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The CMG (CDC45/RecJ, MCM, GINS) complex is a conserved component of the DNA replication system in all archaea and eukaryotes

机译:CMG(CDC45 / RecJ,MCM,GINS)复合物是所有古细菌和真核生物中DNA复制系统的保守组成部分

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Background In eukaryotes, the CMG (CDC45, MCM, GINS) complex containing the replicative helicase MCM is a key player in DNA replication. Archaeal homologs of the eukaryotic MCM and GINS proteins have been identified but until recently no homolog of the CDC45 protein was known. Two recent developments, namely the discovery of archaeal G INS- a ssociated n uclease (GAN) that belongs to the RecJ family of the DHH hydrolase superfamily and the demonstration of homology between the DHH domains of CDC45 and RecJ, show that at least some Archaea possess a full complement of homologs of the CMG complex subunits. Here we present the results of in-depth phylogenomic analysis of RecJ homologs in archaea. Results We confirm and extend the recent hypothesis that CDC45 is the eukaryotic ortholog of the bacterial and archaeal RecJ family nucleases. At least one RecJ homolog was identified in all sequenced archaeal genomes, with the single exception of Caldivirga maquilingensis. These proteins include previously unnoticed remote RecJ homologs with inactivated DHH domain in Thermoproteales. Combined with phylogenetic tree reconstruction of diverse eukaryotic, archaeal and bacterial DHH subfamilies, this analysis yields a complex scenario of RecJ family evolution in Archaea which includes independent inactivation of the nuclease domain in Crenarchaeota and Halobacteria, and loss of this domain in Methanococcales. Conclusions The archaeal complex of a CDC45/RecJ homolog, MCM and GINS is homologous and most likely functionally analogous to the eukaryotic CMG complex, and appears to be a key component of the DNA replication machinery in all Archaea. It is inferred that the last common archaeo-eukaryotic ancestor encoded a CMG complex that contained an active nuclease of the RecJ family. The inactivated RecJ homologs in several archaeal lineages most likely are dedicated structural components of replication complexes. Reviewers This article was reviewed by Prof. Patrick Forterre, Dr. Stephen John Aves (nominated by Dr. Purificacion Lopez-Garcia) and Prof. Martijn Huynen. For the full reviews, see the Reviewers' Comments section.
机译:背景技术在真核生物中,含有复制解旋酶MCM的CMG(CDC45,MCM,GINS)复合物是DNA复制中的关键角色。已经鉴定出真核MCM和GINS蛋白的古细菌同源物,但是直到最近还没有发现CDC45蛋白的同源物。最近的两个发展,即发现古细菌G INS-关联的核酸酶(GAN),它属于DHH水解酶超家族的RecJ家族,以及CDC45和RecJ的DHH域之间同源性的证明,表明至少有一些古细菌拥有CMG复杂亚基的完整同源物。在这里,我们介绍在古细菌中RecJ同源物的深入系统生物学分析的结果。结果我们证实并扩展了CDC45是细菌和古细菌RecJ家族核酸酶的真核直向同源物的最新假说。在所有测序的古细菌基因组中,至少鉴定出一个RecJ同源物,唯一的例外是Caldivirga maquilingensis。这些蛋白质包括以前没有注意到的,在热蛋白酶中具有失活的DHH结构域的远程RecJ同源物。结合各种真核生物,古细菌和细菌DHH亚科的系统树重建,该分析产生了古细菌中RecJ家族进化的复杂情况,包括Crenarchaeota和Halobacteria中核酸酶结构域的独立失活以及甲烷球菌中该结构域的丧失。结论CDC45 / RecJ同源物,MCM和GINS的古细菌复合物与真核CMG复合物同源,并且很可能在功能上类似,并且似乎是所有古细菌DNA复制机制的关键组成部分。可以推断,最后一个常见的古真核祖先编码了一个CMG复合物,其中包含RecJ家族的活性核酸酶。几个古菌谱系中的灭活的RecJ同源物很可能是复制复合体的专用结构组分。审阅者本文由Patrick Forterre教授,Stephen John Aves博士(由Purificacion Lopez-Garcia博士提名)和Martijn Huynen教授审阅。有关完整的评论,请参阅“评论者的评论”部分。

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