Department of Zoology, University of Oxford, South Parks Road, Oxford OX13PS, UK.
Biol Direct. 2010 Feb 4;5:7. doi: 10.1186/1745-6150-5-7.
The transition from prokaryotes to eukaryotes was the most radical change in cell organisation since life began, with the largest ever burst of gene duplication and novelty. According to the coevolutionary theory of eukaryote origins, the fundamental innovations were the concerted origins of the endomembrane system and cytoskeleton, subsequently recruited to form the cell nucleus and coevolving mitotic apparatus, with numerous genetic eukaryotic novelties inevitable consequences of this compartmentation and novel DNA segregation mechanism. Physical and mutational mechanisms of origin of the nucleus are seldom considered beyond the long-standing assumption that it involved wrapping pre-existing endomembranes around chromatin. Discussions on the origin of sex typically overlook its association with protozoan entry into dormant walled cysts and the likely simultaneous coevolutionary, not sequential, origin of mitosis and meiosis.
I elucidate nuclear and mitotic coevolution, explaining the origins of dicer and small centromeric RNAs for positionally controlling centromeric heterochromatin, and how 27 major features of the cell nucleus evolved in four logical stages, making both mechanisms and selective advantages explicit: two initial stages (origin of 30 nm chromatin fibres, enabling DNA compaction; and firmer attachment of endomembranes to heterochromatin) protected DNA and nascent RNA from shearing by novel molecular motors mediating vesicle transport, division, and cytoplasmic motility. Then octagonal nuclear pore complexes (NPCs) arguably evolved from COPII coated vesicle proteins trapped in clumps by Ran GTPase-mediated cisternal fusion that generated the fenestrated nuclear envelope, preventing lethal complete cisternal fusion, and allowing passive protein and RNA exchange. Finally, plugging NPC lumens by an FG-nucleoporin meshwork and adopting karyopherins for nucleocytoplasmic exchange conferred compartmentation advantages. These successive changes took place in naked growing cells, probably as indirect consequences of the origin of phagotrophy. The first eukaryote had 1-2 cilia and also walled resting cysts; I outline how encystation may have promoted the origin of meiotic sex. I also explain why many alternative ideas are inadequate.
Nuclear pore complexes are evolutionary chimaeras of endomembrane- and mitosis-related chromatin-associated proteins. The keys to understanding eukaryogenesis are a proper phylogenetic context and understanding organelle coevolution: how innovations in one cell component caused repercussions on others.
从原核生物到真核生物的转变是生命诞生以来细胞组织发生的最根本变化,伴随着最大规模的基因复制和新颖性爆发。根据真核生物起源的协同进化理论,基本的创新是内质网系统和细胞骨架的协同起源,随后被招募来形成细胞核,并协同进化有丝分裂装置,伴随着许多遗传上的真核新颖性,这是这种分隔和新颖的 DNA 分离机制的必然结果。细胞核起源的物理和突变机制很少被考虑,除了长期以来的假设,即它涉及将预先存在的内质网包裹在染色质周围。关于性起源的讨论通常忽略了它与原生动物进入休眠的有壁孢囊的联系,以及有丝分裂和减数分裂可能同时发生的协同进化,而不是顺序进化。
我阐明了核和有丝分裂的协同进化,解释了 Dicer 和小着丝粒 RNA 用于位置控制着丝粒异染色质的起源,以及细胞核对有丝分裂和减数分裂的 27 个主要特征是如何在四个逻辑阶段进化的,明确了机制和选择优势:两个初始阶段(30nm 染色质纤维的起源,使 DNA 压缩;以及内质网更牢固地附着于异染色质)通过介导囊泡运输、分裂和细胞质运动的新型分子马达,保护 DNA 和新生 RNA 免受剪切。然后,八角形核孔复合体(NPC)可以说是从 COPII 包裹的囊泡蛋白进化而来的,这些蛋白被 Ran GTPase 介导的小泡融合捕获在团块中,从而产生有孔核膜,防止致命的完全小泡融合,并允许被动的蛋白质和 RNA 交换。最后,通过 FG-核孔蛋白网格堵塞 NPC 腔,并采用核质穿梭蛋白进行核质交换,赋予了分隔优势。这些连续的变化发生在裸露的生长细胞中,可能是吞噬作用起源的间接后果。第一个真核生物有 1-2 个纤毛,也有壁状休眠孢囊;我概述了包囊化如何促进减数分裂性的起源。我还解释了为什么许多替代想法是不充分的。
核孔复合体是内质网和有丝分裂相关染色质相关蛋白的进化嵌合体。理解真核生物起源的关键是适当的系统发育背景和细胞器的协同进化:一个细胞成分的创新如何对其他成分产生影响。