National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, Maryland 20894, USA.
Nat Rev Microbiol. 2010 Oct;8(10):731-41. doi: 10.1038/nrmicro2406. Epub 2010 Sep 6.
Recently a novel cell division system comprised of homologues of eukaryotic ESCRT-III (endosomal sorting complex required for transport III) proteins was discovered in the hyperthermophilic crenarchaeote Sulfolobus acidocaldarius. On the basis of this discovery, we undertook a comparative genomic analysis of the machineries for cell division and vesicle formation in Archaea. Archaea possess at least three distinct membrane remodelling systems: the FtsZ-based bacterial-type system, the ESCRT-III-based eukaryote-like system and a putative novel system that uses an archaeal actin-related protein. Many archaeal genomes encode assortments of components from different systems. Evolutionary reconstruction from these findings suggests that the last common ancestor of the extant Archaea possessed a complex membrane remodelling apparatus, different components of which were lost during subsequent evolution of archaeal lineages. By contrast, eukaryotes seem to have inherited all three ancestral systems.
最近,在嗜热古菌 Sulfolobus acidocaldarius 中发现了一种新型的细胞分裂系统,该系统由真核 ESCRT-III(内体运输所需的分选复合物 III)蛋白的同源物组成。基于这一发现,我们对古菌中细胞分裂和囊泡形成的机制进行了比较基因组分析。古菌至少拥有三种不同的膜重塑系统:基于 FtsZ 的细菌型系统、基于 ESCRT-III 的真核样系统和一种可能的新型系统,该系统使用古菌肌动蛋白相关蛋白。许多古菌基因组编码来自不同系统的成分组合。从这些发现进行的进化重建表明,现存古菌的最后共同祖先拥有一个复杂的膜重塑装置,其不同成分在古菌谱系的后续进化过程中丢失了。相比之下,真核生物似乎继承了所有三个祖先系统。