Opperdoes Fred R, Michels Paul A M
Research Unit for Tropical Diseases, Christian de Duve Institute of Cellular Pathology and Laboratory of Biochemistry, Université catholique de Louvain, Avenue Hippocrate 74-75, B-1200 Brussels, Belgium.
Trends Parasitol. 2007 Oct;23(10):470-6. doi: 10.1016/j.pt.2007.08.002. Epub 2007 Sep 7.
Trypanosomes harbour a large number of structural and biochemical peculiarities. Kinetoplast DNA, mitochondrial RNA editing, the sequestration of glycolysis inside glycosomes and unique oxidative-stress protection mechanisms (to name but a few) are found only in the members of the order Kinetoplastida. Thus, it is not surprising that they have provoked much speculation about why and how such oddities have evolved in trypanosomes. However, the true reasons for their existence within the eukaryotic world are still far from clear. Here, Fred Opperdoes and Paul Michels argue that the trypanosome-specific evolution of novel processes and organization could only have been made possible by the acquisition of a large number of foreign genes, which entered a trypanosomatid ancestor through lateral gene transfer. Many different organisms must have served as donors. Some of them were viruses, and others were bacteria, such as cyanobacterial endosymbionts and non-phototrophic bacteria.
锥虫具有大量结构和生化特性。动质体DNA、线粒体RNA编辑、糖酵解被隔离在糖体内部以及独特的氧化应激保护机制(仅列举其中一些)仅在动质体目成员中发现。因此,它们引发了许多关于锥虫中这些奇特现象为何以及如何演化的猜测也就不足为奇了。然而,它们在真核生物世界中存在的真正原因仍远未明确。在此,弗雷德·奥珀多斯和保罗·米歇尔认为,新过程和组织的锥虫特异性进化只有通过获取大量外来基因才有可能实现,这些基因通过横向基因转移进入了一个锥虫祖先。许多不同的生物体一定都充当了供体。其中一些是病毒,另一些是细菌,如蓝藻内共生体和非光合细菌。