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缺乏 tRNAArg-腺嘌呤脱氨酶 TadA:在支原体和其他柔膜体纲生物中将四个 CGN 密码子解码为精氨酸的进化后果。

Life without tRNAArg-adenosine deaminase TadA: evolutionary consequences of decoding the four CGN codons as arginine in Mycoplasmas and other Mollicutes.

机构信息

Laboratory of Extremophiles, Department of Applied Life Sciences, School of Life Sciences, Tokyo University of Pharmacy and Life Sciences, 1432-1 Horinouchi, Hachioji, Tokyo 192-0392, Japan.

出版信息

Nucleic Acids Res. 2013 Jul;41(13):6531-43. doi: 10.1093/nar/gkt356. Epub 2013 May 8.

DOI:10.1093/nar/gkt356
PMID:23658230
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3711424/
Abstract

In most bacteria, two tRNAs decode the four arginine CGN codons. One tRNA harboring a wobble inosine (tRNA(Arg)ICG) reads the CGU, CGC and CGA codons, whereas a second tRNA harboring a wobble cytidine (tRNA(Arg)CCG) reads the remaining CGG codon. The reduced genomes of Mycoplasmas and other Mollicutes lack the gene encoding tRNA(Arg)CCG. This raises the question of how these organisms decode CGG codons. Examination of 36 Mollicute genomes for genes encoding tRNA(Arg) and the TadA enzyme, responsible for wobble inosine formation, suggested an evolutionary scenario where tadA gene mutations first occurred. This allowed the temporary accumulation of non-deaminated tRNA(Arg)ACG, capable of reading all CGN codons. This hypothesis was verified in Mycoplasma capricolum, which contains a small fraction of tRNA(Arg)ACG with a non-deaminated wobble adenosine. Subsets of Mollicutes continued to evolve by losing both the mutated tRNA(Arg)CCG and tadA, and then acquired a new tRNA(Arg)UCG. This permitted further tRNA(Arg)ACG mutations with tRNA(Arg)GCG or its disappearance, leaving a single tRNA(Arg)UCG to decode the four CGN codons. The key point of our model is that the A-to-I deamination activity had to be controlled before the loss of the tadA gene, allowing the stepwise evolution of Mollicutes toward an alternative decoding strategy.

摘要

在大多数细菌中,两种 tRNA 可解码四个精氨酸 CGN 密码子。一种携带摆动次黄嘌呤的 tRNA(tRNA(Arg)ICG)可读取 CGU、CGC 和 CGA 密码子,而另一种携带摆动胞嘧啶的 tRNA(tRNA(Arg)CCG)可读取其余的 CGG 密码子。支原体和其他柔膜体纲的简化基因组缺乏编码 tRNA(Arg)CCG 的基因。这就提出了这些生物体如何解码 CGG 密码子的问题。对 36 种柔膜体纲基因组中编码 tRNA(Arg)和 TadA 酶(负责摆动次黄嘌呤形成)的基因进行检查,表明 TadA 基因突变首先发生的进化情景。这允许暂时积累未经脱氨酶处理的 tRNA(Arg)ACG,能够读取所有 CGN 密码子。这一假说在含有少量未经脱氨酶处理的摆动腺嘌呤 tRNA(Arg)ACG 的支原体 capricolum 中得到了验证。柔膜体纲的一部分继续进化,失去了突变的 tRNA(Arg)CCG 和 TadA,然后获得了新的 tRNA(Arg)UCG。这使得进一步的 tRNA(Arg)ACG 突变成为可能,与 tRNA(Arg)GCG 或其消失,只剩下一个 tRNA(Arg)UCG 来解码四个 CGN 密码子。我们模型的关键点是,在失去 TadA 基因之前,必须控制 A 到 I 的脱氨酶活性,从而允许柔膜体纲朝着替代解码策略逐步进化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f1c/3711424/778e3b495515/gkt356f5p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f1c/3711424/43b80455b24d/gkt356f1p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f1c/3711424/5090eab6806b/gkt356f2p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f1c/3711424/053a6b0c51e9/gkt356f3p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f1c/3711424/e2122690a20e/gkt356f4p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f1c/3711424/778e3b495515/gkt356f5p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f1c/3711424/43b80455b24d/gkt356f1p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f1c/3711424/5090eab6806b/gkt356f2p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f1c/3711424/053a6b0c51e9/gkt356f3p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f1c/3711424/e2122690a20e/gkt356f4p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f1c/3711424/778e3b495515/gkt356f5p.jpg

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