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细菌和古菌中依赖RNA的半胱氨酸生物合成

RNA-Dependent Cysteine Biosynthesis in Bacteria and Archaea.

作者信息

Mukai Takahito, Crnković Ana, Umehara Takuya, Ivanova Natalia N, Kyrpides Nikos C, Söll Dieter

机构信息

Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut, USA.

Department of Biological Science and Technology, Tokyo University of Science, Katsushika-ku, Tokyo, Japan.

出版信息

mBio. 2017 May 9;8(3):e00561-17. doi: 10.1128/mBio.00561-17.

Abstract

The diversity of the genetic code systems used by microbes on earth is yet to be elucidated. It is known that certain methanogenic archaea employ an alternative system for cysteine (Cys) biosynthesis and encoding; tRNA is first acylated with phosphoserine (Sep) by -phosphoseryl-tRNA synthetase (SepRS) and then converted to Cys-tRNA by Sep-tRNA:Cys-tRNA synthase (SepCysS). In this study, we searched all genomic and metagenomic protein sequence data in the Integrated Microbial Genomes (IMG) system and at the NCBI to reveal new clades of SepRS and SepCysS proteins belonging to diverse archaea in the four major groups (DPANN, , TACK, and Asgard) and two groups of bacteria (" Parcubacteria" and ). Bacterial SepRS and SepCysS charged bacterial tRNA species with cysteine Homologs of SepCysE, a scaffold protein facilitating SepRS⋅SepCysS complex assembly in Euryarchaeota class I methanogens, are found in a few groups of TACK and Asgard archaea, whereas the C-terminally truncated homologs exist fused or genetically coupled with diverse SepCysS species. Investigation of the selenocysteine (Sec)- and pyrrolysine (Pyl)-utilizing traits in SepRS-utilizing archaea and bacteria revealed that the archaea carrying full-length SepCysE employ Sec and that SepRS is often found in Pyl-utilizing archaea and bacteria. We discuss possible contributions of the SepRS-SepCysS system for sulfur assimilation, methanogenesis, and other metabolic processes requiring large amounts of iron-sulfur enzymes or Pyl-containing enzymes. Comprehensive analyses of all genomic and metagenomic protein sequence data in public databases revealed the distribution and evolution of an alternative cysteine-encoding system in diverse archaea and bacteria. The finding that the SepRS-SepCysS-SepCysE- and the selenocysteine-encoding systems are shared by the class I methanogens, the AK8/W8A-19 group, and an Asgard archaeon suggests that ancient archaea may have used both systems. In contrast, bacteria may have obtained the SepRS-SepCysS system from archaea. The SepRS-SepCysS system sometimes coexists with a pyrrolysine-encoding system in both archaea and bacteria. Our results provide additional bioinformatic evidence for the contribution of the SepRS-SepCysS system for sulfur assimilation and diverse metabolisms which require vast amounts of iron-sulfur enzymes and proteins. Among these biological activities, methanogenesis, methylamine metabolism, and organohalide respiration may have local and global effects on earth. Taken together, uncultured bacteria and archaea provide an expanded record of the evolution of the genetic code.

摘要

地球上微生物所使用的遗传密码系统的多样性尚待阐明。已知某些产甲烷古菌采用一种替代系统进行半胱氨酸(Cys)的生物合成和编码;首先,磷酸丝氨酸(Sep)由磷酸丝氨酰 - tRNA合成酶(SepRS)酰化到tRNA上,然后通过Sep - tRNA:Cys - tRNA合成酶(SepCysS)转化为Cys - tRNA。在本研究中,我们搜索了综合微生物基因组(IMG)系统和美国国立生物技术信息中心(NCBI)中的所有基因组和宏基因组蛋白质序列数据,以揭示属于四个主要类群(DPANN、 、TACK和阿斯加德)的不同古菌以及两组细菌(“ Parcubacteria”和 )中的SepRS和SepCysS蛋白的新分支。细菌的SepRS和SepCysS用半胱氨酸使细菌tRNA物种带电。在少数TACK和阿斯加德古菌类群中发现了SepCysE的同源物,SepCysE是一种支架蛋白,有助于广古菌纲I类产甲烷菌中SepRS⋅SepCysS复合物的组装,而C末端截短的同源物与不同的SepCysS物种融合或基因偶联存在。对利用SepRS的古菌和细菌中硒代半胱氨酸(Sec)和吡咯赖氨酸(Pyl)利用特性的研究表明,携带全长SepCysE的古菌利用Sec,并且SepRS经常在利用Pyl的古菌和细菌中发现。我们讨论了SepRS - SepCysS系统对硫同化、甲烷生成以及其他需要大量铁硫酶或含Pyl酶的代谢过程的可能贡献。对公共数据库中所有基因组和宏基因组蛋白质序列数据的综合分析揭示了不同古菌和细菌中替代半胱氨酸编码系统的分布和进化。I类产甲烷菌、AK8 / W8A - 19组和一种阿斯加德古菌共享SepRS - SepCysS - SepCysE和硒代半胱氨酸编码系统这一发现表明,古代古菌可能同时使用这两种系统。相比之下,细菌可能从古菌那里获得了SepRS - SepCysS系统。SepRS - SepCysS系统有时在古菌和细菌中都与吡咯赖氨酸编码系统共存。我们的结果为SepRS - SepCysS系统对硫同化和需要大量铁硫酶和蛋白质的多种代谢的贡献提供了额外的生物信息学证据。在这些生物活性中,甲烷生成、甲胺代谢和有机卤化物呼吸可能对地球产生局部和全球影响。总之,未培养的细菌和古菌提供了遗传密码进化的扩展记录。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38c9/5424206/e154608359b6/mbo0021732920001.jpg

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