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固定的tRNA基因组与遗传密码的进化。

Rooted tRNAomes and evolution of the genetic code.

作者信息

Pak Daewoo, Du Nan, Kim Yunsoo, Sun Yanni, Burton Zachary F

机构信息

a Center for Statistical Training and Consulting , Michigan State University , E. Lansing , MI 48824 , USA.

b Computer Science and Engineering , Michigan State University , E. Lansing , MI 48824.

出版信息

Transcription. 2018;9(3):137-151. doi: 10.1080/21541264.2018.1429837. Epub 2018 Feb 6.

DOI:10.1080/21541264.2018.1429837
PMID:29372672
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5927645/
Abstract

We advocate for a tRNA- rather than an mRNA-centric model for evolution of the genetic code. The mechanism for evolution of cloverleaf tRNA provides a root sequence for radiation of tRNAs and suggests a simplified understanding of code evolution. To analyze code sectoring, rooted tRNAomes were compared for several archaeal and one bacterial species. Rooting of tRNAome trees reveals conserved structures, indicating how the code was shaped during evolution and suggesting a model for evolution of a LUCA tRNAome tree. We propose the polyglycine hypothesis that the initial product of the genetic code may have been short chain polyglycine to stabilize protocells. In order to describe how anticodons were allotted in evolution, the sectoring-degeneracy hypothesis is proposed. Based on sectoring, a simple stepwise model is developed, in which the code sectors from a 1→4→8→∼16 letter code. At initial stages of code evolution, we posit strong positive selection for wobble base ambiguity, supporting convergence to 4-codon sectors and ∼16 letters. In a later stage, ∼5-6 letters, including stops, were added through innovating at the anticodon wobble position. In archaea and bacteria, tRNA wobble adenine is negatively selected, shrinking the maximum size of the primordial genetic code to 48 anticodons. Because 64 codons are recognized in mRNA, tRNA-mRNA coevolution requires tRNA wobble position ambiguity leading to degeneracy of the code.

摘要

我们提倡一种以tRNA而非mRNA为中心的遗传密码进化模型。三叶草型tRNA的进化机制为tRNA的辐射提供了一个根序列,并为密码进化提供了一种简化的理解方式。为了分析密码分区,我们比较了几种古菌和一种细菌的有根tRNA组。tRNA组树的生根揭示了保守结构,表明了密码在进化过程中是如何形成的,并提出了一个LUCA tRNA组树的进化模型。我们提出了聚甘氨酸假说,即遗传密码的初始产物可能是短链聚甘氨酸,以稳定原始细胞。为了描述反密码子在进化中是如何分配的,我们提出了分区简并假说。基于分区,我们开发了一个简单的逐步模型,其中密码分区从1→4→8→∼16字母密码。在密码进化的初始阶段,我们假定对摆动碱基模糊性有强烈的正选择,支持向4密码子分区和∼16字母的趋同。在后期阶段,通过在反密码子摆动位置进行创新,增加了包括终止密码子在内的∼5 - 6个字母。在古菌和细菌中,tRNA摆动腺嘌呤受到负选择,将原始遗传密码的最大大小缩小到48个反密码子。因为在mRNA中识别出64个密码子,tRNA - mRNA的共同进化需要tRNA摆动位置的模糊性导致密码的简并。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f2/5927645/6f1d02dcc3d1/ktrn-09-03-1429837-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f2/5927645/81f94116b3a9/ktrn-09-03-1429837-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f2/5927645/955ae02bacf8/ktrn-09-03-1429837-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f2/5927645/b7a99102778f/ktrn-09-03-1429837-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f2/5927645/6ac9d553b6eb/ktrn-09-03-1429837-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f2/5927645/6f1d02dcc3d1/ktrn-09-03-1429837-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f2/5927645/81f94116b3a9/ktrn-09-03-1429837-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f2/5927645/955ae02bacf8/ktrn-09-03-1429837-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f2/5927645/b7a99102778f/ktrn-09-03-1429837-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f2/5927645/6ac9d553b6eb/ktrn-09-03-1429837-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/48f2/5927645/6f1d02dcc3d1/ktrn-09-03-1429837-g005.jpg

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