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How translational accuracy influences reading frame maintenance.

机译:平移精度如何影响阅读框架的维护。

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摘要

Most missense errors have little effect on protein function, since they only exchange one amino acid for another. However, processivity errors, frameshifting or premature termination result in a synthesis of an incomplete peptide. There may be a connection between missense and processivity errors, since processivity errors now appear to result from a second error occurring after recruitment of an errant aminoacyl-tRNA, either spontaneous dissociation causing premature termination or translational frameshifting. This is clearest in programmed translational frameshifting where the mRNA programs errant reading by a near-cognate tRNA; this error promotes a second frameshifting error (a dual-error model of frameshifting). The same mechanism can explain frameshifting by suppressor tRNAs, even those with expanded anticodon loops. The previous model that suppressor tRNAs induce quadruplet translocation now appears incorrect for most, and perhaps for all of them. We suggest that the 'spontaneous' tRNA-induced frameshifting and 'programmed' mRNA-induced frameshifting use the same mechanism, although the frequency of frameshifting is very different. This new model of frameshifting suggests that the tRNA is not acting as the yardstick to measure out the length of the translocation step. Rather, the translocation of 3 nucleotides may be an inherent feature of the ribosome.
机译:大多数错义错误对蛋白质功能的影响很小,因为它们只会将一种氨基酸交换为另一种氨基酸。但是,合成错误,移码或过早终止会导致合成不完整的肽。错义错误与进行性错误之间可能存在联系,因为处理性错误现在似乎是由于错误的氨酰基-tRNA募集后发生的第二种错误导致的,该错误是自发解离导致过早终止或翻译移码。这在程序化翻译移码中最为明显,在该翻译中,mRNA会通过近同源的tRNA产生错误的读数。此错误会引起第二个移码错误(移码的双错误模型)。相同的机制可以解释抑制性tRNA的移码,即使那些反密码子环扩展的tRNA也是如此。抑制性tRNA诱导四联体易位的先前模型现在对于大多数人,也许对所有人而言似乎都是错误的。我们建议“自发” tRNA诱导的移码和“程序化” mRNA诱导的移码使用相同的机制,尽管移码的频率非常不同。这种新的移码模型表明tRNA不能作为衡量易位步骤长度的准绳。相反,3个核苷酸的易位可能是核糖体的固有特征。

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