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Conflict and cooperation in eukaryogenesis: implications for the timing of endosymbiosis and the evolution of sex

机译:真核生物中的冲突与合作:对共生时机和性进化的影响

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Roughly 1.5-2.0 Gya, the eukaryotic cell evolved from an endosymbiosis of an archaeal host and proteobacterial symbionts. The timing of this endosymbiosis relative to the evolution of eukaryotic features remains subject to considerable debate, yet the evolutionary process itself constrains the timing of these events. Endosymbiosis entailed levels-of-selection conflicts, and mechanisms of conflict mediation had to evolve for eukaryogenesis to proceed. The initial mechanisms of conflict mediation (e.g. signalling with calcium and soluble adenylyl cyclase, substrate carriers, adenine nucleotide translocase, uncouplers) led to metabolic homeostasis in the eukaryotic cell. Later mechanisms (e.g. mitochondrial gene loss) contributed to the chimeric eukaryotic genome. These integral features of eukaryotes were derived because of, and therefore subsequent to, endosymbiosis. Perhaps the greatest opportunity for conflict arose with the emergence of eukaryotic sex, involving whole-cell fusion. A simple model demonstrates that competition on the lower level severely hinders the evolution of sex. Cytoplasmic mixing, however, is beneficial for non-cooperative endosymbionts, which could have used their aerobic metabolism to manipulate the life history of the host. While early evolution of sex may have facilitated symbiont acquisition, sex would have also destabilized the subsequent endosymbiosis. More plausibly, the evolution of sex and the true nucleus concluded the transition.
机译:真核细胞大约为1.5-2.0 Gya,由古细菌宿主和蛋白细菌共生体的内共生演化而来。相对于真核生物特征进化而言,这种内共生的时机仍然存在很多争议,但是进化过程本身限制了这些事件的时机。内共生需要选择水平的冲突,而冲突中介的机制必须发展,才能继续进行真核生物。冲突介导的最初机制(例如,钙和可溶性腺苷酸环化酶的信号传导,底物载体,腺嘌呤核苷酸转位酶,解偶联剂)导致真核细胞的代谢稳态。后来的机制(例如线粒体基因丢失)促成了嵌合真核基因组。真核生物的这些不可或缺的特征是由于内共生而衍生的。真核性的出现涉及到全细胞融合,这是发生冲突的最大机会。一个简单的模型表明,较低层次的竞争严重阻碍了性别的演变。然而,细胞质混合对于非合作性内共生体是有益的,它们可以利用它们的有氧代谢来操纵宿主的生活史。尽管性的早期演变可能促进了共生体的获取,但性也会破坏随后的内共生。更有可能的是,性别的进化和真正的细胞核终结了这一转变。

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