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古菌限制修饰系统综述。

A Survey of Archaeal Restriction-Modification Systems.

作者信息

Anton Brian P, Roberts Richard J

机构信息

New England Biolabs, Ipswich, MA 02127, USA.

出版信息

Microorganisms. 2023 Sep 28;11(10):2424. doi: 10.3390/microorganisms11102424.

DOI:10.3390/microorganisms11102424
PMID:37894082
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10609329/
Abstract

When compared with bacteria, relatively little is known about the restriction-modification (RM) systems of archaea, particularly those in taxa outside of the haloarchaea. To improve our understanding of archaeal RM systems, we surveyed REBASE, the restriction enzyme database, to catalog what is known about the genes and activities present in the 519 completely sequenced archaeal genomes currently deposited there. For 49 (9.4%) of these genomes, we also have methylome data from Single-Molecule Real-Time (SMRT) sequencing that reveal the target recognition sites of the active mA and mC DNA methyltransferases (MTases). The gene-finding pipeline employed by REBASE is trained primarily on bacterial examples and so will look for similar genes in archaea. Nonetheless, the organizational structure and protein sequence of RM systems from archaea are highly similar to those of bacteria, with both groups acquiring systems from a shared genetic pool through horizontal gene transfer. As in bacteria, we observe numerous examples of "persistent" DNA MTases conserved within archaeal taxa at different levels. We experimentally validated two homologous members of one of the largest "persistent" MTase groups, revealing that methylation of C(mC)WGG sites may play a key epigenetic role in Crenarchaea. Throughout the archaea, genes encoding mA, mC, and mC DNA MTases, respectively, occur in approximately the ratio 4:2:1.

摘要

与细菌相比,我们对古菌的限制修饰(RM)系统了解相对较少,尤其是那些盐生古菌以外类群中的RM系统。为了增进我们对古菌RM系统的了解,我们调查了限制酶数据库REBASE,以梳理目前保存在该数据库中的519个完全测序古菌基因组中已知的基因和活性。对于其中49个(9.4%)基因组,我们还拥有来自单分子实时(SMRT)测序的甲基化组数据,这些数据揭示了活性mA和mC DNA甲基转移酶(MTases)的靶标识别位点。REBASE采用的基因发现流程主要以细菌实例为训练对象,因此会在古菌中寻找相似基因。尽管如此,古菌RM系统的组织结构和蛋白质序列与细菌的高度相似,两组都是通过水平基因转移从共享基因库中获得系统。与细菌一样,我们在不同水平的古菌类群中观察到许多“持久性”DNA MTases保守的实例。我们通过实验验证了最大的“持久性”MTase组之一的两个同源成员,揭示了C(mC)WGG位点的甲基化可能在泉古菌中发挥关键的表观遗传作用。在整个古菌中,分别编码mA、mC和mC DNA MTases的基因出现的比例约为4:2:1。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e2b/10609329/a168ba0819fa/microorganisms-11-02424-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e2b/10609329/62270ca25ed8/microorganisms-11-02424-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e2b/10609329/a168ba0819fa/microorganisms-11-02424-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e2b/10609329/62270ca25ed8/microorganisms-11-02424-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e2b/10609329/a168ba0819fa/microorganisms-11-02424-g002.jpg

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本文引用的文献

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Genome Res. 2024 Jul 23;34(6):904-913. doi: 10.1101/gr.278294.123.
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Enzymatic methyl sequencing detects DNA methylation at single-base resolution from picograms of DNA.酶促甲基化测序可从皮克级别的DNA中以单碱基分辨率检测DNA甲基化。
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Systematic Analysis of REBASE Identifies Numerous Type I Restriction-Modification Systems with Duplicated, Distinct Specificity Genes That Can Switch System Specificity by Recombination.对REBASE的系统分析鉴定出众多具有重复、独特特异性基因的I型限制修饰系统,这些系统可通过重组切换系统特异性。
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