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病毒及其宿主中dUTPase编码基因的进化与水平转移

Evolution and horizontal transfer of dUTPase-encoding genes in viruses and their hosts.

作者信息

Baldo A M, McClure M A

机构信息

Department of Biological Sciences, University of Nevada-Las Vegas, Las Vegas, Nevada 89154-4004, USA.

出版信息

J Virol. 1999 Sep;73(9):7710-21. doi: 10.1128/JVI.73.9.7710-7721.1999.

Abstract

dUTPase is a ubiquitous and essential enzyme responsible for regulating cellular levels of dUTP. The dut gene exists as single, tandemly duplicated, and tandemly triplicated copies. Crystallized single-copy dUTPases have been shown to assemble as homotrimers. dUTPase is encoded as an auxiliary gene in a number of virus genomes. The origin of viral dut genes has remained unresolved since their initial discovery. A comprehensive analysis of dUTPase amino acid sequence relationships was performed to explore the evolutionary dynamics of dut in viruses and their hosts. Our data set, comprised of 24 host and 51 viral sequences, includes representative sequences from available eukaryotes, archaea, eubacteria cells, and viruses, including herpesviruses. These amino acid sequences were aligned by using a hidden Markov model approach developed to align divergent data. Known secondary structures from single-copy crystals were mapped onto the aligned duplicate and triplicate sequences. We show how duplicated dUTPases might fold into a monomer, and we hypothesize that triplicated dUTPases also assemble as monomers. Phylogenetic analysis revealed at least five viral dUTPase sequence lineages in well-supported monophyletic clusters with eukaryotic, eubacterial, and archaeal hosts. We have identified all five as strong examples of horizontal transfer as well as additional potential transfer of dut genes among eubacteria, between eubacteria and viruses, and between retroviruses. The evidence for horizontal transfers is particularly interesting since eukaryotic dut genes have introns, while DNA virus dut genes do not. This implies that an intermediary retroid agent facilitated the horizontal transfer process between host mRNA and DNA viruses.

摘要

脱氧尿苷三磷酸酶(dUTPase)是一种普遍存在且必不可少的酶,负责调节细胞内dUTP的水平。dut基因以单拷贝、串联重复和串联三倍体拷贝的形式存在。已证明结晶的单拷贝dUTPases会组装成同三聚体。dUTPase在许多病毒基因组中被编码为辅助基因。自首次发现以来,病毒dut基因的起源一直未得到解决。为了探索dut在病毒及其宿主中的进化动态,我们对dUTPase氨基酸序列关系进行了全面分析。我们的数据集由24个宿主序列和51个病毒序列组成,包括来自可用的真核生物、古细菌、真细菌细胞和病毒(包括疱疹病毒)的代表性序列。这些氨基酸序列通过使用一种为比对差异数据而开发的隐马尔可夫模型方法进行比对。将单拷贝晶体的已知二级结构映射到比对后的重复和三倍体序列上。我们展示了重复的dUTPases可能如何折叠成单体,并推测三倍体dUTPases也组装成单体。系统发育分析揭示了在与真核生物、真细菌和古细菌宿主形成的得到充分支持的单系类群中至少有五个病毒dUTPase序列谱系。我们已将所有这五个谱系确定为水平转移的有力实例,以及dut基因在真细菌之间、真细菌与病毒之间以及逆转录病毒之间的其他潜在转移实例。水平转移的证据特别有趣,因为真核生物的dut基因有内含子,而DNA病毒的dut基因没有。这意味着一种中间的类逆转录因子促进了宿主mRNA与DNA病毒之间的水平转移过程。

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