National Center for Biotechnology Information, NLM, National Institutes of Health, Bethesda, Maryland 20894, USA.
Biol Direct. 2012 Feb 13;7:7. doi: 10.1186/1745-6150-7-7.
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 GINS-associated nuclease (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.
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.
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.
在真核生物中,包含复制解旋酶 MCM 的 CMG(CDC45、MCM、GINS)复合物是 DNA 复制的关键因素。已经鉴定出真核生物 MCM 和 GINS 蛋白的古菌同源物,但直到最近还不知道 CDC45 蛋白的同源物。最近的两项发展,即发现属于 DHH 水解酶超家族 RecJ 家族的古菌 GINS 相关核酸内切酶(GAN),以及证明 CDC45 和 RecJ 的 DHH 结构域之间存在同源性,表明至少一些古菌具有 CMG 复合物亚基的完整同源物。在这里,我们展示了古菌 RecJ 同源物的深入系统发育基因组分析结果。
我们证实并扩展了最近的假设,即 CDC45 是细菌和古菌 RecJ 家族核酸酶的真核同源物。在所有测序的古菌基因组中都鉴定到至少一个 RecJ 同源物,只有 Caldivirga maquilingensis 例外。这些蛋白质包括以前未被注意到的在 Thermoproteales 中失活 DHH 结构域的远程 RecJ 同源物。与不同真核生物、古菌和细菌 DHH 亚家族的系统发育树重建相结合,这种分析得出了古菌 RecJ 家族进化的复杂情况,其中包括 Crenarchaeota 和 Halobacteria 中核酸酶结构域的独立失活,以及 Methanococcales 中该结构域的缺失。
古菌的 CDC45/RecJ 同源物、MCM 和 GINS 复合物是同源的,并且很可能在功能上类似于真核生物的 CMG 复合物,并且似乎是所有古菌 DNA 复制机制的关键组成部分。据推断,最后一个共同的古真核祖先编码了一个包含 RecJ 家族活性核酸酶的 CMG 复合物。几个古菌谱系中失活的 RecJ 同源物很可能是复制复合物的专用结构成分。