首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Nonlinearity in genetic decoding: Homologous DNA replicase genes use alternatives of transcriptional slippage or translational frameshifting
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Nonlinearity in genetic decoding: Homologous DNA replicase genes use alternatives of transcriptional slippage or translational frameshifting

机译:基因解码中的非线性:同源DNA复制酶基因使用转录滑移或翻译移码的替代方法

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摘要

The τ and γ subunits of DNA polymerase III are both encoded by a single gene in Escherichia coli and Thermus thermophilus. γ is two-thirds the size of τ and shares virtually all its amino acid sequence with τ. E. coli and T. thermophilus have evolved very different mechanisms for setting the approximate 1:1 ratio between τ and γ. Both mechanisms put ribosomes into alternate reading frames so that stop codons in the new frame serve to make the smaller γ protein. In E. coli, ≈50% of initiating ribosomes translate the dnaX mRNA conventionally to give τ, but the other 50% shift into the −1 reading frame at a specific site (A AAA AAG) in the mRNA to produce γ. In T. thermophilus ribosomal frameshifting is not required: the dnaX mRNA is a heterogeneous population of molecules with different numbers of A residues arising from transcriptional slippage on a run of nine T residues in the DNA template. Translation of the subpopulation containing nine As (or +/− multiples of three As) yields τ. The rest of the population of mRNAs (containing nine +/− nonmultiples of three As) puts ribosomes into the alternate reading frames to produce the γ protein(s). It is surprising that two rather similar dnaX sequences in E. coli and T. thermophilus lead to very different mechanisms of expression.
机译:DNA聚合酶III的τ和γ亚基均由大肠杆菌和嗜热栖热菌中的单个基因编码。 γ的大小为τ的三分之二,并且实际上与τ共享其所有氨基酸序列。大肠杆菌和嗜热链球菌进化出了截然不同的机制来设定τ和γ之间的近似1:1比例。两种机制都将核糖体置于交替的阅读框中,以便新框架中的终止密码子可用于制造较小的γ蛋白。在大肠杆菌中,约50%的起始核糖体按常规翻译dnaX mRNA以产生τ,但其他50%的核糖体在mRNA中的特定位点(A AAA AAG)移入-1阅读框以产生γ。在嗜热衣原体中,不需要核糖体移码:dnaX mRNA是具有不同数量A残基的分子的异质群体,这些残基由DNA模板中9个T残基的转录滑动引起。包含九个As(或三个As的+/-)的亚群的翻译产生τ。其余的mRNA群体(包含三个As的9个+/-非整数)将核糖体置于其他阅读框中,以产生γ蛋白。令人惊讶的是,大肠杆菌和嗜热链球菌中两个相当相似的dnaX序列导致非常不同的表达机制。

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