National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, Maryland, USA; email:
Annu Rev Biomed Data Sci. 2022 Aug 10;5:367-391. doi: 10.1146/annurev-biodatasci-122220-101119. Epub 2022 May 24.
Biological replicators, from genes within a genome to whole organisms, are locked in conflicts. Comparative genomics has revealed a staggering diversity of molecular armaments and mechanisms regulating their deployment, collectively termed biological conflict systems. These encompass toxins used in inter- and intraspecific interactions, self/nonself discrimination, antiviral immune mechanisms, and counter-host effectors deployed by viruses and intragenomic selfish elements. These systems possess shared syntactical features in their organizational logic and a set of effectors targeting genetic information flow through the Central Dogma, certain membranes, and key molecules like NAD. These principles can be exploited to discover new conflict systems through sensitive computational analyses. This has led to significant advances in our understanding of the biology of these systems and furnished new biotechnological reagents for genome editing, sequencing, and beyond. We discuss these advances using specific examples of toxins, restriction-modification, apoptosis, CRISPR/second messenger-regulated systems, and other enigmatic nucleic acid-targeting systems.
生物复制子,从基因组内的基因到整个生物体,都陷入了冲突之中。比较基因组学揭示了令人震惊的分子武器多样性和调节它们部署的机制,统称为生物冲突系统。这些系统包括用于种间和种内相互作用、自我/非自我识别、抗病毒免疫机制以及病毒和基因组内自私元件部署的抗病毒免疫机制。这些系统在其组织逻辑中具有共享的句法特征,以及一组效应物,通过中心法则、某些膜和关键分子(如 NAD)靶向遗传信息流。可以利用这些原则通过敏感的计算分析来发现新的冲突系统。这使得我们对这些系统的生物学有了更深入的了解,并为基因组编辑、测序等提供了新的生物技术试剂。我们将使用毒素、限制修饰、细胞凋亡、CRISPR/第二信使调节系统和其他神秘的核酸靶向系统等特定示例来讨论这些进展。