选择的总准确性取决于tRNA身份,错配类型和错配密码子位置,相差五个数量级。校对和初始选择在较高的初始选择时呈正相关,而在初始选择较低的情况下则不相关,这表明过度激活的校对可以抵消潜在的灾难性初始选择错误。

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