Comparative genomics and evolutionary trajectories of viral ATP dependent DNA-packaging systems.

Genome dynamics Pub Date : 2007-01-01 DOI:10.1159/000107603
A M Burroughs, L M Iyer, L Aravind
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引用次数: 99

Abstract

We present an overview of comparative genomics of ATP-dependent DNA packaging systems of viruses. Several distinct ATPase motors and accessory proteins have been identified in DNA-packaging systems of viruses such as terminase-portal systems, the 29-like packaging apparatus, and packaging systems of lipid inner-membrane-containing viruses. Sequence and structure analysis of these proteins suggest that there were two major independent innovations of ATP-dependent DNA packaging systems in the viral universe. The first of these utilizes a HerA/FtsK superfamily ATPase and is seen in prokaryotic viruses with inner lipid membranes, large eukaryotic nucleo-cytoplasmic DNA viruses (including poxviruses) and a group of eukaryotic mobile DNA transposons. We show that ATPases of the 29-like packaging system are also divergent versions of the HerA/FtsK superfamily that functions in viruses without an inner membrane. The second system, the terminase-portal system, is dominant in prokaryotic tailed viruses and typically functions with linear chromosomes. The large subunit of this system contains a distinct ATPase domain and a C-terminal nuclease domain of the RNAse H fold. We discuss the classification of these ATPases within the P-loop NTPases, genomic demography and positioning of their genes in the viral chromosome. We show that diverse portal proteins utilized by these systems share a common evolutionary origin and might have frequently displaced each other in evolution. Examination of conserved gene neighborhoods indicates repeated acquisition of Helix-turn-Helix domain-containing terminase small subunits and a third accessory component, the MuF protein. Adenoviruses appear to have evolved a third packaging ATPase, unique to their lineage. Relationship between one major type of packaging ATPases and cellular chromosome pumps like FtsK suggests an ancient common origin for viral packaging and cellular chromosome partitioning systems.

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病毒ATP依赖dna包装系统的比较基因组学和进化轨迹。
我们提出的比较基因组学的atp依赖的DNA包装系统的病毒的概述。在病毒的dna包装系统中已经发现了几种不同的atp酶马达和辅助蛋白,如终端-门户系统、29样包装装置和含脂质内膜病毒的包装系统。这些蛋白质的序列和结构分析表明,在病毒世界中,atp依赖的DNA包装系统有两个主要的独立创新。其中第一种利用HerA/FtsK超家族atp酶,见于具有内脂质膜的原核病毒、大型真核核细胞质DNA病毒(包括痘病毒)和一组真核生物可移动DNA转座子。我们发现29样包装系统的atp酶也是在没有内膜的病毒中起作用的HerA/FtsK超家族的不同版本。第二个系统是终端-门户系统,在原核有尾病毒中占主导地位,通常与线性染色体一起起作用。该系统的大亚基包含一个独特的atp酶结构域和RNAse H折叠的c端核酸酶结构域。我们讨论了这些atp酶在p环NTPases中的分类,基因组人口统计学和它们的基因在病毒染色体中的定位。我们表明,这些系统所利用的各种门脉蛋白具有共同的进化起源,并且可能在进化中经常相互取代。对保守基因邻域的检测表明,含有螺旋-转-螺旋结构域的末端酶小亚基和第三个辅助成分MuF蛋白的重复获得。腺病毒似乎进化出了第三种包装三磷酸腺苷酶,这是它们的谱系所独有的。一种主要类型的包装atp酶和细胞染色体泵(如FtsK)之间的关系表明,病毒包装和细胞染色体分配系统有一个古老的共同起源。
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The evolutionary dynamics of transposable elements in eukaryote genomes. SINEs as driving forces in genome evolution. Unstable microsatellite repeats facilitate rapid evolution of coding and regulatory sequences. Satellite DNA evolution. Satellite DNA-mediated effects on genome regulation.
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